Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830005F24Rik |
T |
C |
13: 48,667,937 (GRCm39) |
|
probably benign |
Het |
Acad11 |
T |
C |
9: 103,960,038 (GRCm39) |
F219L |
probably benign |
Het |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Adamts17 |
A |
T |
7: 66,677,641 (GRCm39) |
E518D |
probably damaging |
Het |
Adamts3 |
A |
G |
5: 89,848,346 (GRCm39) |
Y659H |
probably benign |
Het |
Adgrb3 |
T |
C |
1: 25,123,360 (GRCm39) |
R1414G |
probably damaging |
Het |
Apba1 |
T |
A |
19: 23,894,956 (GRCm39) |
I464N |
probably damaging |
Het |
Bcl11a |
A |
G |
11: 24,114,004 (GRCm39) |
E449G |
probably damaging |
Het |
Ccdc162 |
T |
A |
10: 41,463,384 (GRCm39) |
I1453L |
probably benign |
Het |
Ccdc175 |
T |
A |
12: 72,175,080 (GRCm39) |
E531V |
probably benign |
Het |
Cep68 |
A |
T |
11: 20,189,113 (GRCm39) |
|
probably benign |
Het |
Dlgap1 |
C |
A |
17: 70,823,684 (GRCm39) |
T223K |
probably benign |
Het |
Exoc1 |
G |
A |
5: 76,709,290 (GRCm39) |
V24M |
probably damaging |
Het |
Fbxo4 |
A |
G |
15: 3,995,187 (GRCm39) |
*386R |
probably null |
Het |
Gm10100 |
G |
A |
10: 77,562,365 (GRCm39) |
|
probably benign |
Het |
Gpr149 |
A |
G |
3: 62,438,291 (GRCm39) |
V622A |
probably damaging |
Het |
Gpr149 |
A |
C |
3: 62,511,918 (GRCm39) |
M27R |
probably benign |
Het |
Ighv3-6 |
T |
C |
12: 114,251,818 (GRCm39) |
N101D |
probably benign |
Het |
Igkv4-78 |
A |
G |
6: 69,036,755 (GRCm39) |
S93P |
possibly damaging |
Het |
Kmt2c |
A |
T |
5: 25,505,313 (GRCm39) |
W3332R |
probably damaging |
Het |
Marf1 |
T |
C |
16: 13,971,841 (GRCm39) |
|
probably benign |
Het |
Mcrs1 |
A |
G |
15: 99,141,028 (GRCm39) |
I459T |
probably benign |
Het |
Mdn1 |
G |
T |
4: 32,754,437 (GRCm39) |
C4646F |
probably damaging |
Het |
Med17 |
T |
C |
9: 15,182,993 (GRCm39) |
K351E |
possibly damaging |
Het |
Nalcn |
T |
C |
14: 123,558,647 (GRCm39) |
|
probably benign |
Het |
Or14j8 |
C |
A |
17: 38,263,142 (GRCm39) |
A258S |
probably benign |
Het |
Or1e29 |
G |
A |
11: 73,667,307 (GRCm39) |
T282I |
possibly damaging |
Het |
Or1r1 |
A |
T |
11: 73,875,425 (GRCm39) |
V3E |
probably benign |
Het |
Or6c69 |
A |
G |
10: 129,747,398 (GRCm39) |
Y250H |
probably damaging |
Het |
Phrf1 |
C |
T |
7: 140,838,842 (GRCm39) |
|
probably benign |
Het |
Pitpnm1 |
A |
G |
19: 4,153,085 (GRCm39) |
Q135R |
probably benign |
Het |
Prdm16 |
T |
A |
4: 154,613,284 (GRCm39) |
M48L |
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,688,976 (GRCm39) |
E923G |
probably damaging |
Het |
Rp1 |
A |
T |
1: 4,414,886 (GRCm39) |
S2075R |
possibly damaging |
Het |
Sft2d2 |
A |
G |
1: 165,011,553 (GRCm39) |
C114R |
probably damaging |
Het |
Sipa1l2 |
T |
G |
8: 126,191,154 (GRCm39) |
R945S |
probably damaging |
Het |
Slc12a1 |
A |
G |
2: 125,028,561 (GRCm39) |
N517S |
probably damaging |
Het |
Slc44a2 |
T |
G |
9: 21,258,079 (GRCm39) |
L443R |
possibly damaging |
Het |
Smok4a |
T |
C |
17: 13,746,643 (GRCm39) |
|
noncoding transcript |
Het |
Snx18 |
A |
G |
13: 113,754,364 (GRCm39) |
S190P |
probably damaging |
Het |
Thap12 |
A |
G |
7: 98,365,052 (GRCm39) |
N407D |
probably benign |
Het |
Tmc5 |
T |
C |
7: 118,269,956 (GRCm39) |
I902T |
probably benign |
Het |
Ttc27 |
T |
G |
17: 75,136,544 (GRCm39) |
S584A |
probably benign |
Het |
Ttn |
A |
T |
2: 76,779,359 (GRCm39) |
Y1174N |
probably damaging |
Het |
Zbtb44 |
T |
G |
9: 30,975,544 (GRCm39) |
S391R |
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 |
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 |
R7794:Bahcc1
|
UTSW |
11 |
120,163,507 (GRCm39) |
nonsense |
probably null |
|
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 |
|