Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933406P04Rik |
T |
C |
10: 20,187,087 (GRCm39) |
|
probably benign |
Het |
A1cf |
A |
G |
19: 31,912,175 (GRCm39) |
E430G |
probably damaging |
Het |
Aacs |
T |
A |
5: 125,561,590 (GRCm39) |
|
probably null |
Het |
Acot12 |
G |
A |
13: 91,920,886 (GRCm39) |
V331I |
probably benign |
Het |
Acp7 |
A |
G |
7: 28,310,503 (GRCm39) |
W445R |
probably damaging |
Het |
Actl11 |
C |
A |
9: 107,809,135 (GRCm39) |
Q1153K |
probably benign |
Het |
Actr8 |
A |
G |
14: 29,704,601 (GRCm39) |
T34A |
possibly damaging |
Het |
Ahnak |
A |
G |
19: 8,986,351 (GRCm39) |
D2545G |
possibly damaging |
Het |
Ap5z1 |
A |
G |
5: 142,457,991 (GRCm39) |
Y388C |
probably benign |
Het |
Apol7a |
C |
T |
15: 77,273,806 (GRCm39) |
G219S |
probably damaging |
Het |
Arid1b |
T |
A |
17: 5,389,569 (GRCm39) |
I1705N |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,966,058 (GRCm39) |
Q2669R |
probably benign |
Het |
Braf |
A |
T |
6: 39,620,067 (GRCm39) |
S504T |
probably benign |
Het |
Cbl |
A |
T |
9: 44,064,197 (GRCm39) |
Y780N |
probably damaging |
Het |
Cd86 |
T |
C |
16: 36,449,338 (GRCm39) |
I20V |
probably benign |
Het |
Ckmt2 |
G |
A |
13: 92,007,328 (GRCm39) |
R289C |
probably benign |
Het |
Col3a1 |
T |
C |
1: 45,367,648 (GRCm39) |
|
probably null |
Het |
Cyp4f16 |
T |
A |
17: 32,761,942 (GRCm39) |
Y163* |
probably null |
Het |
Dimt1 |
T |
C |
13: 107,089,958 (GRCm39) |
V227A |
possibly damaging |
Het |
Dnah6 |
A |
T |
6: 73,077,095 (GRCm39) |
M2338K |
probably benign |
Het |
Dock4 |
T |
G |
12: 40,719,044 (GRCm39) |
I274S |
probably damaging |
Het |
Enthd1 |
T |
C |
15: 80,336,586 (GRCm39) |
D616G |
probably damaging |
Het |
Fignl2 |
T |
C |
15: 100,951,997 (GRCm39) |
E95G |
probably damaging |
Het |
Foxn1 |
A |
G |
11: 78,249,692 (GRCm39) |
M611T |
probably benign |
Het |
Foxs1 |
T |
C |
2: 152,774,559 (GRCm39) |
S165G |
probably benign |
Het |
Fzd3 |
G |
T |
14: 65,472,956 (GRCm39) |
Q271K |
probably benign |
Het |
Hadhb |
A |
T |
5: 30,371,713 (GRCm39) |
I55F |
probably damaging |
Het |
Hipk3 |
G |
A |
2: 104,264,090 (GRCm39) |
Q824* |
probably null |
Het |
Hps1 |
G |
A |
19: 42,755,624 (GRCm39) |
R201W |
probably damaging |
Het |
Kif21b |
T |
C |
1: 136,099,423 (GRCm39) |
S1477P |
probably damaging |
Het |
Kif26a |
A |
T |
12: 112,123,680 (GRCm39) |
|
probably null |
Het |
Krt90 |
T |
C |
15: 101,469,026 (GRCm39) |
E172G |
possibly damaging |
Het |
Lama4 |
T |
G |
10: 38,951,446 (GRCm39) |
F1064V |
probably damaging |
Het |
Leng9 |
A |
G |
7: 4,151,902 (GRCm39) |
V258A |
probably benign |
Het |
Lgi2 |
A |
C |
5: 52,703,980 (GRCm39) |
V217G |
probably benign |
Het |
Lpgat1 |
T |
C |
1: 191,495,741 (GRCm39) |
I310T |
possibly damaging |
Het |
Ltbp3 |
A |
G |
19: 5,796,995 (GRCm39) |
Y374C |
probably damaging |
Het |
Magi2 |
C |
A |
5: 20,814,324 (GRCm39) |
T1075K |
probably damaging |
Het |
Man2c1 |
T |
C |
9: 57,042,793 (GRCm39) |
I221T |
probably benign |
Het |
Mydgf |
A |
G |
17: 56,486,415 (GRCm39) |
M72T |
possibly damaging |
Het |
Myo1b |
T |
C |
1: 51,815,474 (GRCm39) |
N624S |
probably damaging |
Het |
Myo5c |
T |
A |
9: 75,203,299 (GRCm39) |
M1465K |
probably damaging |
Het |
Nek4 |
A |
T |
14: 30,709,094 (GRCm39) |
D716V |
probably damaging |
Het |
Nfxl1 |
T |
A |
5: 72,686,380 (GRCm39) |
Q607L |
probably benign |
Het |
Nlrp9c |
A |
T |
7: 26,083,862 (GRCm39) |
D572E |
probably benign |
Het |
Nop14 |
G |
T |
5: 34,807,757 (GRCm39) |
Q402K |
possibly damaging |
Het |
Npy5r |
C |
G |
8: 67,134,052 (GRCm39) |
C247S |
probably damaging |
Het |
Nrap |
T |
A |
19: 56,378,255 (GRCm39) |
I19F |
probably damaging |
Het |
Or4c102 |
A |
G |
2: 88,422,352 (GRCm39) |
D68G |
probably damaging |
Het |
Or51t4 |
T |
A |
7: 102,597,721 (GRCm39) |
N16K |
probably damaging |
Het |
Or6z3 |
T |
G |
7: 6,463,744 (GRCm39) |
S79A |
probably damaging |
Het |
Pcdh9 |
A |
T |
14: 94,124,405 (GRCm39) |
Y588* |
probably null |
Het |
Ppp1r12a |
A |
G |
10: 108,096,728 (GRCm39) |
E183G |
probably damaging |
Het |
Ppp2r2b |
T |
A |
18: 42,821,375 (GRCm39) |
H261L |
probably benign |
Het |
Ptch1 |
G |
T |
13: 63,687,656 (GRCm39) |
T374K |
possibly damaging |
Het |
Ptpn13 |
A |
T |
5: 103,713,103 (GRCm39) |
N1742I |
possibly damaging |
Het |
Rab33a |
C |
T |
X: 47,608,521 (GRCm39) |
S15L |
probably benign |
Het |
Ralb |
T |
C |
1: 119,405,744 (GRCm39) |
Y75C |
probably damaging |
Het |
Rassf7 |
T |
A |
7: 140,796,645 (GRCm39) |
V2D |
probably damaging |
Het |
Rbm10 |
A |
G |
X: 20,512,230 (GRCm39) |
N397S |
probably benign |
Het |
Rbm15 |
T |
C |
3: 107,238,197 (GRCm39) |
T734A |
probably benign |
Het |
Rbm8a |
G |
T |
3: 96,539,046 (GRCm39) |
|
probably benign |
Het |
Rock2 |
T |
C |
12: 17,022,986 (GRCm39) |
I1095T |
probably benign |
Het |
Rxfp3 |
T |
A |
15: 11,036,389 (GRCm39) |
T328S |
probably damaging |
Het |
Sec31a |
T |
A |
5: 100,534,054 (GRCm39) |
K505N |
possibly damaging |
Het |
Selenof |
A |
G |
3: 144,302,642 (GRCm39) |
*122W |
probably null |
Het |
Sh3pxd2b |
T |
C |
11: 32,331,441 (GRCm39) |
M55T |
possibly damaging |
Het |
Slc15a2 |
T |
C |
16: 36,574,843 (GRCm39) |
D522G |
probably benign |
Het |
Slc2a1 |
T |
C |
4: 118,993,503 (GRCm39) |
F447L |
probably damaging |
Het |
Slc45a2 |
T |
A |
15: 11,022,214 (GRCm39) |
C319S |
probably null |
Het |
Smad4 |
T |
C |
18: 73,773,333 (GRCm39) |
D551G |
probably benign |
Het |
Smarcc2 |
A |
G |
10: 128,318,662 (GRCm39) |
Y648C |
probably damaging |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Stab2 |
A |
T |
10: 86,721,582 (GRCm39) |
|
probably null |
Het |
Tanc1 |
A |
G |
2: 59,615,731 (GRCm39) |
D246G |
probably damaging |
Het |
Tekt3 |
T |
G |
11: 62,978,024 (GRCm39) |
|
probably null |
Het |
Them5 |
G |
A |
3: 94,253,567 (GRCm39) |
|
probably null |
Het |
Tlr4 |
T |
A |
4: 66,757,717 (GRCm39) |
F170Y |
probably damaging |
Het |
Tmem214 |
T |
G |
5: 31,028,907 (GRCm39) |
Y165* |
probably null |
Het |
Tmem94 |
T |
C |
11: 115,686,971 (GRCm39) |
|
probably null |
Het |
Tom1l1 |
A |
G |
11: 90,547,177 (GRCm39) |
L301S |
possibly damaging |
Het |
Trpm3 |
A |
G |
19: 22,960,076 (GRCm39) |
E1237G |
probably damaging |
Het |
Ube2d1 |
C |
A |
10: 71,092,523 (GRCm39) |
C107F |
probably damaging |
Het |
Ugt3a1 |
C |
T |
15: 9,306,330 (GRCm39) |
R160* |
probably null |
Het |
Vcan |
G |
A |
13: 89,853,782 (GRCm39) |
P393S |
probably damaging |
Het |
Virma |
T |
C |
4: 11,544,954 (GRCm39) |
F1638L |
probably damaging |
Het |
Vmn1r31 |
G |
A |
6: 58,449,043 (GRCm39) |
T274I |
probably damaging |
Het |
Xylt2 |
C |
T |
11: 94,559,035 (GRCm39) |
S445N |
probably damaging |
Het |
Zfp457 |
A |
G |
13: 67,444,375 (GRCm39) |
F43L |
possibly damaging |
Het |
Zfp879 |
T |
A |
11: 50,723,473 (GRCm39) |
M455L |
probably benign |
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 |
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 |
|
R7757:Cep290
|
UTSW |
10 |
100,399,296 (GRCm39) |
missense |
probably benign |
|
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 |
|
|