Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
T |
2: 69,117,022 (GRCm39) |
M542K |
possibly damaging |
Het |
Abcc3 |
T |
A |
11: 94,249,697 (GRCm39) |
I1083F |
probably benign |
Het |
Acsm5 |
A |
G |
7: 119,137,352 (GRCm39) |
|
probably benign |
Het |
Acyp1 |
G |
T |
12: 85,335,053 (GRCm39) |
A22E |
probably benign |
Het |
Afdn |
C |
A |
17: 14,102,695 (GRCm39) |
A1090E |
probably damaging |
Het |
Ahdc1 |
T |
G |
4: 132,791,289 (GRCm39) |
D843E |
possibly damaging |
Het |
Bora |
A |
G |
14: 99,310,080 (GRCm39) |
T470A |
possibly damaging |
Het |
Bzw1 |
T |
A |
1: 58,439,959 (GRCm39) |
S166T |
probably benign |
Het |
Car13 |
A |
G |
3: 14,719,948 (GRCm39) |
H120R |
probably damaging |
Het |
Cstf3 |
G |
A |
2: 104,420,926 (GRCm39) |
⇒1 |
probably benign |
Het |
Dip2a |
T |
C |
10: 76,112,459 (GRCm39) |
N1080D |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,336,233 (GRCm39) |
L91P |
probably benign |
Het |
E2f6 |
A |
G |
12: 16,870,370 (GRCm39) |
D174G |
possibly damaging |
Het |
Emsy |
A |
T |
7: 98,249,931 (GRCm39) |
S785R |
probably benign |
Het |
Fbxl17 |
A |
G |
17: 63,663,806 (GRCm39) |
I561T |
probably damaging |
Het |
Gabra6 |
A |
T |
11: 42,211,868 (GRCm39) |
|
probably null |
Het |
Gm47996 |
C |
G |
1: 151,086,545 (GRCm39) |
P209A |
possibly damaging |
Het |
Hcls1 |
A |
G |
16: 36,782,426 (GRCm39) |
E365G |
probably damaging |
Het |
Hoxa6 |
T |
A |
6: 52,183,548 (GRCm39) |
T166S |
possibly damaging |
Het |
Hydin |
A |
G |
8: 111,235,715 (GRCm39) |
Y1900C |
probably damaging |
Het |
I0C0044D17Rik |
T |
C |
4: 98,708,582 (GRCm39) |
|
probably benign |
Het |
Ifitm7 |
T |
C |
16: 13,801,610 (GRCm39) |
T50A |
probably benign |
Het |
Igkv10-95 |
A |
G |
6: 68,657,811 (GRCm39) |
Q109R |
possibly damaging |
Het |
Il1rap |
A |
T |
16: 26,541,658 (GRCm39) |
H633L |
probably benign |
Het |
Ippk |
C |
T |
13: 49,599,818 (GRCm39) |
P226S |
|
Het |
Kmt2e |
G |
A |
5: 23,669,714 (GRCm39) |
G67D |
probably damaging |
Het |
Kpna6 |
T |
C |
4: 129,541,844 (GRCm39) |
T518A |
probably benign |
Het |
Marchf11 |
A |
G |
15: 26,409,284 (GRCm39) |
I328V |
probably benign |
Het |
Mbtps1 |
A |
G |
8: 120,265,623 (GRCm39) |
I308T |
probably damaging |
Het |
Mug1 |
A |
T |
6: 121,833,247 (GRCm39) |
D284V |
possibly damaging |
Het |
Myo16 |
A |
G |
8: 10,619,913 (GRCm39) |
K1488R |
unknown |
Het |
Myom2 |
G |
A |
8: 15,133,259 (GRCm39) |
G384R |
probably damaging |
Het |
Naa16 |
A |
G |
14: 79,614,934 (GRCm39) |
Y189H |
probably damaging |
Het |
Nav3 |
G |
A |
10: 109,524,717 (GRCm39) |
A2304V |
probably benign |
Het |
Or12e10 |
T |
A |
2: 87,640,818 (GRCm39) |
V218E |
probably damaging |
Het |
Or14c46 |
T |
A |
7: 85,918,341 (GRCm39) |
I219L |
probably damaging |
Het |
Or14j5 |
A |
T |
17: 38,161,678 (GRCm39) |
Q65L |
probably benign |
Het |
Orc5 |
A |
T |
5: 22,738,782 (GRCm39) |
Y160N |
possibly damaging |
Het |
Pan2 |
T |
C |
10: 128,152,396 (GRCm39) |
|
probably null |
Het |
Pcdhb20 |
A |
G |
18: 37,637,485 (GRCm39) |
R4G |
probably benign |
Het |
Poc1b |
A |
G |
10: 98,965,460 (GRCm39) |
S130G |
possibly damaging |
Het |
Psme2b |
A |
G |
11: 48,836,683 (GRCm39) |
V88A |
probably benign |
Het |
Ptpn13 |
C |
T |
5: 103,640,090 (GRCm39) |
T183M |
probably benign |
Het |
Ptpn4 |
T |
C |
1: 119,653,767 (GRCm39) |
E275G |
probably damaging |
Het |
Rab21 |
A |
T |
10: 115,134,762 (GRCm39) |
L119* |
probably null |
Het |
Rep15 |
T |
A |
6: 146,934,638 (GRCm39) |
I159N |
probably damaging |
Het |
Rps6kc1 |
T |
C |
1: 190,515,825 (GRCm39) |
E967G |
probably benign |
Het |
Rptn |
G |
A |
3: 93,303,036 (GRCm39) |
R123K |
probably benign |
Het |
Scn11a |
A |
T |
9: 119,594,580 (GRCm39) |
V1271D |
probably damaging |
Het |
Scn5a |
A |
T |
9: 119,358,153 (GRCm39) |
I696N |
probably damaging |
Het |
Slc25a12 |
T |
C |
2: 71,141,852 (GRCm39) |
E267G |
probably damaging |
Het |
Slc5a4b |
A |
T |
10: 75,898,133 (GRCm39) |
M527K |
probably benign |
Het |
Spata31e4 |
C |
G |
13: 50,856,344 (GRCm39) |
P661A |
probably damaging |
Het |
Speg |
T |
A |
1: 75,365,514 (GRCm39) |
S632T |
probably benign |
Het |
Stard9 |
G |
A |
2: 120,534,911 (GRCm39) |
G3723S |
probably benign |
Het |
Synrg |
G |
T |
11: 83,910,400 (GRCm39) |
M933I |
probably benign |
Het |
Tmem178b |
A |
T |
6: 40,222,551 (GRCm39) |
I89F |
probably damaging |
Het |
Tyr |
C |
T |
7: 87,133,028 (GRCm39) |
|
probably null |
Het |
Usp30 |
T |
A |
5: 114,251,033 (GRCm39) |
C237* |
probably null |
Het |
Xpo6 |
G |
T |
7: 125,760,035 (GRCm39) |
T188K |
probably damaging |
Het |
Zfp382 |
G |
A |
7: 29,831,035 (GRCm39) |
S108N |
possibly damaging |
Het |
Zfp820 |
A |
C |
17: 22,039,109 (GRCm39) |
V73G |
probably damaging |
Het |
|
Other mutations in Bahcc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00341:Bahcc1
|
APN |
11 |
120,163,130 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00536:Bahcc1
|
APN |
11 |
120,175,871 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01339:Bahcc1
|
APN |
11 |
120,180,338 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01695:Bahcc1
|
APN |
11 |
120,167,435 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01744:Bahcc1
|
APN |
11 |
120,162,563 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01769:Bahcc1
|
APN |
11 |
120,171,030 (GRCm39) |
splice site |
probably benign |
|
IGL01982:Bahcc1
|
APN |
11 |
120,178,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02341:Bahcc1
|
APN |
11 |
120,163,346 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:Bahcc1
|
APN |
11 |
120,178,362 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02559:Bahcc1
|
APN |
11 |
120,175,998 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02579:Bahcc1
|
APN |
11 |
120,176,175 (GRCm39) |
splice site |
probably benign |
|
IGL02609:Bahcc1
|
APN |
11 |
120,180,224 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02678:Bahcc1
|
APN |
11 |
120,163,697 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02800:Bahcc1
|
APN |
11 |
120,163,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02963:Bahcc1
|
APN |
11 |
120,165,758 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03128:Bahcc1
|
APN |
11 |
120,159,260 (GRCm39) |
splice site |
probably benign |
|
IGL03242:Bahcc1
|
APN |
11 |
120,159,126 (GRCm39) |
splice site |
probably benign |
|
IGL03248:Bahcc1
|
APN |
11 |
120,159,235 (GRCm39) |
missense |
probably damaging |
1.00 |
Dimensionality
|
UTSW |
11 |
120,163,835 (GRCm39) |
missense |
probably damaging |
1.00 |
G1citation:Bahcc1
|
UTSW |
11 |
120,178,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R0019:Bahcc1
|
UTSW |
11 |
120,180,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Bahcc1
|
UTSW |
11 |
120,159,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Bahcc1
|
UTSW |
11 |
120,159,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R0148:Bahcc1
|
UTSW |
11 |
120,159,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Bahcc1
|
UTSW |
11 |
120,175,900 (GRCm39) |
splice site |
probably benign |
|
R0321:Bahcc1
|
UTSW |
11 |
120,164,251 (GRCm39) |
critical splice donor site |
probably null |
|
R0671:Bahcc1
|
UTSW |
11 |
120,178,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R0737:Bahcc1
|
UTSW |
11 |
120,163,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R1452:Bahcc1
|
UTSW |
11 |
120,173,065 (GRCm39) |
splice site |
probably benign |
|
R1570:Bahcc1
|
UTSW |
11 |
120,163,009 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1914:Bahcc1
|
UTSW |
11 |
120,176,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Bahcc1
|
UTSW |
11 |
120,163,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Bahcc1
|
UTSW |
11 |
120,162,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R2085:Bahcc1
|
UTSW |
11 |
120,178,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R3552:Bahcc1
|
UTSW |
11 |
120,167,598 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3711:Bahcc1
|
UTSW |
11 |
120,165,923 (GRCm39) |
missense |
probably benign |
0.27 |
R3804:Bahcc1
|
UTSW |
11 |
120,174,184 (GRCm39) |
missense |
probably benign |
0.01 |
R4349:Bahcc1
|
UTSW |
11 |
120,150,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R4557:Bahcc1
|
UTSW |
11 |
120,165,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Bahcc1
|
UTSW |
11 |
120,173,051 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Bahcc1
|
UTSW |
11 |
120,173,051 (GRCm39) |
missense |
probably benign |
0.00 |
R4908:Bahcc1
|
UTSW |
11 |
120,178,580 (GRCm39) |
missense |
probably benign |
0.36 |
R4941:Bahcc1
|
UTSW |
11 |
120,177,491 (GRCm39) |
missense |
probably benign |
|
R5217:Bahcc1
|
UTSW |
11 |
120,165,285 (GRCm39) |
nonsense |
probably null |
|
R5241:Bahcc1
|
UTSW |
11 |
120,162,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R5432:Bahcc1
|
UTSW |
11 |
120,178,814 (GRCm39) |
missense |
probably benign |
0.02 |
R5696:Bahcc1
|
UTSW |
11 |
120,164,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5724:Bahcc1
|
UTSW |
11 |
120,176,192 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5725:Bahcc1
|
UTSW |
11 |
120,165,714 (GRCm39) |
missense |
probably benign |
|
R5788:Bahcc1
|
UTSW |
11 |
120,177,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R5893:Bahcc1
|
UTSW |
11 |
120,176,256 (GRCm39) |
missense |
probably damaging |
0.99 |
R5900:Bahcc1
|
UTSW |
11 |
120,175,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Bahcc1
|
UTSW |
11 |
120,180,615 (GRCm39) |
missense |
probably benign |
0.00 |
R6058:Bahcc1
|
UTSW |
11 |
120,178,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R6107:Bahcc1
|
UTSW |
11 |
120,163,714 (GRCm39) |
missense |
probably benign |
0.00 |
R6302:Bahcc1
|
UTSW |
11 |
120,167,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R6525:Bahcc1
|
UTSW |
11 |
120,176,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R6550:Bahcc1
|
UTSW |
11 |
120,167,477 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6822:Bahcc1
|
UTSW |
11 |
120,178,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R6836:Bahcc1
|
UTSW |
11 |
120,162,583 (GRCm39) |
nonsense |
probably null |
|
R6846:Bahcc1
|
UTSW |
11 |
120,162,422 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6916:Bahcc1
|
UTSW |
11 |
120,163,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R6966:Bahcc1
|
UTSW |
11 |
120,173,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R7097:Bahcc1
|
UTSW |
11 |
120,163,472 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7289:Bahcc1
|
UTSW |
11 |
120,171,000 (GRCm39) |
missense |
probably benign |
0.08 |
R7441:Bahcc1
|
UTSW |
11 |
120,177,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R7520:Bahcc1
|
UTSW |
11 |
120,167,031 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7556:Bahcc1
|
UTSW |
11 |
120,178,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R7672:Bahcc1
|
UTSW |
11 |
120,174,172 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7791:Bahcc1
|
UTSW |
11 |
120,159,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R7802:Bahcc1
|
UTSW |
11 |
120,165,518 (GRCm39) |
missense |
probably benign |
0.03 |
R7946:Bahcc1
|
UTSW |
11 |
120,163,325 (GRCm39) |
missense |
probably benign |
|
R7985:Bahcc1
|
UTSW |
11 |
120,163,717 (GRCm39) |
missense |
probably damaging |
0.97 |
R8128:Bahcc1
|
UTSW |
11 |
120,163,216 (GRCm39) |
nonsense |
probably null |
|
R8131:Bahcc1
|
UTSW |
11 |
120,163,664 (GRCm39) |
missense |
probably benign |
0.01 |
R8353:Bahcc1
|
UTSW |
11 |
120,165,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R8439:Bahcc1
|
UTSW |
11 |
120,165,415 (GRCm39) |
missense |
probably benign |
0.01 |
R8710:Bahcc1
|
UTSW |
11 |
120,174,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8799:Bahcc1
|
UTSW |
11 |
120,177,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Bahcc1
|
UTSW |
11 |
120,164,587 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8920:Bahcc1
|
UTSW |
11 |
120,175,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Bahcc1
|
UTSW |
11 |
120,167,591 (GRCm39) |
missense |
probably benign |
0.09 |
R9014:Bahcc1
|
UTSW |
11 |
120,173,048 (GRCm39) |
missense |
probably benign |
|
R9014:Bahcc1
|
UTSW |
11 |
120,163,715 (GRCm39) |
missense |
probably benign |
0.00 |
R9195:Bahcc1
|
UTSW |
11 |
120,167,337 (GRCm39) |
missense |
probably benign |
|
R9216:Bahcc1
|
UTSW |
11 |
120,177,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Bahcc1
|
UTSW |
11 |
120,165,885 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9392:Bahcc1
|
UTSW |
11 |
120,163,513 (GRCm39) |
nonsense |
probably null |
|
R9562:Bahcc1
|
UTSW |
11 |
120,150,035 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9680:Bahcc1
|
UTSW |
11 |
120,163,286 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9797:Bahcc1
|
UTSW |
11 |
120,159,147 (GRCm39) |
nonsense |
probably null |
|
X0026:Bahcc1
|
UTSW |
11 |
120,162,578 (GRCm39) |
missense |
probably benign |
0.20 |
Z1176:Bahcc1
|
UTSW |
11 |
120,175,220 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Bahcc1
|
UTSW |
11 |
120,167,435 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1177:Bahcc1
|
UTSW |
11 |
120,163,747 (GRCm39) |
missense |
possibly damaging |
0.73 |
|