Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Acot6 |
A |
G |
12: 84,155,789 (GRCm39) |
K246E |
probably benign |
Het |
Actl11 |
T |
A |
9: 107,808,615 (GRCm39) |
H979Q |
probably damaging |
Het |
Adal |
T |
A |
2: 120,986,030 (GRCm39) |
|
probably benign |
Het |
Add2 |
G |
A |
6: 86,087,840 (GRCm39) |
V596I |
probably benign |
Het |
Adrb3 |
A |
C |
8: 27,717,798 (GRCm39) |
M217R |
probably damaging |
Het |
Ank1 |
T |
C |
8: 23,631,134 (GRCm39) |
|
probably benign |
Het |
Ank2 |
A |
T |
3: 126,757,094 (GRCm39) |
N1054K |
possibly damaging |
Het |
Ankib1 |
T |
C |
5: 3,763,217 (GRCm39) |
Y504C |
probably damaging |
Het |
Ankrd29 |
T |
C |
18: 12,395,242 (GRCm39) |
K217R |
probably damaging |
Het |
Ankrd45 |
T |
C |
1: 160,982,876 (GRCm39) |
V129A |
probably damaging |
Het |
Aox4 |
A |
T |
1: 58,275,835 (GRCm39) |
D389V |
probably benign |
Het |
Aph1a |
G |
T |
3: 95,802,843 (GRCm39) |
G148W |
probably damaging |
Het |
Arhgef26 |
G |
A |
3: 62,247,806 (GRCm39) |
D297N |
possibly damaging |
Het |
Atxn7l3b |
C |
A |
10: 112,764,649 (GRCm39) |
|
probably benign |
Het |
Auh |
A |
G |
13: 52,995,065 (GRCm39) |
S167P |
probably damaging |
Het |
Bach1 |
A |
T |
16: 87,515,888 (GRCm39) |
K143I |
possibly damaging |
Het |
Bbx |
T |
A |
16: 50,045,101 (GRCm39) |
T487S |
probably damaging |
Het |
Bche |
T |
G |
3: 73,609,177 (GRCm39) |
D83A |
probably benign |
Het |
Bri3bp |
G |
T |
5: 125,518,760 (GRCm39) |
|
probably benign |
Het |
Cd3d |
A |
T |
9: 44,896,296 (GRCm39) |
E28D |
probably damaging |
Het |
Cdc42bpa |
A |
G |
1: 179,965,366 (GRCm39) |
T1028A |
probably damaging |
Het |
Ceacam23 |
A |
G |
7: 17,639,143 (GRCm39) |
|
probably null |
Het |
Celsr2 |
T |
C |
3: 108,319,945 (GRCm39) |
I956V |
possibly damaging |
Het |
Cep95 |
A |
T |
11: 106,707,480 (GRCm39) |
|
probably null |
Het |
Cic |
G |
T |
7: 24,986,535 (GRCm39) |
G1289C |
probably damaging |
Het |
Cndp1 |
A |
G |
18: 84,650,025 (GRCm39) |
Y223H |
probably damaging |
Het |
Cops8 |
A |
G |
1: 90,538,724 (GRCm39) |
D51G |
probably damaging |
Het |
Csgalnact1 |
T |
C |
8: 68,913,623 (GRCm39) |
E194G |
probably benign |
Het |
Ctsm |
A |
G |
13: 61,686,776 (GRCm39) |
Y39H |
probably damaging |
Het |
Dhrs2 |
T |
C |
14: 55,474,722 (GRCm39) |
V119A |
probably damaging |
Het |
Drosha |
T |
A |
15: 12,935,093 (GRCm39) |
M1336K |
probably benign |
Het |
Dsp |
G |
A |
13: 38,381,678 (GRCm39) |
D2808N |
possibly damaging |
Het |
Ehmt1 |
G |
T |
2: 24,767,509 (GRCm39) |
P135T |
probably damaging |
Het |
Epas1 |
A |
G |
17: 87,116,882 (GRCm39) |
N184S |
probably damaging |
Het |
Erich3 |
C |
T |
3: 154,454,025 (GRCm39) |
T597I |
possibly damaging |
Het |
F10 |
T |
C |
8: 13,105,698 (GRCm39) |
V421A |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
Fcgrt |
C |
T |
7: 44,751,372 (GRCm39) |
G192D |
probably benign |
Het |
Fras1 |
A |
G |
5: 96,798,541 (GRCm39) |
E1184G |
possibly damaging |
Het |
Garre1 |
A |
C |
7: 33,945,225 (GRCm39) |
Y552D |
probably damaging |
Het |
Grn |
C |
A |
11: 102,321,380 (GRCm39) |
|
probably benign |
Het |
Gvin-ps5 |
A |
T |
7: 105,928,664 (GRCm39) |
|
noncoding transcript |
Het |
Hadh |
A |
T |
3: 131,029,197 (GRCm39) |
L274* |
probably null |
Het |
Hus1 |
T |
C |
11: 8,956,027 (GRCm39) |
S169G |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,290,554 (GRCm39) |
I3338F |
possibly damaging |
Het |
Ighv11-1 |
T |
G |
12: 113,945,768 (GRCm39) |
E28D |
probably benign |
Het |
Kctd9 |
C |
T |
14: 67,966,805 (GRCm39) |
T106I |
probably damaging |
Het |
Krit1 |
A |
T |
5: 3,872,238 (GRCm39) |
N421I |
probably damaging |
Het |
Lamb1 |
A |
G |
12: 31,376,677 (GRCm39) |
D1619G |
probably damaging |
Het |
Lpar6 |
G |
A |
14: 73,476,147 (GRCm39) |
C36Y |
probably damaging |
Het |
Lrrc37a |
G |
C |
11: 103,347,565 (GRCm39) |
F3043L |
unknown |
Het |
Lrrc46 |
A |
T |
11: 96,931,765 (GRCm39) |
V19D |
probably damaging |
Het |
Mapkap1 |
G |
T |
2: 34,471,303 (GRCm39) |
S197I |
probably damaging |
Het |
Mrps35 |
A |
C |
6: 146,961,645 (GRCm39) |
K173N |
possibly damaging |
Het |
Mtf2 |
A |
G |
5: 108,220,894 (GRCm39) |
|
probably benign |
Het |
Ncf1 |
A |
C |
5: 134,252,267 (GRCm39) |
D261E |
probably damaging |
Het |
Notch1 |
C |
T |
2: 26,371,193 (GRCm39) |
E298K |
probably damaging |
Het |
Nrxn1 |
A |
T |
17: 90,928,274 (GRCm39) |
|
probably benign |
Het |
Or13a18 |
C |
A |
7: 140,190,304 (GRCm39) |
A75E |
possibly damaging |
Het |
Or4x13 |
T |
A |
2: 90,231,107 (GRCm39) |
M34K |
probably benign |
Het |
Or52a33 |
A |
G |
7: 103,289,308 (GRCm39) |
F13S |
probably damaging |
Het |
Or5k3 |
T |
C |
16: 58,969,981 (GRCm39) |
L256P |
probably damaging |
Het |
Or5v1 |
G |
T |
17: 37,810,017 (GRCm39) |
L158F |
probably benign |
Het |
Otud4 |
G |
A |
8: 80,382,318 (GRCm39) |
V176I |
probably damaging |
Het |
Pakap |
T |
A |
4: 57,856,552 (GRCm39) |
V668E |
probably benign |
Het |
Papolg |
T |
C |
11: 23,823,919 (GRCm39) |
|
probably null |
Het |
Pgk2 |
A |
G |
17: 40,518,402 (GRCm39) |
V342A |
probably damaging |
Het |
Phf2 |
G |
A |
13: 48,961,320 (GRCm39) |
A790V |
unknown |
Het |
Prl3d3 |
T |
C |
13: 27,343,072 (GRCm39) |
I86T |
possibly damaging |
Het |
Prss8 |
G |
T |
7: 127,525,635 (GRCm39) |
Q295K |
probably benign |
Het |
Ptpre |
C |
T |
7: 135,270,861 (GRCm39) |
H346Y |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Pwwp3a |
T |
C |
10: 80,068,702 (GRCm39) |
L282P |
probably benign |
Het |
Qrfpr |
A |
G |
3: 36,276,285 (GRCm39) |
V35A |
probably damaging |
Het |
Rpf1 |
A |
G |
3: 146,212,293 (GRCm39) |
L349S |
probably damaging |
Het |
Rpl41 |
G |
T |
10: 128,384,652 (GRCm39) |
|
probably null |
Het |
Rprd2 |
G |
C |
3: 95,672,632 (GRCm39) |
R924G |
probably benign |
Het |
Serpini1 |
T |
A |
3: 75,521,795 (GRCm39) |
N95K |
probably benign |
Het |
Sfxn1 |
A |
T |
13: 54,242,933 (GRCm39) |
T64S |
probably benign |
Het |
Siae |
T |
G |
9: 37,557,816 (GRCm39) |
I541S |
possibly damaging |
Het |
Slc25a4 |
T |
A |
8: 46,660,509 (GRCm39) |
K296N |
probably benign |
Het |
Slc37a1 |
A |
G |
17: 31,541,120 (GRCm39) |
N204S |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,413,800 (GRCm39) |
N976S |
probably benign |
Het |
Smarcal1 |
T |
C |
1: 72,672,019 (GRCm39) |
S847P |
possibly damaging |
Het |
Smg1 |
A |
T |
7: 117,757,323 (GRCm39) |
|
probably benign |
Het |
Smg1 |
C |
T |
7: 117,807,274 (GRCm39) |
A168T |
probably benign |
Het |
Sptlc1 |
A |
G |
13: 53,505,692 (GRCm39) |
I242T |
probably damaging |
Het |
St8sia2 |
T |
C |
7: 73,616,709 (GRCm39) |
I89V |
possibly damaging |
Het |
Supt20 |
A |
T |
3: 54,602,555 (GRCm39) |
|
probably benign |
Het |
Tep1 |
T |
C |
14: 51,076,457 (GRCm39) |
D1659G |
probably benign |
Het |
Tex10 |
C |
A |
4: 48,458,525 (GRCm39) |
|
probably benign |
Het |
Thbs3 |
CAGAAG |
CAG |
3: 89,130,409 (GRCm39) |
|
probably benign |
Het |
Tmbim6 |
C |
A |
15: 99,299,950 (GRCm39) |
S22* |
probably null |
Het |
Tmc2 |
A |
T |
2: 130,043,961 (GRCm39) |
K65M |
possibly damaging |
Het |
Tmod1 |
A |
G |
4: 46,090,872 (GRCm39) |
S142G |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trmt6 |
T |
C |
2: 132,650,191 (GRCm39) |
R349G |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,537,586 (GRCm39) |
T26454S |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,605,122 (GRCm39) |
V16555I |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,384,042 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
C |
2: 69,850,790 (GRCm39) |
|
probably benign |
Het |
Vmn1r17 |
A |
C |
6: 57,337,460 (GRCm39) |
F253V |
possibly damaging |
Het |
Vmn1r201 |
G |
T |
13: 22,659,622 (GRCm39) |
A279S |
possibly damaging |
Het |
Vmn2r17 |
A |
T |
5: 109,575,739 (GRCm39) |
R203S |
probably benign |
Het |
Vwa5a |
A |
G |
9: 38,633,926 (GRCm39) |
E43G |
probably benign |
Het |
Wdr86 |
C |
T |
5: 24,917,843 (GRCm39) |
|
probably null |
Het |
Wdsub1 |
A |
T |
2: 59,700,758 (GRCm39) |
|
probably benign |
Het |
Zcchc7 |
T |
C |
4: 44,931,039 (GRCm39) |
L76P |
probably damaging |
Het |
Zfp108 |
G |
T |
7: 23,960,163 (GRCm39) |
K251N |
probably benign |
Het |
Zfp263 |
T |
C |
16: 3,566,992 (GRCm39) |
C148R |
probably damaging |
Het |
Zfp687 |
A |
C |
3: 94,917,697 (GRCm39) |
F692V |
probably 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 |
R5059:Prkdc
|
UTSW |
16 |
15,655,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Prkdc
|
UTSW |
16 |
15,589,912 (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 |
|
|