Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406B18Rik |
T |
C |
7: 43,147,273 (GRCm39) |
I320V |
possibly damaging |
Het |
Adat2 |
A |
G |
10: 13,429,020 (GRCm39) |
K4R |
probably benign |
Het |
Adgb |
G |
A |
10: 10,311,754 (GRCm39) |
L226F |
probably damaging |
Het |
Adgrb3 |
C |
T |
1: 25,137,978 (GRCm39) |
V1192I |
probably damaging |
Het |
Ahsa2 |
T |
A |
11: 23,446,750 (GRCm39) |
N71I |
possibly damaging |
Het |
Amigo2 |
T |
G |
15: 97,143,223 (GRCm39) |
T400P |
probably damaging |
Het |
Ankhd1 |
A |
T |
18: 36,789,826 (GRCm39) |
Q466L |
|
Het |
Auh |
T |
C |
13: 53,073,049 (GRCm39) |
I111V |
probably benign |
Het |
Brwd1 |
A |
G |
16: 95,835,039 (GRCm39) |
F942L |
probably damaging |
Het |
C1qtnf7 |
A |
G |
5: 43,773,486 (GRCm39) |
N262D |
probably damaging |
Het |
Cdh9 |
T |
A |
15: 16,856,316 (GRCm39) |
S785R |
probably damaging |
Het |
Celsr3 |
A |
G |
9: 108,714,851 (GRCm39) |
T2046A |
possibly damaging |
Het |
Cep170b |
T |
C |
12: 112,711,099 (GRCm39) |
V1493A |
probably damaging |
Het |
Chd2 |
T |
A |
7: 73,091,390 (GRCm39) |
H1617L |
probably damaging |
Het |
Ciao3 |
C |
T |
17: 26,001,103 (GRCm39) |
P452S |
probably benign |
Het |
Clnk |
T |
C |
5: 38,864,041 (GRCm39) |
D404G |
probably damaging |
Het |
Col18a1 |
C |
T |
10: 76,902,839 (GRCm39) |
G795D |
probably damaging |
Het |
Csf3r |
T |
A |
4: 125,931,449 (GRCm39) |
Y477* |
probably null |
Het |
Dnah17 |
T |
A |
11: 118,001,373 (GRCm39) |
K857* |
probably null |
Het |
Dnah2 |
T |
G |
11: 69,326,130 (GRCm39) |
I3674L |
probably damaging |
Het |
Dnah6 |
A |
C |
6: 73,072,189 (GRCm39) |
I2431S |
possibly damaging |
Het |
Eml6 |
T |
A |
11: 29,752,501 (GRCm39) |
I971F |
possibly damaging |
Het |
Fam135b |
A |
T |
15: 71,335,172 (GRCm39) |
I674N |
probably damaging |
Het |
Fancc |
T |
A |
13: 63,465,372 (GRCm39) |
|
probably null |
Het |
Gabrb2 |
A |
C |
11: 42,517,569 (GRCm39) |
K464Q |
probably benign |
Het |
Gbp4 |
T |
A |
5: 105,270,848 (GRCm39) |
D261V |
possibly damaging |
Het |
Gdf3 |
A |
G |
6: 122,583,875 (GRCm39) |
V164A |
probably benign |
Het |
Gm19410 |
A |
G |
8: 36,263,513 (GRCm39) |
D978G |
probably damaging |
Het |
Gm20730 |
C |
T |
6: 43,058,708 (GRCm39) |
G35R |
probably null |
Het |
Grin2b |
G |
A |
6: 135,900,362 (GRCm39) |
T173I |
probably damaging |
Het |
Gtf3c3 |
A |
T |
1: 54,462,731 (GRCm39) |
V344E |
possibly damaging |
Het |
Hsd3b5 |
A |
G |
3: 98,537,420 (GRCm39) |
I32T |
probably damaging |
Het |
Ido1 |
G |
C |
8: 25,083,204 (GRCm39) |
L74V |
probably damaging |
Het |
Igkv1-88 |
T |
A |
6: 68,839,357 (GRCm39) |
D85V |
probably damaging |
Het |
Il22ra1 |
A |
G |
4: 135,464,770 (GRCm39) |
I159V |
probably benign |
Het |
Iqgap1 |
A |
T |
7: 80,379,848 (GRCm39) |
F1175Y |
probably damaging |
Het |
Iqgap1 |
A |
G |
7: 80,401,094 (GRCm39) |
V531A |
probably benign |
Het |
Itga1 |
T |
A |
13: 115,133,458 (GRCm39) |
Q484L |
probably null |
Het |
Itga11 |
A |
T |
9: 62,651,300 (GRCm39) |
E281V |
probably benign |
Het |
Kpna3 |
T |
C |
14: 61,610,411 (GRCm39) |
N343S |
possibly damaging |
Het |
Larp1b |
A |
G |
3: 40,987,969 (GRCm39) |
K64E |
possibly damaging |
Het |
Larp1b |
A |
G |
3: 40,990,251 (GRCm39) |
N133S |
probably benign |
Het |
Lctl |
T |
A |
9: 64,029,392 (GRCm39) |
L161H |
probably damaging |
Het |
Mlip |
A |
G |
9: 77,137,765 (GRCm39) |
S381P |
probably damaging |
Het |
Mroh9 |
A |
G |
1: 162,873,601 (GRCm39) |
I518T |
probably benign |
Het |
Mst1r |
A |
G |
9: 107,797,211 (GRCm39) |
Q1360R |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,418,629 (GRCm39) |
C3858* |
probably null |
Het |
Naip1 |
A |
T |
13: 100,562,284 (GRCm39) |
H960Q |
probably benign |
Het |
Neo1 |
A |
T |
9: 58,791,786 (GRCm39) |
S1321T |
probably benign |
Het |
Nid2 |
C |
A |
14: 19,852,598 (GRCm39) |
T1102K |
probably damaging |
Het |
Nsmaf |
C |
T |
4: 6,408,563 (GRCm39) |
V739M |
probably damaging |
Het |
Or1o2 |
T |
G |
17: 37,542,341 (GRCm39) |
K307Q |
probably benign |
Het |
Or4k15 |
T |
G |
14: 50,364,446 (GRCm39) |
S137R |
probably benign |
Het |
Or5ar1 |
T |
A |
2: 85,672,001 (GRCm39) |
M45L |
probably benign |
Het |
Or5b110-ps1 |
A |
G |
19: 13,259,954 (GRCm39) |
I156T |
probably damaging |
Het |
Or5d39 |
T |
C |
2: 87,979,862 (GRCm39) |
Q167R |
probably benign |
Het |
Osbpl9 |
G |
A |
4: 108,943,536 (GRCm39) |
P159S |
probably damaging |
Het |
Parpbp |
A |
G |
10: 87,929,499 (GRCm39) |
S450P |
probably damaging |
Het |
Pdgfrb |
A |
G |
18: 61,197,118 (GRCm39) |
T185A |
probably benign |
Het |
Pkd1 |
T |
C |
17: 24,812,476 (GRCm39) |
V3803A |
probably damaging |
Het |
Plau |
A |
T |
14: 20,889,534 (GRCm39) |
K200* |
probably null |
Het |
Plce1 |
A |
T |
19: 38,513,109 (GRCm39) |
Q136L |
probably benign |
Het |
Plekhd1 |
C |
T |
12: 80,769,219 (GRCm39) |
T493I |
probably benign |
Het |
Pofut1 |
T |
C |
2: 153,101,338 (GRCm39) |
S31P |
unknown |
Het |
Prlr |
T |
A |
15: 10,326,010 (GRCm39) |
I243N |
probably damaging |
Het |
Ptgis |
A |
G |
2: 167,065,908 (GRCm39) |
L174P |
probably damaging |
Het |
Ralgapb |
T |
A |
2: 158,292,190 (GRCm39) |
I792K |
probably damaging |
Het |
Retreg3 |
C |
T |
11: 100,993,806 (GRCm39) |
S136N |
probably damaging |
Het |
Rigi |
T |
A |
4: 40,229,653 (GRCm39) |
I89F |
possibly damaging |
Het |
Rnf213 |
C |
T |
11: 119,358,123 (GRCm39) |
T4291M |
|
Het |
Rtn1 |
A |
G |
12: 72,350,917 (GRCm39) |
Y431H |
probably damaging |
Het |
Rwdd3 |
A |
G |
3: 120,965,253 (GRCm39) |
|
probably benign |
Het |
Scyl3 |
A |
T |
1: 163,777,907 (GRCm39) |
|
probably null |
Het |
Sh2b2 |
G |
T |
5: 136,248,511 (GRCm39) |
Q510K |
probably damaging |
Het |
Sh2b3 |
G |
A |
5: 121,956,763 (GRCm39) |
P333S |
probably benign |
Het |
Sirpd |
A |
G |
3: 15,385,545 (GRCm39) |
V119A |
probably damaging |
Het |
Slc27a6 |
A |
T |
18: 58,742,255 (GRCm39) |
N490Y |
probably damaging |
Het |
Slc45a1 |
C |
T |
4: 150,723,002 (GRCm39) |
R294Q |
probably benign |
Het |
Sorl1 |
A |
C |
9: 41,888,878 (GRCm39) |
I1974S |
possibly damaging |
Het |
Specc1l |
C |
A |
10: 75,099,120 (GRCm39) |
N857K |
probably benign |
Het |
Speg |
T |
C |
1: 75,405,886 (GRCm39) |
L3030P |
probably damaging |
Het |
Spsb1 |
A |
C |
4: 149,991,357 (GRCm39) |
D70E |
probably benign |
Het |
Srsf11 |
A |
G |
3: 157,722,062 (GRCm39) |
S270P |
unknown |
Het |
Ssr3 |
A |
C |
3: 65,295,213 (GRCm39) |
V100G |
probably damaging |
Het |
Synpo |
G |
A |
18: 60,737,547 (GRCm39) |
T133I |
probably damaging |
Het |
Tas2r120 |
T |
G |
6: 132,634,773 (GRCm39) |
V285G |
probably benign |
Het |
Tenm4 |
T |
A |
7: 96,495,133 (GRCm39) |
V1187D |
probably damaging |
Het |
Tmed8 |
C |
A |
12: 87,228,162 (GRCm39) |
|
probably null |
Het |
Tmem51 |
G |
A |
4: 141,764,875 (GRCm39) |
T61M |
probably damaging |
Het |
Tonsl |
A |
T |
15: 76,514,807 (GRCm39) |
D1132E |
probably benign |
Het |
Tor1aip1 |
C |
T |
1: 155,883,330 (GRCm39) |
V358I |
possibly damaging |
Het |
Txlna |
A |
T |
4: 129,524,112 (GRCm39) |
M415K |
probably damaging |
Het |
Tyms |
T |
A |
5: 30,278,558 (GRCm39) |
|
probably benign |
Het |
Uggt2 |
G |
T |
14: 119,326,681 (GRCm39) |
L177I |
probably benign |
Het |
Uqcrh |
T |
C |
4: 115,927,076 (GRCm39) |
H74R |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,909,699 (GRCm39) |
S33T |
probably benign |
Het |
Zfp553 |
T |
A |
7: 126,835,188 (GRCm39) |
C248S |
probably damaging |
Het |
Zfp574 |
G |
A |
7: 24,780,001 (GRCm39) |
C341Y |
possibly damaging |
Het |
Zfp729b |
T |
C |
13: 67,739,617 (GRCm39) |
T883A |
possibly damaging |
Het |
Zfp738 |
T |
A |
13: 67,818,322 (GRCm39) |
K556N |
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 |
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 |
|
|