Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
A |
G |
9: 46,221,552 (GRCm39) |
|
probably benign |
Het |
4933411K16Rik |
T |
C |
19: 42,041,489 (GRCm39) |
Y207H |
probably damaging |
Het |
Abcc1 |
T |
A |
16: 14,266,298 (GRCm39) |
L832Q |
probably damaging |
Het |
Acan |
T |
A |
7: 78,750,552 (GRCm39) |
H1774Q |
probably benign |
Het |
Adss2 |
T |
C |
1: 177,599,760 (GRCm39) |
T275A |
probably benign |
Het |
Ano5 |
G |
A |
7: 51,233,523 (GRCm39) |
R595H |
probably damaging |
Het |
Araf |
G |
T |
X: 20,725,943 (GRCm39) |
R522L |
probably damaging |
Het |
Arhgef28 |
C |
T |
13: 98,102,054 (GRCm39) |
V807I |
possibly damaging |
Het |
Bin1 |
T |
C |
18: 32,545,757 (GRCm39) |
I103T |
probably damaging |
Het |
C4b |
C |
T |
17: 34,958,995 (GRCm39) |
R478Q |
probably benign |
Het |
Cacna1b |
G |
A |
2: 24,568,047 (GRCm39) |
P1015S |
probably benign |
Het |
Capn1 |
A |
G |
19: 6,057,528 (GRCm39) |
|
probably null |
Het |
Cfap126 |
T |
C |
1: 170,953,386 (GRCm39) |
|
probably benign |
Het |
Chn1 |
T |
C |
2: 73,509,951 (GRCm39) |
|
probably benign |
Het |
Cldn8 |
T |
C |
16: 88,359,289 (GRCm39) |
E212G |
probably benign |
Het |
Cpb1 |
T |
C |
3: 20,317,696 (GRCm39) |
N249S |
probably damaging |
Het |
Cxcr6 |
A |
T |
9: 123,639,412 (GRCm39) |
I138F |
probably benign |
Het |
Dab2ip |
G |
A |
2: 35,608,803 (GRCm39) |
R579H |
probably damaging |
Het |
Dcaf8 |
T |
C |
1: 172,021,422 (GRCm39) |
M538T |
probably benign |
Het |
Dhrs4 |
T |
G |
14: 55,725,107 (GRCm39) |
L201V |
probably damaging |
Het |
Dnah12 |
C |
T |
14: 26,431,403 (GRCm39) |
A407V |
probably benign |
Het |
Elavl3 |
T |
A |
9: 21,937,461 (GRCm39) |
|
probably benign |
Het |
Elp4 |
T |
C |
2: 105,662,506 (GRCm39) |
H88R |
probably benign |
Het |
Ercc3 |
T |
C |
18: 32,394,350 (GRCm39) |
|
probably benign |
Het |
Eri1 |
A |
G |
8: 35,936,335 (GRCm39) |
S329P |
possibly damaging |
Het |
Erich2 |
A |
T |
2: 70,343,117 (GRCm39) |
|
probably benign |
Het |
Esyt1 |
A |
G |
10: 128,348,297 (GRCm39) |
S864P |
possibly damaging |
Het |
Fam170b |
A |
G |
14: 32,557,588 (GRCm39) |
E141G |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,486,427 (GRCm39) |
Y3304C |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,151,415 (GRCm39) |
T2531A |
probably benign |
Het |
Fgfr3 |
T |
C |
5: 33,887,094 (GRCm39) |
V166A |
probably damaging |
Het |
Glt8d2 |
T |
C |
10: 82,495,372 (GRCm39) |
D194G |
probably damaging |
Het |
Gpr89 |
A |
G |
3: 96,812,526 (GRCm39) |
I5T |
probably benign |
Het |
Gpx6 |
A |
T |
13: 21,503,090 (GRCm39) |
H168L |
probably benign |
Het |
Gusb |
T |
C |
5: 130,027,385 (GRCm39) |
T307A |
probably benign |
Het |
Hjurp |
A |
T |
1: 88,202,772 (GRCm39) |
Y71N |
possibly damaging |
Het |
Ifngr1 |
A |
G |
10: 19,477,193 (GRCm39) |
D118G |
probably benign |
Het |
Ipcef1 |
A |
T |
10: 6,885,173 (GRCm39) |
|
probably null |
Het |
Kbtbd3 |
A |
T |
9: 4,330,276 (GRCm39) |
T217S |
probably benign |
Het |
Kmt5a |
GAA |
GA |
5: 124,597,948 (GRCm39) |
|
probably null |
Het |
Lrp1 |
T |
C |
10: 127,374,880 (GRCm39) |
D4526G |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 42,213,674 (GRCm39) |
V46D |
probably damaging |
Het |
Lsm8 |
T |
A |
6: 18,849,658 (GRCm39) |
M22K |
probably benign |
Het |
Map1lc3b |
C |
T |
8: 122,323,339 (GRCm39) |
R70C |
possibly damaging |
Het |
Meiob |
T |
A |
17: 25,032,026 (GRCm39) |
S14T |
possibly damaging |
Het |
Mkx |
G |
T |
18: 6,992,330 (GRCm39) |
Y183* |
probably null |
Het |
Mrs2 |
T |
C |
13: 25,189,017 (GRCm39) |
Y99C |
probably benign |
Het |
Mycbpap |
T |
C |
11: 94,396,387 (GRCm39) |
K151R |
probably benign |
Het |
Neb |
T |
G |
2: 52,218,746 (GRCm39) |
Q88P |
probably damaging |
Het |
Noc4l |
T |
A |
5: 110,797,944 (GRCm39) |
H319L |
probably damaging |
Het |
Nt5c2 |
G |
A |
19: 46,893,417 (GRCm39) |
T122I |
probably damaging |
Het |
Nuggc |
A |
T |
14: 65,861,582 (GRCm39) |
N476I |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,921,862 (GRCm39) |
H5978L |
probably benign |
Het |
Oc90 |
G |
T |
15: 65,748,370 (GRCm39) |
A412D |
probably damaging |
Het |
Or2l13b |
T |
A |
16: 19,349,133 (GRCm39) |
D179V |
possibly damaging |
Het |
Or3a4 |
A |
G |
11: 73,944,650 (GRCm39) |
*312Q |
probably null |
Het |
Or4a76 |
A |
G |
2: 89,460,358 (GRCm39) |
S295P |
possibly damaging |
Het |
Or5w18 |
T |
G |
2: 87,633,212 (GRCm39) |
S160A |
probably benign |
Het |
Or7a42 |
T |
A |
10: 78,791,682 (GRCm39) |
S214R |
probably benign |
Het |
Or8k33 |
A |
T |
2: 86,384,096 (GRCm39) |
V124E |
probably damaging |
Het |
Pdzrn3 |
A |
T |
6: 101,127,930 (GRCm39) |
V912E |
probably benign |
Het |
Phactr1 |
T |
A |
13: 43,248,466 (GRCm39) |
Y387N |
probably damaging |
Het |
Picalm |
T |
A |
7: 89,779,859 (GRCm39) |
C27S |
probably benign |
Het |
Pkd1l1 |
T |
A |
11: 8,891,077 (GRCm39) |
I314F |
possibly damaging |
Het |
Pold2 |
T |
C |
11: 5,824,175 (GRCm39) |
E210G |
possibly damaging |
Het |
Ptprz1 |
C |
T |
6: 23,049,523 (GRCm39) |
|
probably benign |
Het |
Rac1 |
G |
T |
5: 143,493,093 (GRCm39) |
A165E |
probably damaging |
Het |
Rpap3 |
G |
T |
15: 97,584,364 (GRCm39) |
T360K |
possibly damaging |
Het |
Scn9a |
G |
A |
2: 66,357,232 (GRCm39) |
T1012I |
probably benign |
Het |
Sdad1 |
A |
G |
5: 92,457,682 (GRCm39) |
I20T |
possibly damaging |
Het |
Setbp1 |
T |
G |
18: 78,903,127 (GRCm39) |
K180T |
probably damaging |
Het |
Sgpl1 |
T |
C |
10: 60,938,368 (GRCm39) |
N475S |
probably damaging |
Het |
Shroom3 |
T |
C |
5: 93,090,693 (GRCm39) |
S1148P |
possibly damaging |
Het |
Sin3a |
T |
A |
9: 57,026,442 (GRCm39) |
H1119Q |
possibly damaging |
Het |
Slc26a7 |
T |
A |
4: 14,506,489 (GRCm39) |
Y620F |
probably benign |
Het |
Slc4a1 |
T |
C |
11: 102,251,997 (GRCm39) |
I36V |
probably benign |
Het |
Smarca2 |
C |
G |
19: 26,608,501 (GRCm39) |
P263A |
possibly damaging |
Het |
Sp100 |
T |
C |
1: 85,591,242 (GRCm39) |
|
probably benign |
Het |
Spag6l |
A |
G |
16: 16,598,478 (GRCm39) |
|
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,071,498 (GRCm39) |
N1491S |
probably damaging |
Het |
Tbl1xr1 |
T |
G |
3: 22,245,115 (GRCm39) |
V155G |
possibly damaging |
Het |
Tmc1 |
A |
G |
19: 20,845,719 (GRCm39) |
I168T |
probably damaging |
Het |
Tmem87b |
G |
A |
2: 128,668,313 (GRCm39) |
|
probably null |
Het |
Tnfrsf9 |
T |
A |
4: 151,017,561 (GRCm39) |
|
probably null |
Het |
Tnni3k |
T |
C |
3: 154,645,295 (GRCm39) |
D530G |
probably damaging |
Het |
Vmn1r209 |
G |
A |
13: 22,989,934 (GRCm39) |
S252F |
probably damaging |
Het |
Zbtb3 |
A |
T |
19: 8,780,714 (GRCm39) |
N109I |
probably damaging |
Het |
Zdhhc17 |
T |
G |
10: 110,782,071 (GRCm39) |
H541P |
probably damaging |
Het |
Zfp84 |
A |
G |
7: 29,476,039 (GRCm39) |
I244V |
possibly damaging |
Het |
Zyx |
A |
G |
6: 42,333,246 (GRCm39) |
Y393C |
probably damaging |
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 |
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 |
|
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 |
|
|