Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrd1 |
T |
A |
5: 129,255,143 (GRCm39) |
S597T |
possibly damaging |
Het |
Btnl9 |
T |
C |
11: 49,071,409 (GRCm39) |
D138G |
probably benign |
Het |
Cep135 |
T |
A |
5: 76,788,829 (GRCm39) |
*1141K |
probably null |
Het |
Ctnnd2 |
A |
T |
15: 30,480,974 (GRCm39) |
Q74L |
probably damaging |
Het |
Cyp2j13 |
A |
T |
4: 95,950,294 (GRCm39) |
W236R |
probably benign |
Het |
Dixdc1 |
A |
T |
9: 50,606,803 (GRCm39) |
I271N |
possibly damaging |
Het |
Dlec1 |
A |
G |
9: 118,957,182 (GRCm39) |
|
probably null |
Het |
Dnah9 |
C |
A |
11: 66,016,061 (GRCm39) |
|
probably benign |
Het |
Dop1a |
A |
T |
9: 86,404,920 (GRCm39) |
Y275F |
probably damaging |
Het |
Dysf |
T |
A |
6: 84,187,811 (GRCm39) |
*2105R |
probably null |
Het |
Eif4a1 |
A |
T |
11: 69,563,129 (GRCm39) |
D25E |
possibly damaging |
Het |
Fras1 |
T |
A |
5: 96,883,139 (GRCm39) |
I2557N |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm12253 |
G |
T |
11: 58,325,727 (GRCm39) |
|
probably null |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Hsd17b7 |
A |
G |
1: 169,787,035 (GRCm39) |
V254A |
probably benign |
Het |
Kif21a |
T |
A |
15: 90,840,633 (GRCm39) |
D143V |
probably damaging |
Het |
Lrrc9 |
T |
C |
12: 72,557,186 (GRCm39) |
V1417A |
possibly damaging |
Het |
Macf1 |
C |
T |
4: 123,274,237 (GRCm39) |
A4926T |
possibly damaging |
Het |
Mef2a |
A |
C |
7: 66,914,620 (GRCm39) |
S91R |
probably damaging |
Het |
Myh7 |
A |
G |
14: 55,222,916 (GRCm39) |
|
probably null |
Het |
Or6c65 |
T |
A |
10: 129,603,973 (GRCm39) |
F203I |
probably benign |
Het |
Pbx2 |
A |
G |
17: 34,813,024 (GRCm39) |
D160G |
probably damaging |
Het |
Pcdhb17 |
T |
C |
18: 37,619,790 (GRCm39) |
F527L |
probably benign |
Het |
Ppm1b |
T |
C |
17: 85,301,489 (GRCm39) |
L123P |
probably damaging |
Het |
Ppm1k |
T |
A |
6: 57,499,813 (GRCm39) |
K154N |
probably benign |
Het |
Ppp2r1a |
T |
G |
17: 21,185,731 (GRCm39) |
*590G |
probably null |
Het |
Rrbp1 |
A |
G |
2: 143,832,081 (GRCm39) |
S29P |
probably damaging |
Het |
Senp5 |
A |
G |
16: 31,784,634 (GRCm39) |
Y673H |
probably damaging |
Het |
Serpina3j |
T |
A |
12: 104,281,473 (GRCm39) |
|
probably benign |
Het |
Serpinc1 |
A |
G |
1: 160,817,116 (GRCm39) |
E70G |
probably damaging |
Het |
Sp140l2 |
A |
G |
1: 85,231,907 (GRCm39) |
|
probably benign |
Het |
Stag3 |
A |
G |
5: 138,287,492 (GRCm39) |
Q139R |
probably damaging |
Het |
Sva |
T |
A |
6: 42,019,104 (GRCm39) |
H91Q |
probably benign |
Het |
Tmem263 |
C |
T |
10: 84,950,295 (GRCm39) |
Q29* |
probably null |
Het |
Tpp1 |
T |
C |
7: 105,400,857 (GRCm39) |
N57D |
probably benign |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r27 |
T |
A |
6: 124,177,484 (GRCm39) |
I507L |
probably benign |
Het |
Wdr11 |
A |
T |
7: 129,234,046 (GRCm39) |
|
probably null |
Het |
Zfp236 |
C |
T |
18: 82,700,344 (GRCm39) |
E42K |
probably damaging |
Het |
|
Other mutations in Raver1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02863:Raver1
|
APN |
9 |
20,987,267 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03128:Raver1
|
APN |
9 |
20,992,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R0265:Raver1
|
UTSW |
9 |
20,986,955 (GRCm39) |
missense |
probably benign |
0.43 |
R1017:Raver1
|
UTSW |
9 |
20,990,886 (GRCm39) |
splice site |
probably benign |
|
R3177:Raver1
|
UTSW |
9 |
20,990,573 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3277:Raver1
|
UTSW |
9 |
20,990,573 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4092:Raver1
|
UTSW |
9 |
20,992,568 (GRCm39) |
missense |
probably damaging |
0.99 |
R4463:Raver1
|
UTSW |
9 |
21,003,123 (GRCm39) |
missense |
probably benign |
0.01 |
R5302:Raver1
|
UTSW |
9 |
20,986,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Raver1
|
UTSW |
9 |
21,001,608 (GRCm39) |
missense |
probably damaging |
0.98 |
R6021:Raver1
|
UTSW |
9 |
20,987,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R7065:Raver1
|
UTSW |
9 |
21,001,590 (GRCm39) |
missense |
probably benign |
0.00 |
R7833:Raver1
|
UTSW |
9 |
20,992,610 (GRCm39) |
missense |
probably benign |
0.11 |
R8480:Raver1
|
UTSW |
9 |
21,001,576 (GRCm39) |
missense |
probably benign |
0.29 |
R9662:Raver1
|
UTSW |
9 |
20,992,550 (GRCm39) |
missense |
probably benign |
0.40 |
|