Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
C |
10: 79,849,165 (GRCm39) |
V1842A |
probably damaging |
Het |
Abi3 |
A |
T |
11: 95,732,934 (GRCm39) |
F13L |
probably benign |
Het |
Adgre4 |
A |
G |
17: 56,125,758 (GRCm39) |
K538R |
probably benign |
Het |
Bcas3 |
C |
T |
11: 85,342,581 (GRCm39) |
H191Y |
probably benign |
Het |
Bicdl2 |
A |
G |
17: 23,886,538 (GRCm39) |
T376A |
probably benign |
Het |
Ceacam18 |
C |
A |
7: 43,286,497 (GRCm39) |
N123K |
possibly damaging |
Het |
Celsr3 |
C |
T |
9: 108,709,224 (GRCm39) |
R1357C |
possibly damaging |
Het |
Chek2 |
T |
C |
5: 110,989,148 (GRCm39) |
|
probably benign |
Het |
Chmp7 |
A |
G |
14: 69,958,684 (GRCm39) |
V210A |
probably benign |
Het |
Chrm2 |
A |
G |
6: 36,500,290 (GRCm39) |
K49R |
probably damaging |
Het |
Ciao2b |
T |
C |
8: 105,368,282 (GRCm39) |
N14S |
probably damaging |
Het |
Daam1 |
T |
A |
12: 71,999,233 (GRCm39) |
L623* |
probably null |
Het |
Ddx31 |
T |
A |
2: 28,753,782 (GRCm39) |
C448S |
probably damaging |
Het |
Dnah7a |
A |
G |
1: 53,586,331 (GRCm39) |
S1507P |
probably damaging |
Het |
Dnah8 |
C |
A |
17: 30,965,928 (GRCm39) |
T2420K |
probably damaging |
Het |
Dyrk3 |
C |
T |
1: 131,057,432 (GRCm39) |
R247H |
probably damaging |
Het |
Exoc4 |
A |
G |
6: 33,242,934 (GRCm39) |
E49G |
probably damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Foxj3 |
A |
G |
4: 119,476,596 (GRCm39) |
E258G |
probably damaging |
Het |
Gata4 |
C |
T |
14: 63,478,075 (GRCm39) |
A175T |
probably benign |
Het |
Helz2 |
C |
T |
2: 180,877,321 (GRCm39) |
E1106K |
probably damaging |
Het |
Hip1 |
G |
T |
5: 135,465,252 (GRCm39) |
S385R |
probably benign |
Het |
Igsf9 |
C |
T |
1: 172,312,078 (GRCm39) |
T8I |
probably benign |
Het |
Insyn2b |
G |
A |
11: 34,352,788 (GRCm39) |
E277K |
probably damaging |
Het |
Katnal2 |
A |
G |
18: 77,105,190 (GRCm39) |
Y86H |
possibly damaging |
Het |
Kcnh6 |
A |
T |
11: 105,918,417 (GRCm39) |
I756F |
possibly damaging |
Het |
Kdm5b |
C |
T |
1: 134,535,432 (GRCm39) |
R570* |
probably null |
Het |
Kif16b |
T |
A |
2: 142,582,889 (GRCm39) |
R545S |
probably damaging |
Het |
Kif21b |
T |
A |
1: 136,100,030 (GRCm39) |
I1528N |
possibly damaging |
Het |
Kmt2a |
T |
C |
9: 44,730,571 (GRCm39) |
|
probably benign |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Melk |
C |
T |
4: 44,363,730 (GRCm39) |
T592M |
probably damaging |
Het |
Mknk2 |
T |
C |
10: 80,507,597 (GRCm39) |
T60A |
probably benign |
Het |
Ncoa6 |
T |
C |
2: 155,248,907 (GRCm39) |
K1466E |
probably damaging |
Het |
Ntsr2 |
A |
C |
12: 16,704,083 (GRCm39) |
T109P |
probably damaging |
Het |
Nup214 |
C |
A |
2: 31,907,158 (GRCm39) |
S995Y |
unknown |
Het |
Or2a5 |
A |
T |
6: 42,873,454 (GRCm39) |
Q23L |
probably benign |
Het |
Pclo |
T |
A |
5: 14,762,750 (GRCm39) |
L456* |
probably null |
Het |
Pde5a |
A |
G |
3: 122,541,825 (GRCm39) |
D105G |
probably damaging |
Het |
Pik3c3 |
C |
A |
18: 30,456,597 (GRCm39) |
P709H |
probably damaging |
Het |
R3hdm4 |
C |
T |
10: 79,748,292 (GRCm39) |
E162K |
possibly damaging |
Het |
Rab3c |
T |
C |
13: 110,198,497 (GRCm39) |
N179S |
possibly damaging |
Het |
Setdb2 |
T |
A |
14: 59,646,885 (GRCm39) |
R559S |
probably benign |
Het |
Sf3b1 |
A |
G |
1: 55,042,469 (GRCm39) |
Y474H |
probably benign |
Het |
Slc6a6 |
G |
T |
6: 91,712,155 (GRCm39) |
W228L |
probably benign |
Het |
Slc8a2 |
T |
G |
7: 15,891,228 (GRCm39) |
I750S |
probably damaging |
Het |
Slco2b1 |
T |
A |
7: 99,309,251 (GRCm39) |
I194L |
unknown |
Het |
Smarcd1 |
C |
T |
15: 99,601,128 (GRCm39) |
Q45* |
probably null |
Het |
Srsf12 |
A |
T |
4: 33,209,330 (GRCm39) |
N9Y |
probably damaging |
Het |
St7 |
T |
C |
6: 17,819,317 (GRCm39) |
S74P |
probably damaging |
Het |
Stxbp5l |
T |
A |
16: 36,994,688 (GRCm39) |
E739V |
probably damaging |
Het |
Sun3 |
T |
A |
11: 8,981,496 (GRCm39) |
Q36L |
possibly damaging |
Het |
Tbc1d32 |
T |
C |
10: 56,047,033 (GRCm39) |
H545R |
possibly damaging |
Het |
Tcp11 |
A |
T |
17: 28,296,994 (GRCm39) |
C133S |
probably benign |
Het |
Tm6sf2 |
T |
C |
8: 70,526,939 (GRCm39) |
V36A |
possibly damaging |
Het |
Tmem108 |
T |
C |
9: 103,376,717 (GRCm39) |
Y244C |
probably damaging |
Het |
Tra2a |
A |
T |
6: 49,227,949 (GRCm39) |
|
probably benign |
Het |
Trpm3 |
A |
T |
19: 22,903,332 (GRCm39) |
I1031F |
probably damaging |
Het |
Ttll3 |
A |
G |
6: 113,378,292 (GRCm39) |
K381E |
probably benign |
Het |
Uaca |
T |
C |
9: 60,778,430 (GRCm39) |
V937A |
probably benign |
Het |
Umod |
C |
T |
7: 119,071,577 (GRCm39) |
G388D |
probably damaging |
Het |
Vmn2r90 |
G |
A |
17: 17,924,412 (GRCm39) |
|
probably null |
Het |
Zbtb47 |
T |
A |
9: 121,594,661 (GRCm39) |
F540Y |
probably damaging |
Het |
Zfp644 |
G |
A |
5: 106,783,541 (GRCm39) |
T1002I |
probably damaging |
Het |
Zfp738 |
A |
G |
13: 67,819,131 (GRCm39) |
Y287H |
probably damaging |
Het |
Zfyve16 |
T |
C |
13: 92,644,771 (GRCm39) |
T1144A |
probably benign |
Het |
Zgrf1 |
T |
C |
3: 127,361,352 (GRCm39) |
|
probably null |
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 |
PIT4453001:Srcap
|
UTSW |
7 |
127,148,492 (GRCm39) |
missense |
possibly damaging |
0.52 |
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 |
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 |
|
|