Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Adamts20 |
G |
A |
15: 94,227,928 (GRCm39) |
R1040* |
probably null |
Het |
Akt1 |
A |
G |
12: 112,628,634 (GRCm39) |
L52P |
probably damaging |
Het |
Alk |
T |
A |
17: 72,176,742 (GRCm39) |
T1521S |
probably benign |
Het |
Armt1 |
A |
G |
10: 4,403,488 (GRCm39) |
N191S |
probably damaging |
Het |
Ascl1 |
T |
G |
10: 87,328,562 (GRCm39) |
N130T |
probably damaging |
Het |
Cd86 |
T |
C |
16: 36,449,377 (GRCm39) |
M7V |
possibly damaging |
Het |
Cep57 |
A |
T |
9: 13,722,057 (GRCm39) |
S304R |
possibly damaging |
Het |
Cep57l1 |
A |
T |
10: 41,616,918 (GRCm39) |
I123N |
possibly damaging |
Het |
Cers6 |
A |
G |
2: 68,692,008 (GRCm39) |
N10S |
probably benign |
Het |
Chrng |
A |
G |
1: 87,139,074 (GRCm39) |
D475G |
probably damaging |
Het |
Crabp1 |
T |
A |
9: 54,680,129 (GRCm39) |
V128E |
probably damaging |
Het |
Csnk2a1-ps3 |
T |
C |
1: 156,352,425 (GRCm39) |
Y209H |
probably damaging |
Het |
Dcdc2a |
T |
C |
13: 25,240,354 (GRCm39) |
V34A |
possibly damaging |
Het |
Eeig1 |
G |
A |
2: 32,450,102 (GRCm39) |
V117I |
probably benign |
Het |
Fbn1 |
A |
G |
2: 125,308,532 (GRCm39) |
C177R |
possibly damaging |
Het |
Fras1 |
A |
G |
5: 96,857,844 (GRCm39) |
D2046G |
probably benign |
Het |
Glul |
T |
C |
1: 153,783,087 (GRCm39) |
I220T |
probably benign |
Het |
Gpc6 |
C |
T |
14: 118,202,182 (GRCm39) |
T464M |
probably damaging |
Het |
Gpm6a |
T |
C |
8: 55,511,833 (GRCm39) |
S236P |
probably damaging |
Het |
H2-K2 |
G |
T |
17: 34,218,304 (GRCm39) |
T204K |
probably benign |
Het |
H2-K2 |
T |
C |
17: 34,218,305 (GRCm39) |
T204A |
probably benign |
Het |
Hecw2 |
T |
C |
1: 53,963,135 (GRCm39) |
H792R |
possibly damaging |
Het |
Herc4 |
T |
A |
10: 63,110,821 (GRCm39) |
I244K |
possibly damaging |
Het |
Hsd11b2 |
G |
T |
8: 106,249,966 (GRCm39) |
R359L |
possibly damaging |
Het |
Igsf9 |
G |
A |
1: 172,312,456 (GRCm39) |
E56K |
probably damaging |
Het |
Il9 |
T |
C |
13: 56,628,495 (GRCm39) |
T65A |
possibly damaging |
Het |
Kcnip1 |
T |
C |
11: 33,592,478 (GRCm39) |
T102A |
probably damaging |
Het |
L3mbtl2 |
T |
C |
15: 81,551,555 (GRCm39) |
S74P |
probably benign |
Het |
Lamc2 |
C |
T |
1: 153,012,575 (GRCm39) |
D700N |
probably benign |
Het |
Ldb2 |
T |
C |
5: 44,633,905 (GRCm39) |
T322A |
possibly damaging |
Het |
Lix1 |
A |
T |
17: 17,664,012 (GRCm39) |
I117F |
probably damaging |
Het |
Map2 |
T |
A |
1: 66,454,573 (GRCm39) |
D1154E |
probably benign |
Het |
Marco |
A |
T |
1: 120,404,435 (GRCm39) |
I425N |
probably damaging |
Het |
Mark4 |
T |
C |
7: 19,160,310 (GRCm39) |
E650G |
probably benign |
Het |
Mink1 |
A |
G |
11: 70,502,546 (GRCm39) |
T1086A |
possibly damaging |
Het |
Nxf1 |
G |
A |
19: 8,745,186 (GRCm39) |
V479M |
probably damaging |
Het |
Or10v1 |
T |
A |
19: 11,873,388 (GRCm39) |
M1K |
probably null |
Het |
Or11g2 |
T |
C |
14: 50,856,158 (GRCm39) |
F160L |
probably benign |
Het |
Or2n1e |
A |
G |
17: 38,586,150 (GRCm39) |
T163A |
probably damaging |
Het |
Or5h23 |
T |
C |
16: 58,906,273 (GRCm39) |
D191G |
probably damaging |
Het |
Or5h23 |
A |
G |
16: 58,906,792 (GRCm39) |
V18A |
probably benign |
Het |
Or6c5 |
T |
C |
10: 129,074,329 (GRCm39) |
S104P |
probably damaging |
Het |
Otx2 |
T |
C |
14: 48,896,215 (GRCm39) |
D281G |
probably damaging |
Het |
Pcdhga3 |
A |
T |
18: 37,808,141 (GRCm39) |
D198V |
probably damaging |
Het |
Ppp1r13l |
T |
C |
7: 19,104,500 (GRCm39) |
V273A |
probably benign |
Het |
Ppp6r2 |
T |
C |
15: 89,137,455 (GRCm39) |
|
probably null |
Het |
Pramel51 |
T |
A |
12: 88,143,995 (GRCm39) |
I273F |
possibly damaging |
Het |
Prg4 |
C |
T |
1: 150,327,197 (GRCm39) |
G873D |
probably damaging |
Het |
Ptprq |
T |
C |
10: 107,471,135 (GRCm39) |
N1422S |
probably benign |
Het |
Rbm27 |
A |
T |
18: 42,460,570 (GRCm39) |
K839M |
probably damaging |
Het |
Rere |
A |
T |
4: 150,553,255 (GRCm39) |
N149I |
probably damaging |
Het |
Ret |
A |
G |
6: 118,156,280 (GRCm39) |
L340S |
probably benign |
Het |
Sel1l2 |
T |
A |
2: 140,082,889 (GRCm39) |
D583V |
possibly damaging |
Het |
Shroom1 |
A |
T |
11: 53,354,308 (GRCm39) |
D76V |
possibly damaging |
Het |
Slc5a3 |
C |
A |
16: 91,875,963 (GRCm39) |
S673R |
probably benign |
Het |
Spink1 |
A |
T |
18: 43,861,247 (GRCm39) |
I74N |
probably damaging |
Het |
Tbc1d1 |
T |
A |
5: 64,435,352 (GRCm39) |
S497T |
probably damaging |
Het |
Trim3 |
C |
T |
7: 105,260,278 (GRCm39) |
R741Q |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,747,022 (GRCm39) |
C4676R |
probably benign |
Het |
Ubqlnl |
G |
A |
7: 103,797,959 (GRCm39) |
P513S |
probably benign |
Het |
Unc13d |
C |
T |
11: 115,964,394 (GRCm39) |
|
probably null |
Het |
Vmn1r125 |
TGG |
TG |
7: 21,006,144 (GRCm39) |
|
probably null |
Het |
Vmn2r7 |
A |
T |
3: 64,632,436 (GRCm39) |
C9S |
probably benign |
Het |
Xdh |
T |
A |
17: 74,213,264 (GRCm39) |
M829L |
probably damaging |
Het |
Zcrb1 |
A |
G |
15: 93,285,463 (GRCm39) |
F173L |
probably benign |
Het |
Zfp41 |
T |
C |
15: 75,490,372 (GRCm39) |
V108A |
probably damaging |
Het |
Zfp438 |
T |
C |
18: 5,213,209 (GRCm39) |
E583G |
probably damaging |
Het |
Zfp628 |
T |
C |
7: 4,923,917 (GRCm39) |
L713P |
probably damaging |
Het |
Zfp664 |
T |
A |
5: 124,963,042 (GRCm39) |
C145* |
probably null |
Het |
Zfp683 |
T |
C |
4: 133,786,042 (GRCm39) |
C390R |
probably damaging |
Het |
Zfp941 |
G |
A |
7: 140,392,010 (GRCm39) |
P450S |
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 |
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 |
|