Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930453N24Rik |
G |
T |
16: 64,586,823 (GRCm39) |
N300K |
possibly damaging |
Het |
A130010J15Rik |
G |
A |
1: 192,857,065 (GRCm39) |
R139H |
probably benign |
Het |
Aanat |
A |
C |
11: 116,487,681 (GRCm39) |
T127P |
possibly damaging |
Het |
Acp4 |
G |
A |
7: 43,906,733 (GRCm39) |
|
probably benign |
Het |
Arhgef5 |
T |
G |
6: 43,250,527 (GRCm39) |
I426S |
probably benign |
Het |
Bcl2a1a |
T |
C |
9: 88,839,185 (GRCm39) |
S28P |
probably benign |
Het |
Cd163 |
T |
C |
6: 124,288,384 (GRCm39) |
S272P |
possibly damaging |
Het |
Cdk13 |
C |
A |
13: 17,978,542 (GRCm39) |
R232L |
unknown |
Het |
Clrn2 |
A |
G |
5: 45,611,331 (GRCm39) |
D60G |
possibly damaging |
Het |
Cnot6l |
A |
G |
5: 96,230,749 (GRCm39) |
L406P |
probably damaging |
Het |
Cspg4 |
T |
G |
9: 56,797,622 (GRCm39) |
V1362G |
probably benign |
Het |
Cspp1 |
C |
T |
1: 10,196,639 (GRCm39) |
S939L |
probably benign |
Het |
Dcaf1 |
C |
T |
9: 106,713,818 (GRCm39) |
T145I |
probably benign |
Het |
Ddx28 |
T |
C |
8: 106,736,733 (GRCm39) |
S442G |
probably benign |
Het |
Dnajc3 |
A |
T |
14: 119,209,775 (GRCm39) |
R283S |
probably benign |
Het |
Dsc1 |
G |
A |
18: 20,232,087 (GRCm39) |
T307I |
possibly damaging |
Het |
Elovl5 |
T |
C |
9: 77,868,291 (GRCm39) |
Y68H |
probably damaging |
Het |
Fam25a |
G |
A |
14: 34,077,266 (GRCm39) |
T17I |
probably damaging |
Het |
Fryl |
T |
C |
5: 73,216,879 (GRCm39) |
E2137G |
probably damaging |
Het |
Gm10142 |
A |
G |
10: 77,551,762 (GRCm39) |
Q41R |
unknown |
Het |
Grm1 |
T |
C |
10: 10,564,775 (GRCm39) |
T1178A |
possibly damaging |
Het |
Hhip |
A |
T |
8: 80,723,363 (GRCm39) |
H430Q |
probably damaging |
Het |
Hip1 |
A |
G |
5: 135,478,676 (GRCm39) |
F178L |
probably damaging |
Het |
Impa1 |
T |
A |
3: 10,393,430 (GRCm39) |
I58L |
probably benign |
Het |
Irak4 |
T |
A |
15: 94,451,812 (GRCm39) |
V135E |
probably benign |
Het |
Jup |
A |
C |
11: 100,274,237 (GRCm39) |
L151R |
probably damaging |
Het |
Lrrn4cl |
T |
A |
19: 8,829,419 (GRCm39) |
N132K |
probably damaging |
Het |
Mapkbp1 |
C |
A |
2: 119,851,664 (GRCm39) |
R863S |
probably benign |
Het |
Or8k16 |
T |
C |
2: 85,519,866 (GRCm39) |
F31S |
probably damaging |
Het |
Pramel14 |
T |
A |
4: 143,719,520 (GRCm39) |
M282L |
probably benign |
Het |
Rasa4 |
A |
G |
5: 136,124,383 (GRCm39) |
D144G |
probably benign |
Het |
Rrs1 |
T |
A |
1: 9,616,390 (GRCm39) |
S214R |
probably benign |
Het |
Rsf1 |
CGGC |
CGGCGGCGGGGGC |
7: 97,229,139 (GRCm39) |
|
probably benign |
Het |
Rtca |
T |
A |
3: 116,293,225 (GRCm39) |
R195S |
probably benign |
Het |
Scaper |
A |
T |
9: 55,771,835 (GRCm39) |
S360R |
probably benign |
Het |
Scarb1 |
A |
T |
5: 125,371,194 (GRCm39) |
F293I |
possibly damaging |
Het |
Snapc1 |
T |
C |
12: 74,017,115 (GRCm39) |
|
probably null |
Het |
Speer4a3 |
AACT |
A |
5: 26,155,849 (GRCm39) |
|
probably benign |
Het |
Spta1 |
T |
C |
1: 174,032,925 (GRCm39) |
V994A |
probably damaging |
Het |
Synpo2 |
T |
C |
3: 122,911,366 (GRCm39) |
E93G |
probably damaging |
Het |
Ubr4 |
A |
G |
4: 139,191,341 (GRCm39) |
T985A |
unknown |
Het |
Vmn2r15 |
A |
G |
5: 109,440,598 (GRCm39) |
V420A |
probably benign |
Het |
Vmn2r6 |
A |
G |
3: 64,464,081 (GRCm39) |
V251A |
probably benign |
Het |
Zfyve16 |
A |
T |
13: 92,659,311 (GRCm39) |
I200N |
possibly damaging |
Het |
|
Other mutations in Vmn1r18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01129:Vmn1r18
|
APN |
6 |
57,367,482 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01301:Vmn1r18
|
APN |
6 |
57,366,652 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01996:Vmn1r18
|
APN |
6 |
57,367,001 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02017:Vmn1r18
|
APN |
6 |
57,366,741 (GRCm39) |
missense |
probably benign |
0.01 |
R1908:Vmn1r18
|
UTSW |
6 |
57,367,026 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4200:Vmn1r18
|
UTSW |
6 |
57,367,101 (GRCm39) |
missense |
probably benign |
0.01 |
R4288:Vmn1r18
|
UTSW |
6 |
57,367,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Vmn1r18
|
UTSW |
6 |
57,367,069 (GRCm39) |
missense |
probably benign |
0.11 |
R6029:Vmn1r18
|
UTSW |
6 |
57,367,451 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6767:Vmn1r18
|
UTSW |
6 |
57,367,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R7174:Vmn1r18
|
UTSW |
6 |
57,366,609 (GRCm39) |
splice site |
probably null |
|
R7229:Vmn1r18
|
UTSW |
6 |
57,367,083 (GRCm39) |
missense |
probably benign |
0.14 |
R7332:Vmn1r18
|
UTSW |
6 |
57,367,503 (GRCm39) |
missense |
probably benign |
0.06 |
R7425:Vmn1r18
|
UTSW |
6 |
57,367,551 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R9428:Vmn1r18
|
UTSW |
6 |
57,367,535 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9561:Vmn1r18
|
UTSW |
6 |
57,367,202 (GRCm39) |
missense |
probably benign |
0.01 |
|