Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
A |
12: 71,236,187 (GRCm39) |
M1179I |
probably benign |
Het |
6430550D23Rik |
T |
C |
2: 155,845,351 (GRCm39) |
T18A |
possibly damaging |
Het |
Acox2 |
T |
C |
14: 8,230,166 (GRCm38) |
N659S |
probably damaging |
Het |
Agk |
T |
C |
6: 40,353,212 (GRCm39) |
V192A |
possibly damaging |
Het |
Ap3b1 |
T |
A |
13: 94,664,666 (GRCm39) |
|
probably null |
Het |
Bche |
T |
A |
3: 73,608,454 (GRCm39) |
D324V |
probably damaging |
Het |
Bsn |
A |
G |
9: 107,991,939 (GRCm39) |
I1271T |
possibly damaging |
Het |
Capn12 |
T |
C |
7: 28,582,246 (GRCm39) |
L120P |
probably damaging |
Het |
Ckap4 |
T |
C |
10: 84,364,331 (GRCm39) |
E244G |
probably damaging |
Het |
Clcn7 |
T |
C |
17: 25,375,796 (GRCm39) |
Y545H |
probably damaging |
Het |
Cmya5 |
T |
A |
13: 93,234,780 (GRCm39) |
T103S |
possibly damaging |
Het |
Cplane1 |
A |
T |
15: 8,281,711 (GRCm39) |
E2850V |
unknown |
Het |
Cpne9 |
G |
A |
6: 113,261,406 (GRCm39) |
V121M |
possibly damaging |
Het |
Csmd2 |
T |
A |
4: 128,377,249 (GRCm39) |
I2043N |
|
Het |
Disc1 |
A |
G |
8: 125,814,243 (GRCm39) |
T36A |
probably benign |
Het |
Disp2 |
T |
C |
2: 118,621,391 (GRCm39) |
Y708H |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,670,793 (GRCm39) |
V635A |
probably benign |
Het |
Dnah3 |
A |
T |
7: 119,570,438 (GRCm39) |
|
probably null |
Het |
Dync1li1 |
A |
G |
9: 114,538,345 (GRCm39) |
H234R |
possibly damaging |
Het |
Egfr |
T |
C |
11: 16,839,966 (GRCm39) |
V660A |
possibly damaging |
Het |
Epb42 |
T |
C |
2: 120,858,200 (GRCm39) |
R253G |
possibly damaging |
Het |
Fat2 |
T |
A |
11: 55,202,247 (GRCm39) |
T276S |
probably benign |
Het |
Fcho2 |
A |
G |
13: 98,901,011 (GRCm39) |
|
probably null |
Het |
Ginm1 |
A |
T |
10: 7,655,119 (GRCm39) |
I41N |
probably damaging |
Het |
Gm4744 |
A |
G |
6: 40,927,367 (GRCm39) |
|
probably benign |
Het |
Gm49368 |
C |
T |
7: 127,711,398 (GRCm39) |
R701C |
probably damaging |
Het |
Gpr37 |
T |
A |
6: 25,688,207 (GRCm39) |
I297F |
probably benign |
Het |
Gprc5a |
T |
A |
6: 135,056,342 (GRCm39) |
I263N |
possibly damaging |
Het |
Gys2 |
A |
T |
6: 142,400,177 (GRCm39) |
S345T |
probably benign |
Het |
Hk2 |
T |
C |
6: 82,719,896 (GRCm39) |
M255V |
possibly damaging |
Het |
Ibtk |
A |
C |
9: 85,579,290 (GRCm39) |
S1202A |
possibly damaging |
Het |
Il23r |
T |
G |
6: 67,400,965 (GRCm39) |
D455A |
probably benign |
Het |
Irs2 |
T |
A |
8: 11,056,522 (GRCm39) |
K637* |
probably null |
Het |
Jak2 |
T |
C |
19: 29,260,946 (GRCm39) |
V314A |
probably benign |
Het |
Mei1 |
C |
T |
15: 81,966,824 (GRCm39) |
|
probably benign |
Het |
Mill1 |
T |
C |
7: 17,996,391 (GRCm39) |
M69T |
probably benign |
Het |
Mms22l |
T |
C |
4: 24,598,884 (GRCm39) |
|
probably null |
Het |
Mup8 |
C |
A |
4: 60,220,332 (GRCm39) |
Q133H |
probably benign |
Het |
Mup8 |
T |
A |
4: 60,220,333 (GRCm39) |
Q133L |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,429,055 (GRCm39) |
Y2374N |
probably damaging |
Het |
Nbeal1 |
A |
T |
1: 60,296,609 (GRCm39) |
K1166N |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,755,191 (GRCm39) |
R8S |
probably benign |
Het |
Nrcam |
C |
T |
12: 44,596,681 (GRCm39) |
Q25* |
probably null |
Het |
Nudt16 |
A |
C |
9: 105,008,760 (GRCm39) |
M47R |
probably damaging |
Het |
Nup62 |
T |
C |
7: 44,478,419 (GRCm39) |
S145P |
probably benign |
Het |
Or10d1 |
A |
G |
9: 39,483,761 (GRCm39) |
W265R |
probably benign |
Het |
Or4c117 |
T |
C |
2: 88,955,333 (GRCm39) |
I247M |
possibly damaging |
Het |
Osbpl1a |
A |
T |
18: 13,066,657 (GRCm39) |
V34D |
probably benign |
Het |
Otogl |
T |
A |
10: 107,712,782 (GRCm39) |
N521Y |
probably damaging |
Het |
Pcdhb14 |
T |
A |
18: 37,582,887 (GRCm39) |
D664E |
possibly damaging |
Het |
Pex5l |
T |
C |
3: 33,136,300 (GRCm39) |
|
probably benign |
Het |
Pkhd1 |
A |
G |
1: 20,632,639 (GRCm39) |
L592P |
probably damaging |
Het |
Plxdc2 |
A |
G |
2: 16,734,187 (GRCm39) |
H480R |
probably benign |
Het |
Rnf216 |
T |
A |
5: 143,065,991 (GRCm39) |
K532N |
probably damaging |
Het |
Schip1 |
C |
A |
3: 68,525,028 (GRCm39) |
Q358K |
probably damaging |
Het |
Sdc2 |
A |
T |
15: 33,028,233 (GRCm39) |
E117V |
possibly damaging |
Het |
Septin11 |
A |
T |
5: 93,319,323 (GRCm39) |
|
probably null |
Het |
Shprh |
A |
T |
10: 11,037,924 (GRCm39) |
E420V |
probably benign |
Het |
Ska1 |
T |
A |
18: 74,330,044 (GRCm39) |
H232L |
probably benign |
Het |
Slc36a4 |
A |
G |
9: 15,630,956 (GRCm39) |
N25S |
possibly damaging |
Het |
Slitrk3 |
G |
A |
3: 72,958,172 (GRCm39) |
T200M |
probably damaging |
Het |
Smad2 |
C |
T |
18: 76,421,084 (GRCm39) |
H138Y |
probably benign |
Het |
Snx21 |
T |
C |
2: 164,628,085 (GRCm39) |
S34P |
probably damaging |
Het |
Sos2 |
A |
G |
12: 69,695,359 (GRCm39) |
V126A |
probably damaging |
Het |
Srcap |
C |
T |
7: 127,129,966 (GRCm39) |
T596I |
probably damaging |
Het |
Stk31 |
T |
G |
6: 49,383,877 (GRCm39) |
|
probably null |
Het |
Stox1 |
T |
C |
10: 62,499,743 (GRCm39) |
D939G |
probably damaging |
Het |
Syne2 |
G |
T |
12: 76,108,553 (GRCm39) |
C979F |
possibly damaging |
Het |
Tanc2 |
C |
A |
11: 105,667,684 (GRCm39) |
N88K |
possibly damaging |
Het |
Tll2 |
A |
T |
19: 41,084,447 (GRCm39) |
V677E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,748,834 (GRCm39) |
T4072A |
probably benign |
Het |
Unc13b |
CAGAGC |
CAGAGCGAGAGC |
4: 43,177,341 (GRCm39) |
|
probably benign |
Het |
Unc13b |
CGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGC |
CGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGCCAGAGC |
4: 43,177,312 (GRCm39) |
|
probably benign |
Het |
Unc13b |
AGAGCC |
AGAGCCCGAGCC |
4: 43,177,330 (GRCm39) |
|
probably benign |
Het |
Vmn2r43 |
A |
T |
7: 8,258,253 (GRCm39) |
F320Y |
possibly damaging |
Het |
Zscan4f |
G |
T |
7: 11,135,205 (GRCm39) |
G204* |
probably null |
Het |
|
Other mutations in Cep290 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00430:Cep290
|
APN |
10 |
100,344,586 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00499:Cep290
|
APN |
10 |
100,379,189 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00547:Cep290
|
APN |
10 |
100,346,570 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00573:Cep290
|
APN |
10 |
100,376,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00646:Cep290
|
APN |
10 |
100,337,016 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00755:Cep290
|
APN |
10 |
100,366,966 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00835:Cep290
|
APN |
10 |
100,399,242 (GRCm39) |
nonsense |
probably null |
|
IGL00846:Cep290
|
APN |
10 |
100,376,195 (GRCm39) |
splice site |
probably benign |
|
IGL00985:Cep290
|
APN |
10 |
100,403,023 (GRCm39) |
splice site |
probably benign |
|
IGL01687:Cep290
|
APN |
10 |
100,336,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01782:Cep290
|
APN |
10 |
100,380,987 (GRCm39) |
nonsense |
probably null |
|
IGL02010:Cep290
|
APN |
10 |
100,397,207 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02010:Cep290
|
APN |
10 |
100,344,569 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02036:Cep290
|
APN |
10 |
100,393,962 (GRCm39) |
nonsense |
probably null |
|
IGL02039:Cep290
|
APN |
10 |
100,350,464 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02532:Cep290
|
APN |
10 |
100,380,927 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02950:Cep290
|
APN |
10 |
100,376,191 (GRCm39) |
splice site |
probably benign |
|
IGL03105:Cep290
|
APN |
10 |
100,387,686 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03179:Cep290
|
APN |
10 |
100,403,950 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL03271:Cep290
|
APN |
10 |
100,373,663 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03401:Cep290
|
APN |
10 |
100,336,127 (GRCm39) |
missense |
probably benign |
0.27 |
PIT4687001:Cep290
|
UTSW |
10 |
100,373,453 (GRCm39) |
missense |
probably benign |
0.28 |
R0025:Cep290
|
UTSW |
10 |
100,373,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R0127:Cep290
|
UTSW |
10 |
100,372,787 (GRCm39) |
splice site |
probably benign |
|
R0254:Cep290
|
UTSW |
10 |
100,350,436 (GRCm39) |
missense |
probably benign |
0.31 |
R0295:Cep290
|
UTSW |
10 |
100,373,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R0371:Cep290
|
UTSW |
10 |
100,354,426 (GRCm39) |
splice site |
probably benign |
|
R0390:Cep290
|
UTSW |
10 |
100,344,620 (GRCm39) |
missense |
probably benign |
0.09 |
R0399:Cep290
|
UTSW |
10 |
100,390,262 (GRCm39) |
splice site |
probably benign |
|
R0413:Cep290
|
UTSW |
10 |
100,359,176 (GRCm39) |
nonsense |
probably null |
|
R0427:Cep290
|
UTSW |
10 |
100,352,041 (GRCm39) |
missense |
probably benign |
0.01 |
R0472:Cep290
|
UTSW |
10 |
100,387,317 (GRCm39) |
missense |
probably benign |
0.19 |
R0485:Cep290
|
UTSW |
10 |
100,385,206 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0635:Cep290
|
UTSW |
10 |
100,328,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Cep290
|
UTSW |
10 |
100,404,675 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0972:Cep290
|
UTSW |
10 |
100,354,624 (GRCm39) |
missense |
probably benign |
0.08 |
R1238:Cep290
|
UTSW |
10 |
100,353,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R1297:Cep290
|
UTSW |
10 |
100,374,962 (GRCm39) |
splice site |
probably benign |
|
R1368:Cep290
|
UTSW |
10 |
100,330,828 (GRCm39) |
splice site |
probably benign |
|
R1394:Cep290
|
UTSW |
10 |
100,373,391 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1437:Cep290
|
UTSW |
10 |
100,407,963 (GRCm39) |
missense |
probably benign |
0.00 |
R1493:Cep290
|
UTSW |
10 |
100,398,043 (GRCm39) |
missense |
probably benign |
0.21 |
R1496:Cep290
|
UTSW |
10 |
100,374,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R1539:Cep290
|
UTSW |
10 |
100,332,690 (GRCm39) |
missense |
probably benign |
0.06 |
R1598:Cep290
|
UTSW |
10 |
100,385,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1616:Cep290
|
UTSW |
10 |
100,404,698 (GRCm39) |
missense |
probably benign |
|
R1712:Cep290
|
UTSW |
10 |
100,390,361 (GRCm39) |
missense |
probably benign |
0.02 |
R1753:Cep290
|
UTSW |
10 |
100,349,843 (GRCm39) |
missense |
probably benign |
|
R1773:Cep290
|
UTSW |
10 |
100,346,435 (GRCm39) |
missense |
probably benign |
|
R1775:Cep290
|
UTSW |
10 |
100,332,672 (GRCm39) |
missense |
probably damaging |
0.98 |
R1799:Cep290
|
UTSW |
10 |
100,352,058 (GRCm39) |
missense |
probably benign |
0.00 |
R1937:Cep290
|
UTSW |
10 |
100,333,815 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1991:Cep290
|
UTSW |
10 |
100,367,046 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2031:Cep290
|
UTSW |
10 |
100,348,262 (GRCm39) |
critical splice donor site |
probably null |
|
R2164:Cep290
|
UTSW |
10 |
100,354,657 (GRCm39) |
missense |
probably damaging |
0.96 |
R2393:Cep290
|
UTSW |
10 |
100,397,100 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2403:Cep290
|
UTSW |
10 |
100,373,299 (GRCm39) |
missense |
probably benign |
0.19 |
R3612:Cep290
|
UTSW |
10 |
100,377,443 (GRCm39) |
nonsense |
probably null |
|
R3800:Cep290
|
UTSW |
10 |
100,408,803 (GRCm39) |
missense |
probably damaging |
0.97 |
R4005:Cep290
|
UTSW |
10 |
100,374,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R4039:Cep290
|
UTSW |
10 |
100,348,263 (GRCm39) |
critical splice donor site |
probably null |
|
R4259:Cep290
|
UTSW |
10 |
100,350,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R4260:Cep290
|
UTSW |
10 |
100,350,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R4319:Cep290
|
UTSW |
10 |
100,374,909 (GRCm39) |
missense |
probably benign |
0.09 |
R4329:Cep290
|
UTSW |
10 |
100,373,530 (GRCm39) |
missense |
probably damaging |
0.98 |
R4573:Cep290
|
UTSW |
10 |
100,354,712 (GRCm39) |
missense |
probably benign |
|
R4614:Cep290
|
UTSW |
10 |
100,395,549 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4614:Cep290
|
UTSW |
10 |
100,344,602 (GRCm39) |
missense |
probably benign |
|
R4708:Cep290
|
UTSW |
10 |
100,359,126 (GRCm39) |
missense |
probably benign |
0.02 |
R4727:Cep290
|
UTSW |
10 |
100,399,132 (GRCm39) |
missense |
probably benign |
0.05 |
R4825:Cep290
|
UTSW |
10 |
100,324,210 (GRCm39) |
missense |
probably damaging |
0.96 |
R4839:Cep290
|
UTSW |
10 |
100,344,648 (GRCm39) |
missense |
probably damaging |
0.99 |
R4858:Cep290
|
UTSW |
10 |
100,330,773 (GRCm39) |
missense |
probably benign |
0.31 |
R4871:Cep290
|
UTSW |
10 |
100,384,776 (GRCm39) |
missense |
probably benign |
0.22 |
R5094:Cep290
|
UTSW |
10 |
100,402,892 (GRCm39) |
missense |
probably damaging |
0.97 |
R5103:Cep290
|
UTSW |
10 |
100,374,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R5499:Cep290
|
UTSW |
10 |
100,373,515 (GRCm39) |
missense |
probably damaging |
0.99 |
R5505:Cep290
|
UTSW |
10 |
100,335,048 (GRCm39) |
critical splice donor site |
probably null |
|
R5615:Cep290
|
UTSW |
10 |
100,367,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R5815:Cep290
|
UTSW |
10 |
100,393,970 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5883:Cep290
|
UTSW |
10 |
100,359,261 (GRCm39) |
missense |
probably benign |
0.44 |
R5889:Cep290
|
UTSW |
10 |
100,334,936 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5928:Cep290
|
UTSW |
10 |
100,387,692 (GRCm39) |
missense |
probably damaging |
0.99 |
R5992:Cep290
|
UTSW |
10 |
100,379,183 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6000:Cep290
|
UTSW |
10 |
100,377,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R6213:Cep290
|
UTSW |
10 |
100,359,222 (GRCm39) |
missense |
probably benign |
0.06 |
R6274:Cep290
|
UTSW |
10 |
100,366,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R6285:Cep290
|
UTSW |
10 |
100,359,191 (GRCm39) |
missense |
probably benign |
0.17 |
R6306:Cep290
|
UTSW |
10 |
100,367,028 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6593:Cep290
|
UTSW |
10 |
100,344,638 (GRCm39) |
missense |
probably benign |
0.01 |
R6649:Cep290
|
UTSW |
10 |
100,354,393 (GRCm39) |
missense |
probably benign |
0.28 |
R6692:Cep290
|
UTSW |
10 |
100,405,006 (GRCm39) |
splice site |
probably null |
|
R6788:Cep290
|
UTSW |
10 |
100,324,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R6847:Cep290
|
UTSW |
10 |
100,399,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R6947:Cep290
|
UTSW |
10 |
100,365,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R7035:Cep290
|
UTSW |
10 |
100,334,933 (GRCm39) |
missense |
probably benign |
0.07 |
R7073:Cep290
|
UTSW |
10 |
100,374,865 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7114:Cep290
|
UTSW |
10 |
100,379,220 (GRCm39) |
missense |
probably damaging |
0.98 |
R7256:Cep290
|
UTSW |
10 |
100,382,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R7258:Cep290
|
UTSW |
10 |
100,334,970 (GRCm39) |
missense |
probably benign |
0.01 |
R7311:Cep290
|
UTSW |
10 |
100,373,580 (GRCm39) |
missense |
probably damaging |
0.98 |
R7505:Cep290
|
UTSW |
10 |
100,352,127 (GRCm39) |
missense |
probably benign |
0.01 |
R7615:Cep290
|
UTSW |
10 |
100,328,543 (GRCm39) |
missense |
probably benign |
0.03 |
R7643:Cep290
|
UTSW |
10 |
100,373,415 (GRCm39) |
missense |
probably benign |
|
R7662:Cep290
|
UTSW |
10 |
100,373,665 (GRCm39) |
missense |
probably benign |
0.21 |
R7663:Cep290
|
UTSW |
10 |
100,390,398 (GRCm39) |
critical splice donor site |
probably null |
|
R7685:Cep290
|
UTSW |
10 |
100,375,919 (GRCm39) |
missense |
probably benign |
0.19 |
R7699:Cep290
|
UTSW |
10 |
100,376,231 (GRCm39) |
missense |
probably benign |
0.33 |
R7717:Cep290
|
UTSW |
10 |
100,328,543 (GRCm39) |
missense |
probably benign |
0.03 |
R7747:Cep290
|
UTSW |
10 |
100,394,038 (GRCm39) |
nonsense |
probably null |
|
R7843:Cep290
|
UTSW |
10 |
100,352,050 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7905:Cep290
|
UTSW |
10 |
100,390,352 (GRCm39) |
missense |
probably benign |
|
R8078:Cep290
|
UTSW |
10 |
100,408,749 (GRCm39) |
missense |
probably benign |
0.04 |
R8081:Cep290
|
UTSW |
10 |
100,394,038 (GRCm39) |
nonsense |
probably null |
|
R8094:Cep290
|
UTSW |
10 |
100,380,793 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8266:Cep290
|
UTSW |
10 |
100,395,533 (GRCm39) |
missense |
probably benign |
0.08 |
R8305:Cep290
|
UTSW |
10 |
100,380,796 (GRCm39) |
missense |
probably benign |
0.09 |
R8325:Cep290
|
UTSW |
10 |
100,353,670 (GRCm39) |
missense |
probably benign |
0.03 |
R8372:Cep290
|
UTSW |
10 |
100,385,203 (GRCm39) |
missense |
probably benign |
0.00 |
R8443:Cep290
|
UTSW |
10 |
100,331,706 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8497:Cep290
|
UTSW |
10 |
100,387,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R8778:Cep290
|
UTSW |
10 |
100,350,374 (GRCm39) |
nonsense |
probably null |
|
R8975:Cep290
|
UTSW |
10 |
100,349,782 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9146:Cep290
|
UTSW |
10 |
100,377,665 (GRCm39) |
missense |
probably benign |
0.44 |
R9264:Cep290
|
UTSW |
10 |
100,333,878 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9374:Cep290
|
UTSW |
10 |
100,372,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R9448:Cep290
|
UTSW |
10 |
100,395,546 (GRCm39) |
missense |
probably benign |
0.32 |
R9499:Cep290
|
UTSW |
10 |
100,372,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R9507:Cep290
|
UTSW |
10 |
100,330,785 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9539:Cep290
|
UTSW |
10 |
100,404,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9547:Cep290
|
UTSW |
10 |
100,380,841 (GRCm39) |
missense |
probably benign |
0.00 |
R9551:Cep290
|
UTSW |
10 |
100,372,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R9657:Cep290
|
UTSW |
10 |
100,351,003 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9731:Cep290
|
UTSW |
10 |
100,346,404 (GRCm39) |
missense |
probably damaging |
0.98 |
R9756:Cep290
|
UTSW |
10 |
100,352,034 (GRCm39) |
missense |
probably damaging |
0.97 |
R9777:Cep290
|
UTSW |
10 |
100,354,529 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Cep290
|
UTSW |
10 |
100,385,236 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1177:Cep290
|
UTSW |
10 |
100,374,859 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1177:Cep290
|
UTSW |
10 |
100,333,806 (GRCm39) |
missense |
probably benign |
|
|