Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
T |
C |
5: 64,053,833 (GRCm39) |
|
probably benign |
Het |
4933412E24Rik |
T |
A |
15: 59,888,134 (GRCm39) |
E102V |
probably damaging |
Het |
Adcy9 |
A |
G |
16: 4,129,452 (GRCm39) |
L715P |
probably damaging |
Het |
Adgre4 |
T |
C |
17: 56,109,218 (GRCm39) |
|
probably benign |
Het |
Amer2 |
A |
G |
14: 60,616,000 (GRCm39) |
D65G |
probably damaging |
Het |
Atad2b |
C |
A |
12: 4,989,689 (GRCm39) |
N133K |
possibly damaging |
Het |
AW551984 |
C |
A |
9: 39,504,325 (GRCm39) |
R547L |
probably damaging |
Het |
B3galt6 |
A |
G |
4: 156,076,464 (GRCm39) |
Y204H |
probably benign |
Het |
Btnl2 |
T |
C |
17: 34,577,039 (GRCm39) |
W65R |
probably damaging |
Het |
Camk1g |
T |
C |
1: 193,042,115 (GRCm39) |
T45A |
possibly damaging |
Het |
Caps2 |
C |
A |
10: 112,018,391 (GRCm39) |
Y180* |
probably null |
Het |
Ccdc181 |
T |
A |
1: 164,107,865 (GRCm39) |
S183T |
probably damaging |
Het |
Cdc14b |
A |
G |
13: 64,394,422 (GRCm39) |
|
probably benign |
Het |
Cfap54 |
T |
A |
10: 92,881,140 (GRCm39) |
K349N |
probably damaging |
Het |
Copa |
T |
A |
1: 171,918,800 (GRCm39) |
C127S |
probably damaging |
Het |
Crbn |
T |
C |
6: 106,767,827 (GRCm39) |
Q221R |
probably benign |
Het |
Dapk2 |
T |
G |
9: 66,161,893 (GRCm39) |
V267G |
probably damaging |
Het |
Ddb1 |
T |
C |
19: 10,603,335 (GRCm39) |
L881P |
probably damaging |
Het |
Decr1 |
T |
A |
4: 15,930,972 (GRCm39) |
D120V |
probably damaging |
Het |
Dennd1c |
C |
T |
17: 57,373,562 (GRCm39) |
G637D |
possibly damaging |
Het |
Dhrs3 |
A |
G |
4: 144,646,016 (GRCm39) |
D108G |
possibly damaging |
Het |
Disp1 |
T |
C |
1: 182,868,806 (GRCm39) |
K1205E |
probably benign |
Het |
Dnajc13 |
G |
T |
9: 104,097,097 (GRCm39) |
N510K |
possibly damaging |
Het |
Dusp6 |
T |
C |
10: 99,099,944 (GRCm39) |
Y131H |
probably damaging |
Het |
Eif2b2 |
A |
T |
12: 85,266,435 (GRCm39) |
M34L |
probably benign |
Het |
Epsti1 |
A |
T |
14: 78,211,953 (GRCm39) |
|
probably benign |
Het |
Errfi1 |
G |
A |
4: 150,951,816 (GRCm39) |
E415K |
probably damaging |
Het |
Ext1 |
T |
C |
15: 53,208,000 (GRCm39) |
N254D |
possibly damaging |
Het |
Gm7337 |
A |
C |
5: 87,999,416 (GRCm39) |
|
noncoding transcript |
Het |
Hnrnpu |
T |
C |
1: 178,158,690 (GRCm39) |
|
probably benign |
Het |
Hyal3 |
T |
A |
9: 107,464,005 (GRCm39) |
C407S |
probably damaging |
Het |
Insr |
T |
G |
8: 3,211,416 (GRCm39) |
N1141T |
possibly damaging |
Het |
Ipo9 |
T |
C |
1: 135,337,214 (GRCm39) |
T174A |
probably benign |
Het |
Iqgap1 |
G |
A |
7: 80,402,086 (GRCm39) |
A393V |
probably benign |
Het |
Irak2 |
G |
T |
6: 113,649,721 (GRCm39) |
A119S |
probably benign |
Het |
Itgb2l |
A |
G |
16: 96,238,589 (GRCm39) |
L70P |
probably damaging |
Het |
Itsn1 |
C |
A |
16: 91,649,932 (GRCm39) |
S202* |
probably null |
Het |
Ivd |
T |
C |
2: 118,692,650 (GRCm39) |
|
probably null |
Het |
Leprot |
C |
T |
4: 101,515,090 (GRCm39) |
T89I |
probably damaging |
Het |
Lratd2 |
A |
T |
15: 60,695,296 (GRCm39) |
V150E |
probably damaging |
Het |
Mill2 |
A |
C |
7: 18,590,099 (GRCm39) |
E127A |
probably benign |
Het |
Msh6 |
T |
C |
17: 88,292,909 (GRCm39) |
Y555H |
probably damaging |
Het |
Myo18b |
A |
C |
5: 112,840,594 (GRCm39) |
S2400A |
probably damaging |
Het |
Naa25 |
A |
G |
5: 121,573,135 (GRCm39) |
|
probably null |
Het |
Nop2 |
A |
G |
6: 125,111,555 (GRCm39) |
N96S |
probably benign |
Het |
Nup155 |
G |
T |
15: 8,177,867 (GRCm39) |
R1083S |
possibly damaging |
Het |
Nusap1 |
A |
T |
2: 119,460,885 (GRCm39) |
Q126L |
possibly damaging |
Het |
Or11g24 |
T |
A |
14: 50,662,488 (GRCm39) |
C171S |
probably damaging |
Het |
Or13c7b |
T |
A |
4: 43,820,544 (GRCm39) |
K272N |
probably benign |
Het |
Or2z2 |
T |
C |
11: 58,346,053 (GRCm39) |
T241A |
probably damaging |
Het |
Or4c52 |
T |
G |
2: 89,845,365 (GRCm39) |
Y30* |
probably null |
Het |
Or5al1 |
T |
C |
2: 85,990,439 (GRCm39) |
I92V |
probably benign |
Het |
Or6x1 |
G |
T |
9: 40,098,901 (GRCm39) |
Q163H |
probably benign |
Het |
Or7a35 |
C |
A |
10: 78,853,438 (GRCm39) |
T94N |
probably benign |
Het |
Pde5a |
T |
A |
3: 122,575,277 (GRCm39) |
L356* |
probably null |
Het |
Pdik1l |
A |
G |
4: 134,011,561 (GRCm39) |
L94S |
probably damaging |
Het |
Pkdrej |
T |
A |
15: 85,700,818 (GRCm39) |
D1706V |
probably damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,368,924 (GRCm39) |
I856M |
probably damaging |
Het |
Prkcz |
A |
T |
4: 155,374,981 (GRCm39) |
D114E |
probably benign |
Het |
Prss59 |
A |
G |
6: 40,903,003 (GRCm39) |
M123T |
probably benign |
Het |
Psap |
T |
C |
10: 60,113,575 (GRCm39) |
L4P |
possibly damaging |
Het |
Ptprk |
T |
C |
10: 28,468,822 (GRCm39) |
V1402A |
probably benign |
Het |
Rai14 |
T |
C |
15: 10,633,250 (GRCm39) |
T47A |
possibly damaging |
Het |
Ralgapa1 |
A |
T |
12: 55,756,371 (GRCm39) |
N1075K |
probably damaging |
Het |
Rlf |
A |
G |
4: 121,006,044 (GRCm39) |
S979P |
probably damaging |
Het |
Rps2 |
G |
T |
17: 24,939,952 (GRCm39) |
A129S |
probably benign |
Het |
Serinc2 |
A |
G |
4: 130,154,528 (GRCm39) |
S175P |
probably benign |
Het |
Skic2 |
C |
T |
17: 35,066,789 (GRCm39) |
W88* |
probably null |
Het |
Socs5 |
A |
T |
17: 87,442,146 (GRCm39) |
Q362L |
probably damaging |
Het |
Srbd1 |
A |
T |
17: 86,437,643 (GRCm39) |
D233E |
probably benign |
Het |
Srgap3 |
A |
G |
6: 112,706,619 (GRCm39) |
V826A |
probably benign |
Het |
Tacr2 |
A |
G |
10: 62,101,024 (GRCm39) |
D378G |
probably benign |
Het |
Taok2 |
A |
G |
7: 126,474,347 (GRCm39) |
I294T |
possibly damaging |
Het |
Tert |
A |
G |
13: 73,775,528 (GRCm39) |
E93G |
possibly damaging |
Het |
Tns2 |
A |
G |
15: 102,021,771 (GRCm39) |
E1118G |
possibly damaging |
Het |
Topaz1 |
T |
C |
9: 122,578,446 (GRCm39) |
I452T |
probably benign |
Het |
Trak1 |
C |
T |
9: 121,280,800 (GRCm39) |
|
probably benign |
Het |
Ttc22 |
A |
T |
4: 106,480,276 (GRCm39) |
I177F |
probably damaging |
Het |
Tuba8 |
A |
G |
6: 121,199,697 (GRCm39) |
D127G |
possibly damaging |
Het |
Tulp4 |
A |
G |
17: 6,248,983 (GRCm39) |
M1V |
probably null |
Het |
Urb1 |
A |
G |
16: 90,594,791 (GRCm39) |
L247P |
probably damaging |
Het |
Usp32 |
A |
G |
11: 84,916,362 (GRCm39) |
W861R |
probably damaging |
Het |
Vmn1r48 |
G |
A |
6: 90,013,360 (GRCm39) |
T155I |
probably benign |
Het |
Vmn2r117 |
A |
G |
17: 23,679,352 (GRCm39) |
L624P |
probably damaging |
Het |
Vmn2r86 |
T |
C |
10: 130,291,673 (GRCm39) |
R31G |
probably damaging |
Het |
Vstm5 |
T |
G |
9: 15,168,594 (GRCm39) |
S53A |
probably benign |
Het |
Wnt5a |
T |
C |
14: 28,244,445 (GRCm39) |
Y231H |
probably benign |
Het |
Yeats2 |
T |
C |
16: 20,012,395 (GRCm39) |
V531A |
probably damaging |
Het |
Zw10 |
T |
C |
9: 48,988,860 (GRCm39) |
Y709H |
probably damaging |
Het |
|
Other mutations in Cep350 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00764:Cep350
|
APN |
1 |
155,816,492 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00821:Cep350
|
APN |
1 |
155,737,950 (GRCm39) |
missense |
probably benign |
|
IGL00837:Cep350
|
APN |
1 |
155,829,137 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00977:Cep350
|
APN |
1 |
155,808,611 (GRCm39) |
missense |
probably null |
0.99 |
IGL01544:Cep350
|
APN |
1 |
155,828,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01616:Cep350
|
APN |
1 |
155,828,993 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01695:Cep350
|
APN |
1 |
155,819,904 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01902:Cep350
|
APN |
1 |
155,737,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01977:Cep350
|
APN |
1 |
155,787,714 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02388:Cep350
|
APN |
1 |
155,829,499 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02475:Cep350
|
APN |
1 |
155,738,341 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02528:Cep350
|
APN |
1 |
155,770,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02598:Cep350
|
APN |
1 |
155,738,713 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02676:Cep350
|
APN |
1 |
155,737,977 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02728:Cep350
|
APN |
1 |
155,828,968 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02744:Cep350
|
APN |
1 |
155,807,279 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02817:Cep350
|
APN |
1 |
155,804,588 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02892:Cep350
|
APN |
1 |
155,744,552 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03156:Cep350
|
APN |
1 |
155,733,788 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03166:Cep350
|
APN |
1 |
155,739,346 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL03216:Cep350
|
APN |
1 |
155,736,373 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03268:Cep350
|
APN |
1 |
155,829,295 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03358:Cep350
|
APN |
1 |
155,804,285 (GRCm39) |
missense |
probably benign |
|
primed
|
UTSW |
1 |
155,829,334 (GRCm39) |
missense |
probably damaging |
0.98 |
stoked
|
UTSW |
1 |
155,791,321 (GRCm39) |
missense |
probably benign |
0.03 |
NA:Cep350
|
UTSW |
1 |
155,834,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Cep350
|
UTSW |
1 |
155,804,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Cep350
|
UTSW |
1 |
155,804,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Cep350
|
UTSW |
1 |
155,786,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R0066:Cep350
|
UTSW |
1 |
155,786,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R0172:Cep350
|
UTSW |
1 |
155,829,193 (GRCm39) |
missense |
probably benign |
0.00 |
R0365:Cep350
|
UTSW |
1 |
155,782,317 (GRCm39) |
missense |
probably benign |
0.00 |
R0472:Cep350
|
UTSW |
1 |
155,790,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R0502:Cep350
|
UTSW |
1 |
155,776,629 (GRCm39) |
splice site |
probably null |
|
R0538:Cep350
|
UTSW |
1 |
155,724,366 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0547:Cep350
|
UTSW |
1 |
155,777,181 (GRCm39) |
splice site |
probably null |
|
R0565:Cep350
|
UTSW |
1 |
155,836,941 (GRCm39) |
splice site |
probably benign |
|
R0607:Cep350
|
UTSW |
1 |
155,747,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Cep350
|
UTSW |
1 |
155,816,458 (GRCm39) |
splice site |
probably null |
|
R0675:Cep350
|
UTSW |
1 |
155,835,499 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0828:Cep350
|
UTSW |
1 |
155,828,992 (GRCm39) |
missense |
probably benign |
0.00 |
R0863:Cep350
|
UTSW |
1 |
155,737,981 (GRCm39) |
missense |
probably benign |
0.00 |
R0969:Cep350
|
UTSW |
1 |
155,816,572 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1102:Cep350
|
UTSW |
1 |
155,807,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1186:Cep350
|
UTSW |
1 |
155,751,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R1552:Cep350
|
UTSW |
1 |
155,786,484 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1560:Cep350
|
UTSW |
1 |
155,804,825 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1698:Cep350
|
UTSW |
1 |
155,829,104 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1729:Cep350
|
UTSW |
1 |
155,787,727 (GRCm39) |
missense |
probably benign |
0.17 |
R1735:Cep350
|
UTSW |
1 |
155,828,960 (GRCm39) |
missense |
probably damaging |
0.99 |
R1740:Cep350
|
UTSW |
1 |
155,804,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Cep350
|
UTSW |
1 |
155,804,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R1844:Cep350
|
UTSW |
1 |
155,724,374 (GRCm39) |
missense |
probably damaging |
0.99 |
R1848:Cep350
|
UTSW |
1 |
155,829,397 (GRCm39) |
missense |
probably benign |
0.28 |
R1988:Cep350
|
UTSW |
1 |
155,808,850 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2008:Cep350
|
UTSW |
1 |
155,790,467 (GRCm39) |
missense |
probably benign |
0.16 |
R2241:Cep350
|
UTSW |
1 |
155,834,302 (GRCm39) |
splice site |
probably null |
|
R2245:Cep350
|
UTSW |
1 |
155,754,766 (GRCm39) |
missense |
probably benign |
0.10 |
R2402:Cep350
|
UTSW |
1 |
155,738,882 (GRCm39) |
missense |
probably benign |
|
R2566:Cep350
|
UTSW |
1 |
155,835,464 (GRCm39) |
critical splice donor site |
probably null |
|
R3160:Cep350
|
UTSW |
1 |
155,738,910 (GRCm39) |
missense |
probably benign |
0.00 |
R3769:Cep350
|
UTSW |
1 |
155,828,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R4035:Cep350
|
UTSW |
1 |
155,835,541 (GRCm39) |
missense |
probably benign |
0.06 |
R4158:Cep350
|
UTSW |
1 |
155,808,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R4160:Cep350
|
UTSW |
1 |
155,808,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R4213:Cep350
|
UTSW |
1 |
155,811,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R4483:Cep350
|
UTSW |
1 |
155,802,214 (GRCm39) |
missense |
probably benign |
0.01 |
R4648:Cep350
|
UTSW |
1 |
155,778,344 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4694:Cep350
|
UTSW |
1 |
155,804,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4836:Cep350
|
UTSW |
1 |
155,804,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:Cep350
|
UTSW |
1 |
155,804,240 (GRCm39) |
missense |
probably benign |
0.00 |
R4969:Cep350
|
UTSW |
1 |
155,736,025 (GRCm39) |
missense |
probably damaging |
0.99 |
R5014:Cep350
|
UTSW |
1 |
155,803,952 (GRCm39) |
missense |
probably benign |
0.00 |
R5027:Cep350
|
UTSW |
1 |
155,809,100 (GRCm39) |
missense |
probably benign |
0.01 |
R5144:Cep350
|
UTSW |
1 |
155,786,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R5153:Cep350
|
UTSW |
1 |
155,811,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R5165:Cep350
|
UTSW |
1 |
155,804,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5182:Cep350
|
UTSW |
1 |
155,733,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R5445:Cep350
|
UTSW |
1 |
155,770,469 (GRCm39) |
missense |
probably benign |
0.01 |
R5738:Cep350
|
UTSW |
1 |
155,741,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R5809:Cep350
|
UTSW |
1 |
155,809,087 (GRCm39) |
missense |
probably damaging |
0.98 |
R5855:Cep350
|
UTSW |
1 |
155,829,508 (GRCm39) |
missense |
probably benign |
0.00 |
R6103:Cep350
|
UTSW |
1 |
155,800,322 (GRCm39) |
missense |
probably benign |
0.05 |
R6139:Cep350
|
UTSW |
1 |
155,829,025 (GRCm39) |
missense |
probably benign |
0.03 |
R6285:Cep350
|
UTSW |
1 |
155,829,120 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6430:Cep350
|
UTSW |
1 |
155,770,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R6446:Cep350
|
UTSW |
1 |
155,737,900 (GRCm39) |
missense |
probably benign |
|
R6520:Cep350
|
UTSW |
1 |
155,809,082 (GRCm39) |
missense |
probably benign |
0.02 |
R6712:Cep350
|
UTSW |
1 |
155,733,852 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6940:Cep350
|
UTSW |
1 |
155,804,297 (GRCm39) |
missense |
probably benign |
0.01 |
R7020:Cep350
|
UTSW |
1 |
155,804,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R7056:Cep350
|
UTSW |
1 |
155,724,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7141:Cep350
|
UTSW |
1 |
155,790,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R7215:Cep350
|
UTSW |
1 |
155,770,453 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7247:Cep350
|
UTSW |
1 |
155,786,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R7272:Cep350
|
UTSW |
1 |
155,829,334 (GRCm39) |
missense |
probably damaging |
0.98 |
R7336:Cep350
|
UTSW |
1 |
155,738,022 (GRCm39) |
missense |
probably benign |
0.17 |
R7361:Cep350
|
UTSW |
1 |
155,777,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R7390:Cep350
|
UTSW |
1 |
155,741,833 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7402:Cep350
|
UTSW |
1 |
155,803,961 (GRCm39) |
missense |
probably benign |
0.00 |
R7428:Cep350
|
UTSW |
1 |
155,770,365 (GRCm39) |
missense |
probably benign |
0.00 |
R7440:Cep350
|
UTSW |
1 |
155,816,518 (GRCm39) |
missense |
probably damaging |
0.98 |
R7520:Cep350
|
UTSW |
1 |
155,791,375 (GRCm39) |
missense |
probably benign |
0.05 |
R7529:Cep350
|
UTSW |
1 |
155,737,669 (GRCm39) |
missense |
probably benign |
0.08 |
R7635:Cep350
|
UTSW |
1 |
155,754,767 (GRCm39) |
nonsense |
probably null |
|
R7806:Cep350
|
UTSW |
1 |
155,737,809 (GRCm39) |
missense |
probably benign |
0.00 |
R8100:Cep350
|
UTSW |
1 |
155,829,148 (GRCm39) |
missense |
probably damaging |
0.97 |
R8192:Cep350
|
UTSW |
1 |
155,816,529 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8193:Cep350
|
UTSW |
1 |
155,737,825 (GRCm39) |
missense |
probably benign |
0.01 |
R8351:Cep350
|
UTSW |
1 |
155,747,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R8406:Cep350
|
UTSW |
1 |
155,798,164 (GRCm39) |
missense |
probably benign |
0.00 |
R8451:Cep350
|
UTSW |
1 |
155,747,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R8467:Cep350
|
UTSW |
1 |
155,791,321 (GRCm39) |
missense |
probably benign |
0.03 |
R8543:Cep350
|
UTSW |
1 |
155,738,122 (GRCm39) |
missense |
probably damaging |
0.98 |
R8714:Cep350
|
UTSW |
1 |
155,736,477 (GRCm39) |
missense |
probably damaging |
0.98 |
R8810:Cep350
|
UTSW |
1 |
155,803,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R8837:Cep350
|
UTSW |
1 |
155,737,518 (GRCm39) |
missense |
probably benign |
0.09 |
R8933:Cep350
|
UTSW |
1 |
155,739,161 (GRCm39) |
missense |
probably benign |
0.01 |
R9043:Cep350
|
UTSW |
1 |
155,773,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R9050:Cep350
|
UTSW |
1 |
155,738,687 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9067:Cep350
|
UTSW |
1 |
155,737,485 (GRCm39) |
missense |
probably benign |
0.00 |
R9105:Cep350
|
UTSW |
1 |
155,835,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R9295:Cep350
|
UTSW |
1 |
155,738,051 (GRCm39) |
nonsense |
probably null |
|
R9304:Cep350
|
UTSW |
1 |
155,829,464 (GRCm39) |
missense |
probably damaging |
0.98 |
R9456:Cep350
|
UTSW |
1 |
155,744,457 (GRCm39) |
missense |
probably benign |
0.00 |
R9575:Cep350
|
UTSW |
1 |
155,751,113 (GRCm39) |
missense |
probably benign |
0.03 |
R9715:Cep350
|
UTSW |
1 |
155,751,107 (GRCm39) |
missense |
probably benign |
0.00 |
R9749:Cep350
|
UTSW |
1 |
155,828,985 (GRCm39) |
missense |
probably benign |
0.02 |
R9758:Cep350
|
UTSW |
1 |
155,770,433 (GRCm39) |
missense |
probably damaging |
0.96 |
R9767:Cep350
|
UTSW |
1 |
155,739,018 (GRCm39) |
missense |
probably benign |
0.01 |
RF020:Cep350
|
UTSW |
1 |
155,791,224 (GRCm39) |
missense |
probably benign |
0.34 |
X0018:Cep350
|
UTSW |
1 |
155,829,032 (GRCm39) |
missense |
probably benign |
0.13 |
|