Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010109A12Rik |
G |
A |
5: 93,354,416 (GRCm39) |
|
probably null |
Het |
2410004P03Rik |
C |
T |
12: 17,057,149 (GRCm39) |
S116N |
probably damaging |
Het |
3425401B19Rik |
T |
C |
14: 32,385,026 (GRCm39) |
D313G |
possibly damaging |
Het |
AA986860 |
A |
G |
1: 130,671,284 (GRCm39) |
E502G |
possibly damaging |
Het |
Adamts20 |
T |
A |
15: 94,189,468 (GRCm39) |
K1462* |
probably null |
Het |
Adgrg6 |
A |
C |
10: 14,326,321 (GRCm39) |
|
probably null |
Het |
Ankrd13d |
G |
A |
19: 4,331,013 (GRCm39) |
H165Y |
probably damaging |
Het |
Arap3 |
T |
C |
18: 38,121,941 (GRCm39) |
|
probably null |
Het |
Arhgap33 |
A |
G |
7: 30,223,560 (GRCm39) |
V823A |
probably damaging |
Het |
Aup1 |
C |
A |
6: 83,031,776 (GRCm39) |
P34T |
unknown |
Het |
Bcl2l2 |
C |
T |
14: 55,121,836 (GRCm39) |
|
probably benign |
Het |
Bicc1 |
T |
C |
10: 70,782,823 (GRCm39) |
T515A |
probably benign |
Het |
Ccdc73 |
A |
C |
2: 104,759,901 (GRCm39) |
K106Q |
probably damaging |
Het |
Celsr3 |
G |
A |
9: 108,707,177 (GRCm39) |
R1220Q |
possibly damaging |
Het |
Cercam |
A |
G |
2: 29,761,298 (GRCm39) |
D104G |
probably benign |
Het |
Champ1 |
A |
G |
8: 13,929,990 (GRCm39) |
H716R |
probably damaging |
Het |
Cntrl |
A |
T |
2: 35,006,810 (GRCm39) |
I159F |
probably damaging |
Het |
Col11a1 |
T |
C |
3: 113,896,221 (GRCm39) |
I507T |
unknown |
Het |
Cped1 |
T |
C |
6: 22,143,973 (GRCm39) |
I573T |
probably damaging |
Het |
Crot |
C |
T |
5: 9,018,869 (GRCm39) |
|
probably null |
Het |
D1Pas1 |
T |
A |
1: 186,700,874 (GRCm39) |
S268T |
probably benign |
Het |
Efcab3 |
T |
G |
11: 104,733,429 (GRCm39) |
I2011S |
probably damaging |
Het |
Erich6 |
A |
G |
3: 58,526,349 (GRCm39) |
V551A |
probably damaging |
Het |
Fbxo32 |
T |
C |
15: 58,054,757 (GRCm39) |
N192S |
probably damaging |
Het |
Fgd6 |
T |
C |
10: 93,880,778 (GRCm39) |
V544A |
probably damaging |
Het |
Fnbp1 |
C |
T |
2: 30,926,159 (GRCm39) |
G552E |
probably damaging |
Het |
Gjb5 |
A |
T |
4: 127,249,955 (GRCm39) |
V63D |
probably damaging |
Het |
Gm10053 |
T |
C |
19: 24,853,403 (GRCm39) |
I96T |
probably benign |
Het |
Gm38119 |
T |
C |
3: 92,645,328 (GRCm39) |
S89G |
unknown |
Het |
Gpn2 |
A |
G |
4: 133,313,356 (GRCm39) |
I183V |
probably benign |
Het |
Greb1 |
C |
T |
12: 16,724,796 (GRCm39) |
V1793M |
probably benign |
Het |
H2-Q7 |
A |
G |
17: 35,659,037 (GRCm39) |
I163V |
probably benign |
Het |
Hrh2 |
T |
C |
13: 54,368,549 (GRCm39) |
V175A |
possibly damaging |
Het |
Hsd3b3 |
C |
T |
3: 98,651,214 (GRCm39) |
V79I |
possibly damaging |
Het |
Itgb7 |
T |
C |
15: 102,125,039 (GRCm39) |
I727M |
possibly damaging |
Het |
Kcnj16 |
T |
A |
11: 110,915,569 (GRCm39) |
F77Y |
probably damaging |
Het |
Lilra6 |
T |
A |
7: 3,915,995 (GRCm39) |
Q288L |
probably benign |
Het |
Lrrc37 |
A |
T |
11: 103,505,081 (GRCm39) |
S2296T |
probably damaging |
Het |
Malrd1 |
G |
A |
2: 16,079,646 (GRCm39) |
V1788M |
unknown |
Het |
Mau2 |
T |
C |
8: 70,479,373 (GRCm39) |
I349V |
possibly damaging |
Het |
Mbnl3 |
C |
T |
X: 50,219,211 (GRCm39) |
R181H |
probably damaging |
Het |
Mfsd6 |
T |
C |
1: 52,715,706 (GRCm39) |
T524A |
probably benign |
Het |
Mical2 |
G |
T |
7: 111,933,046 (GRCm39) |
R740L |
probably benign |
Het |
Mknk1 |
G |
A |
4: 115,735,269 (GRCm39) |
C379Y |
possibly damaging |
Het |
Mta3 |
A |
T |
17: 84,099,165 (GRCm39) |
K410* |
probably null |
Het |
Myb |
A |
C |
10: 21,032,324 (GRCm39) |
I19S |
possibly damaging |
Het |
Ncor2 |
A |
G |
5: 125,104,102 (GRCm39) |
F996S |
|
Het |
Nlrp1a |
T |
C |
11: 71,014,234 (GRCm39) |
M339V |
possibly damaging |
Het |
Or2n1d |
C |
T |
17: 38,646,285 (GRCm39) |
P79L |
probably benign |
Het |
Or56b35 |
A |
G |
7: 104,963,654 (GRCm39) |
K148E |
probably damaging |
Het |
Pcdhga5 |
C |
T |
18: 37,829,835 (GRCm39) |
T761I |
possibly damaging |
Het |
Pcmtd2 |
T |
C |
2: 181,493,452 (GRCm39) |
L219P |
possibly damaging |
Het |
Pfdn1 |
C |
T |
18: 36,565,358 (GRCm39) |
|
probably null |
Het |
Pkn3 |
G |
A |
2: 29,980,596 (GRCm39) |
C829Y |
probably benign |
Het |
Pld1 |
T |
C |
3: 28,141,338 (GRCm39) |
S634P |
possibly damaging |
Het |
Pofut2 |
T |
G |
10: 77,098,304 (GRCm39) |
V139G |
possibly damaging |
Het |
Prdm12 |
C |
A |
2: 31,543,883 (GRCm39) |
|
probably null |
Het |
Prkar2b |
C |
A |
12: 32,110,937 (GRCm39) |
A49S |
probably benign |
Het |
Prmt1 |
A |
T |
7: 44,633,560 (GRCm39) |
|
probably null |
Het |
Rab39 |
A |
T |
9: 53,597,700 (GRCm39) |
D188E |
probably benign |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Scgb1b19 |
A |
G |
7: 32,986,923 (GRCm39) |
I25V |
probably benign |
Het |
Scn9a |
A |
T |
2: 66,314,642 (GRCm39) |
I1692N |
probably damaging |
Het |
Sdk1 |
G |
T |
5: 142,070,246 (GRCm39) |
G1137V |
probably damaging |
Het |
Sec16b |
A |
G |
1: 157,393,042 (GRCm39) |
T950A |
possibly damaging |
Het |
Senp2 |
G |
T |
16: 21,857,372 (GRCm39) |
R398L |
probably damaging |
Het |
Sfswap |
G |
T |
5: 129,627,657 (GRCm39) |
|
probably null |
Het |
Sh3rf1 |
A |
G |
8: 61,806,787 (GRCm39) |
T362A |
probably damaging |
Het |
Slc17a1 |
A |
T |
13: 24,072,035 (GRCm39) |
I418F |
probably benign |
Het |
Slc1a4 |
A |
T |
11: 20,258,587 (GRCm39) |
M284K |
probably damaging |
Het |
Slc5a2 |
A |
T |
7: 127,865,567 (GRCm39) |
|
probably null |
Het |
Slco5a1 |
A |
G |
1: 13,060,346 (GRCm39) |
V125A |
probably benign |
Het |
Smu1 |
A |
G |
4: 40,748,600 (GRCm39) |
V230A |
probably benign |
Het |
Sp4 |
A |
G |
12: 118,218,139 (GRCm39) |
|
probably null |
Het |
Stbd1 |
A |
G |
5: 92,753,416 (GRCm39) |
K302R |
probably damaging |
Het |
Stx2 |
A |
T |
5: 129,063,481 (GRCm39) |
V268D |
probably benign |
Het |
Tbc1d9b |
G |
A |
11: 50,052,447 (GRCm39) |
A885T |
probably benign |
Het |
Tbce |
T |
A |
13: 14,181,063 (GRCm39) |
D267V |
possibly damaging |
Het |
Tert |
T |
C |
13: 73,775,725 (GRCm39) |
Y159H |
probably damaging |
Het |
Thbs2 |
T |
A |
17: 14,890,301 (GRCm39) |
I1102F |
possibly damaging |
Het |
Tmprss7 |
G |
C |
16: 45,503,873 (GRCm39) |
A183G |
probably benign |
Het |
Top3b |
C |
A |
16: 16,705,585 (GRCm39) |
P450Q |
probably benign |
Het |
Trpm6 |
A |
T |
19: 18,727,409 (GRCm39) |
|
probably null |
Het |
Ube4a |
T |
C |
9: 44,837,271 (GRCm39) |
D988G |
probably damaging |
Het |
Vmn1r158 |
A |
T |
7: 22,489,725 (GRCm39) |
S161R |
probably benign |
Het |
Vps41 |
T |
C |
13: 19,025,422 (GRCm39) |
|
probably null |
Het |
Zfp354c |
TCACACTCGGCACA |
TCACA |
11: 50,706,067 (GRCm39) |
|
probably benign |
Het |
Zfp617 |
T |
A |
8: 72,682,033 (GRCm39) |
|
probably null |
Het |
Zfp808 |
C |
T |
13: 62,319,319 (GRCm39) |
H183Y |
probably benign |
Het |
Zfy1 |
A |
T |
Y: 725,496 (GRCm39) |
C756* |
probably null |
Het |
Zswim2 |
A |
T |
2: 83,745,951 (GRCm39) |
Y496N |
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 |
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 |
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 |
|
|