Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
C |
5: 8,944,166 (GRCm39) |
|
probably null |
Het |
Ankib1 |
A |
T |
5: 3,784,194 (GRCm39) |
|
probably benign |
Het |
Birc2 |
T |
C |
9: 7,860,733 (GRCm39) |
Y195C |
probably damaging |
Het |
Cand2 |
T |
C |
6: 115,759,755 (GRCm39) |
I142T |
probably benign |
Het |
Cdh15 |
T |
C |
8: 123,592,062 (GRCm39) |
|
probably benign |
Het |
Ceacam5 |
G |
A |
7: 17,479,534 (GRCm39) |
G217D |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,917,385 (GRCm39) |
H25L |
unknown |
Het |
Cfap95 |
A |
G |
19: 23,630,100 (GRCm39) |
|
probably benign |
Het |
Col22a1 |
A |
G |
15: 71,778,889 (GRCm39) |
V266A |
probably benign |
Het |
D3Ertd751e |
A |
G |
3: 41,703,132 (GRCm39) |
D69G |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,622,164 (GRCm39) |
I1518V |
probably damaging |
Het |
Entpd8 |
A |
G |
2: 24,974,358 (GRCm39) |
K381R |
probably benign |
Het |
Fli1 |
T |
A |
9: 32,335,397 (GRCm39) |
K345I |
probably damaging |
Het |
G6pd2 |
T |
C |
5: 61,967,281 (GRCm39) |
V352A |
probably damaging |
Het |
Gbp11 |
C |
T |
5: 105,475,482 (GRCm39) |
|
probably null |
Het |
Gm11992 |
A |
G |
11: 9,018,383 (GRCm39) |
*292W |
probably null |
Het |
Ifnar2 |
T |
A |
16: 91,188,599 (GRCm39) |
|
probably benign |
Het |
Impg1 |
T |
C |
9: 80,230,111 (GRCm39) |
K661R |
probably benign |
Het |
Inf2 |
G |
T |
12: 112,578,290 (GRCm39) |
E651* |
probably null |
Het |
Ints1 |
A |
G |
5: 139,753,258 (GRCm39) |
|
probably benign |
Het |
Iqcf4 |
T |
C |
9: 106,447,832 (GRCm39) |
K26E |
probably benign |
Het |
Map4k3 |
A |
G |
17: 80,951,613 (GRCm39) |
V289A |
probably benign |
Het |
Mis18bp1 |
T |
C |
12: 65,205,215 (GRCm39) |
K319R |
possibly damaging |
Het |
Nubpl |
T |
C |
12: 52,352,638 (GRCm39) |
V291A |
probably damaging |
Het |
Or4f56 |
A |
G |
2: 111,703,295 (GRCm39) |
F302L |
probably benign |
Het |
Or4k15c |
C |
T |
14: 50,321,454 (GRCm39) |
R228H |
probably benign |
Het |
Or8b57 |
A |
G |
9: 40,003,324 (GRCm39) |
S313P |
possibly damaging |
Het |
Or8k38 |
T |
C |
2: 86,488,551 (GRCm39) |
N84D |
probably benign |
Het |
Otof |
A |
G |
5: 30,598,723 (GRCm39) |
S29P |
probably benign |
Het |
Pcca |
A |
G |
14: 122,927,545 (GRCm39) |
D436G |
possibly damaging |
Het |
Rasef |
T |
A |
4: 73,645,882 (GRCm39) |
T496S |
probably damaging |
Het |
Saa2 |
A |
G |
7: 46,402,896 (GRCm39) |
D49G |
probably benign |
Het |
Scart1 |
T |
A |
7: 139,804,552 (GRCm39) |
|
probably null |
Het |
Scn2a |
A |
G |
2: 65,547,852 (GRCm39) |
I1015V |
probably benign |
Het |
Sim2 |
T |
C |
16: 93,907,119 (GRCm39) |
Y154H |
possibly damaging |
Het |
Spag17 |
A |
G |
3: 100,002,865 (GRCm39) |
H1863R |
probably benign |
Het |
Supt16 |
C |
T |
14: 52,414,489 (GRCm39) |
E438K |
probably benign |
Het |
Svil |
A |
G |
18: 5,064,501 (GRCm39) |
E1111G |
probably benign |
Het |
Vmn1r205 |
T |
C |
13: 22,776,273 (GRCm39) |
I276M |
probably benign |
Het |
Vps13d |
A |
T |
4: 144,882,776 (GRCm39) |
I939N |
possibly damaging |
Het |
Zc3h11a |
T |
C |
1: 133,553,600 (GRCm39) |
M515V |
probably benign |
Het |
Zfp457 |
T |
C |
13: 67,442,330 (GRCm39) |
T82A |
possibly damaging |
Het |
|
Other mutations in Trabd2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01404:Trabd2b
|
APN |
4 |
114,457,153 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01866:Trabd2b
|
APN |
4 |
114,266,117 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03056:Trabd2b
|
APN |
4 |
114,266,535 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03167:Trabd2b
|
APN |
4 |
114,467,195 (GRCm39) |
missense |
probably benign |
|
E0374:Trabd2b
|
UTSW |
4 |
114,457,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R0645:Trabd2b
|
UTSW |
4 |
114,443,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Trabd2b
|
UTSW |
4 |
114,437,519 (GRCm39) |
missense |
probably benign |
0.00 |
R0833:Trabd2b
|
UTSW |
4 |
114,437,519 (GRCm39) |
missense |
probably benign |
0.00 |
R1580:Trabd2b
|
UTSW |
4 |
114,437,531 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1599:Trabd2b
|
UTSW |
4 |
114,266,178 (GRCm39) |
missense |
probably damaging |
0.99 |
R2132:Trabd2b
|
UTSW |
4 |
114,467,205 (GRCm39) |
missense |
probably benign |
|
R2133:Trabd2b
|
UTSW |
4 |
114,467,205 (GRCm39) |
missense |
probably benign |
|
R2204:Trabd2b
|
UTSW |
4 |
114,460,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R2518:Trabd2b
|
UTSW |
4 |
114,457,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R4940:Trabd2b
|
UTSW |
4 |
114,266,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R4994:Trabd2b
|
UTSW |
4 |
114,264,052 (GRCm39) |
missense |
probably benign |
0.05 |
R5104:Trabd2b
|
UTSW |
4 |
114,264,114 (GRCm39) |
missense |
probably benign |
0.21 |
R5219:Trabd2b
|
UTSW |
4 |
114,460,007 (GRCm39) |
missense |
probably damaging |
0.97 |
R6456:Trabd2b
|
UTSW |
4 |
114,443,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R7148:Trabd2b
|
UTSW |
4 |
114,266,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R7192:Trabd2b
|
UTSW |
4 |
114,467,217 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7195:Trabd2b
|
UTSW |
4 |
114,266,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Trabd2b
|
UTSW |
4 |
114,467,194 (GRCm39) |
missense |
probably benign |
0.00 |
R8490:Trabd2b
|
UTSW |
4 |
114,460,113 (GRCm39) |
missense |
probably damaging |
0.99 |
R8717:Trabd2b
|
UTSW |
4 |
114,460,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R9203:Trabd2b
|
UTSW |
4 |
114,460,122 (GRCm39) |
missense |
probably damaging |
0.99 |
|