Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1b |
G |
A |
15: 101,108,720 (GRCm39) |
V499M |
possibly damaging |
Het |
Adam5 |
G |
A |
8: 25,294,475 (GRCm39) |
Q375* |
probably null |
Het |
Adgrf1 |
G |
A |
17: 43,606,055 (GRCm39) |
E60K |
probably benign |
Het |
Alb |
T |
C |
5: 90,610,630 (GRCm39) |
V70A |
probably damaging |
Het |
Aph1b |
T |
A |
9: 66,695,709 (GRCm39) |
|
probably benign |
Het |
Aste1 |
G |
A |
9: 105,274,189 (GRCm39) |
R143Q |
possibly damaging |
Het |
Aste1 |
A |
T |
9: 105,274,995 (GRCm39) |
T351S |
probably damaging |
Het |
Bace2 |
T |
A |
16: 97,214,670 (GRCm39) |
L286Q |
probably damaging |
Het |
Bach1 |
G |
A |
16: 87,516,163 (GRCm39) |
G235R |
probably damaging |
Het |
Bpnt2 |
C |
T |
4: 4,769,376 (GRCm39) |
M246I |
probably benign |
Het |
Brwd1 |
A |
T |
16: 95,848,630 (GRCm39) |
H516Q |
probably damaging |
Het |
Cc2d2a |
C |
A |
5: 43,842,486 (GRCm39) |
|
probably null |
Het |
Cdh22 |
T |
A |
2: 164,988,646 (GRCm39) |
E236D |
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,917,286 (GRCm39) |
S229* |
probably null |
Het |
Celsr2 |
T |
A |
3: 108,306,218 (GRCm39) |
T2029S |
probably benign |
Het |
Col11a1 |
A |
G |
3: 113,975,043 (GRCm39) |
D1234G |
probably benign |
Het |
Cplane1 |
C |
A |
15: 8,216,942 (GRCm39) |
P720Q |
possibly damaging |
Het |
Cpt2 |
A |
G |
4: 107,764,957 (GRCm39) |
I269T |
probably damaging |
Het |
Dcaf7 |
T |
A |
11: 105,945,619 (GRCm39) |
S323T |
probably benign |
Het |
Ddias |
G |
T |
7: 92,508,608 (GRCm39) |
Q436K |
probably benign |
Het |
Dlec1 |
G |
A |
9: 118,972,335 (GRCm39) |
|
probably null |
Het |
Dock5 |
T |
A |
14: 68,073,859 (GRCm39) |
I294F |
probably benign |
Het |
Fat2 |
A |
T |
11: 55,173,794 (GRCm39) |
D2306E |
possibly damaging |
Het |
Gm4787 |
T |
A |
12: 81,424,280 (GRCm39) |
D626V |
probably damaging |
Het |
Gm6563 |
A |
G |
19: 23,653,290 (GRCm39) |
T27A |
probably benign |
Het |
Hadhb |
T |
C |
5: 30,373,568 (GRCm39) |
|
probably null |
Het |
Hsph1 |
A |
T |
5: 149,551,029 (GRCm39) |
W406R |
probably null |
Het |
Ighv1-66 |
C |
T |
12: 115,557,002 (GRCm39) |
G27R |
possibly damaging |
Het |
Krt26 |
T |
C |
11: 99,228,426 (GRCm39) |
E102G |
probably damaging |
Het |
Krt34 |
T |
A |
11: 99,930,971 (GRCm39) |
|
probably null |
Het |
Krt36 |
T |
C |
11: 99,993,635 (GRCm39) |
D401G |
possibly damaging |
Het |
Loxhd1 |
G |
A |
18: 77,518,827 (GRCm39) |
G326S |
probably damaging |
Het |
Lrrc8b |
A |
G |
5: 105,633,802 (GRCm39) |
N758S |
probably damaging |
Het |
Mrtfb |
A |
T |
16: 13,202,056 (GRCm39) |
|
probably null |
Het |
Muc4 |
C |
T |
16: 32,574,421 (GRCm39) |
T957I |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,358,743 (GRCm39) |
Y831C |
probably damaging |
Het |
Nfatc1 |
A |
T |
18: 80,678,859 (GRCm39) |
V829E |
probably benign |
Het |
Nmnat1 |
G |
A |
4: 149,557,827 (GRCm39) |
L72F |
possibly damaging |
Het |
Or4f14d |
A |
T |
2: 111,960,330 (GRCm39) |
D275E |
possibly damaging |
Het |
Pcdh7 |
T |
A |
5: 58,286,407 (GRCm39) |
V1161E |
probably damaging |
Het |
Recql4 |
G |
T |
15: 76,588,705 (GRCm39) |
H1035Q |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,411,284 (GRCm39) |
M814K |
probably benign |
Het |
Sh3d19 |
T |
G |
3: 85,992,184 (GRCm39) |
W71G |
probably benign |
Het |
Sidt1 |
T |
C |
16: 44,065,529 (GRCm39) |
Y759C |
probably damaging |
Het |
Spg11 |
G |
T |
2: 121,943,560 (GRCm39) |
D197E |
probably damaging |
Het |
Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
Ssc5d |
A |
T |
7: 4,939,328 (GRCm39) |
D588V |
probably damaging |
Het |
Supt20 |
C |
A |
3: 54,614,537 (GRCm39) |
T181K |
probably damaging |
Het |
Szt2 |
A |
T |
4: 118,244,015 (GRCm39) |
S1363R |
probably benign |
Het |
Tbcel |
G |
A |
9: 42,375,169 (GRCm39) |
|
probably null |
Het |
Ube2e3 |
T |
C |
2: 78,749,158 (GRCm39) |
L169P |
probably damaging |
Het |
Wrn |
A |
G |
8: 33,778,796 (GRCm39) |
F595S |
probably benign |
Het |
Zfp473 |
G |
T |
7: 44,382,323 (GRCm39) |
P670Q |
probably damaging |
Het |
Zw10 |
C |
T |
9: 48,986,299 (GRCm39) |
A660V |
probably benign |
Het |
|
Other mutations in Raver1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01923:Raver1
|
APN |
9 |
20,990,536 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
R9662:Raver1
|
UTSW |
9 |
20,992,550 (GRCm39) |
missense |
probably benign |
0.40 |
|