Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
T |
C |
10: 10,225,321 (GRCm39) |
Y1415C |
probably damaging |
Het |
Adgrf1 |
T |
C |
17: 43,614,563 (GRCm39) |
S216P |
probably damaging |
Het |
Ankrd12 |
T |
C |
17: 66,338,428 (GRCm39) |
D197G |
probably damaging |
Het |
Aoc3 |
C |
A |
11: 101,222,488 (GRCm39) |
H198Q |
probably damaging |
Het |
Aox1 |
C |
A |
1: 58,143,640 (GRCm39) |
H1253N |
probably benign |
Het |
Arg1 |
T |
A |
10: 24,798,536 (GRCm39) |
E38V |
possibly damaging |
Het |
Baz2b |
T |
A |
2: 59,738,087 (GRCm39) |
M1741L |
probably benign |
Het |
Bend4 |
T |
C |
5: 67,574,915 (GRCm39) |
E322G |
probably damaging |
Het |
Brpf1 |
T |
C |
6: 113,294,639 (GRCm39) |
V661A |
possibly damaging |
Het |
C2cd3 |
A |
T |
7: 100,104,160 (GRCm39) |
T2058S |
probably damaging |
Het |
Camk4 |
T |
C |
18: 33,309,266 (GRCm39) |
V223A |
probably damaging |
Het |
Casp1 |
C |
T |
9: 5,306,742 (GRCm39) |
R395C |
probably damaging |
Het |
Ccdc180 |
T |
G |
4: 45,923,244 (GRCm39) |
I1066S |
probably damaging |
Het |
Ccne1 |
A |
G |
7: 37,798,744 (GRCm39) |
F292L |
probably damaging |
Het |
Ccz1 |
A |
T |
5: 143,949,628 (GRCm39) |
M100K |
probably damaging |
Het |
Cep128 |
T |
C |
12: 91,226,936 (GRCm39) |
T678A |
probably benign |
Het |
Crip3 |
A |
G |
17: 46,741,673 (GRCm39) |
|
probably benign |
Het |
Ddx60 |
A |
G |
8: 62,474,348 (GRCm39) |
M1479V |
possibly damaging |
Het |
Defb40 |
T |
A |
8: 19,025,093 (GRCm39) |
I38F |
probably benign |
Het |
Dnajb2 |
C |
T |
1: 75,220,198 (GRCm39) |
T221I |
possibly damaging |
Het |
Dpysl3 |
T |
C |
18: 43,467,079 (GRCm39) |
I279V |
probably damaging |
Het |
Echs1 |
G |
A |
7: 139,692,499 (GRCm39) |
|
probably benign |
Het |
Efl1 |
T |
A |
7: 82,320,835 (GRCm39) |
N89K |
probably damaging |
Het |
Extl3 |
T |
C |
14: 65,313,443 (GRCm39) |
T580A |
probably benign |
Het |
Fam171a2 |
C |
T |
11: 102,330,982 (GRCm39) |
G193E |
probably damaging |
Het |
Fam234a |
A |
T |
17: 26,435,591 (GRCm39) |
D264E |
probably benign |
Het |
Fbxw20 |
A |
T |
9: 109,063,763 (GRCm39) |
V3D |
possibly damaging |
Het |
Fig4 |
G |
A |
10: 41,109,586 (GRCm39) |
P637L |
probably benign |
Het |
Fnbp1l |
G |
A |
3: 122,339,964 (GRCm39) |
T496I |
probably benign |
Het |
Fry |
T |
C |
5: 150,325,108 (GRCm39) |
V1175A |
possibly damaging |
Het |
Gm5617 |
C |
T |
9: 48,406,968 (GRCm39) |
A34V |
possibly damaging |
Het |
Gnai1 |
A |
T |
5: 18,496,596 (GRCm39) |
V109E |
probably benign |
Het |
H2-K2 |
A |
T |
17: 34,216,298 (GRCm39) |
Y283N |
probably benign |
Het |
Hectd2 |
A |
T |
19: 36,582,682 (GRCm39) |
I471F |
probably damaging |
Het |
Hsdl2 |
T |
C |
4: 59,612,812 (GRCm39) |
|
probably null |
Het |
Igkv3-1 |
T |
C |
6: 70,681,028 (GRCm39) |
S76P |
probably damaging |
Het |
Krt15 |
A |
T |
11: 100,022,897 (GRCm39) |
S439R |
probably benign |
Het |
Lama2 |
TTTGCGCATT |
TTT |
10: 26,919,639 (GRCm39) |
|
probably null |
Het |
Lima1 |
G |
A |
15: 99,717,457 (GRCm39) |
T23I |
probably benign |
Het |
Map4k1 |
C |
A |
7: 28,688,195 (GRCm39) |
H248Q |
probably damaging |
Het |
Mcf2l |
C |
A |
8: 13,063,972 (GRCm39) |
T1004K |
probably damaging |
Het |
Meak7 |
T |
G |
8: 120,499,262 (GRCm39) |
T77P |
probably benign |
Het |
Micall1 |
T |
A |
15: 79,007,146 (GRCm39) |
|
probably benign |
Het |
Ms4a14 |
A |
G |
19: 11,278,976 (GRCm39) |
I1194T |
probably benign |
Het |
Mtor |
T |
C |
4: 148,539,273 (GRCm39) |
*257Q |
probably null |
Het |
Mucl3 |
G |
A |
17: 35,948,468 (GRCm39) |
T377I |
possibly damaging |
Het |
Ncan |
T |
A |
8: 70,556,705 (GRCm39) |
T961S |
probably benign |
Het |
Odad4 |
A |
G |
11: 100,441,147 (GRCm39) |
N126S |
probably damaging |
Het |
Or10z1 |
A |
T |
1: 174,078,262 (GRCm39) |
I77N |
probably damaging |
Het |
Or1e29 |
T |
A |
11: 73,667,372 (GRCm39) |
L260F |
probably benign |
Het |
Or1f19 |
T |
C |
16: 3,410,706 (GRCm39) |
S149P |
probably damaging |
Het |
Or2t49 |
T |
A |
11: 58,392,735 (GRCm39) |
I216F |
probably damaging |
Het |
Or8h10 |
T |
G |
2: 86,808,693 (GRCm39) |
Y149S |
probably damaging |
Het |
Or9e1 |
T |
A |
11: 58,732,033 (GRCm39) |
L31H |
possibly damaging |
Het |
Pcdhgb2 |
A |
G |
18: 37,825,153 (GRCm39) |
R715G |
probably benign |
Het |
Pik3c3 |
T |
C |
18: 30,477,131 (GRCm39) |
|
probably null |
Het |
Pkhd1l1 |
A |
T |
15: 44,354,497 (GRCm39) |
D296V |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,908,125 (GRCm39) |
I1189V |
probably damaging |
Het |
Psg18 |
A |
T |
7: 18,087,409 (GRCm39) |
L83Q |
possibly damaging |
Het |
Rps6kc1 |
A |
G |
1: 190,532,515 (GRCm39) |
W496R |
probably damaging |
Het |
Setd5 |
C |
T |
6: 113,126,527 (GRCm39) |
T1188I |
probably damaging |
Het |
Slc4a3 |
T |
C |
1: 75,531,729 (GRCm39) |
F899L |
probably damaging |
Het |
Slitrk6 |
T |
C |
14: 110,989,315 (GRCm39) |
T131A |
probably damaging |
Het |
Speg |
G |
T |
1: 75,398,379 (GRCm39) |
R1942L |
probably damaging |
Het |
Sulf2 |
C |
A |
2: 165,923,524 (GRCm39) |
R565L |
probably benign |
Het |
Tcerg1 |
T |
C |
18: 42,657,046 (GRCm39) |
M176T |
unknown |
Het |
Tfcp2l1 |
T |
C |
1: 118,597,239 (GRCm39) |
I440T |
possibly damaging |
Het |
Tgm7 |
A |
T |
2: 120,929,445 (GRCm39) |
|
probably null |
Het |
Tjp2 |
C |
A |
19: 24,099,484 (GRCm39) |
G433V |
probably damaging |
Het |
Tmc7 |
C |
T |
7: 118,142,565 (GRCm39) |
G608R |
probably damaging |
Het |
Tmed4 |
A |
G |
11: 6,224,456 (GRCm39) |
F68S |
possibly damaging |
Het |
Tmem30b |
G |
A |
12: 73,592,686 (GRCm39) |
P143L |
probably damaging |
Het |
Tnfrsf23 |
C |
T |
7: 143,235,217 (GRCm39) |
C49Y |
probably damaging |
Het |
Tnni3k |
A |
T |
3: 154,492,445 (GRCm39) |
|
probably null |
Het |
Trav12-2 |
G |
T |
14: 53,854,150 (GRCm39) |
M41I |
probably benign |
Het |
Trim6 |
T |
A |
7: 103,881,692 (GRCm39) |
Y314* |
probably null |
Het |
Utp25 |
A |
G |
1: 192,796,072 (GRCm39) |
Y686H |
probably damaging |
Het |
Vmn2r118 |
A |
G |
17: 55,899,894 (GRCm39) |
V670A |
probably damaging |
Het |
Zfp438 |
A |
T |
18: 5,213,154 (GRCm39) |
D601E |
probably benign |
Het |
Zfp606 |
T |
A |
7: 12,226,983 (GRCm39) |
I310N |
possibly 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 |
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 |
|
|