Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad11 |
T |
C |
9: 103,991,684 (GRCm39) |
M573T |
probably benign |
Het |
Ank3 |
A |
G |
10: 69,851,422 (GRCm39) |
T1162A |
possibly damaging |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
Arpp21 |
T |
A |
9: 111,972,595 (GRCm39) |
D232V |
probably damaging |
Het |
Atg2a |
T |
C |
19: 6,304,414 (GRCm39) |
Y1144H |
probably damaging |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Brs3 |
T |
C |
X: 56,092,449 (GRCm39) |
I311T |
probably benign |
Het |
Cenpf |
C |
T |
1: 189,379,046 (GRCm39) |
V2915I |
probably benign |
Het |
Cep170 |
G |
T |
1: 176,602,245 (GRCm39) |
T287K |
probably benign |
Het |
Chst2 |
G |
A |
9: 95,287,611 (GRCm39) |
T245I |
probably damaging |
Het |
Cnot4 |
C |
T |
6: 35,055,092 (GRCm39) |
V66I |
probably damaging |
Het |
Cntn4 |
A |
G |
6: 106,656,353 (GRCm39) |
T885A |
probably benign |
Het |
Col20a1 |
C |
T |
2: 180,634,703 (GRCm39) |
T131I |
possibly damaging |
Het |
Coro7 |
G |
T |
16: 4,446,683 (GRCm39) |
|
probably benign |
Het |
Cpne8 |
C |
A |
15: 90,532,831 (GRCm39) |
|
probably benign |
Het |
Dbnl |
G |
A |
11: 5,749,247 (GRCm39) |
G356E |
probably benign |
Het |
Ddx31 |
T |
A |
2: 28,749,002 (GRCm39) |
I266N |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,580,159 (GRCm39) |
I1592N |
probably damaging |
Het |
Dok6 |
A |
T |
18: 89,492,130 (GRCm39) |
L149Q |
probably damaging |
Het |
Eri2 |
G |
A |
7: 119,390,346 (GRCm39) |
T94I |
probably benign |
Het |
Ermp1 |
A |
G |
19: 29,594,079 (GRCm39) |
V697A |
probably benign |
Het |
Foxc1 |
C |
T |
13: 31,991,648 (GRCm39) |
T153M |
probably damaging |
Het |
Fry |
A |
G |
5: 150,326,985 (GRCm39) |
I1224V |
probably benign |
Het |
Fzd5 |
G |
A |
1: 64,774,813 (GRCm39) |
T316M |
probably damaging |
Het |
Gcm1 |
G |
T |
9: 77,966,861 (GRCm39) |
V27L |
probably benign |
Het |
Gm5773 |
A |
T |
3: 93,681,348 (GRCm39) |
D340V |
probably benign |
Het |
Gucy2d |
T |
A |
7: 98,100,815 (GRCm39) |
H379Q |
probably benign |
Het |
Hectd1 |
T |
A |
12: 51,847,738 (GRCm39) |
M392L |
probably benign |
Het |
Itpr2 |
A |
C |
6: 146,287,469 (GRCm39) |
D452E |
probably benign |
Het |
Krtap2-4 |
G |
C |
11: 99,505,505 (GRCm39) |
|
probably benign |
Het |
Lrit1 |
T |
C |
14: 36,783,710 (GRCm39) |
V346A |
possibly damaging |
Het |
Lrrk1 |
A |
G |
7: 65,912,185 (GRCm39) |
S1792P |
probably benign |
Het |
Marveld2 |
A |
T |
13: 100,737,129 (GRCm39) |
V168E |
probably benign |
Het |
Ms4a4b |
T |
A |
19: 11,438,629 (GRCm39) |
D149E |
probably damaging |
Het |
Myom2 |
G |
A |
8: 15,164,278 (GRCm39) |
D1058N |
probably benign |
Het |
Ncam2 |
C |
T |
16: 81,234,571 (GRCm39) |
P142L |
probably damaging |
Het |
Nek9 |
A |
G |
12: 85,379,330 (GRCm39) |
L192P |
probably damaging |
Het |
Nol10 |
T |
C |
12: 17,418,390 (GRCm39) |
|
probably null |
Het |
Nrcam |
T |
C |
12: 44,591,538 (GRCm39) |
V194A |
probably damaging |
Het |
Nudt6 |
A |
G |
3: 37,466,549 (GRCm39) |
V82A |
probably benign |
Het |
Odf2l |
A |
T |
3: 144,856,809 (GRCm39) |
N492I |
probably damaging |
Het |
Or2a12 |
T |
C |
6: 42,904,764 (GRCm39) |
S200P |
probably damaging |
Het |
Or51f1d |
T |
C |
7: 102,701,189 (GRCm39) |
I228T |
probably benign |
Het |
Pkn3 |
T |
C |
2: 29,972,840 (GRCm39) |
V276A |
probably damaging |
Het |
Prl3b1 |
T |
G |
13: 27,431,886 (GRCm39) |
L137R |
possibly damaging |
Het |
Rab11fip2 |
A |
G |
19: 59,925,762 (GRCm39) |
F10L |
probably damaging |
Het |
Rab3b |
T |
A |
4: 108,786,649 (GRCm39) |
V133E |
probably damaging |
Het |
Rnf111 |
A |
T |
9: 70,383,520 (GRCm39) |
S138T |
probably damaging |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Runx1t1 |
A |
G |
4: 13,835,767 (GRCm39) |
T75A |
probably benign |
Het |
Ryr2 |
T |
G |
13: 11,753,242 (GRCm39) |
K1693T |
probably damaging |
Het |
Serpina1d |
T |
A |
12: 103,732,037 (GRCm39) |
D274V |
possibly damaging |
Het |
Setd2 |
T |
G |
9: 110,385,486 (GRCm39) |
|
probably null |
Het |
Sh3tc2 |
A |
G |
18: 62,141,646 (GRCm39) |
Y1109C |
probably damaging |
Het |
Sik3 |
C |
G |
9: 46,132,387 (GRCm39) |
H1276Q |
probably benign |
Het |
Slc22a2 |
A |
G |
17: 12,833,713 (GRCm39) |
|
probably benign |
Het |
Slc35f4 |
A |
T |
14: 49,551,091 (GRCm39) |
W108R |
probably damaging |
Het |
Slc4a1ap |
A |
G |
5: 31,691,524 (GRCm39) |
E440G |
probably damaging |
Het |
Slc6a4 |
A |
G |
11: 76,904,201 (GRCm39) |
T219A |
probably benign |
Het |
Stxbp5 |
C |
A |
10: 9,688,042 (GRCm39) |
V420F |
possibly damaging |
Het |
Svil |
T |
G |
18: 5,094,640 (GRCm39) |
V1440G |
possibly damaging |
Het |
Tas2r126 |
A |
T |
6: 42,411,961 (GRCm39) |
T165S |
probably benign |
Het |
Tbck |
T |
C |
3: 132,430,677 (GRCm39) |
|
probably null |
Het |
Tnxb |
T |
A |
17: 34,908,539 (GRCm39) |
D1520E |
probably benign |
Het |
Top1mt |
C |
T |
15: 75,539,750 (GRCm39) |
R287H |
possibly damaging |
Het |
Trdn |
A |
G |
10: 33,133,091 (GRCm39) |
K314E |
probably benign |
Het |
Troap |
T |
A |
15: 98,975,779 (GRCm39) |
C233S |
probably benign |
Het |
Usp28 |
T |
C |
9: 48,947,247 (GRCm39) |
M571T |
probably damaging |
Het |
Vac14 |
A |
G |
8: 111,438,319 (GRCm39) |
H644R |
probably damaging |
Het |
Vipr1 |
C |
T |
9: 121,494,930 (GRCm39) |
P327L |
possibly damaging |
Het |
Vmn1r31 |
C |
T |
6: 58,449,029 (GRCm39) |
V279I |
probably damaging |
Het |
Vmn1r69 |
G |
A |
7: 10,314,678 (GRCm39) |
R18W |
probably benign |
Het |
Vmn2r18 |
G |
T |
5: 151,499,190 (GRCm39) |
Q425K |
probably benign |
Het |
Vmn2r60 |
T |
C |
7: 41,786,094 (GRCm39) |
V299A |
probably damaging |
Het |
Vps13b |
A |
T |
15: 35,430,437 (GRCm39) |
|
probably benign |
Het |
Zfp157 |
A |
G |
5: 138,443,102 (GRCm39) |
D31G |
probably damaging |
Het |
Zfp385c |
A |
C |
11: 100,521,532 (GRCm39) |
V176G |
probably benign |
Het |
Zfp831 |
A |
G |
2: 174,545,870 (GRCm39) |
H1325R |
possibly damaging |
Het |
|
Other mutations in Sdha |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0270:Sdha
|
UTSW |
13 |
74,480,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R0480:Sdha
|
UTSW |
13 |
74,475,452 (GRCm39) |
missense |
probably benign |
0.36 |
R0960:Sdha
|
UTSW |
13 |
74,471,303 (GRCm39) |
splice site |
probably benign |
|
R1883:Sdha
|
UTSW |
13 |
74,481,255 (GRCm39) |
missense |
probably damaging |
0.98 |
R2068:Sdha
|
UTSW |
13 |
74,472,087 (GRCm39) |
splice site |
probably null |
|
R3881:Sdha
|
UTSW |
13 |
74,487,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R3894:Sdha
|
UTSW |
13 |
74,482,510 (GRCm39) |
missense |
probably benign |
0.03 |
R4063:Sdha
|
UTSW |
13 |
74,472,077 (GRCm39) |
intron |
probably benign |
|
R4384:Sdha
|
UTSW |
13 |
74,475,104 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5046:Sdha
|
UTSW |
13 |
74,475,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R5432:Sdha
|
UTSW |
13 |
74,475,068 (GRCm39) |
missense |
probably damaging |
0.97 |
R5521:Sdha
|
UTSW |
13 |
74,498,218 (GRCm39) |
intron |
probably benign |
|
R5645:Sdha
|
UTSW |
13 |
74,471,958 (GRCm39) |
critical splice donor site |
probably null |
|
R5770:Sdha
|
UTSW |
13 |
74,471,239 (GRCm39) |
nonsense |
probably null |
|
R5797:Sdha
|
UTSW |
13 |
74,482,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R5920:Sdha
|
UTSW |
13 |
74,475,044 (GRCm39) |
critical splice donor site |
probably null |
|
R6450:Sdha
|
UTSW |
13 |
74,482,412 (GRCm39) |
splice site |
probably null |
|
R7677:Sdha
|
UTSW |
13 |
74,481,172 (GRCm39) |
nonsense |
probably null |
|
R7793:Sdha
|
UTSW |
13 |
74,479,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R8284:Sdha
|
UTSW |
13 |
74,479,416 (GRCm39) |
critical splice donor site |
probably null |
|
R8912:Sdha
|
UTSW |
13 |
74,475,323 (GRCm39) |
intron |
probably benign |
|
R8923:Sdha
|
UTSW |
13 |
74,487,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R9256:Sdha
|
UTSW |
13 |
74,475,483 (GRCm39) |
intron |
probably benign |
|
R9281:Sdha
|
UTSW |
13 |
74,472,056 (GRCm39) |
nonsense |
probably null |
|
R9296:Sdha
|
UTSW |
13 |
74,472,062 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Sdha
|
UTSW |
13 |
74,498,312 (GRCm39) |
missense |
unknown |
|
Z1177:Sdha
|
UTSW |
13 |
74,487,751 (GRCm39) |
missense |
probably damaging |
1.00 |
|