Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr1b |
T |
C |
1: 36,740,911 (GRCm39) |
Y171C |
possibly damaging |
Het |
Ap1g1 |
G |
A |
8: 110,560,122 (GRCm39) |
S281N |
probably benign |
Het |
Ccdc137 |
T |
C |
11: 120,352,844 (GRCm39) |
F196S |
probably damaging |
Het |
Ccdc18 |
C |
T |
5: 108,296,838 (GRCm39) |
Q214* |
probably null |
Het |
Ccrl2 |
T |
C |
9: 110,884,422 (GRCm39) |
I359V |
probably benign |
Het |
Cdh20 |
C |
T |
1: 104,869,868 (GRCm39) |
T196I |
probably damaging |
Het |
Cfap20dc |
T |
C |
14: 8,482,521 (GRCm38) |
T551A |
probably benign |
Het |
Col6a3 |
G |
T |
1: 90,714,361 (GRCm39) |
T1683K |
unknown |
Het |
Copa |
A |
G |
1: 171,938,285 (GRCm39) |
I524V |
probably benign |
Het |
Cyld |
A |
T |
8: 89,457,383 (GRCm39) |
R536* |
probably null |
Het |
Dock10 |
T |
A |
1: 80,544,472 (GRCm39) |
E905V |
probably benign |
Het |
Dock5 |
A |
G |
14: 68,012,031 (GRCm39) |
F1348L |
probably benign |
Het |
Efcab3 |
A |
T |
11: 105,002,629 (GRCm39) |
K5664I |
probably damaging |
Het |
Gm5174 |
C |
A |
10: 86,492,144 (GRCm39) |
|
noncoding transcript |
Het |
Gm9892 |
A |
T |
8: 52,649,435 (GRCm39) |
|
noncoding transcript |
Het |
Grm4 |
A |
G |
17: 27,721,709 (GRCm39) |
I144T |
probably damaging |
Het |
Kcnv1 |
G |
A |
15: 44,977,840 (GRCm39) |
T66M |
probably damaging |
Het |
Krt28 |
G |
T |
11: 99,265,376 (GRCm39) |
S97Y |
probably damaging |
Het |
Map3k6 |
T |
C |
4: 132,979,258 (GRCm39) |
Y1204H |
possibly damaging |
Het |
Mfsd2b |
G |
T |
12: 4,924,356 (GRCm39) |
|
probably benign |
Het |
Nav3 |
T |
C |
10: 109,605,157 (GRCm39) |
D972G |
probably damaging |
Het |
Or2ak6 |
T |
G |
11: 58,593,277 (GRCm39) |
L250R |
probably damaging |
Het |
Or2y3 |
C |
T |
17: 38,393,321 (GRCm39) |
V183I |
probably benign |
Het |
Or5d39 |
T |
C |
2: 87,979,632 (GRCm39) |
T244A |
probably benign |
Het |
Prex1 |
G |
A |
2: 166,412,256 (GRCm39) |
R392W |
probably damaging |
Het |
Ptpn5 |
C |
T |
7: 46,741,296 (GRCm39) |
W38* |
probably null |
Het |
Rab3gap1 |
T |
C |
1: 127,865,304 (GRCm39) |
|
probably null |
Het |
Rfx7 |
A |
G |
9: 72,499,051 (GRCm39) |
T72A |
possibly damaging |
Het |
Scn7a |
T |
C |
2: 66,572,345 (GRCm39) |
I209V |
probably benign |
Het |
Sh3d21 |
C |
T |
4: 126,044,511 (GRCm39) |
|
probably benign |
Het |
Slc27a1 |
A |
G |
8: 72,037,617 (GRCm39) |
T535A |
probably benign |
Het |
Slc5a5 |
A |
G |
8: 71,342,930 (GRCm39) |
V210A |
probably benign |
Het |
Snx25 |
A |
G |
8: 46,558,291 (GRCm39) |
C239R |
probably damaging |
Het |
Sp5 |
T |
C |
2: 70,307,382 (GRCm39) |
F356L |
probably damaging |
Het |
Spaca9 |
T |
C |
2: 28,582,998 (GRCm39) |
I141V |
probably benign |
Het |
Tbcd |
T |
A |
11: 121,485,107 (GRCm39) |
L763H |
probably damaging |
Het |
Thnsl1 |
A |
G |
2: 21,217,059 (GRCm39) |
E271G |
probably benign |
Het |
Vmn1r79 |
T |
A |
7: 11,910,971 (GRCm39) |
C284* |
probably null |
Het |
Vwa5a |
T |
C |
9: 38,649,112 (GRCm39) |
|
probably benign |
Het |
Zar1 |
T |
C |
5: 72,737,736 (GRCm39) |
E121G |
possibly damaging |
Het |
Zscan29 |
C |
T |
2: 120,995,275 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Arfgef3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00769:Arfgef3
|
APN |
10 |
18,536,352 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00835:Arfgef3
|
APN |
10 |
18,537,106 (GRCm39) |
missense |
probably benign |
|
IGL00961:Arfgef3
|
APN |
10 |
18,486,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01400:Arfgef3
|
APN |
10 |
18,528,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01501:Arfgef3
|
APN |
10 |
18,476,308 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01595:Arfgef3
|
APN |
10 |
18,470,660 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01695:Arfgef3
|
APN |
10 |
18,479,167 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01774:Arfgef3
|
APN |
10 |
18,619,363 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02348:Arfgef3
|
APN |
10 |
18,467,095 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02371:Arfgef3
|
APN |
10 |
18,522,287 (GRCm39) |
missense |
probably benign |
|
IGL02400:Arfgef3
|
APN |
10 |
18,522,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02630:Arfgef3
|
APN |
10 |
18,537,140 (GRCm39) |
splice site |
probably benign |
|
IGL02815:Arfgef3
|
APN |
10 |
18,528,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03178:Arfgef3
|
APN |
10 |
18,488,973 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03182:Arfgef3
|
APN |
10 |
18,476,292 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Arfgef3
|
APN |
10 |
18,467,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Arfgef3
|
APN |
10 |
18,540,660 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03410:Arfgef3
|
APN |
10 |
18,476,238 (GRCm39) |
missense |
probably damaging |
1.00 |
Bow-wow
|
UTSW |
10 |
18,522,478 (GRCm39) |
nonsense |
probably null |
|
R0098:Arfgef3
|
UTSW |
10 |
18,465,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Arfgef3
|
UTSW |
10 |
18,465,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0141:Arfgef3
|
UTSW |
10 |
18,473,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Arfgef3
|
UTSW |
10 |
18,523,663 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0164:Arfgef3
|
UTSW |
10 |
18,523,663 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0241:Arfgef3
|
UTSW |
10 |
18,474,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Arfgef3
|
UTSW |
10 |
18,468,029 (GRCm39) |
missense |
probably damaging |
0.98 |
R0352:Arfgef3
|
UTSW |
10 |
18,537,135 (GRCm39) |
missense |
probably benign |
0.17 |
R0415:Arfgef3
|
UTSW |
10 |
18,488,875 (GRCm39) |
splice site |
probably benign |
|
R0417:Arfgef3
|
UTSW |
10 |
18,479,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Arfgef3
|
UTSW |
10 |
18,553,563 (GRCm39) |
splice site |
probably benign |
|
R0507:Arfgef3
|
UTSW |
10 |
18,467,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Arfgef3
|
UTSW |
10 |
18,475,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0582:Arfgef3
|
UTSW |
10 |
18,487,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Arfgef3
|
UTSW |
10 |
18,473,179 (GRCm39) |
missense |
probably benign |
0.31 |
R0826:Arfgef3
|
UTSW |
10 |
18,465,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R0919:Arfgef3
|
UTSW |
10 |
18,465,483 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0980:Arfgef3
|
UTSW |
10 |
18,467,866 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1027:Arfgef3
|
UTSW |
10 |
18,467,123 (GRCm39) |
missense |
probably benign |
0.02 |
R1140:Arfgef3
|
UTSW |
10 |
18,473,096 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1491:Arfgef3
|
UTSW |
10 |
18,522,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1493:Arfgef3
|
UTSW |
10 |
18,506,627 (GRCm39) |
missense |
probably damaging |
0.96 |
R1529:Arfgef3
|
UTSW |
10 |
18,488,970 (GRCm39) |
nonsense |
probably null |
|
R1564:Arfgef3
|
UTSW |
10 |
18,467,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Arfgef3
|
UTSW |
10 |
18,500,896 (GRCm39) |
missense |
probably null |
0.15 |
R1868:Arfgef3
|
UTSW |
10 |
18,537,135 (GRCm39) |
missense |
probably benign |
0.17 |
R1876:Arfgef3
|
UTSW |
10 |
18,473,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Arfgef3
|
UTSW |
10 |
18,528,511 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2211:Arfgef3
|
UTSW |
10 |
18,467,993 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2316:Arfgef3
|
UTSW |
10 |
18,492,701 (GRCm39) |
missense |
probably benign |
0.19 |
R2393:Arfgef3
|
UTSW |
10 |
18,473,535 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2407:Arfgef3
|
UTSW |
10 |
18,553,614 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3076:Arfgef3
|
UTSW |
10 |
18,479,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R3077:Arfgef3
|
UTSW |
10 |
18,479,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R3963:Arfgef3
|
UTSW |
10 |
18,468,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R4201:Arfgef3
|
UTSW |
10 |
18,495,530 (GRCm39) |
missense |
probably benign |
0.01 |
R4241:Arfgef3
|
UTSW |
10 |
18,500,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R4395:Arfgef3
|
UTSW |
10 |
18,473,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4455:Arfgef3
|
UTSW |
10 |
18,483,423 (GRCm39) |
missense |
probably benign |
0.18 |
R4480:Arfgef3
|
UTSW |
10 |
18,476,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R4499:Arfgef3
|
UTSW |
10 |
18,484,091 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4589:Arfgef3
|
UTSW |
10 |
18,521,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4635:Arfgef3
|
UTSW |
10 |
18,510,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Arfgef3
|
UTSW |
10 |
18,529,995 (GRCm39) |
missense |
probably benign |
|
R4801:Arfgef3
|
UTSW |
10 |
18,467,654 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Arfgef3
|
UTSW |
10 |
18,467,654 (GRCm39) |
missense |
probably benign |
0.00 |
R4807:Arfgef3
|
UTSW |
10 |
18,522,385 (GRCm39) |
missense |
probably benign |
|
R4828:Arfgef3
|
UTSW |
10 |
18,528,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R4861:Arfgef3
|
UTSW |
10 |
18,483,479 (GRCm39) |
missense |
probably benign |
0.01 |
R4861:Arfgef3
|
UTSW |
10 |
18,483,479 (GRCm39) |
missense |
probably benign |
0.01 |
R4917:Arfgef3
|
UTSW |
10 |
18,492,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R4918:Arfgef3
|
UTSW |
10 |
18,492,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R4922:Arfgef3
|
UTSW |
10 |
18,467,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R4929:Arfgef3
|
UTSW |
10 |
18,506,599 (GRCm39) |
missense |
probably benign |
0.00 |
R4937:Arfgef3
|
UTSW |
10 |
18,465,454 (GRCm39) |
missense |
probably damaging |
0.98 |
R5290:Arfgef3
|
UTSW |
10 |
18,476,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R5410:Arfgef3
|
UTSW |
10 |
18,486,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R5807:Arfgef3
|
UTSW |
10 |
18,523,546 (GRCm39) |
splice site |
probably null |
|
R5832:Arfgef3
|
UTSW |
10 |
18,506,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R5887:Arfgef3
|
UTSW |
10 |
18,483,413 (GRCm39) |
nonsense |
probably null |
|
R6272:Arfgef3
|
UTSW |
10 |
18,522,711 (GRCm39) |
missense |
probably benign |
0.00 |
R6302:Arfgef3
|
UTSW |
10 |
18,528,589 (GRCm39) |
missense |
probably damaging |
0.97 |
R6397:Arfgef3
|
UTSW |
10 |
18,483,413 (GRCm39) |
nonsense |
probably null |
|
R6495:Arfgef3
|
UTSW |
10 |
18,486,950 (GRCm39) |
critical splice donor site |
probably null |
|
R6707:Arfgef3
|
UTSW |
10 |
18,496,903 (GRCm39) |
missense |
probably benign |
0.11 |
R6814:Arfgef3
|
UTSW |
10 |
18,470,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Arfgef3
|
UTSW |
10 |
18,540,637 (GRCm39) |
critical splice donor site |
probably null |
|
R6870:Arfgef3
|
UTSW |
10 |
18,522,478 (GRCm39) |
nonsense |
probably null |
|
R6941:Arfgef3
|
UTSW |
10 |
18,501,203 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7094:Arfgef3
|
UTSW |
10 |
18,522,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Arfgef3
|
UTSW |
10 |
18,475,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Arfgef3
|
UTSW |
10 |
18,522,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R7247:Arfgef3
|
UTSW |
10 |
18,501,139 (GRCm39) |
missense |
probably benign |
0.00 |
R7249:Arfgef3
|
UTSW |
10 |
18,506,583 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7318:Arfgef3
|
UTSW |
10 |
18,506,211 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7391:Arfgef3
|
UTSW |
10 |
18,522,007 (GRCm39) |
missense |
probably benign |
0.05 |
R7527:Arfgef3
|
UTSW |
10 |
18,522,377 (GRCm39) |
missense |
probably benign |
|
R7618:Arfgef3
|
UTSW |
10 |
18,522,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Arfgef3
|
UTSW |
10 |
18,470,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R7851:Arfgef3
|
UTSW |
10 |
18,468,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R8112:Arfgef3
|
UTSW |
10 |
18,528,379 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8133:Arfgef3
|
UTSW |
10 |
18,486,951 (GRCm39) |
critical splice donor site |
probably null |
|
R8242:Arfgef3
|
UTSW |
10 |
18,505,824 (GRCm39) |
missense |
probably benign |
0.25 |
R8369:Arfgef3
|
UTSW |
10 |
18,465,477 (GRCm39) |
missense |
probably benign |
0.34 |
R8396:Arfgef3
|
UTSW |
10 |
18,528,280 (GRCm39) |
critical splice donor site |
probably null |
|
R8553:Arfgef3
|
UTSW |
10 |
18,479,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:Arfgef3
|
UTSW |
10 |
18,522,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R8821:Arfgef3
|
UTSW |
10 |
18,528,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8831:Arfgef3
|
UTSW |
10 |
18,528,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8918:Arfgef3
|
UTSW |
10 |
18,511,453 (GRCm39) |
missense |
probably benign |
0.01 |
R8929:Arfgef3
|
UTSW |
10 |
18,479,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9001:Arfgef3
|
UTSW |
10 |
18,522,476 (GRCm39) |
missense |
probably benign |
0.32 |
R9077:Arfgef3
|
UTSW |
10 |
18,500,899 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9258:Arfgef3
|
UTSW |
10 |
18,465,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R9267:Arfgef3
|
UTSW |
10 |
18,475,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R9358:Arfgef3
|
UTSW |
10 |
18,492,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9388:Arfgef3
|
UTSW |
10 |
18,505,877 (GRCm39) |
missense |
probably benign |
0.35 |
R9389:Arfgef3
|
UTSW |
10 |
18,479,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Arfgef3
|
UTSW |
10 |
18,522,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9713:Arfgef3
|
UTSW |
10 |
18,528,556 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Arfgef3
|
UTSW |
10 |
18,528,374 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Arfgef3
|
UTSW |
10 |
18,510,600 (GRCm39) |
missense |
probably benign |
0.26 |
Z1176:Arfgef3
|
UTSW |
10 |
18,484,106 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Arfgef3
|
UTSW |
10 |
18,467,185 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arfgef3
|
UTSW |
10 |
18,503,376 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arfgef3
|
UTSW |
10 |
18,483,524 (GRCm39) |
missense |
probably damaging |
1.00 |
|