Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
C |
T |
7: 41,275,298 (GRCm39) |
Q334* |
probably null |
Het |
Aadacl2fm2 |
A |
T |
3: 59,652,972 (GRCm39) |
D137V |
probably damaging |
Het |
Adam28 |
T |
C |
14: 68,868,116 (GRCm39) |
T410A |
probably benign |
Het |
Ano10 |
T |
C |
9: 122,030,754 (GRCm39) |
|
probably benign |
Het |
Bmpr2 |
T |
A |
1: 59,906,596 (GRCm39) |
V563E |
probably damaging |
Het |
Ccdc47 |
A |
G |
11: 106,095,811 (GRCm39) |
L295P |
probably damaging |
Het |
Cdhr1 |
T |
C |
14: 36,812,554 (GRCm39) |
T210A |
probably benign |
Het |
Col16a1 |
G |
A |
4: 129,960,486 (GRCm39) |
A408T |
unknown |
Het |
Csnk1g2 |
A |
G |
10: 80,475,906 (GRCm39) |
K415R |
probably damaging |
Het |
Cyp2c29 |
G |
T |
19: 39,279,311 (GRCm39) |
A103S |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Dsg1b |
A |
T |
18: 20,527,498 (GRCm39) |
I210F |
possibly damaging |
Het |
Fhod1 |
T |
A |
8: 106,056,869 (GRCm39) |
D1002V |
probably damaging |
Het |
Gm5592 |
G |
A |
7: 40,938,010 (GRCm39) |
V431I |
probably benign |
Het |
Gtpbp4 |
A |
T |
13: 9,040,773 (GRCm39) |
C174* |
probably null |
Het |
Il2ra |
A |
G |
2: 11,685,173 (GRCm39) |
K170E |
probably benign |
Het |
Itch |
T |
C |
2: 155,005,315 (GRCm39) |
|
probably benign |
Het |
Jazf1 |
A |
C |
6: 52,754,640 (GRCm39) |
D145E |
probably damaging |
Het |
Kank2 |
G |
T |
9: 21,691,858 (GRCm39) |
A469E |
possibly damaging |
Het |
Kirrel3 |
A |
G |
9: 34,902,269 (GRCm39) |
I125V |
probably benign |
Het |
Klra9 |
G |
T |
6: 130,155,995 (GRCm39) |
Y253* |
probably null |
Het |
Krtap27-1 |
C |
T |
16: 88,467,941 (GRCm39) |
S201N |
probably benign |
Het |
Map3k20 |
T |
C |
2: 72,228,758 (GRCm39) |
S326P |
probably damaging |
Het |
Mkks |
C |
A |
2: 136,716,206 (GRCm39) |
V565F |
probably damaging |
Het |
Ntaq1 |
T |
G |
15: 58,013,994 (GRCm39) |
|
probably null |
Het |
Or5c1 |
A |
G |
2: 37,221,837 (GRCm39) |
D26G |
possibly damaging |
Het |
Or5k8 |
A |
T |
16: 58,644,889 (GRCm39) |
I61N |
probably damaging |
Het |
Or5w11 |
T |
C |
2: 87,459,493 (GRCm39) |
S229P |
possibly damaging |
Het |
Pacsin3 |
A |
T |
2: 91,090,514 (GRCm39) |
|
probably null |
Het |
Pdcd7 |
A |
G |
9: 65,264,057 (GRCm39) |
E434G |
probably damaging |
Het |
Plekhb2 |
T |
C |
1: 34,903,564 (GRCm39) |
F102L |
probably benign |
Het |
Ppp1r9a |
A |
G |
6: 5,057,458 (GRCm39) |
D191G |
probably benign |
Het |
Psmd3 |
A |
G |
11: 98,576,466 (GRCm39) |
T123A |
probably benign |
Het |
Ptprq |
C |
T |
10: 107,541,444 (GRCm39) |
V361M |
probably benign |
Het |
Rnf123 |
G |
A |
9: 107,933,252 (GRCm39) |
H1162Y |
probably benign |
Het |
Sema4f |
A |
G |
6: 82,894,851 (GRCm39) |
V448A |
probably benign |
Het |
Tcf12 |
A |
T |
9: 71,775,550 (GRCm39) |
M400K |
probably damaging |
Het |
Tcl1b2 |
G |
T |
12: 105,119,261 (GRCm39) |
E50* |
probably null |
Het |
Thada |
A |
C |
17: 84,736,601 (GRCm39) |
D893E |
probably benign |
Het |
Trim24 |
G |
A |
6: 37,880,587 (GRCm39) |
|
probably null |
Het |
Ttll5 |
T |
C |
12: 86,071,050 (GRCm39) |
S1308P |
probably benign |
Het |
Ubtfl1 |
T |
A |
9: 18,320,925 (GRCm39) |
I151N |
possibly damaging |
Het |
Vmn2r70 |
A |
T |
7: 85,214,157 (GRCm39) |
F332I |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,307,488 (GRCm39) |
D238G |
probably damaging |
Het |
Zfp639 |
A |
G |
3: 32,573,810 (GRCm39) |
H145R |
possibly damaging |
Het |
|
Other mutations in Raver2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00325:Raver2
|
APN |
4 |
100,960,065 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00778:Raver2
|
APN |
4 |
100,953,468 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01363:Raver2
|
APN |
4 |
100,977,780 (GRCm39) |
splice site |
probably benign |
|
IGL02631:Raver2
|
APN |
4 |
100,953,499 (GRCm39) |
missense |
probably damaging |
0.96 |
R0071:Raver2
|
UTSW |
4 |
100,977,642 (GRCm39) |
splice site |
probably benign |
|
R0071:Raver2
|
UTSW |
4 |
100,977,642 (GRCm39) |
splice site |
probably benign |
|
R0792:Raver2
|
UTSW |
4 |
100,960,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R1450:Raver2
|
UTSW |
4 |
100,993,349 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2044:Raver2
|
UTSW |
4 |
100,960,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R5127:Raver2
|
UTSW |
4 |
100,960,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5162:Raver2
|
UTSW |
4 |
100,959,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R5342:Raver2
|
UTSW |
4 |
100,959,889 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5557:Raver2
|
UTSW |
4 |
100,993,336 (GRCm39) |
missense |
probably benign |
0.04 |
R6190:Raver2
|
UTSW |
4 |
100,990,814 (GRCm39) |
missense |
probably benign |
0.00 |
R6248:Raver2
|
UTSW |
4 |
100,991,320 (GRCm39) |
splice site |
probably null |
|
R6640:Raver2
|
UTSW |
4 |
100,988,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R6852:Raver2
|
UTSW |
4 |
100,990,787 (GRCm39) |
missense |
probably benign |
0.00 |
R7196:Raver2
|
UTSW |
4 |
100,960,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R7449:Raver2
|
UTSW |
4 |
100,959,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R7459:Raver2
|
UTSW |
4 |
100,964,410 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8025:Raver2
|
UTSW |
4 |
100,960,162 (GRCm39) |
nonsense |
probably null |
|
R8843:Raver2
|
UTSW |
4 |
100,994,942 (GRCm39) |
missense |
probably damaging |
0.96 |
R8898:Raver2
|
UTSW |
4 |
100,964,399 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9290:Raver2
|
UTSW |
4 |
100,977,387 (GRCm39) |
intron |
probably benign |
|
RF017:Raver2
|
UTSW |
4 |
100,960,195 (GRCm39) |
missense |
probably damaging |
0.99 |
|