Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
C |
16: 4,669,799 (GRCm39) |
V788A |
possibly damaging |
Het |
Abca15 |
A |
T |
7: 120,002,217 (GRCm39) |
K1577* |
probably null |
Het |
Arhgap12 |
T |
C |
18: 6,111,803 (GRCm39) |
E187G |
probably damaging |
Het |
Arhgef10 |
T |
A |
8: 15,025,005 (GRCm39) |
Y398N |
probably damaging |
Het |
Baz2b |
C |
T |
2: 59,731,874 (GRCm39) |
V2055I |
probably benign |
Het |
Btnl4 |
T |
C |
17: 34,688,353 (GRCm39) |
D475G |
probably damaging |
Het |
C1qtnf12 |
T |
A |
4: 156,050,070 (GRCm39) |
F190Y |
probably damaging |
Het |
Cacul1 |
A |
G |
19: 60,522,683 (GRCm39) |
S284P |
probably damaging |
Het |
Ccdc166 |
C |
A |
15: 75,853,820 (GRCm39) |
V87L |
possibly damaging |
Het |
Ceacam13 |
C |
T |
7: 17,747,032 (GRCm39) |
P162S |
probably damaging |
Het |
Chd5 |
T |
C |
4: 152,462,664 (GRCm39) |
S1372P |
probably damaging |
Het |
Chil3 |
C |
A |
3: 106,067,730 (GRCm39) |
R145L |
probably benign |
Het |
Cyp4f40 |
T |
C |
17: 32,894,923 (GRCm39) |
S454P |
probably benign |
Het |
Defa3 |
T |
A |
8: 21,778,213 (GRCm39) |
C66S |
probably damaging |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Glmp |
C |
A |
3: 88,235,349 (GRCm39) |
N260K |
probably benign |
Het |
Gsap |
T |
A |
5: 21,486,016 (GRCm39) |
L653Q |
probably damaging |
Het |
Il18rap |
T |
A |
1: 40,564,255 (GRCm39) |
Y124* |
probably null |
Het |
Lao1 |
A |
C |
4: 118,820,948 (GRCm39) |
K58T |
probably damaging |
Het |
Lepr |
T |
A |
4: 101,622,487 (GRCm39) |
|
probably null |
Het |
Mrgpra3 |
G |
C |
7: 47,239,781 (GRCm39) |
I48M |
probably benign |
Het |
Nck2 |
T |
G |
1: 43,593,511 (GRCm39) |
N239K |
probably benign |
Het |
Optc |
A |
T |
1: 133,825,554 (GRCm39) |
V324E |
possibly damaging |
Het |
Or12k7 |
A |
T |
2: 36,958,794 (GRCm39) |
Y159F |
probably damaging |
Het |
Or4p8 |
A |
G |
2: 88,727,278 (GRCm39) |
I221T |
probably benign |
Het |
Or51b6 |
G |
A |
7: 103,555,908 (GRCm39) |
W84* |
probably null |
Het |
Otog |
T |
C |
7: 45,923,205 (GRCm39) |
S1027P |
probably damaging |
Het |
Plbd2 |
A |
G |
5: 120,641,407 (GRCm39) |
F84L |
probably benign |
Het |
Plxnb1 |
T |
C |
9: 108,935,838 (GRCm39) |
L110P |
probably damaging |
Het |
Prnp |
T |
C |
2: 131,778,708 (GRCm39) |
V120A |
possibly damaging |
Het |
Ptprh |
C |
A |
7: 4,552,370 (GRCm39) |
E965* |
probably null |
Het |
Reln |
T |
C |
5: 22,239,568 (GRCm39) |
T900A |
probably damaging |
Het |
Stt3a |
A |
G |
9: 36,646,682 (GRCm39) |
Y644H |
probably damaging |
Het |
Sulf2 |
A |
G |
2: 165,929,039 (GRCm39) |
Y311H |
probably damaging |
Het |
Tbc1d32 |
A |
T |
10: 56,056,626 (GRCm39) |
I438N |
probably damaging |
Het |
Tbcd |
T |
C |
11: 121,387,937 (GRCm39) |
V356A |
possibly damaging |
Het |
Tecta |
T |
C |
9: 42,303,425 (GRCm39) |
N69S |
probably damaging |
Het |
Topaz1 |
T |
C |
9: 122,631,023 (GRCm39) |
V1618A |
probably benign |
Het |
Usp48 |
C |
T |
4: 137,352,587 (GRCm39) |
T627I |
possibly damaging |
Het |
Vcl |
T |
C |
14: 21,037,143 (GRCm39) |
V247A |
probably damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,693,277 (GRCm39) |
L441P |
probably damaging |
Het |
Zfp869 |
C |
T |
8: 70,159,175 (GRCm39) |
G466D |
probably damaging |
Het |
|
Other mutations in Cep250 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Cep250
|
APN |
2 |
155,833,249 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01077:Cep250
|
APN |
2 |
155,804,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Cep250
|
APN |
2 |
155,840,313 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01400:Cep250
|
APN |
2 |
155,840,211 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01570:Cep250
|
APN |
2 |
155,809,583 (GRCm39) |
splice site |
probably benign |
|
IGL01583:Cep250
|
APN |
2 |
155,818,069 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01590:Cep250
|
APN |
2 |
155,834,237 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01647:Cep250
|
APN |
2 |
155,825,296 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01959:Cep250
|
APN |
2 |
155,825,279 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02066:Cep250
|
APN |
2 |
155,818,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02219:Cep250
|
APN |
2 |
155,833,514 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02322:Cep250
|
APN |
2 |
155,832,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02728:Cep250
|
APN |
2 |
155,825,198 (GRCm39) |
unclassified |
probably benign |
|
IGL02955:Cep250
|
APN |
2 |
155,817,676 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03369:Cep250
|
APN |
2 |
155,832,191 (GRCm39) |
missense |
probably benign |
0.00 |
R0366:Cep250
|
UTSW |
2 |
155,830,321 (GRCm39) |
missense |
probably benign |
0.00 |
R0403:Cep250
|
UTSW |
2 |
155,834,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R0441:Cep250
|
UTSW |
2 |
155,813,924 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0482:Cep250
|
UTSW |
2 |
155,806,894 (GRCm39) |
splice site |
probably benign |
|
R0507:Cep250
|
UTSW |
2 |
155,834,452 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0614:Cep250
|
UTSW |
2 |
155,812,017 (GRCm39) |
nonsense |
probably null |
|
R0855:Cep250
|
UTSW |
2 |
155,806,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Cep250
|
UTSW |
2 |
155,806,209 (GRCm39) |
splice site |
probably benign |
|
R1137:Cep250
|
UTSW |
2 |
155,832,760 (GRCm39) |
missense |
probably benign |
0.05 |
R1270:Cep250
|
UTSW |
2 |
155,832,601 (GRCm39) |
missense |
probably benign |
0.01 |
R1313:Cep250
|
UTSW |
2 |
155,813,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R1313:Cep250
|
UTSW |
2 |
155,813,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R1470:Cep250
|
UTSW |
2 |
155,832,995 (GRCm39) |
missense |
probably damaging |
0.99 |
R1470:Cep250
|
UTSW |
2 |
155,832,995 (GRCm39) |
missense |
probably damaging |
0.99 |
R1703:Cep250
|
UTSW |
2 |
155,807,466 (GRCm39) |
missense |
probably benign |
0.23 |
R1705:Cep250
|
UTSW |
2 |
155,805,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1740:Cep250
|
UTSW |
2 |
155,815,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R1796:Cep250
|
UTSW |
2 |
155,834,107 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1897:Cep250
|
UTSW |
2 |
155,818,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1900:Cep250
|
UTSW |
2 |
155,827,294 (GRCm39) |
critical splice donor site |
probably null |
|
R1958:Cep250
|
UTSW |
2 |
155,818,301 (GRCm39) |
splice site |
probably null |
|
R1974:Cep250
|
UTSW |
2 |
155,831,424 (GRCm39) |
missense |
probably damaging |
0.96 |
R2015:Cep250
|
UTSW |
2 |
155,823,373 (GRCm39) |
missense |
probably damaging |
0.96 |
R2033:Cep250
|
UTSW |
2 |
155,812,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R2224:Cep250
|
UTSW |
2 |
155,833,737 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2266:Cep250
|
UTSW |
2 |
155,818,090 (GRCm39) |
missense |
probably benign |
0.13 |
R2278:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2332:Cep250
|
UTSW |
2 |
155,832,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2366:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2385:Cep250
|
UTSW |
2 |
155,816,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R2830:Cep250
|
UTSW |
2 |
155,825,236 (GRCm39) |
missense |
probably benign |
0.00 |
R2895:Cep250
|
UTSW |
2 |
155,834,042 (GRCm39) |
missense |
probably benign |
0.00 |
R2965:Cep250
|
UTSW |
2 |
155,836,798 (GRCm39) |
missense |
probably benign |
0.44 |
R2966:Cep250
|
UTSW |
2 |
155,836,798 (GRCm39) |
missense |
probably benign |
0.44 |
R3016:Cep250
|
UTSW |
2 |
155,833,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R3052:Cep250
|
UTSW |
2 |
155,832,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R3424:Cep250
|
UTSW |
2 |
155,823,381 (GRCm39) |
missense |
probably benign |
0.02 |
R3930:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4085:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4087:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4090:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4110:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4355:Cep250
|
UTSW |
2 |
155,833,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4601:Cep250
|
UTSW |
2 |
155,803,973 (GRCm39) |
missense |
probably benign |
0.10 |
R4721:Cep250
|
UTSW |
2 |
155,812,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Cep250
|
UTSW |
2 |
155,830,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5053:Cep250
|
UTSW |
2 |
155,804,848 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5090:Cep250
|
UTSW |
2 |
155,818,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R5744:Cep250
|
UTSW |
2 |
155,823,394 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5775:Cep250
|
UTSW |
2 |
155,811,294 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5986:Cep250
|
UTSW |
2 |
155,821,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R6112:Cep250
|
UTSW |
2 |
155,836,503 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6152:Cep250
|
UTSW |
2 |
155,823,358 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6823:Cep250
|
UTSW |
2 |
155,823,379 (GRCm39) |
missense |
probably benign |
0.02 |
R6900:Cep250
|
UTSW |
2 |
155,838,190 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7107:Cep250
|
UTSW |
2 |
155,837,314 (GRCm39) |
missense |
probably benign |
0.00 |
R7131:Cep250
|
UTSW |
2 |
155,806,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R7178:Cep250
|
UTSW |
2 |
155,815,375 (GRCm39) |
nonsense |
probably null |
|
R7241:Cep250
|
UTSW |
2 |
155,833,472 (GRCm39) |
missense |
probably benign |
0.20 |
R7264:Cep250
|
UTSW |
2 |
155,821,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R7290:Cep250
|
UTSW |
2 |
155,834,682 (GRCm39) |
missense |
probably benign |
0.03 |
R7367:Cep250
|
UTSW |
2 |
155,811,227 (GRCm39) |
missense |
probably benign |
0.00 |
R7397:Cep250
|
UTSW |
2 |
155,823,331 (GRCm39) |
missense |
probably damaging |
0.99 |
R7768:Cep250
|
UTSW |
2 |
155,827,929 (GRCm39) |
missense |
|
|
R7823:Cep250
|
UTSW |
2 |
155,807,336 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8152:Cep250
|
UTSW |
2 |
155,811,227 (GRCm39) |
missense |
probably benign |
0.00 |
R8331:Cep250
|
UTSW |
2 |
155,832,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R8559:Cep250
|
UTSW |
2 |
155,834,656 (GRCm39) |
missense |
probably damaging |
0.99 |
R8972:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8973:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8974:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8975:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8976:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9072:Cep250
|
UTSW |
2 |
155,834,035 (GRCm39) |
missense |
probably benign |
0.01 |
R9123:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9127:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9128:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9167:Cep250
|
UTSW |
2 |
155,828,920 (GRCm39) |
missense |
|
|
R9189:Cep250
|
UTSW |
2 |
155,818,350 (GRCm39) |
missense |
probably benign |
0.00 |
R9198:Cep250
|
UTSW |
2 |
155,830,354 (GRCm39) |
critical splice donor site |
probably null |
|
R9227:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9228:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9292:Cep250
|
UTSW |
2 |
155,832,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R9516:Cep250
|
UTSW |
2 |
155,833,459 (GRCm39) |
missense |
probably benign |
0.00 |
R9723:Cep250
|
UTSW |
2 |
155,823,337 (GRCm39) |
missense |
probably benign |
0.00 |
R9760:Cep250
|
UTSW |
2 |
155,818,473 (GRCm39) |
missense |
probably benign |
0.02 |
X0061:Cep250
|
UTSW |
2 |
155,803,905 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Cep250
|
UTSW |
2 |
155,818,387 (GRCm39) |
missense |
probably benign |
0.03 |
|