Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cd300ld2 |
T |
C |
11: 114,904,586 (GRCm39) |
T94A |
probably damaging |
Het |
Cdc42bpg |
G |
A |
19: 6,372,856 (GRCm39) |
S1515N |
probably damaging |
Het |
Ckb |
T |
C |
12: 111,637,681 (GRCm39) |
E150G |
probably benign |
Het |
Clec2m |
A |
G |
6: 129,300,013 (GRCm39) |
I155T |
possibly damaging |
Het |
Cobl |
T |
A |
11: 12,204,327 (GRCm39) |
M785L |
possibly damaging |
Het |
Col6a5 |
T |
C |
9: 105,758,982 (GRCm39) |
N2075D |
probably damaging |
Het |
Commd7 |
G |
C |
2: 153,461,447 (GRCm39) |
|
probably benign |
Het |
Corin |
G |
A |
5: 72,458,993 (GRCm39) |
R927* |
probably null |
Het |
Dync2i1 |
C |
T |
12: 116,219,696 (GRCm39) |
R82H |
probably damaging |
Het |
Ift122 |
A |
T |
6: 115,852,286 (GRCm39) |
|
probably null |
Het |
Il1b |
G |
A |
2: 129,209,927 (GRCm39) |
T83I |
probably benign |
Het |
Ints4 |
T |
C |
7: 97,157,099 (GRCm39) |
|
probably null |
Het |
Mtmr3 |
T |
C |
11: 4,442,859 (GRCm39) |
K392E |
probably damaging |
Het |
Or5t9 |
A |
G |
2: 86,659,888 (GRCm39) |
H264R |
probably damaging |
Het |
Pde3a |
T |
C |
6: 141,422,458 (GRCm39) |
|
probably benign |
Het |
Pde6h |
A |
C |
6: 136,936,368 (GRCm39) |
K37T |
probably damaging |
Het |
Plat |
C |
A |
8: 23,266,879 (GRCm39) |
D290E |
probably damaging |
Het |
Polk |
A |
C |
13: 96,644,760 (GRCm39) |
L122R |
probably damaging |
Het |
Ppp1r3g |
T |
A |
13: 36,153,418 (GRCm39) |
D279E |
probably benign |
Het |
Ptpru |
T |
C |
4: 131,535,651 (GRCm39) |
E370G |
possibly damaging |
Het |
Ralgapa2 |
T |
C |
2: 146,292,478 (GRCm39) |
Y187C |
probably benign |
Het |
Rps6ka2 |
C |
T |
17: 7,549,157 (GRCm39) |
|
probably benign |
Het |
Slit3 |
T |
C |
11: 35,012,462 (GRCm39) |
S41P |
possibly damaging |
Het |
Smarca5 |
A |
T |
8: 81,431,343 (GRCm39) |
L958Q |
probably damaging |
Het |
Snx9 |
T |
C |
17: 5,952,636 (GRCm39) |
|
probably benign |
Het |
Stkld1 |
A |
T |
2: 26,830,050 (GRCm39) |
N72I |
probably damaging |
Het |
Strc |
C |
A |
2: 121,197,132 (GRCm39) |
D1532Y |
probably damaging |
Het |
Sucla2 |
C |
T |
14: 73,798,074 (GRCm39) |
|
probably benign |
Het |
Svil |
T |
G |
18: 5,063,777 (GRCm39) |
|
probably benign |
Het |
Traf3ip1 |
T |
A |
1: 91,428,506 (GRCm39) |
D122E |
unknown |
Het |
Vmn2r7 |
A |
T |
3: 64,614,559 (GRCm39) |
D509E |
possibly damaging |
Het |
Vps52 |
C |
A |
17: 34,180,213 (GRCm39) |
Q306K |
probably benign |
Het |
Zfp407 |
C |
T |
18: 84,577,898 (GRCm39) |
A1072T |
probably benign |
Het |
Zfp418 |
C |
A |
7: 7,184,561 (GRCm39) |
Q175K |
probably benign |
Het |
Zxdc |
T |
C |
6: 90,355,885 (GRCm39) |
S465P |
probably damaging |
Het |
|
Other mutations in Msh6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01691:Msh6
|
APN |
17 |
88,292,907 (GRCm39) |
missense |
probably benign |
|
IGL01834:Msh6
|
APN |
17 |
88,293,140 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01904:Msh6
|
APN |
17 |
88,292,160 (GRCm39) |
missense |
probably benign |
|
IGL01957:Msh6
|
APN |
17 |
88,292,519 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02117:Msh6
|
APN |
17 |
88,298,234 (GRCm39) |
unclassified |
probably benign |
|
IGL02234:Msh6
|
APN |
17 |
88,294,229 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02512:Msh6
|
APN |
17 |
88,292,160 (GRCm39) |
missense |
probably benign |
|
IGL02651:Msh6
|
APN |
17 |
88,296,943 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03381:Msh6
|
APN |
17 |
88,292,537 (GRCm39) |
missense |
probably damaging |
1.00 |
medea
|
UTSW |
17 |
88,287,651 (GRCm39) |
nonsense |
probably null |
|
medusa
|
UTSW |
17 |
88,295,891 (GRCm39) |
unclassified |
probably benign |
|
PIT4449001:Msh6
|
UTSW |
17 |
88,293,616 (GRCm39) |
missense |
probably damaging |
0.96 |
R0196:Msh6
|
UTSW |
17 |
88,287,788 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0324:Msh6
|
UTSW |
17 |
88,294,048 (GRCm39) |
nonsense |
probably null |
|
R0492:Msh6
|
UTSW |
17 |
88,282,679 (GRCm39) |
missense |
probably benign |
|
R0711:Msh6
|
UTSW |
17 |
88,294,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R1454:Msh6
|
UTSW |
17 |
88,292,186 (GRCm39) |
missense |
probably benign |
0.00 |
R1740:Msh6
|
UTSW |
17 |
88,293,150 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1770:Msh6
|
UTSW |
17 |
88,287,651 (GRCm39) |
nonsense |
probably null |
|
R1771:Msh6
|
UTSW |
17 |
88,291,950 (GRCm39) |
missense |
probably benign |
0.17 |
R1919:Msh6
|
UTSW |
17 |
88,292,553 (GRCm39) |
missense |
probably benign |
0.01 |
R1926:Msh6
|
UTSW |
17 |
88,293,653 (GRCm39) |
missense |
probably benign |
|
R2026:Msh6
|
UTSW |
17 |
88,297,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R2095:Msh6
|
UTSW |
17 |
88,295,661 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2097:Msh6
|
UTSW |
17 |
88,292,844 (GRCm39) |
missense |
probably benign |
0.00 |
R2149:Msh6
|
UTSW |
17 |
88,293,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R2156:Msh6
|
UTSW |
17 |
88,293,568 (GRCm39) |
nonsense |
probably null |
|
R2167:Msh6
|
UTSW |
17 |
88,296,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R2382:Msh6
|
UTSW |
17 |
88,292,159 (GRCm39) |
missense |
probably benign |
|
R3005:Msh6
|
UTSW |
17 |
88,295,713 (GRCm39) |
missense |
probably benign |
0.34 |
R3160:Msh6
|
UTSW |
17 |
88,292,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Msh6
|
UTSW |
17 |
88,292,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Msh6
|
UTSW |
17 |
88,292,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R3774:Msh6
|
UTSW |
17 |
88,293,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R3775:Msh6
|
UTSW |
17 |
88,293,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R4350:Msh6
|
UTSW |
17 |
88,292,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R4424:Msh6
|
UTSW |
17 |
88,298,217 (GRCm39) |
nonsense |
probably null |
|
R4499:Msh6
|
UTSW |
17 |
88,287,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Msh6
|
UTSW |
17 |
88,292,234 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4668:Msh6
|
UTSW |
17 |
88,292,234 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4669:Msh6
|
UTSW |
17 |
88,292,234 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4849:Msh6
|
UTSW |
17 |
88,290,947 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5137:Msh6
|
UTSW |
17 |
88,287,716 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5472:Msh6
|
UTSW |
17 |
88,291,989 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5594:Msh6
|
UTSW |
17 |
88,293,497 (GRCm39) |
missense |
probably benign |
0.00 |
R5607:Msh6
|
UTSW |
17 |
88,294,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R5608:Msh6
|
UTSW |
17 |
88,294,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R5660:Msh6
|
UTSW |
17 |
88,292,147 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6243:Msh6
|
UTSW |
17 |
88,290,999 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6279:Msh6
|
UTSW |
17 |
88,287,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R6357:Msh6
|
UTSW |
17 |
88,291,888 (GRCm39) |
nonsense |
probably null |
|
R6399:Msh6
|
UTSW |
17 |
88,294,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R6453:Msh6
|
UTSW |
17 |
88,293,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R6646:Msh6
|
UTSW |
17 |
88,293,870 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7404:Msh6
|
UTSW |
17 |
88,282,548 (GRCm39) |
|
|
|
R7837:Msh6
|
UTSW |
17 |
88,292,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R8004:Msh6
|
UTSW |
17 |
88,294,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R8296:Msh6
|
UTSW |
17 |
88,294,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R8326:Msh6
|
UTSW |
17 |
88,294,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R8377:Msh6
|
UTSW |
17 |
88,292,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R8715:Msh6
|
UTSW |
17 |
88,293,195 (GRCm39) |
missense |
probably benign |
|
R9752:Msh6
|
UTSW |
17 |
88,293,963 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Msh6
|
UTSW |
17 |
88,298,042 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Msh6
|
UTSW |
17 |
88,293,609 (GRCm39) |
missense |
probably damaging |
1.00 |
|