Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430033K04Rik |
T |
C |
5: 138,645,821 (GRCm39) |
C569R |
probably damaging |
Het |
Acadsb |
T |
A |
7: 131,031,784 (GRCm39) |
W207R |
probably damaging |
Het |
Apbb2 |
C |
T |
5: 66,608,810 (GRCm39) |
|
probably null |
Het |
Atad2b |
T |
C |
12: 5,007,558 (GRCm39) |
V415A |
probably damaging |
Het |
Ccdc150 |
G |
A |
1: 54,303,116 (GRCm39) |
|
probably null |
Het |
Cep20 |
TTGTG |
TTG |
16: 14,118,009 (GRCm39) |
|
probably null |
Het |
Chd7 |
A |
G |
4: 8,828,274 (GRCm39) |
T1072A |
probably damaging |
Het |
Depdc1b |
T |
A |
13: 108,460,580 (GRCm39) |
F63L |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,349,344 (GRCm39) |
V2431M |
probably damaging |
Het |
Dnajc14 |
A |
G |
10: 128,643,359 (GRCm39) |
E427G |
probably damaging |
Het |
Flnc |
A |
G |
6: 29,458,882 (GRCm39) |
E2421G |
probably damaging |
Het |
Kcna4 |
T |
C |
2: 107,126,894 (GRCm39) |
S543P |
probably damaging |
Het |
Lrrc30 |
T |
A |
17: 67,939,681 (GRCm39) |
|
probably benign |
Het |
Ndrg3 |
C |
G |
2: 156,782,294 (GRCm39) |
A191P |
probably damaging |
Het |
Or1o4 |
T |
C |
17: 37,590,666 (GRCm39) |
Y215C |
probably damaging |
Het |
Or5aq7 |
C |
T |
2: 86,938,330 (GRCm39) |
V134I |
probably benign |
Het |
Or5p5 |
A |
G |
7: 107,413,961 (GRCm39) |
T57A |
possibly damaging |
Het |
Pls1 |
A |
G |
9: 95,636,798 (GRCm39) |
I558T |
probably damaging |
Het |
Rnf34 |
T |
C |
5: 122,999,839 (GRCm39) |
F32L |
probably benign |
Het |
Serpinb9g |
A |
T |
13: 33,676,834 (GRCm39) |
L205F |
probably benign |
Het |
Tbc1d24 |
T |
A |
17: 24,427,303 (GRCm39) |
I220F |
probably damaging |
Het |
Thsd7b |
A |
T |
1: 129,744,385 (GRCm39) |
T758S |
probably benign |
Het |
Trak1 |
A |
G |
9: 121,282,562 (GRCm39) |
|
probably null |
Het |
Ttn |
G |
C |
2: 76,556,407 (GRCm39) |
F30199L |
probably benign |
Het |
Ttn |
T |
G |
2: 76,556,406 (GRCm39) |
S30200R |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,202,447 (GRCm39) |
D1050G |
possibly damaging |
Het |
Veph1 |
T |
A |
3: 66,033,312 (GRCm39) |
S605C |
probably benign |
Het |
Wbp1 |
A |
G |
6: 83,096,982 (GRCm39) |
|
probably benign |
Het |
Ythdc2 |
C |
A |
18: 45,019,469 (GRCm39) |
Q1413K |
possibly 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 |
R1065:Msh6
|
UTSW |
17 |
88,295,891 (GRCm39) |
unclassified |
probably benign |
|
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 |
|
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 |
|