Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
T |
C |
17: 84,983,667 (GRCm39) |
D124G |
possibly damaging |
Het |
Ackr3 |
C |
G |
1: 90,141,923 (GRCm39) |
N127K |
probably damaging |
Het |
AL732309.1 |
A |
C |
2: 25,136,151 (GRCm39) |
M21R |
possibly damaging |
Het |
Ankrd52 |
C |
A |
10: 128,222,032 (GRCm39) |
T552K |
possibly damaging |
Het |
Arhgap28 |
T |
C |
17: 68,202,879 (GRCm39) |
|
probably null |
Het |
Arid5b |
A |
T |
10: 67,964,752 (GRCm39) |
N306K |
probably benign |
Het |
C1qtnf3 |
A |
C |
15: 10,952,707 (GRCm39) |
K56N |
probably benign |
Het |
C2 |
C |
T |
17: 35,100,664 (GRCm39) |
G52D |
probably benign |
Het |
Casz1 |
C |
T |
4: 149,031,490 (GRCm39) |
T1247M |
probably damaging |
Het |
Cc2d2b |
A |
G |
19: 40,797,552 (GRCm39) |
D778G |
unknown |
Het |
Cdh5 |
A |
G |
8: 104,869,425 (GRCm39) |
D717G |
probably damaging |
Het |
Clca3a2 |
G |
A |
3: 144,514,372 (GRCm39) |
A445V |
probably damaging |
Het |
Clca3b |
T |
A |
3: 144,547,181 (GRCm39) |
M319L |
possibly damaging |
Het |
Csmd1 |
G |
A |
8: 16,108,721 (GRCm39) |
S1894L |
probably damaging |
Het |
Csnk1g3 |
A |
G |
18: 54,052,090 (GRCm39) |
T220A |
probably damaging |
Het |
Cyp2d10 |
T |
G |
15: 82,287,961 (GRCm39) |
T381P |
probably damaging |
Het |
Ddb2 |
G |
A |
2: 91,067,229 (GRCm39) |
|
probably benign |
Het |
Ddx24 |
C |
A |
12: 103,382,518 (GRCm39) |
L688F |
probably damaging |
Het |
Dennd4c |
T |
C |
4: 86,747,975 (GRCm39) |
L1615P |
unknown |
Het |
Dnah8 |
T |
A |
17: 31,003,099 (GRCm39) |
D3599E |
probably benign |
Het |
Dst |
T |
C |
1: 34,045,305 (GRCm39) |
S13P |
possibly damaging |
Het |
Efcab12 |
T |
C |
6: 115,800,555 (GRCm39) |
D156G |
probably benign |
Het |
Enpp2 |
A |
G |
15: 54,741,170 (GRCm39) |
|
probably null |
Het |
Ephx2 |
A |
G |
14: 66,322,803 (GRCm39) |
V490A |
probably damaging |
Het |
Etnppl |
A |
G |
3: 130,423,224 (GRCm39) |
N308D |
probably damaging |
Het |
F5 |
TCAGAAGACCTCCTCCCCAGACCTGGGCCAGGTGCCCCTTTCTCCAGATGACAACCAGAAGACCTCCTCCCCAGACCTGGGTCAGGTGTCCCTTTCTCCAGATGATAACCAGAAGACCTCCTCCCCAGACCTGGGTCAGGTGCCCCTTTCTCTAGATGACAACCAGAAGACGACCTCCCCAGACCTGGGTCAGGTGCCCCTTTCTCCAGATGACAACCAGA |
TCAGAAGACCTCCTCCCCAGACCTGGGTCAGGTGTCCCTTTCTCCAGATGATAACCAGAAGACCTCCTCCCCAGACCTGGGTCAGGTGCCCCTTTCTCTAGATGACAACCAGAAGACGACCTCCCCAGACCTGGGTCAGGTGCCCCTTTCTCCAGATGACAACCAGA |
1: 164,021,150 (GRCm39) |
|
probably benign |
Het |
Fam162b |
A |
T |
10: 51,466,282 (GRCm39) |
|
probably null |
Het |
Fancl |
A |
G |
11: 26,353,362 (GRCm39) |
E86G |
probably damaging |
Het |
Flii |
G |
A |
11: 60,609,866 (GRCm39) |
T615I |
probably benign |
Het |
Fndc7 |
G |
T |
3: 108,779,537 (GRCm39) |
Q336K |
probably benign |
Het |
Gm26661 |
T |
C |
14: 7,791,911 (GRCm38) |
C109R |
unknown |
Het |
H2-DMb1 |
T |
C |
17: 34,378,436 (GRCm39) |
|
probably null |
Het |
H2-T10 |
C |
T |
17: 36,430,189 (GRCm39) |
G251R |
probably damaging |
Het |
Harbi1 |
T |
C |
2: 91,551,044 (GRCm39) |
I339T |
probably benign |
Het |
Hsp90aa1 |
A |
G |
12: 110,661,659 (GRCm39) |
M119T |
unknown |
Het |
Ighe |
T |
A |
12: 113,235,954 (GRCm39) |
Y124F |
|
Het |
Ighv7-1 |
T |
C |
12: 113,860,149 (GRCm39) |
Y81C |
probably damaging |
Het |
Ilkap |
A |
T |
1: 91,313,115 (GRCm39) |
|
probably null |
Het |
Inpp5a |
A |
G |
7: 139,105,586 (GRCm39) |
D179G |
probably damaging |
Het |
Itgad |
A |
T |
7: 127,788,979 (GRCm39) |
D510V |
probably damaging |
Het |
Kcnn2 |
A |
T |
18: 45,693,138 (GRCm39) |
H238L |
probably benign |
Het |
Kctd17 |
T |
A |
15: 78,319,842 (GRCm39) |
C189S |
probably damaging |
Het |
Larp4b |
C |
A |
13: 9,208,616 (GRCm39) |
A423E |
probably benign |
Het |
Llgl2 |
A |
G |
11: 115,741,556 (GRCm39) |
E562G |
possibly damaging |
Het |
Macf1 |
T |
C |
4: 123,268,218 (GRCm39) |
T6734A |
probably benign |
Het |
Maz |
G |
A |
7: 126,623,765 (GRCm39) |
T377M |
probably damaging |
Het |
Mmrn1 |
G |
T |
6: 60,921,917 (GRCm39) |
G125* |
probably null |
Het |
Mvp |
A |
G |
7: 126,592,781 (GRCm39) |
S377P |
probably benign |
Het |
Nin |
C |
T |
12: 70,090,508 (GRCm39) |
R969Q |
|
Het |
Nktr |
C |
T |
9: 121,556,427 (GRCm39) |
T35I |
probably damaging |
Het |
Nktr |
T |
A |
9: 121,577,357 (GRCm39) |
M475K |
possibly damaging |
Het |
Nod2 |
T |
A |
8: 89,379,694 (GRCm39) |
V65D |
probably damaging |
Het |
Opa1 |
A |
T |
16: 29,405,799 (GRCm39) |
E121D |
probably benign |
Het |
Or10w3 |
C |
T |
19: 13,704,270 (GRCm39) |
A215V |
probably benign |
Het |
Or1r1 |
A |
G |
11: 73,874,669 (GRCm39) |
V255A |
probably benign |
Het |
Or2n1c |
T |
C |
17: 38,519,607 (GRCm39) |
V157A |
probably benign |
Het |
Or4a76 |
A |
T |
2: 89,460,447 (GRCm39) |
I265N |
possibly damaging |
Het |
Or5ac21 |
T |
C |
16: 59,123,611 (GRCm39) |
F32L |
probably benign |
Het |
Or5b123 |
A |
G |
19: 13,596,942 (GRCm39) |
I96V |
probably benign |
Het |
Or6c88 |
T |
A |
10: 129,406,718 (GRCm39) |
S65T |
probably damaging |
Het |
Or7e174 |
A |
T |
9: 20,012,726 (GRCm39) |
I224F |
possibly damaging |
Het |
Osbpl2 |
A |
G |
2: 179,791,994 (GRCm39) |
T233A |
probably benign |
Het |
Pcp4l1 |
G |
A |
1: 171,002,034 (GRCm39) |
A42V |
possibly damaging |
Het |
Plekhh3 |
T |
A |
11: 101,061,600 (GRCm39) |
D38V |
possibly damaging |
Het |
Prtg |
C |
T |
9: 72,798,122 (GRCm39) |
A696V |
probably damaging |
Het |
Ptpn14 |
T |
G |
1: 189,595,621 (GRCm39) |
V748G |
possibly damaging |
Het |
Reg2 |
A |
T |
6: 78,383,137 (GRCm39) |
D28V |
probably benign |
Het |
Rhpn1 |
A |
T |
15: 75,576,246 (GRCm39) |
I2F |
possibly damaging |
Het |
Rundc3a |
A |
G |
11: 102,290,799 (GRCm39) |
E294G |
possibly damaging |
Het |
Scara3 |
T |
A |
14: 66,168,865 (GRCm39) |
I251L |
probably benign |
Het |
Slc23a2 |
G |
A |
2: 131,931,043 (GRCm39) |
T152I |
probably damaging |
Het |
Slc39a2 |
T |
G |
14: 52,131,650 (GRCm39) |
S74A |
possibly damaging |
Het |
Tmprss15 |
T |
C |
16: 78,758,907 (GRCm39) |
Y937C |
probably damaging |
Het |
Tpp2 |
T |
C |
1: 44,017,938 (GRCm39) |
L779S |
probably damaging |
Het |
Tssk2 |
T |
C |
16: 17,717,227 (GRCm39) |
V210A |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,725,937 (GRCm39) |
T6100S |
unknown |
Het |
Tufm |
G |
A |
7: 126,088,759 (GRCm39) |
E317K |
possibly damaging |
Het |
Wdfy4 |
A |
G |
14: 32,769,271 (GRCm39) |
S2219P |
|
Het |
Wtap |
T |
C |
17: 13,199,833 (GRCm39) |
N50S |
possibly damaging |
Het |
|
Other mutations in Vinac1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01318:Vinac1
|
APN |
2 |
128,880,622 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02423:Vinac1
|
APN |
2 |
128,889,968 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02730:Vinac1
|
APN |
2 |
128,880,646 (GRCm39) |
missense |
possibly damaging |
0.57 |
PIT4677001:Vinac1
|
UTSW |
2 |
128,880,636 (GRCm39) |
missense |
|
|
R0019:Vinac1
|
UTSW |
2 |
128,880,946 (GRCm39) |
missense |
probably benign |
0.26 |
R3946:Vinac1
|
UTSW |
2 |
128,881,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Vinac1
|
UTSW |
2 |
128,880,150 (GRCm39) |
missense |
probably benign |
0.02 |
R4819:Vinac1
|
UTSW |
2 |
128,882,721 (GRCm39) |
missense |
probably damaging |
0.96 |
R5634:Vinac1
|
UTSW |
2 |
128,881,406 (GRCm39) |
missense |
probably benign |
|
R6019:Vinac1
|
UTSW |
2 |
128,879,610 (GRCm39) |
missense |
probably benign |
|
R6241:Vinac1
|
UTSW |
2 |
128,879,301 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6285:Vinac1
|
UTSW |
2 |
128,879,719 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6377:Vinac1
|
UTSW |
2 |
128,878,731 (GRCm39) |
missense |
unknown |
|
R6464:Vinac1
|
UTSW |
2 |
128,881,465 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6724:Vinac1
|
UTSW |
2 |
128,879,976 (GRCm39) |
missense |
probably benign |
0.23 |
R7050:Vinac1
|
UTSW |
2 |
128,869,891 (GRCm39) |
splice site |
probably null |
|
R7130:Vinac1
|
UTSW |
2 |
128,881,101 (GRCm39) |
missense |
|
|
R7199:Vinac1
|
UTSW |
2 |
128,880,238 (GRCm39) |
missense |
|
|
R7355:Vinac1
|
UTSW |
2 |
128,879,149 (GRCm39) |
missense |
unknown |
|
R7407:Vinac1
|
UTSW |
2 |
128,880,729 (GRCm39) |
missense |
|
|
R7634:Vinac1
|
UTSW |
2 |
128,880,192 (GRCm39) |
missense |
|
|
R7688:Vinac1
|
UTSW |
2 |
128,880,964 (GRCm39) |
nonsense |
probably null |
|
R7889:Vinac1
|
UTSW |
2 |
128,878,914 (GRCm39) |
missense |
unknown |
|
R7894:Vinac1
|
UTSW |
2 |
128,879,049 (GRCm39) |
missense |
unknown |
|
R8242:Vinac1
|
UTSW |
2 |
128,881,313 (GRCm39) |
nonsense |
probably null |
|
R8373:Vinac1
|
UTSW |
2 |
128,880,091 (GRCm39) |
missense |
|
|
R8927:Vinac1
|
UTSW |
2 |
128,882,789 (GRCm39) |
missense |
|
|
R8928:Vinac1
|
UTSW |
2 |
128,882,789 (GRCm39) |
missense |
|
|
R9231:Vinac1
|
UTSW |
2 |
128,879,340 (GRCm39) |
missense |
unknown |
|
R9504:Vinac1
|
UTSW |
2 |
128,881,189 (GRCm39) |
missense |
|
|
R9505:Vinac1
|
UTSW |
2 |
128,878,838 (GRCm39) |
missense |
unknown |
|
R9608:Vinac1
|
UTSW |
2 |
128,878,550 (GRCm39) |
nonsense |
probably null |
|
R9682:Vinac1
|
UTSW |
2 |
128,875,529 (GRCm39) |
missense |
unknown |
|
R9760:Vinac1
|
UTSW |
2 |
128,880,499 (GRCm39) |
missense |
|
|
RF002:Vinac1
|
UTSW |
2 |
128,880,714 (GRCm39) |
missense |
|
|
X0066:Vinac1
|
UTSW |
2 |
128,880,987 (GRCm39) |
missense |
probably benign |
0.33 |
|