Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
G |
3: 121,898,965 (GRCm39) |
I649S |
probably damaging |
Het |
Abcc2 |
T |
A |
19: 43,792,221 (GRCm39) |
L334* |
probably null |
Het |
Adam28 |
A |
T |
14: 68,872,325 (GRCm39) |
S306T |
probably benign |
Het |
Adam34 |
T |
A |
8: 44,104,349 (GRCm39) |
D432V |
probably damaging |
Het |
Adcy7 |
A |
G |
8: 89,050,264 (GRCm39) |
Y723C |
probably benign |
Het |
Adgre5 |
T |
A |
8: 84,451,089 (GRCm39) |
M713L |
probably benign |
Het |
Aebp2 |
C |
A |
6: 140,583,412 (GRCm39) |
C295* |
probably null |
Het |
Amn1 |
G |
T |
6: 149,072,357 (GRCm39) |
Q127K |
probably benign |
Het |
Atcay |
C |
T |
10: 81,046,383 (GRCm39) |
V314M |
probably damaging |
Het |
Atp1a1 |
T |
C |
3: 101,488,495 (GRCm39) |
E847G |
probably benign |
Het |
Atp2b1 |
A |
G |
10: 98,852,840 (GRCm39) |
E1039G |
probably benign |
Het |
Caskin1 |
A |
G |
17: 24,718,266 (GRCm39) |
Y292C |
probably damaging |
Het |
Cftr |
A |
G |
6: 18,214,105 (GRCm39) |
T94A |
probably damaging |
Het |
Ciart |
T |
A |
3: 95,787,788 (GRCm39) |
K182M |
probably damaging |
Het |
Col1a2 |
A |
C |
6: 4,527,079 (GRCm39) |
S603R |
possibly damaging |
Het |
Cspp1 |
C |
A |
1: 10,145,097 (GRCm39) |
S298R |
possibly damaging |
Het |
Cul7 |
T |
A |
17: 46,962,746 (GRCm39) |
C126S |
probably damaging |
Het |
Cyp2c55 |
A |
T |
19: 39,000,235 (GRCm39) |
I145F |
probably damaging |
Het |
Cypt4 |
G |
C |
9: 24,536,770 (GRCm39) |
A87P |
probably damaging |
Het |
Disp2 |
G |
A |
2: 118,618,125 (GRCm39) |
V224M |
probably benign |
Het |
Dlgap5 |
TTC |
T |
14: 47,638,979 (GRCm39) |
|
probably null |
Het |
Dock1 |
A |
G |
7: 134,754,029 (GRCm39) |
K1602R |
probably benign |
Het |
Ears2 |
T |
C |
7: 121,647,562 (GRCm39) |
I241V |
probably benign |
Het |
Eml6 |
T |
C |
11: 29,752,489 (GRCm39) |
T975A |
probably damaging |
Het |
Ephb2 |
T |
C |
4: 136,388,121 (GRCm39) |
T660A |
probably benign |
Het |
Fbxw7 |
G |
A |
3: 84,872,621 (GRCm39) |
V268M |
|
Het |
Gart |
A |
G |
16: 91,433,426 (GRCm39) |
F289S |
probably damaging |
Het |
Gmcl1 |
G |
T |
6: 86,681,520 (GRCm39) |
N391K |
probably benign |
Het |
Greb1l |
A |
C |
18: 10,533,031 (GRCm39) |
Q975P |
probably damaging |
Het |
Greb1l |
G |
T |
18: 10,533,032 (GRCm39) |
Q975H |
probably benign |
Het |
Grik5 |
C |
A |
7: 24,710,119 (GRCm39) |
R872L |
probably damaging |
Het |
Hmox2 |
T |
A |
16: 4,582,921 (GRCm39) |
I218N |
probably damaging |
Het |
Hook1 |
A |
T |
4: 95,903,089 (GRCm39) |
D526V |
probably damaging |
Het |
Ifna4 |
A |
T |
4: 88,760,191 (GRCm39) |
N32Y |
probably damaging |
Het |
Ighg2b |
T |
A |
12: 113,270,492 (GRCm39) |
N213Y |
unknown |
Het |
Itih4 |
G |
A |
14: 30,623,127 (GRCm39) |
V900I |
probably benign |
Het |
Itpr2 |
A |
T |
6: 146,274,671 (GRCm39) |
F837Y |
probably damaging |
Het |
Kif3a |
T |
C |
11: 53,469,941 (GRCm39) |
V147A |
probably benign |
Het |
Klra9 |
T |
A |
6: 130,168,284 (GRCm39) |
|
probably benign |
Het |
Lamp3 |
G |
T |
16: 19,492,210 (GRCm39) |
Q345K |
probably benign |
Het |
Ltbp3 |
G |
A |
19: 5,807,822 (GRCm39) |
E1188K |
probably damaging |
Het |
Med1 |
T |
A |
11: 98,049,243 (GRCm39) |
I518L |
probably benign |
Het |
Mis18bp1 |
T |
C |
12: 65,205,447 (GRCm39) |
T242A |
probably damaging |
Het |
Nemp1 |
T |
A |
10: 127,532,123 (GRCm39) |
F392Y |
probably benign |
Het |
Obscn |
C |
A |
11: 58,951,802 (GRCm39) |
G3984W |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,960,660 (GRCm39) |
H3217L |
possibly damaging |
Het |
Or10ak7 |
A |
G |
4: 118,791,823 (GRCm39) |
M74T |
probably benign |
Het |
Or13j1 |
A |
G |
4: 43,706,464 (GRCm39) |
Y35H |
probably damaging |
Het |
Or2d3b |
C |
T |
7: 106,514,136 (GRCm39) |
H244Y |
probably damaging |
Het |
Or2d3c |
T |
C |
7: 106,526,049 (GRCm39) |
I206V |
probably benign |
Het |
Or5l14 |
C |
T |
2: 87,792,802 (GRCm39) |
V145M |
possibly damaging |
Het |
P4ha1 |
G |
T |
10: 59,186,294 (GRCm39) |
A258S |
probably benign |
Het |
Parn |
T |
C |
16: 13,425,145 (GRCm39) |
I423V |
probably benign |
Het |
Pcdh20 |
C |
A |
14: 88,704,744 (GRCm39) |
S852I |
probably damaging |
Het |
Pcnx3 |
A |
G |
19: 5,722,784 (GRCm39) |
|
probably null |
Het |
Pcsk1 |
A |
T |
13: 75,260,769 (GRCm39) |
I331F |
probably damaging |
Het |
Pkd1l2 |
G |
T |
8: 117,748,761 (GRCm39) |
S1803R |
probably benign |
Het |
Pkd1l3 |
C |
A |
8: 110,387,433 (GRCm39) |
N1792K |
probably damaging |
Het |
Plekhg1 |
C |
A |
10: 3,913,469 (GRCm39) |
Q1119K |
|
Het |
Prr30 |
T |
A |
14: 101,436,371 (GRCm39) |
T64S |
probably benign |
Het |
Rec114 |
T |
C |
9: 58,567,653 (GRCm39) |
N111S |
probably benign |
Het |
Reck |
G |
A |
4: 43,895,850 (GRCm39) |
V79I |
probably benign |
Het |
Rexo1 |
A |
G |
10: 80,386,231 (GRCm39) |
F276L |
probably damaging |
Het |
Rgs6 |
T |
C |
12: 83,138,553 (GRCm39) |
Y296H |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 142,197,793 (GRCm39) |
R2149G |
probably benign |
Het |
Slc20a2 |
C |
A |
8: 23,025,398 (GRCm39) |
F33L |
probably damaging |
Het |
Spopl |
T |
A |
2: 23,435,461 (GRCm39) |
T25S |
probably damaging |
Het |
Srek1 |
A |
C |
13: 103,881,291 (GRCm39) |
|
probably null |
Het |
St8sia1 |
C |
T |
6: 142,774,978 (GRCm39) |
W200* |
probably null |
Het |
Tas2r106 |
A |
T |
6: 131,655,465 (GRCm39) |
F129I |
possibly damaging |
Het |
Tbrg4 |
A |
T |
11: 6,570,857 (GRCm39) |
L205Q |
probably damaging |
Het |
Tchh |
C |
A |
3: 93,353,187 (GRCm39) |
R876S |
unknown |
Het |
Thap12 |
G |
T |
7: 98,364,245 (GRCm39) |
A138S |
probably benign |
Het |
Tjp1 |
C |
T |
7: 64,993,362 (GRCm39) |
|
probably null |
Het |
Traf4 |
G |
A |
11: 78,052,360 (GRCm39) |
P95L |
probably benign |
Het |
Trappc9 |
ATCTC |
ATCTCTC |
15: 72,903,447 (GRCm39) |
|
probably null |
Het |
Usp20 |
G |
A |
2: 30,907,498 (GRCm39) |
V677M |
possibly damaging |
Het |
Usp50 |
C |
A |
2: 126,625,236 (GRCm39) |
|
probably benign |
Het |
Vmn1r21 |
T |
C |
6: 57,821,307 (GRCm39) |
T46A |
probably benign |
Het |
Vmn2r54 |
T |
A |
7: 12,363,669 (GRCm39) |
H408L |
probably benign |
Het |
Zfp266 |
T |
C |
9: 20,417,299 (GRCm39) |
T30A |
probably benign |
Het |
Zfp536 |
T |
C |
7: 37,179,182 (GRCm39) |
H1141R |
probably benign |
Het |
|
Other mutations in Srcap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Srcap
|
APN |
7 |
127,141,885 (GRCm39) |
splice site |
probably benign |
|
IGL00475:Srcap
|
APN |
7 |
127,152,093 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01064:Srcap
|
APN |
7 |
127,159,064 (GRCm39) |
unclassified |
probably benign |
|
IGL01129:Srcap
|
APN |
7 |
127,120,823 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01670:Srcap
|
APN |
7 |
127,127,604 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01861:Srcap
|
APN |
7 |
127,124,457 (GRCm39) |
splice site |
probably benign |
|
IGL02237:Srcap
|
APN |
7 |
127,133,864 (GRCm39) |
splice site |
probably benign |
|
IGL02665:Srcap
|
APN |
7 |
127,140,075 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02688:Srcap
|
APN |
7 |
127,141,625 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02744:Srcap
|
APN |
7 |
127,133,838 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02810:Srcap
|
APN |
7 |
127,120,835 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03184:Srcap
|
APN |
7 |
127,129,674 (GRCm39) |
unclassified |
probably benign |
|
IGL03309:Srcap
|
APN |
7 |
127,129,965 (GRCm39) |
missense |
probably damaging |
0.99 |
R1340:Srcap
|
UTSW |
7 |
127,159,910 (GRCm39) |
intron |
probably benign |
|
R1401:Srcap
|
UTSW |
7 |
127,159,124 (GRCm39) |
unclassified |
probably benign |
|
R1455:Srcap
|
UTSW |
7 |
127,129,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R1470:Srcap
|
UTSW |
7 |
127,158,899 (GRCm39) |
unclassified |
probably benign |
|
R1470:Srcap
|
UTSW |
7 |
127,158,899 (GRCm39) |
unclassified |
probably benign |
|
R1761:Srcap
|
UTSW |
7 |
127,134,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Srcap
|
UTSW |
7 |
127,133,994 (GRCm39) |
missense |
probably damaging |
0.99 |
R2483:Srcap
|
UTSW |
7 |
127,141,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R2892:Srcap
|
UTSW |
7 |
127,138,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R2893:Srcap
|
UTSW |
7 |
127,138,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R3623:Srcap
|
UTSW |
7 |
127,141,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R3976:Srcap
|
UTSW |
7 |
127,148,411 (GRCm39) |
missense |
probably benign |
0.18 |
R4001:Srcap
|
UTSW |
7 |
127,131,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4015:Srcap
|
UTSW |
7 |
127,124,595 (GRCm39) |
missense |
probably benign |
0.27 |
R4581:Srcap
|
UTSW |
7 |
127,157,482 (GRCm39) |
unclassified |
probably benign |
|
R4643:Srcap
|
UTSW |
7 |
127,140,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4644:Srcap
|
UTSW |
7 |
127,151,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R4690:Srcap
|
UTSW |
7 |
127,137,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R4693:Srcap
|
UTSW |
7 |
127,137,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Srcap
|
UTSW |
7 |
127,140,731 (GRCm39) |
missense |
probably benign |
0.13 |
R4728:Srcap
|
UTSW |
7 |
127,140,096 (GRCm39) |
critical splice donor site |
probably null |
|
R4740:Srcap
|
UTSW |
7 |
127,148,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R4752:Srcap
|
UTSW |
7 |
127,158,172 (GRCm39) |
unclassified |
probably benign |
|
R4834:Srcap
|
UTSW |
7 |
127,156,782 (GRCm39) |
critical splice donor site |
probably null |
|
R4837:Srcap
|
UTSW |
7 |
127,158,134 (GRCm39) |
unclassified |
probably benign |
|
R4884:Srcap
|
UTSW |
7 |
127,121,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4889:Srcap
|
UTSW |
7 |
127,137,719 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5088:Srcap
|
UTSW |
7 |
127,140,833 (GRCm39) |
missense |
probably benign |
0.02 |
R5102:Srcap
|
UTSW |
7 |
127,129,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R5358:Srcap
|
UTSW |
7 |
127,139,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R5372:Srcap
|
UTSW |
7 |
127,156,785 (GRCm39) |
splice site |
probably null |
|
R5397:Srcap
|
UTSW |
7 |
127,152,468 (GRCm39) |
critical splice donor site |
probably null |
|
R5481:Srcap
|
UTSW |
7 |
127,131,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5566:Srcap
|
UTSW |
7 |
127,124,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R5584:Srcap
|
UTSW |
7 |
127,127,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R5693:Srcap
|
UTSW |
7 |
127,118,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Srcap
|
UTSW |
7 |
127,158,994 (GRCm39) |
unclassified |
probably benign |
|
R5805:Srcap
|
UTSW |
7 |
127,141,211 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5806:Srcap
|
UTSW |
7 |
127,158,335 (GRCm39) |
unclassified |
probably benign |
|
R5921:Srcap
|
UTSW |
7 |
127,158,005 (GRCm39) |
unclassified |
probably benign |
|
R5942:Srcap
|
UTSW |
7 |
127,137,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Srcap
|
UTSW |
7 |
127,137,922 (GRCm39) |
missense |
probably benign |
0.01 |
R6057:Srcap
|
UTSW |
7 |
127,140,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R6113:Srcap
|
UTSW |
7 |
127,159,453 (GRCm39) |
unclassified |
probably benign |
|
R6150:Srcap
|
UTSW |
7 |
127,134,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R6212:Srcap
|
UTSW |
7 |
127,148,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Srcap
|
UTSW |
7 |
127,129,626 (GRCm39) |
unclassified |
probably benign |
|
R6437:Srcap
|
UTSW |
7 |
127,127,722 (GRCm39) |
splice site |
probably null |
|
R6492:Srcap
|
UTSW |
7 |
127,121,317 (GRCm39) |
nonsense |
probably null |
|
R6537:Srcap
|
UTSW |
7 |
127,141,392 (GRCm39) |
missense |
probably damaging |
0.97 |
R6659:Srcap
|
UTSW |
7 |
127,141,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R6713:Srcap
|
UTSW |
7 |
127,134,089 (GRCm39) |
missense |
probably benign |
0.28 |
R6717:Srcap
|
UTSW |
7 |
127,157,482 (GRCm39) |
unclassified |
probably benign |
|
R6941:Srcap
|
UTSW |
7 |
127,141,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R7068:Srcap
|
UTSW |
7 |
127,141,115 (GRCm39) |
missense |
probably benign |
0.00 |
R7097:Srcap
|
UTSW |
7 |
127,138,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R7394:Srcap
|
UTSW |
7 |
127,134,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R7426:Srcap
|
UTSW |
7 |
127,137,689 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7434:Srcap
|
UTSW |
7 |
127,159,414 (GRCm39) |
missense |
unknown |
|
R7559:Srcap
|
UTSW |
7 |
127,129,722 (GRCm39) |
missense |
unknown |
|
R7638:Srcap
|
UTSW |
7 |
127,137,920 (GRCm39) |
missense |
probably benign |
0.39 |
R7677:Srcap
|
UTSW |
7 |
127,158,980 (GRCm39) |
missense |
unknown |
|
R7715:Srcap
|
UTSW |
7 |
127,148,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R7757:Srcap
|
UTSW |
7 |
127,129,966 (GRCm39) |
missense |
probably damaging |
0.99 |
R7811:Srcap
|
UTSW |
7 |
127,141,221 (GRCm39) |
missense |
probably damaging |
0.97 |
R7821:Srcap
|
UTSW |
7 |
127,129,499 (GRCm39) |
unclassified |
probably benign |
|
R7869:Srcap
|
UTSW |
7 |
127,138,366 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7870:Srcap
|
UTSW |
7 |
127,159,730 (GRCm39) |
missense |
unknown |
|
R7941:Srcap
|
UTSW |
7 |
127,157,462 (GRCm39) |
unclassified |
probably benign |
|
R7994:Srcap
|
UTSW |
7 |
127,140,930 (GRCm39) |
missense |
probably benign |
0.00 |
R8035:Srcap
|
UTSW |
7 |
127,141,784 (GRCm39) |
missense |
probably benign |
0.05 |
R8066:Srcap
|
UTSW |
7 |
127,120,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R8066:Srcap
|
UTSW |
7 |
127,139,484 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8168:Srcap
|
UTSW |
7 |
127,141,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R8194:Srcap
|
UTSW |
7 |
127,138,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R8288:Srcap
|
UTSW |
7 |
127,130,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Srcap
|
UTSW |
7 |
127,124,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R8308:Srcap
|
UTSW |
7 |
127,152,353 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8309:Srcap
|
UTSW |
7 |
127,148,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R8311:Srcap
|
UTSW |
7 |
127,156,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R8321:Srcap
|
UTSW |
7 |
127,140,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8365:Srcap
|
UTSW |
7 |
127,148,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Srcap
|
UTSW |
7 |
127,141,560 (GRCm39) |
missense |
probably benign |
0.00 |
R8815:Srcap
|
UTSW |
7 |
127,158,037 (GRCm39) |
missense |
unknown |
|
R8817:Srcap
|
UTSW |
7 |
127,152,395 (GRCm39) |
missense |
probably benign |
0.23 |
R8924:Srcap
|
UTSW |
7 |
127,158,204 (GRCm39) |
missense |
unknown |
|
R8933:Srcap
|
UTSW |
7 |
127,151,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8961:Srcap
|
UTSW |
7 |
127,141,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R9000:Srcap
|
UTSW |
7 |
127,130,943 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9098:Srcap
|
UTSW |
7 |
127,151,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R9124:Srcap
|
UTSW |
7 |
127,159,874 (GRCm39) |
missense |
unknown |
|
R9163:Srcap
|
UTSW |
7 |
127,121,162 (GRCm39) |
missense |
unknown |
|
R9332:Srcap
|
UTSW |
7 |
127,158,812 (GRCm39) |
missense |
unknown |
|
R9389:Srcap
|
UTSW |
7 |
127,141,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R9464:Srcap
|
UTSW |
7 |
127,137,273 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9467:Srcap
|
UTSW |
7 |
127,139,531 (GRCm39) |
missense |
probably damaging |
0.98 |
R9554:Srcap
|
UTSW |
7 |
127,151,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R9596:Srcap
|
UTSW |
7 |
127,131,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R9597:Srcap
|
UTSW |
7 |
127,121,219 (GRCm39) |
missense |
possibly damaging |
0.91 |
X0025:Srcap
|
UTSW |
7 |
127,159,277 (GRCm39) |
unclassified |
probably benign |
|
|