Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bche |
T |
C |
3: 73,609,262 (GRCm39) |
T55A |
probably benign |
Het |
Ccdc177 |
T |
C |
12: 80,804,372 (GRCm39) |
D634G |
unknown |
Het |
Cnot2 |
T |
C |
10: 116,328,241 (GRCm39) |
T498A |
possibly damaging |
Het |
Dock10 |
C |
T |
1: 80,507,905 (GRCm39) |
V1669M |
probably damaging |
Het |
Emilin2 |
T |
C |
17: 71,581,124 (GRCm39) |
E534G |
probably benign |
Het |
Flt4 |
G |
A |
11: 49,521,400 (GRCm39) |
R440H |
probably benign |
Het |
Gm10073 |
T |
C |
8: 107,299,951 (GRCm39) |
Y11C |
probably benign |
Het |
Krt31 |
T |
C |
11: 99,939,221 (GRCm39) |
Y232C |
probably damaging |
Het |
Muc19 |
G |
A |
15: 91,756,694 (GRCm39) |
|
noncoding transcript |
Het |
Myof |
A |
G |
19: 37,960,641 (GRCm39) |
S467P |
probably benign |
Het |
Nup88 |
C |
T |
11: 70,860,714 (GRCm39) |
V22I |
probably benign |
Het |
Or4f14 |
G |
T |
2: 111,742,762 (GRCm39) |
P171Q |
probably damaging |
Het |
Or6c6c |
A |
T |
10: 129,541,445 (GRCm39) |
T233S |
probably benign |
Het |
Or8h9 |
A |
G |
2: 86,789,392 (GRCm39) |
S137P |
possibly damaging |
Het |
Prag1 |
C |
T |
8: 36,606,722 (GRCm39) |
P821L |
probably damaging |
Het |
Pramel22 |
C |
T |
4: 143,382,007 (GRCm39) |
G230S |
possibly damaging |
Het |
Tap2 |
G |
A |
17: 34,424,393 (GRCm39) |
|
probably benign |
Het |
Tmem68 |
A |
T |
4: 3,569,624 (GRCm39) |
I22N |
possibly damaging |
Het |
Usp17le |
A |
G |
7: 104,418,408 (GRCm39) |
W245R |
probably benign |
Het |
Xpo5 |
G |
T |
17: 46,550,446 (GRCm39) |
C976F |
probably damaging |
Het |
Xrcc1 |
T |
C |
7: 24,264,979 (GRCm39) |
S94P |
possibly damaging |
Het |
Zfp524 |
T |
A |
7: 5,021,091 (GRCm39) |
N206K |
possibly damaging |
Het |
|
Other mutations in Ighv10-3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02130:Ighv10-3
|
APN |
12 |
114,487,121 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03154:Ighv10-3
|
APN |
12 |
114,487,507 (GRCm39) |
start codon destroyed |
probably benign |
0.08 |
R0392:Ighv10-3
|
UTSW |
12 |
114,487,460 (GRCm39) |
critical splice donor site |
probably benign |
|
R4342:Ighv10-3
|
UTSW |
12 |
114,487,124 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5288:Ighv10-3
|
UTSW |
12 |
114,487,125 (GRCm39) |
missense |
probably benign |
0.00 |
R6330:Ighv10-3
|
UTSW |
12 |
114,487,086 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7676:Ighv10-3
|
UTSW |
12 |
114,487,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9718:Ighv10-3
|
UTSW |
12 |
114,487,254 (GRCm39) |
missense |
probably benign |
0.01 |
|