Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
A |
T |
3: 124,210,482 (GRCm39) |
H143Q |
probably benign |
Het |
Abca3 |
C |
T |
17: 24,593,274 (GRCm39) |
R224C |
probably damaging |
Het |
Adcy8 |
A |
T |
15: 64,659,207 (GRCm39) |
W528R |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 76,071,665 (GRCm39) |
E329G |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 31,060,403 (GRCm39) |
R141Q |
probably damaging |
Het |
Ampd2 |
A |
T |
3: 107,986,549 (GRCm39) |
M245K |
probably damaging |
Het |
Apob |
G |
A |
12: 8,055,219 (GRCm39) |
|
probably null |
Het |
Apool |
C |
T |
X: 111,259,540 (GRCm39) |
Q60* |
probably null |
Het |
Aqp1 |
A |
T |
6: 55,322,520 (GRCm39) |
I172F |
probably damaging |
Het |
Atp7a |
A |
G |
X: 105,153,374 (GRCm39) |
D1092G |
probably benign |
Het |
Ccdc83 |
A |
T |
7: 89,899,737 (GRCm39) |
F45Y |
probably damaging |
Het |
Cct8l1 |
G |
A |
5: 25,721,881 (GRCm39) |
V199I |
probably benign |
Het |
Cdc23 |
C |
A |
18: 34,784,742 (GRCm39) |
V7L |
unknown |
Het |
Cdc25a |
T |
A |
9: 109,713,208 (GRCm39) |
C227S |
possibly damaging |
Het |
Ces1a |
A |
G |
8: 93,759,303 (GRCm39) |
S278P |
possibly damaging |
Het |
Cfap65 |
A |
T |
1: 74,962,137 (GRCm39) |
S695T |
probably benign |
Het |
Col13a1 |
A |
G |
10: 61,709,797 (GRCm39) |
|
silent |
Het |
Ctps1 |
A |
T |
4: 120,411,170 (GRCm39) |
L282Q |
probably damaging |
Het |
Cyp2a22 |
A |
T |
7: 26,631,906 (GRCm39) |
F450Y |
probably benign |
Het |
Cyp2d10 |
C |
T |
15: 82,287,954 (GRCm39) |
R383H |
probably benign |
Het |
Dennd3 |
G |
A |
15: 73,419,144 (GRCm39) |
R645H |
probably damaging |
Het |
Dnaaf5 |
G |
T |
5: 139,159,962 (GRCm39) |
R620L |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 118,046,188 (GRCm39) |
L1750* |
probably null |
Het |
Dnah9 |
A |
G |
11: 65,740,866 (GRCm39) |
F4107L |
probably damaging |
Het |
Dnaja3 |
A |
T |
16: 4,514,289 (GRCm39) |
T274S |
probably damaging |
Het |
Dot1l |
A |
G |
10: 80,620,480 (GRCm39) |
D514G |
possibly damaging |
Het |
Dst |
A |
C |
1: 34,334,344 (GRCm39) |
K4857N |
probably damaging |
Het |
Dysf |
A |
T |
6: 84,114,254 (GRCm39) |
K1226M |
probably damaging |
Het |
Enpep |
T |
A |
3: 129,097,404 (GRCm39) |
Q409L |
probably damaging |
Het |
Fign |
A |
T |
2: 63,810,037 (GRCm39) |
L411* |
probably null |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Fryl |
G |
A |
5: 73,232,110 (GRCm39) |
P1550L |
probably damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
H2ab3 |
T |
C |
X: 119,222,543 (GRCm39) |
T84A |
probably damaging |
Het |
Hal |
A |
T |
10: 93,349,904 (GRCm39) |
I555F |
probably damaging |
Het |
Hibadh |
C |
T |
6: 52,597,079 (GRCm39) |
V122M |
possibly damaging |
Het |
Hsd3b3 |
T |
C |
3: 98,649,340 (GRCm39) |
T328A |
possibly damaging |
Het |
Ifi44 |
T |
C |
3: 151,455,269 (GRCm39) |
|
probably benign |
Het |
Ifi47 |
A |
G |
11: 48,986,361 (GRCm39) |
T43A |
probably benign |
Het |
Inf2 |
A |
T |
12: 112,578,473 (GRCm39) |
|
probably null |
Het |
Itga10 |
C |
T |
3: 96,559,527 (GRCm39) |
Q475* |
probably null |
Het |
Itga6 |
T |
A |
2: 71,656,779 (GRCm39) |
D344E |
probably benign |
Het |
Kcnmb4 |
T |
C |
10: 116,309,102 (GRCm39) |
T109A |
probably benign |
Het |
Kif19a |
G |
A |
11: 114,658,053 (GRCm39) |
M37I |
probably benign |
Het |
Kiss1r |
C |
A |
10: 79,754,596 (GRCm39) |
S30* |
probably null |
Het |
Lrrc66 |
G |
A |
5: 73,765,354 (GRCm39) |
P563L |
probably damaging |
Het |
Mamdc2 |
T |
C |
19: 23,356,160 (GRCm39) |
D96G |
probably benign |
Het |
Map3k12 |
A |
T |
15: 102,410,267 (GRCm39) |
|
probably null |
Het |
Mc3r |
A |
T |
2: 172,091,533 (GRCm39) |
I252F |
possibly damaging |
Het |
Metrn |
C |
T |
17: 26,015,613 (GRCm39) |
G34D |
probably damaging |
Het |
Mipep |
A |
G |
14: 61,046,462 (GRCm39) |
E328G |
probably benign |
Het |
Mrtfa |
A |
G |
15: 80,906,627 (GRCm39) |
V91A |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,412,999 (GRCm39) |
T1982S |
unknown |
Het |
Myh8 |
A |
T |
11: 67,196,742 (GRCm39) |
T1792S |
possibly damaging |
Het |
Myo1a |
T |
C |
10: 127,543,288 (GRCm39) |
|
probably null |
Het |
Myo5a |
T |
A |
9: 75,081,438 (GRCm39) |
S1008T |
probably benign |
Het |
Ncald |
A |
T |
15: 37,397,478 (GRCm39) |
H67Q |
probably damaging |
Het |
Nudt5 |
T |
A |
2: 5,869,198 (GRCm39) |
H141Q |
probably benign |
Het |
Numbl |
G |
A |
7: 26,980,415 (GRCm39) |
D466N |
probably damaging |
Het |
Nup210 |
T |
A |
6: 91,032,309 (GRCm39) |
I20F |
probably benign |
Het |
Odad1 |
T |
A |
7: 45,578,514 (GRCm39) |
M29K |
probably benign |
Het |
Or10ak12 |
A |
C |
4: 118,666,057 (GRCm39) |
W319G |
possibly damaging |
Het |
Or10p21 |
T |
C |
10: 128,847,213 (GRCm39) |
Y20H |
possibly damaging |
Het |
Or14c46 |
A |
G |
7: 85,918,799 (GRCm39) |
I66T |
probably damaging |
Het |
Or51l14 |
A |
T |
7: 103,100,617 (GRCm39) |
E24D |
probably benign |
Het |
Or52e8b |
A |
T |
7: 104,673,260 (GRCm39) |
M309K |
probably benign |
Het |
Or52n2c |
A |
C |
7: 104,574,700 (GRCm39) |
N90K |
probably benign |
Het |
Or7h8 |
A |
T |
9: 20,123,878 (GRCm39) |
I78F |
possibly damaging |
Het |
Or8h10 |
A |
T |
2: 86,808,666 (GRCm39) |
V158D |
possibly damaging |
Het |
Papolg |
G |
A |
11: 23,817,331 (GRCm39) |
T153I |
possibly damaging |
Het |
Pappa |
A |
G |
4: 65,123,365 (GRCm39) |
H900R |
probably benign |
Het |
Pcdh17 |
T |
C |
14: 84,770,782 (GRCm39) |
S1087P |
probably benign |
Het |
Phf11a |
T |
G |
14: 59,521,849 (GRCm39) |
L107F |
possibly damaging |
Het |
Phlpp2 |
A |
T |
8: 110,652,461 (GRCm39) |
I602F |
probably damaging |
Het |
Pik3c2g |
T |
A |
6: 139,665,873 (GRCm39) |
C65S |
probably null |
Het |
Pilra |
A |
G |
5: 137,833,674 (GRCm39) |
F131L |
probably damaging |
Het |
Pomt2 |
A |
C |
12: 87,180,234 (GRCm39) |
C256G |
probably damaging |
Het |
Ppl |
A |
T |
16: 4,906,742 (GRCm39) |
S1184R |
probably benign |
Het |
Prkaa1 |
G |
T |
15: 5,206,392 (GRCm39) |
R416L |
possibly damaging |
Het |
Prmt2 |
C |
T |
10: 76,058,390 (GRCm39) |
V140I |
probably damaging |
Het |
Prodh |
A |
T |
16: 17,895,653 (GRCm39) |
|
probably null |
Het |
Psg29 |
T |
A |
7: 16,945,763 (GRCm39) |
D444E |
probably damaging |
Het |
Ptgs1 |
A |
T |
2: 36,141,272 (GRCm39) |
N573I |
probably damaging |
Het |
Rbm38 |
C |
T |
2: 172,863,875 (GRCm39) |
P15S |
probably benign |
Het |
Riox2 |
T |
C |
16: 59,312,236 (GRCm39) |
S458P |
possibly damaging |
Het |
Rnase4 |
T |
C |
14: 51,342,702 (GRCm39) |
V142A |
possibly damaging |
Het |
Rnf138 |
A |
G |
18: 21,159,204 (GRCm39) |
N244S |
probably benign |
Het |
Rnf40 |
T |
C |
7: 127,196,458 (GRCm39) |
L802P |
probably damaging |
Het |
Sfxn4 |
C |
T |
19: 60,839,450 (GRCm39) |
V203M |
probably damaging |
Het |
Skor2 |
G |
T |
18: 76,946,649 (GRCm39) |
E124* |
probably null |
Het |
Slc4a2 |
G |
A |
5: 24,643,760 (GRCm39) |
S855N |
probably benign |
Het |
Slc8a2 |
T |
C |
7: 15,884,508 (GRCm39) |
L626P |
possibly damaging |
Het |
Slco4c1 |
G |
A |
1: 96,768,953 (GRCm39) |
P303L |
probably damaging |
Het |
Slirp |
A |
G |
12: 87,490,784 (GRCm39) |
T29A |
probably damaging |
Het |
Snrpd3 |
G |
T |
10: 75,355,227 (GRCm39) |
C20F |
possibly damaging |
Het |
Spag17 |
T |
A |
3: 99,987,434 (GRCm39) |
Y1575N |
possibly damaging |
Het |
St8sia4 |
G |
A |
1: 95,594,910 (GRCm39) |
A26V |
probably benign |
Het |
Stab2 |
A |
T |
10: 86,699,422 (GRCm39) |
I481N |
probably benign |
Het |
Tenm2 |
T |
A |
11: 35,959,208 (GRCm39) |
T1114S |
probably damaging |
Het |
Tgm1 |
A |
G |
14: 55,947,392 (GRCm39) |
V323A |
probably damaging |
Het |
Tmco4 |
A |
G |
4: 138,785,433 (GRCm39) |
H501R |
probably damaging |
Het |
Tob1 |
A |
T |
11: 94,104,567 (GRCm39) |
R34S |
possibly damaging |
Het |
Trhr2 |
C |
T |
8: 123,084,110 (GRCm39) |
V297I |
probably benign |
Het |
Trim30d |
A |
C |
7: 104,137,165 (GRCm39) |
V13G |
probably damaging |
Het |
Trpm3 |
T |
C |
19: 22,862,713 (GRCm39) |
V485A |
possibly damaging |
Het |
Trrap |
T |
C |
5: 144,787,989 (GRCm39) |
I3518T |
probably damaging |
Het |
Ttc27 |
T |
C |
17: 75,054,750 (GRCm39) |
L352P |
probably damaging |
Het |
Ush1g |
A |
G |
11: 115,209,123 (GRCm39) |
L357P |
possibly damaging |
Het |
Usp24 |
A |
G |
4: 106,277,644 (GRCm39) |
H2258R |
probably benign |
Het |
Vcam1 |
A |
G |
3: 115,918,037 (GRCm39) |
V308A |
probably damaging |
Het |
Vdr |
A |
G |
15: 97,755,459 (GRCm39) |
S355P |
probably benign |
Het |
Vldlr |
T |
C |
19: 27,215,677 (GRCm39) |
S184P |
probably damaging |
Het |
Xpo4 |
C |
A |
14: 57,822,098 (GRCm39) |
A1073S |
probably benign |
Het |
Zfand2b |
A |
G |
1: 75,147,634 (GRCm39) |
D224G |
probably benign |
Het |
Zfp263 |
A |
G |
16: 3,564,704 (GRCm39) |
R240G |
possibly damaging |
Het |
|
Other mutations in Prkdc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Prkdc
|
APN |
16 |
15,515,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00225:Prkdc
|
APN |
16 |
15,627,508 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL00481:Prkdc
|
APN |
16 |
15,608,330 (GRCm39) |
missense |
probably benign |
0.41 |
IGL00488:Prkdc
|
APN |
16 |
15,593,711 (GRCm39) |
splice site |
probably null |
|
IGL00489:Prkdc
|
APN |
16 |
15,617,790 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL00579:Prkdc
|
APN |
16 |
15,482,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00587:Prkdc
|
APN |
16 |
15,470,222 (GRCm39) |
splice site |
probably benign |
|
IGL00666:Prkdc
|
APN |
16 |
15,554,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00675:Prkdc
|
APN |
16 |
15,605,022 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00708:Prkdc
|
APN |
16 |
15,597,290 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00725:Prkdc
|
APN |
16 |
15,634,503 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00818:Prkdc
|
APN |
16 |
15,577,618 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00917:Prkdc
|
APN |
16 |
15,557,428 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00990:Prkdc
|
APN |
16 |
15,519,979 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01126:Prkdc
|
APN |
16 |
15,487,185 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01141:Prkdc
|
APN |
16 |
15,544,568 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01306:Prkdc
|
APN |
16 |
15,485,595 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01326:Prkdc
|
APN |
16 |
15,647,556 (GRCm39) |
missense |
probably benign |
|
IGL01335:Prkdc
|
APN |
16 |
15,634,760 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01419:Prkdc
|
APN |
16 |
15,653,030 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01434:Prkdc
|
APN |
16 |
15,531,451 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01554:Prkdc
|
APN |
16 |
15,470,166 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01671:Prkdc
|
APN |
16 |
15,485,609 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01871:Prkdc
|
APN |
16 |
15,600,951 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01874:Prkdc
|
APN |
16 |
15,552,858 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01930:Prkdc
|
APN |
16 |
15,516,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01984:Prkdc
|
APN |
16 |
15,526,643 (GRCm39) |
missense |
probably benign |
|
IGL02121:Prkdc
|
APN |
16 |
15,535,048 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02152:Prkdc
|
APN |
16 |
15,487,149 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02172:Prkdc
|
APN |
16 |
15,627,623 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02336:Prkdc
|
APN |
16 |
15,603,843 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02336:Prkdc
|
APN |
16 |
15,603,842 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02393:Prkdc
|
APN |
16 |
15,634,622 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02406:Prkdc
|
APN |
16 |
15,488,399 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02500:Prkdc
|
APN |
16 |
15,532,146 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02568:Prkdc
|
APN |
16 |
15,544,406 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02579:Prkdc
|
APN |
16 |
15,488,465 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02652:Prkdc
|
APN |
16 |
15,600,951 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02661:Prkdc
|
APN |
16 |
15,587,689 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02685:Prkdc
|
APN |
16 |
15,653,907 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02741:Prkdc
|
APN |
16 |
15,570,590 (GRCm39) |
splice site |
probably benign |
|
IGL02803:Prkdc
|
APN |
16 |
15,651,530 (GRCm39) |
splice site |
probably benign |
|
IGL02866:Prkdc
|
APN |
16 |
15,649,191 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02882:Prkdc
|
APN |
16 |
15,469,383 (GRCm39) |
nonsense |
probably null |
|
IGL02989:Prkdc
|
APN |
16 |
15,617,880 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03053:Prkdc
|
APN |
16 |
15,652,030 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03071:Prkdc
|
APN |
16 |
15,617,848 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03091:Prkdc
|
APN |
16 |
15,523,174 (GRCm39) |
splice site |
probably benign |
|
IGL03100:Prkdc
|
APN |
16 |
15,531,499 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03128:Prkdc
|
APN |
16 |
15,518,608 (GRCm39) |
splice site |
probably benign |
|
IGL03168:Prkdc
|
APN |
16 |
15,652,030 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03204:Prkdc
|
APN |
16 |
15,587,665 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03390:Prkdc
|
APN |
16 |
15,488,490 (GRCm39) |
nonsense |
probably null |
|
anhimid
|
UTSW |
16 |
15,543,325 (GRCm39) |
critical splice donor site |
probably null |
|
anhinga
|
UTSW |
16 |
15,526,796 (GRCm39) |
critical splice donor site |
probably null |
|
Bushtit
|
UTSW |
16 |
15,570,628 (GRCm39) |
missense |
probably damaging |
0.97 |
clover
|
UTSW |
16 |
15,520,020 (GRCm39) |
splice site |
probably benign |
|
crackle
|
UTSW |
16 |
15,603,914 (GRCm39) |
critical splice donor site |
probably null |
|
Daffy
|
UTSW |
16 |
15,647,561 (GRCm39) |
missense |
possibly damaging |
0.86 |
darter
|
UTSW |
16 |
15,591,477 (GRCm39) |
missense |
possibly damaging |
0.93 |
Elmer_fudd
|
UTSW |
16 |
15,625,922 (GRCm39) |
missense |
probably benign |
0.01 |
envenomation
|
UTSW |
16 |
15,653,091 (GRCm39) |
nonsense |
probably null |
|
hobgoblin
|
UTSW |
16 |
15,633,850 (GRCm39) |
missense |
probably damaging |
1.00 |
Incubus
|
UTSW |
16 |
15,490,191 (GRCm39) |
missense |
probably damaging |
1.00 |
liming
|
UTSW |
16 |
15,570,693 (GRCm39) |
nonsense |
probably null |
|
newt
|
UTSW |
16 |
15,545,590 (GRCm39) |
missense |
probably benign |
0.04 |
ornithorhynchus
|
UTSW |
16 |
15,634,523 (GRCm39) |
critical splice donor site |
probably null |
|
primitive
|
UTSW |
16 |
15,653,022 (GRCm39) |
frame shift |
probably null |
|
roadrunner
|
UTSW |
16 |
15,651,751 (GRCm39) |
missense |
probably damaging |
1.00 |
Schreier
|
UTSW |
16 |
15,488,392 (GRCm39) |
missense |
probably benign |
0.00 |
screamer
|
UTSW |
16 |
15,649,146 (GRCm39) |
nonsense |
probably null |
|
Screamer10
|
UTSW |
16 |
15,585,889 (GRCm39) |
missense |
probably damaging |
0.98 |
screamer2
|
UTSW |
16 |
15,470,416 (GRCm39) |
critical splice donor site |
probably null |
|
screamer3
|
UTSW |
16 |
15,558,196 (GRCm39) |
critical splice donor site |
probably null |
|
screamer4
|
UTSW |
16 |
15,600,943 (GRCm39) |
missense |
probably benign |
0.00 |
screamer5
|
UTSW |
16 |
15,505,268 (GRCm39) |
missense |
probably benign |
|
screamer6
|
UTSW |
16 |
15,577,469 (GRCm39) |
missense |
probably damaging |
1.00 |
screamer7
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
Screamer8
|
UTSW |
16 |
15,537,297 (GRCm39) |
missense |
probably benign |
0.00 |
Screamer9
|
UTSW |
16 |
15,552,786 (GRCm39) |
missense |
probably benign |
0.01 |
Tweetie
|
UTSW |
16 |
15,535,665 (GRCm39) |
missense |
probably damaging |
1.00 |
updock
|
UTSW |
16 |
15,612,958 (GRCm39) |
missense |
probably benign |
|
ANU23:Prkdc
|
UTSW |
16 |
15,485,595 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0008:Prkdc
|
UTSW |
16 |
15,526,565 (GRCm39) |
splice site |
probably benign |
|
R0018:Prkdc
|
UTSW |
16 |
15,544,406 (GRCm39) |
missense |
probably benign |
0.03 |
R0018:Prkdc
|
UTSW |
16 |
15,544,406 (GRCm39) |
missense |
probably benign |
0.03 |
R0069:Prkdc
|
UTSW |
16 |
15,544,368 (GRCm39) |
missense |
probably benign |
0.03 |
R0125:Prkdc
|
UTSW |
16 |
15,516,871 (GRCm39) |
missense |
probably damaging |
0.98 |
R0131:Prkdc
|
UTSW |
16 |
15,531,517 (GRCm39) |
missense |
probably benign |
0.09 |
R0131:Prkdc
|
UTSW |
16 |
15,531,517 (GRCm39) |
missense |
probably benign |
0.09 |
R0132:Prkdc
|
UTSW |
16 |
15,531,517 (GRCm39) |
missense |
probably benign |
0.09 |
R0137:Prkdc
|
UTSW |
16 |
15,558,196 (GRCm39) |
critical splice donor site |
probably null |
|
R0334:Prkdc
|
UTSW |
16 |
15,554,663 (GRCm39) |
missense |
probably benign |
0.00 |
R0373:Prkdc
|
UTSW |
16 |
15,609,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Prkdc
|
UTSW |
16 |
15,651,604 (GRCm39) |
missense |
probably damaging |
0.97 |
R0511:Prkdc
|
UTSW |
16 |
15,649,146 (GRCm39) |
nonsense |
probably null |
|
R0538:Prkdc
|
UTSW |
16 |
15,651,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R0595:Prkdc
|
UTSW |
16 |
15,625,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Prkdc
|
UTSW |
16 |
15,589,921 (GRCm39) |
missense |
probably damaging |
0.98 |
R0616:Prkdc
|
UTSW |
16 |
15,508,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Prkdc
|
UTSW |
16 |
15,628,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R0694:Prkdc
|
UTSW |
16 |
15,586,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R0702:Prkdc
|
UTSW |
16 |
15,603,835 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0965:Prkdc
|
UTSW |
16 |
15,647,580 (GRCm39) |
missense |
probably benign |
|
R1027:Prkdc
|
UTSW |
16 |
15,468,576 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1029:Prkdc
|
UTSW |
16 |
15,472,613 (GRCm39) |
splice site |
probably benign |
|
R1033:Prkdc
|
UTSW |
16 |
15,585,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R1067:Prkdc
|
UTSW |
16 |
15,570,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R1116:Prkdc
|
UTSW |
16 |
15,600,943 (GRCm39) |
missense |
probably benign |
0.00 |
R1187:Prkdc
|
UTSW |
16 |
15,577,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R1226:Prkdc
|
UTSW |
16 |
15,491,861 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1279:Prkdc
|
UTSW |
16 |
15,508,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R1304:Prkdc
|
UTSW |
16 |
15,577,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R1314:Prkdc
|
UTSW |
16 |
15,482,091 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1351:Prkdc
|
UTSW |
16 |
15,485,564 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1509:Prkdc
|
UTSW |
16 |
15,549,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Prkdc
|
UTSW |
16 |
15,505,268 (GRCm39) |
missense |
probably benign |
|
R1531:Prkdc
|
UTSW |
16 |
15,589,970 (GRCm39) |
missense |
probably benign |
0.01 |
R1579:Prkdc
|
UTSW |
16 |
15,493,192 (GRCm39) |
missense |
probably benign |
0.00 |
R1669:Prkdc
|
UTSW |
16 |
15,551,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R1682:Prkdc
|
UTSW |
16 |
15,494,853 (GRCm39) |
missense |
probably benign |
0.19 |
R1713:Prkdc
|
UTSW |
16 |
15,612,958 (GRCm39) |
missense |
probably benign |
|
R1762:Prkdc
|
UTSW |
16 |
15,455,825 (GRCm39) |
missense |
probably benign |
|
R1789:Prkdc
|
UTSW |
16 |
15,557,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Prkdc
|
UTSW |
16 |
15,577,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Prkdc
|
UTSW |
16 |
15,625,922 (GRCm39) |
missense |
probably benign |
0.01 |
R1887:Prkdc
|
UTSW |
16 |
15,647,499 (GRCm39) |
missense |
probably benign |
0.00 |
R1891:Prkdc
|
UTSW |
16 |
15,543,300 (GRCm39) |
missense |
probably benign |
0.02 |
R1921:Prkdc
|
UTSW |
16 |
15,532,079 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1922:Prkdc
|
UTSW |
16 |
15,532,130 (GRCm39) |
missense |
probably benign |
0.00 |
R1929:Prkdc
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
R1939:Prkdc
|
UTSW |
16 |
15,653,777 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2021:Prkdc
|
UTSW |
16 |
15,494,873 (GRCm39) |
missense |
probably benign |
0.00 |
R2033:Prkdc
|
UTSW |
16 |
15,505,216 (GRCm39) |
splice site |
probably benign |
|
R2056:Prkdc
|
UTSW |
16 |
15,545,469 (GRCm39) |
missense |
probably benign |
0.03 |
R2057:Prkdc
|
UTSW |
16 |
15,545,469 (GRCm39) |
missense |
probably benign |
0.03 |
R2058:Prkdc
|
UTSW |
16 |
15,545,469 (GRCm39) |
missense |
probably benign |
0.03 |
R2082:Prkdc
|
UTSW |
16 |
15,533,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Prkdc
|
UTSW |
16 |
15,505,254 (GRCm39) |
missense |
probably benign |
0.01 |
R2124:Prkdc
|
UTSW |
16 |
15,537,297 (GRCm39) |
missense |
probably benign |
0.00 |
R2164:Prkdc
|
UTSW |
16 |
15,523,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Prkdc
|
UTSW |
16 |
15,552,786 (GRCm39) |
missense |
probably benign |
0.01 |
R2191:Prkdc
|
UTSW |
16 |
15,516,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R2270:Prkdc
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
R2271:Prkdc
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
R2272:Prkdc
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
R2356:Prkdc
|
UTSW |
16 |
15,502,068 (GRCm39) |
missense |
probably benign |
|
R2852:Prkdc
|
UTSW |
16 |
15,470,416 (GRCm39) |
critical splice donor site |
probably null |
|
R3115:Prkdc
|
UTSW |
16 |
15,482,222 (GRCm39) |
missense |
probably benign |
0.01 |
R3116:Prkdc
|
UTSW |
16 |
15,482,222 (GRCm39) |
missense |
probably benign |
0.01 |
R3499:Prkdc
|
UTSW |
16 |
15,585,889 (GRCm39) |
missense |
probably damaging |
0.98 |
R3687:Prkdc
|
UTSW |
16 |
15,617,831 (GRCm39) |
missense |
probably benign |
|
R3834:Prkdc
|
UTSW |
16 |
15,609,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3835:Prkdc
|
UTSW |
16 |
15,609,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3961:Prkdc
|
UTSW |
16 |
15,647,475 (GRCm39) |
splice site |
probably null |
|
R4151:Prkdc
|
UTSW |
16 |
15,634,637 (GRCm39) |
missense |
probably benign |
|
R4233:Prkdc
|
UTSW |
16 |
15,653,783 (GRCm39) |
missense |
probably benign |
0.11 |
R4281:Prkdc
|
UTSW |
16 |
15,623,963 (GRCm39) |
splice site |
probably null |
|
R4296:Prkdc
|
UTSW |
16 |
15,555,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R4344:Prkdc
|
UTSW |
16 |
15,585,886 (GRCm39) |
missense |
probably damaging |
0.98 |
R4424:Prkdc
|
UTSW |
16 |
15,653,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R4424:Prkdc
|
UTSW |
16 |
15,591,603 (GRCm39) |
missense |
probably damaging |
0.98 |
R4497:Prkdc
|
UTSW |
16 |
15,518,517 (GRCm39) |
missense |
probably benign |
0.43 |
R4549:Prkdc
|
UTSW |
16 |
15,554,734 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4594:Prkdc
|
UTSW |
16 |
15,585,830 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4603:Prkdc
|
UTSW |
16 |
15,628,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R4615:Prkdc
|
UTSW |
16 |
15,480,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R4648:Prkdc
|
UTSW |
16 |
15,634,638 (GRCm39) |
missense |
probably benign |
0.05 |
R4662:Prkdc
|
UTSW |
16 |
15,551,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R4680:Prkdc
|
UTSW |
16 |
15,589,894 (GRCm39) |
missense |
probably benign |
0.00 |
R4700:Prkdc
|
UTSW |
16 |
15,519,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Prkdc
|
UTSW |
16 |
15,628,701 (GRCm39) |
missense |
probably benign |
0.32 |
R4720:Prkdc
|
UTSW |
16 |
15,485,579 (GRCm39) |
missense |
probably benign |
|
R4785:Prkdc
|
UTSW |
16 |
15,466,840 (GRCm39) |
missense |
probably benign |
0.21 |
R4822:Prkdc
|
UTSW |
16 |
15,468,576 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4829:Prkdc
|
UTSW |
16 |
15,519,939 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4981:Prkdc
|
UTSW |
16 |
15,496,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Prkdc
|
UTSW |
16 |
15,491,861 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5059:Prkdc
|
UTSW |
16 |
15,655,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R5115:Prkdc
|
UTSW |
16 |
15,608,444 (GRCm39) |
missense |
probably benign |
|
R5151:Prkdc
|
UTSW |
16 |
15,533,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5165:Prkdc
|
UTSW |
16 |
15,496,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R5215:Prkdc
|
UTSW |
16 |
15,589,985 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5270:Prkdc
|
UTSW |
16 |
15,552,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R5278:Prkdc
|
UTSW |
16 |
15,532,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5351:Prkdc
|
UTSW |
16 |
15,649,176 (GRCm39) |
missense |
probably benign |
0.03 |
R5416:Prkdc
|
UTSW |
16 |
15,623,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R5418:Prkdc
|
UTSW |
16 |
15,612,961 (GRCm39) |
missense |
probably benign |
0.20 |
R5437:Prkdc
|
UTSW |
16 |
15,587,739 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5452:Prkdc
|
UTSW |
16 |
15,586,501 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5518:Prkdc
|
UTSW |
16 |
15,496,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Prkdc
|
UTSW |
16 |
15,469,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R5589:Prkdc
|
UTSW |
16 |
15,524,655 (GRCm39) |
missense |
probably benign |
0.02 |
R5618:Prkdc
|
UTSW |
16 |
15,627,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R5640:Prkdc
|
UTSW |
16 |
15,647,633 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5661:Prkdc
|
UTSW |
16 |
15,628,634 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5771:Prkdc
|
UTSW |
16 |
15,482,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Prkdc
|
UTSW |
16 |
15,597,252 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5783:Prkdc
|
UTSW |
16 |
15,535,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R5792:Prkdc
|
UTSW |
16 |
15,634,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Prkdc
|
UTSW |
16 |
15,555,698 (GRCm39) |
nonsense |
probably null |
|
R5826:Prkdc
|
UTSW |
16 |
15,551,962 (GRCm39) |
missense |
probably benign |
|
R5883:Prkdc
|
UTSW |
16 |
15,533,778 (GRCm39) |
missense |
probably benign |
|
R5895:Prkdc
|
UTSW |
16 |
15,570,693 (GRCm39) |
nonsense |
probably null |
|
R5998:Prkdc
|
UTSW |
16 |
15,601,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Prkdc
|
UTSW |
16 |
15,647,561 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6120:Prkdc
|
UTSW |
16 |
15,557,335 (GRCm39) |
missense |
probably benign |
0.00 |
R6145:Prkdc
|
UTSW |
16 |
15,589,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Prkdc
|
UTSW |
16 |
15,608,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R6293:Prkdc
|
UTSW |
16 |
15,605,019 (GRCm39) |
missense |
probably benign |
0.00 |
R6321:Prkdc
|
UTSW |
16 |
15,532,783 (GRCm39) |
missense |
probably benign |
|
R6376:Prkdc
|
UTSW |
16 |
15,587,749 (GRCm39) |
missense |
probably benign |
0.06 |
R6387:Prkdc
|
UTSW |
16 |
15,516,679 (GRCm39) |
missense |
probably benign |
0.01 |
R6406:Prkdc
|
UTSW |
16 |
15,535,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R6469:Prkdc
|
UTSW |
16 |
15,612,939 (GRCm39) |
missense |
probably benign |
0.10 |
R6486:Prkdc
|
UTSW |
16 |
15,570,628 (GRCm39) |
missense |
probably damaging |
0.97 |
R6665:Prkdc
|
UTSW |
16 |
15,603,914 (GRCm39) |
critical splice donor site |
probably null |
|
R6703:Prkdc
|
UTSW |
16 |
15,488,392 (GRCm39) |
missense |
probably benign |
0.00 |
R6774:Prkdc
|
UTSW |
16 |
15,543,325 (GRCm39) |
critical splice donor site |
probably null |
|
R6854:Prkdc
|
UTSW |
16 |
15,469,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R6878:Prkdc
|
UTSW |
16 |
15,594,936 (GRCm39) |
missense |
probably benign |
0.31 |
R6882:Prkdc
|
UTSW |
16 |
15,626,020 (GRCm39) |
missense |
probably benign |
0.33 |
R6882:Prkdc
|
UTSW |
16 |
15,601,127 (GRCm39) |
critical splice donor site |
probably null |
|
R6949:Prkdc
|
UTSW |
16 |
15,617,853 (GRCm39) |
missense |
probably benign |
|
R6950:Prkdc
|
UTSW |
16 |
15,633,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Prkdc
|
UTSW |
16 |
15,587,830 (GRCm39) |
missense |
probably benign |
0.00 |
R7064:Prkdc
|
UTSW |
16 |
15,608,317 (GRCm39) |
missense |
probably benign |
0.00 |
R7097:Prkdc
|
UTSW |
16 |
15,507,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R7201:Prkdc
|
UTSW |
16 |
15,516,667 (GRCm39) |
missense |
probably benign |
0.12 |
R7235:Prkdc
|
UTSW |
16 |
15,532,127 (GRCm39) |
missense |
probably benign |
|
R7283:Prkdc
|
UTSW |
16 |
15,535,628 (GRCm39) |
missense |
probably benign |
0.00 |
R7401:Prkdc
|
UTSW |
16 |
15,466,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R7525:Prkdc
|
UTSW |
16 |
15,490,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R7647:Prkdc
|
UTSW |
16 |
15,555,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Prkdc
|
UTSW |
16 |
15,649,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7803:Prkdc
|
UTSW |
16 |
15,623,960 (GRCm39) |
missense |
probably null |
0.05 |
R7858:Prkdc
|
UTSW |
16 |
15,507,141 (GRCm39) |
missense |
probably benign |
0.11 |
R7872:Prkdc
|
UTSW |
16 |
15,532,870 (GRCm39) |
missense |
probably benign |
0.05 |
R7896:Prkdc
|
UTSW |
16 |
15,526,767 (GRCm39) |
missense |
probably damaging |
0.97 |
R8032:Prkdc
|
UTSW |
16 |
15,597,315 (GRCm39) |
missense |
probably benign |
0.00 |
R8055:Prkdc
|
UTSW |
16 |
15,634,749 (GRCm39) |
missense |
probably benign |
0.09 |
R8153:Prkdc
|
UTSW |
16 |
15,482,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R8281:Prkdc
|
UTSW |
16 |
15,523,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8302:Prkdc
|
UTSW |
16 |
15,653,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R8322:Prkdc
|
UTSW |
16 |
15,532,005 (GRCm39) |
splice site |
probably benign |
|
R8401:Prkdc
|
UTSW |
16 |
15,591,477 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8440:Prkdc
|
UTSW |
16 |
15,653,022 (GRCm39) |
frame shift |
probably null |
|
R8458:Prkdc
|
UTSW |
16 |
15,608,540 (GRCm39) |
critical splice donor site |
probably null |
|
R8472:Prkdc
|
UTSW |
16 |
15,469,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R8478:Prkdc
|
UTSW |
16 |
15,466,788 (GRCm39) |
missense |
probably benign |
0.00 |
R8515:Prkdc
|
UTSW |
16 |
15,482,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R8546:Prkdc
|
UTSW |
16 |
15,480,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R8678:Prkdc
|
UTSW |
16 |
15,526,796 (GRCm39) |
critical splice donor site |
probably null |
|
R8739:Prkdc
|
UTSW |
16 |
15,626,068 (GRCm39) |
missense |
probably benign |
0.01 |
R8749:Prkdc
|
UTSW |
16 |
15,601,029 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8836:Prkdc
|
UTSW |
16 |
15,545,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8904:Prkdc
|
UTSW |
16 |
15,545,590 (GRCm39) |
missense |
probably benign |
0.04 |
R8952:Prkdc
|
UTSW |
16 |
15,491,624 (GRCm39) |
intron |
probably benign |
|
R8971:Prkdc
|
UTSW |
16 |
15,493,229 (GRCm39) |
missense |
probably null |
0.99 |
R8974:Prkdc
|
UTSW |
16 |
15,617,726 (GRCm39) |
splice site |
probably null |
|
R9052:Prkdc
|
UTSW |
16 |
15,508,160 (GRCm39) |
missense |
probably benign |
0.05 |
R9069:Prkdc
|
UTSW |
16 |
15,653,091 (GRCm39) |
nonsense |
probably null |
|
R9200:Prkdc
|
UTSW |
16 |
15,523,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R9235:Prkdc
|
UTSW |
16 |
15,651,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R9278:Prkdc
|
UTSW |
16 |
15,634,523 (GRCm39) |
critical splice donor site |
probably null |
|
R9309:Prkdc
|
UTSW |
16 |
15,526,792 (GRCm39) |
nonsense |
probably null |
|
R9386:Prkdc
|
UTSW |
16 |
15,496,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R9452:Prkdc
|
UTSW |
16 |
15,485,465 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9500:Prkdc
|
UTSW |
16 |
15,657,079 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9608:Prkdc
|
UTSW |
16 |
15,548,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Prkdc
|
UTSW |
16 |
15,548,334 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9636:Prkdc
|
UTSW |
16 |
15,548,341 (GRCm39) |
missense |
probably benign |
0.19 |
R9656:Prkdc
|
UTSW |
16 |
15,617,818 (GRCm39) |
missense |
probably benign |
0.00 |
R9674:Prkdc
|
UTSW |
16 |
15,533,819 (GRCm39) |
missense |
probably damaging |
0.98 |
R9760:Prkdc
|
UTSW |
16 |
15,657,044 (GRCm39) |
nonsense |
probably null |
|
X0023:Prkdc
|
UTSW |
16 |
15,558,142 (GRCm39) |
missense |
probably benign |
|
Z1176:Prkdc
|
UTSW |
16 |
15,505,286 (GRCm39) |
nonsense |
probably null |
|
|