Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss2 |
C |
A |
2: 155,398,324 (GRCm39) |
H348Q |
probably benign |
Het |
Ago1 |
T |
A |
4: 126,357,516 (GRCm39) |
Y53F |
probably benign |
Het |
Arrdc5 |
A |
G |
17: 56,601,342 (GRCm39) |
L261P |
probably benign |
Het |
Asb2 |
C |
A |
12: 103,290,138 (GRCm39) |
W551L |
possibly damaging |
Het |
Atl2 |
T |
C |
17: 80,160,232 (GRCm39) |
I452V |
probably benign |
Het |
Atxn7l3 |
T |
C |
11: 102,183,545 (GRCm39) |
S203G |
probably benign |
Het |
C6 |
T |
C |
15: 4,826,454 (GRCm39) |
V679A |
probably benign |
Het |
Cd163 |
A |
T |
6: 124,297,469 (GRCm39) |
N872Y |
probably damaging |
Het |
Cdkal1 |
C |
A |
13: 29,658,607 (GRCm39) |
V380F |
probably damaging |
Het |
Ceacam11 |
A |
T |
7: 17,709,536 (GRCm39) |
I245L |
probably benign |
Het |
Ceacam16 |
G |
T |
7: 19,592,656 (GRCm39) |
T84K |
possibly damaging |
Het |
Ceacam2 |
T |
A |
7: 25,227,351 (GRCm39) |
Q172L |
probably benign |
Het |
Chga |
T |
G |
12: 102,527,720 (GRCm39) |
S125A |
possibly damaging |
Het |
Col9a1 |
T |
C |
1: 24,236,048 (GRCm39) |
|
probably null |
Het |
Crybg3 |
C |
A |
16: 59,380,547 (GRCm39) |
A236S |
probably benign |
Het |
Csmd1 |
A |
G |
8: 15,960,528 (GRCm39) |
Y3296H |
probably damaging |
Het |
Cyp2j8 |
C |
A |
4: 96,358,807 (GRCm39) |
V371L |
possibly damaging |
Het |
Des |
C |
A |
1: 75,337,137 (GRCm39) |
L26M |
unknown |
Het |
Edc3 |
A |
G |
9: 57,623,484 (GRCm39) |
S140G |
possibly damaging |
Het |
Fam161a |
C |
T |
11: 22,970,092 (GRCm39) |
T90I |
probably benign |
Het |
Fancm |
T |
C |
12: 65,173,522 (GRCm39) |
Y1945H |
probably damaging |
Het |
Fbn2 |
C |
T |
18: 58,257,318 (GRCm39) |
V350I |
probably benign |
Het |
Git2 |
A |
G |
5: 114,899,649 (GRCm39) |
C235R |
possibly damaging |
Het |
Gk2 |
T |
C |
5: 97,604,341 (GRCm39) |
K166E |
probably benign |
Het |
Gm12258 |
G |
A |
11: 58,750,112 (GRCm39) |
R429H |
unknown |
Het |
Gm7247 |
T |
G |
14: 51,666,210 (GRCm39) |
|
probably benign |
Het |
Gmppa |
A |
G |
1: 75,414,932 (GRCm39) |
Y59C |
probably damaging |
Het |
Has1 |
G |
T |
17: 18,070,321 (GRCm39) |
A200E |
possibly damaging |
Het |
Hbs1l |
T |
C |
10: 21,234,711 (GRCm39) |
I588T |
possibly damaging |
Het |
Helz2 |
A |
G |
2: 180,874,560 (GRCm39) |
V1978A |
possibly damaging |
Het |
Hoxb9 |
T |
C |
11: 96,165,557 (GRCm39) |
Y209H |
probably damaging |
Het |
Hps5 |
T |
C |
7: 46,421,345 (GRCm39) |
D706G |
probably benign |
Het |
Hydin |
T |
C |
8: 111,035,720 (GRCm39) |
V137A |
probably benign |
Het |
Ifngr2 |
T |
C |
16: 91,359,847 (GRCm39) |
I318T |
probably benign |
Het |
Iqgap3 |
C |
T |
3: 88,020,532 (GRCm39) |
T1290I |
probably damaging |
Het |
Jrk |
A |
T |
15: 74,578,988 (GRCm39) |
V99E |
probably benign |
Het |
Kalrn |
G |
A |
16: 34,025,696 (GRCm39) |
T931M |
probably damaging |
Het |
Kalrn |
G |
A |
16: 34,018,830 (GRCm39) |
P1311S |
probably benign |
Het |
Kirrel3 |
A |
G |
9: 34,850,561 (GRCm39) |
|
probably benign |
Het |
Klk1b9 |
T |
C |
7: 43,443,782 (GRCm39) |
F99L |
possibly damaging |
Het |
Lamb3 |
T |
C |
1: 193,013,124 (GRCm39) |
C450R |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,815,661 (GRCm39) |
S1182T |
probably benign |
Het |
Map1a |
T |
C |
2: 121,138,125 (GRCm39) |
V2933A |
probably damaging |
Het |
Map2k5 |
A |
T |
9: 63,250,667 (GRCm39) |
|
probably null |
Het |
Mcm6 |
A |
G |
1: 128,283,248 (GRCm39) |
|
probably null |
Het |
Mmp17 |
G |
A |
5: 129,683,378 (GRCm39) |
V505M |
probably damaging |
Het |
Mpped2 |
A |
G |
2: 106,575,065 (GRCm39) |
D50G |
probably damaging |
Het |
Mtf1 |
T |
A |
4: 124,715,023 (GRCm39) |
L216* |
probably null |
Het |
Niban2 |
A |
T |
2: 32,811,105 (GRCm39) |
M372L |
probably benign |
Het |
Obscn |
T |
C |
11: 58,890,638 (GRCm39) |
E7298G |
unknown |
Het |
Or52ab7 |
A |
T |
7: 102,978,212 (GRCm39) |
H173L |
possibly damaging |
Het |
Or56a3 |
T |
C |
7: 104,735,763 (GRCm39) |
L280P |
probably damaging |
Het |
Or6c205 |
T |
C |
10: 129,086,883 (GRCm39) |
L160P |
probably benign |
Het |
Or7d9 |
A |
G |
9: 20,197,358 (GRCm39) |
D129G |
probably damaging |
Het |
Otulinl |
T |
A |
15: 27,664,884 (GRCm39) |
H24L |
probably benign |
Het |
Pax2 |
G |
A |
19: 44,777,215 (GRCm39) |
|
probably null |
Het |
Pcnt |
T |
A |
10: 76,244,675 (GRCm39) |
E1135V |
probably damaging |
Het |
Pgap3 |
A |
T |
11: 98,281,924 (GRCm39) |
V129D |
probably benign |
Het |
Polq |
A |
G |
16: 36,860,869 (GRCm39) |
N497S |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,227,122 (GRCm39) |
T1138A |
|
Het |
Prickle4 |
A |
G |
17: 48,001,587 (GRCm39) |
L32P |
|
Het |
Prl2c2 |
C |
T |
13: 13,171,896 (GRCm39) |
G158R |
probably damaging |
Het |
Psd3 |
A |
G |
8: 68,210,750 (GRCm39) |
I752T |
probably benign |
Het |
Sag |
A |
T |
1: 87,756,158 (GRCm39) |
Y255F |
probably benign |
Het |
Scn7a |
A |
T |
2: 66,506,199 (GRCm39) |
D1563E |
probably damaging |
Het |
Secisbp2 |
A |
G |
13: 51,837,404 (GRCm39) |
N855S |
probably benign |
Het |
Setd2 |
T |
C |
9: 110,421,467 (GRCm39) |
V2011A |
probably benign |
Het |
Slc30a6 |
T |
C |
17: 74,730,112 (GRCm39) |
V334A |
probably damaging |
Het |
Spen |
A |
G |
4: 141,204,520 (GRCm39) |
V1369A |
unknown |
Het |
Stac2 |
T |
C |
11: 97,932,373 (GRCm39) |
T207A |
probably benign |
Het |
Syne2 |
T |
C |
12: 75,952,067 (GRCm39) |
V445A |
probably benign |
Het |
Tas2r131 |
C |
A |
6: 132,934,467 (GRCm39) |
W114L |
probably damaging |
Het |
Tgfbrap1 |
G |
A |
1: 43,088,959 (GRCm39) |
R815* |
probably null |
Het |
Trpv2 |
A |
T |
11: 62,481,112 (GRCm39) |
I404L |
probably benign |
Het |
Zfp236 |
G |
A |
18: 82,617,122 (GRCm39) |
T1791M |
probably damaging |
Het |
|
Other mutations in Bche |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00338:Bche
|
APN |
3 |
73,608,640 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01420:Bche
|
APN |
3 |
73,609,342 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02433:Bche
|
APN |
3 |
73,609,262 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02734:Bche
|
APN |
3 |
73,609,409 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03095:Bche
|
APN |
3 |
73,609,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03227:Bche
|
APN |
3 |
73,608,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R0056:Bche
|
UTSW |
3 |
73,608,654 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1780:Bche
|
UTSW |
3 |
73,607,953 (GRCm39) |
missense |
probably benign |
0.00 |
R1984:Bche
|
UTSW |
3 |
73,609,160 (GRCm39) |
missense |
probably benign |
|
R1984:Bche
|
UTSW |
3 |
73,609,159 (GRCm39) |
missense |
probably benign |
0.03 |
R2403:Bche
|
UTSW |
3 |
73,608,805 (GRCm39) |
missense |
probably damaging |
0.96 |
R4989:Bche
|
UTSW |
3 |
73,609,177 (GRCm39) |
missense |
probably benign |
0.02 |
R5231:Bche
|
UTSW |
3 |
73,608,194 (GRCm39) |
missense |
probably benign |
0.07 |
R5363:Bche
|
UTSW |
3 |
73,607,972 (GRCm39) |
missense |
probably damaging |
0.98 |
R5987:Bche
|
UTSW |
3 |
73,556,011 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6164:Bche
|
UTSW |
3 |
73,608,389 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6381:Bche
|
UTSW |
3 |
73,609,132 (GRCm39) |
missense |
probably benign |
0.00 |
R6571:Bche
|
UTSW |
3 |
73,608,824 (GRCm39) |
missense |
probably benign |
0.08 |
R6801:Bche
|
UTSW |
3 |
73,609,133 (GRCm39) |
missense |
probably benign |
|
R6935:Bche
|
UTSW |
3 |
73,609,133 (GRCm39) |
missense |
probably benign |
|
R7275:Bche
|
UTSW |
3 |
73,607,969 (GRCm39) |
missense |
probably benign |
0.19 |
R7499:Bche
|
UTSW |
3 |
73,609,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R7543:Bche
|
UTSW |
3 |
73,609,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R7757:Bche
|
UTSW |
3 |
73,608,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Bche
|
UTSW |
3 |
73,609,149 (GRCm39) |
missense |
probably damaging |
0.98 |
R8944:Bche
|
UTSW |
3 |
73,608,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R8947:Bche
|
UTSW |
3 |
73,608,761 (GRCm39) |
missense |
probably damaging |
0.97 |
R8964:Bche
|
UTSW |
3 |
73,608,406 (GRCm39) |
missense |
probably benign |
0.00 |
R9402:Bche
|
UTSW |
3 |
73,608,656 (GRCm39) |
missense |
probably benign |
0.06 |
|