Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310061N02Rik |
T |
C |
16: 88,504,342 (GRCm39) |
T152A |
probably benign |
Het |
Abca1 |
T |
C |
4: 53,067,155 (GRCm39) |
I1351V |
probably benign |
Het |
Acap1 |
A |
T |
11: 69,778,043 (GRCm39) |
|
probably benign |
Het |
Als2cl |
T |
C |
9: 110,720,935 (GRCm39) |
L521P |
probably damaging |
Het |
Ankrd50 |
T |
C |
3: 38,510,384 (GRCm39) |
D661G |
probably benign |
Het |
Atp6v1b2 |
T |
A |
8: 69,556,112 (GRCm39) |
N262K |
probably damaging |
Het |
Baz1a |
T |
A |
12: 54,945,491 (GRCm39) |
D1288V |
possibly damaging |
Het |
Bbs1 |
A |
T |
19: 4,945,057 (GRCm39) |
D371E |
probably benign |
Het |
Bphl |
A |
G |
13: 34,248,029 (GRCm39) |
|
probably benign |
Het |
Caskin2 |
C |
A |
11: 115,691,820 (GRCm39) |
R988S |
probably damaging |
Het |
Cbr1 |
C |
A |
16: 93,406,875 (GRCm39) |
T197N |
probably damaging |
Het |
Ccdc88c |
T |
C |
12: 100,901,999 (GRCm39) |
E1213G |
possibly damaging |
Het |
Ccna1 |
A |
G |
3: 54,957,169 (GRCm39) |
F83L |
probably damaging |
Het |
Cep89 |
C |
A |
7: 35,127,687 (GRCm39) |
T543K |
possibly damaging |
Het |
Cmtm7 |
T |
C |
9: 114,610,738 (GRCm39) |
M45V |
probably benign |
Het |
Col16a1 |
T |
A |
4: 129,946,650 (GRCm39) |
V91E |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,845,326 (GRCm39) |
N920S |
probably benign |
Het |
Cyp26b1 |
A |
G |
6: 84,554,190 (GRCm39) |
|
probably benign |
Het |
Dao |
T |
A |
5: 114,158,024 (GRCm39) |
H215Q |
probably damaging |
Het |
Dido1 |
T |
C |
2: 180,313,617 (GRCm39) |
D885G |
probably benign |
Het |
Dlx4 |
T |
G |
11: 95,032,055 (GRCm39) |
M240L |
probably benign |
Het |
Dnah5 |
C |
T |
15: 28,295,071 (GRCm39) |
P1351L |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,015,717 (GRCm39) |
|
probably benign |
Het |
Dock5 |
A |
T |
14: 68,083,491 (GRCm39) |
D139E |
probably benign |
Het |
Dynlt5 |
T |
C |
4: 102,859,649 (GRCm39) |
|
probably benign |
Het |
Fam234b |
T |
C |
6: 135,195,821 (GRCm39) |
|
probably benign |
Het |
Fat2 |
T |
C |
11: 55,180,112 (GRCm39) |
T1410A |
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,815,269 (GRCm39) |
N3667K |
probably benign |
Het |
Gm5114 |
T |
C |
7: 39,057,880 (GRCm39) |
I580V |
probably benign |
Het |
Hapln1 |
A |
T |
13: 89,755,988 (GRCm39) |
Y264F |
probably benign |
Het |
Heatr5a |
A |
G |
12: 51,972,188 (GRCm39) |
V694A |
probably benign |
Het |
Hps1 |
A |
G |
19: 42,759,550 (GRCm39) |
|
probably benign |
Het |
Igsf9b |
G |
T |
9: 27,245,681 (GRCm39) |
R1216L |
possibly damaging |
Het |
Il4ra |
G |
T |
7: 125,168,242 (GRCm39) |
C87F |
probably damaging |
Het |
Kmt5b |
A |
G |
19: 3,836,465 (GRCm39) |
M1V |
probably null |
Het |
Krit1 |
A |
G |
5: 3,872,178 (GRCm39) |
E401G |
probably damaging |
Het |
Lamp1 |
T |
C |
8: 13,224,491 (GRCm39) |
V385A |
probably damaging |
Het |
Ly6g5b |
A |
G |
17: 35,333,567 (GRCm39) |
Y82H |
probably damaging |
Het |
Mapre2 |
A |
G |
18: 23,937,232 (GRCm39) |
I25V |
probably benign |
Het |
Mep1a |
A |
G |
17: 43,808,777 (GRCm39) |
|
probably benign |
Het |
Mkrn1 |
A |
G |
6: 39,376,209 (GRCm39) |
W466R |
probably benign |
Het |
Muc2 |
C |
A |
7: 141,302,691 (GRCm39) |
F11L |
probably benign |
Het |
Nebl |
T |
A |
2: 17,397,794 (GRCm39) |
M501L |
probably benign |
Het |
Oga |
A |
T |
19: 45,760,327 (GRCm39) |
I277N |
probably damaging |
Het |
Or11g2 |
A |
G |
14: 50,855,789 (GRCm39) |
I37V |
probably benign |
Het |
Or4p18 |
A |
G |
2: 88,232,699 (GRCm39) |
V193A |
probably benign |
Het |
Or5w8 |
A |
G |
2: 87,687,827 (GRCm39) |
I103V |
probably benign |
Het |
Or8g32 |
A |
G |
9: 39,305,238 (GRCm39) |
I50M |
probably benign |
Het |
Pkd1l2 |
A |
G |
8: 117,776,787 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,418,001 (GRCm39) |
M2886V |
probably damaging |
Het |
Pop5 |
T |
A |
5: 115,378,230 (GRCm39) |
L58H |
probably damaging |
Het |
Prkch |
C |
A |
12: 73,768,561 (GRCm39) |
H444N |
possibly damaging |
Het |
Reln |
T |
C |
5: 22,209,134 (GRCm39) |
D1148G |
probably damaging |
Het |
Rffl |
G |
A |
11: 82,703,458 (GRCm39) |
T120M |
probably damaging |
Het |
Rmdn2 |
A |
T |
17: 79,977,998 (GRCm39) |
S320C |
probably damaging |
Het |
Rrbp1 |
C |
T |
2: 143,831,864 (GRCm39) |
R101H |
probably benign |
Het |
Rtf1 |
G |
A |
2: 119,557,224 (GRCm39) |
R443H |
probably damaging |
Het |
Serac1 |
G |
T |
17: 6,099,115 (GRCm39) |
L559I |
probably damaging |
Het |
Slc12a1 |
A |
G |
2: 125,061,682 (GRCm39) |
R958G |
probably damaging |
Het |
Slc15a3 |
T |
A |
19: 10,833,350 (GRCm39) |
W456R |
probably damaging |
Het |
Slc28a2b |
T |
A |
2: 122,347,550 (GRCm39) |
|
probably null |
Het |
Slc35f5 |
C |
T |
1: 125,503,942 (GRCm39) |
P290L |
probably damaging |
Het |
Slc35g2 |
C |
T |
9: 100,435,170 (GRCm39) |
R167Q |
probably benign |
Het |
Spag4 |
T |
C |
2: 155,909,962 (GRCm39) |
V302A |
probably damaging |
Het |
Spire2 |
A |
C |
8: 124,084,836 (GRCm39) |
|
probably benign |
Het |
Sptbn2 |
G |
T |
19: 4,774,772 (GRCm39) |
V142L |
probably damaging |
Het |
Syt17 |
T |
A |
7: 118,009,164 (GRCm39) |
D352V |
probably damaging |
Het |
Tars3 |
A |
T |
7: 65,314,717 (GRCm39) |
D425V |
probably benign |
Het |
Thsd7a |
A |
G |
6: 12,554,907 (GRCm39) |
S326P |
probably benign |
Het |
Tnpo2 |
T |
C |
8: 85,767,257 (GRCm39) |
S64P |
probably damaging |
Het |
Tonsl |
G |
T |
15: 76,517,685 (GRCm39) |
A678D |
probably benign |
Het |
Trim12c |
A |
G |
7: 103,990,113 (GRCm39) |
|
probably null |
Het |
Tsc22d1 |
A |
G |
14: 76,656,421 (GRCm39) |
T885A |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,572,542 (GRCm39) |
D26117G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,707,355 (GRCm39) |
|
probably benign |
Het |
Ugt3a1 |
T |
C |
15: 9,306,342 (GRCm39) |
F164L |
probably benign |
Het |
Vmn2r89 |
A |
G |
14: 51,693,160 (GRCm39) |
N170S |
probably damaging |
Het |
Vrk2 |
G |
T |
11: 26,484,313 (GRCm39) |
|
probably benign |
Het |
Wt1 |
C |
A |
2: 104,963,802 (GRCm39) |
D207E |
probably damaging |
Het |
Zbtb46 |
G |
A |
2: 181,053,608 (GRCm39) |
A368V |
probably benign |
Het |
Zc3h13 |
A |
T |
14: 75,560,694 (GRCm39) |
D428V |
unknown |
Het |
Zcchc8 |
C |
G |
5: 123,845,400 (GRCm39) |
G320A |
probably damaging |
Het |
Znfx1 |
T |
C |
2: 166,886,130 (GRCm39) |
E810G |
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 |
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 |
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 |
|
|