Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930402F06Rik |
C |
T |
2: 35,265,906 (GRCm39) |
V255I |
possibly damaging |
Het |
Acvrl1 |
T |
A |
15: 101,035,477 (GRCm39) |
N334K |
probably damaging |
Het |
Arhgef5 |
T |
A |
6: 43,257,585 (GRCm39) |
I1284N |
probably damaging |
Het |
Asns |
C |
A |
6: 7,682,002 (GRCm39) |
R236L |
probably damaging |
Het |
Barx2 |
T |
C |
9: 31,770,090 (GRCm39) |
E146G |
probably damaging |
Het |
Ccl7 |
A |
G |
11: 81,936,661 (GRCm39) |
S18G |
probably benign |
Het |
Cilp |
A |
T |
9: 65,185,284 (GRCm39) |
T460S |
probably benign |
Het |
Cpa5 |
A |
G |
6: 30,626,290 (GRCm39) |
Y217C |
possibly damaging |
Het |
Dgkh |
T |
A |
14: 78,832,931 (GRCm39) |
|
probably benign |
Het |
Dmc1 |
T |
C |
15: 79,446,746 (GRCm39) |
T276A |
probably benign |
Het |
Fryl |
G |
A |
5: 73,234,038 (GRCm39) |
P1496S |
probably benign |
Het |
Gstm2 |
T |
C |
3: 107,891,521 (GRCm39) |
Y93C |
possibly damaging |
Het |
Htra1 |
A |
G |
7: 130,583,444 (GRCm39) |
I355V |
probably benign |
Het |
Ifi214 |
G |
T |
1: 173,354,082 (GRCm39) |
T196K |
possibly damaging |
Het |
Ms4a5 |
T |
C |
19: 11,256,742 (GRCm39) |
T52A |
probably benign |
Het |
Mtx3 |
T |
C |
13: 92,984,391 (GRCm39) |
F191L |
probably damaging |
Het |
Padi2 |
A |
G |
4: 140,654,424 (GRCm39) |
M192V |
probably benign |
Het |
Pdcl3 |
C |
A |
1: 39,034,976 (GRCm39) |
Q178K |
probably benign |
Het |
Rap1gap2 |
G |
A |
11: 74,326,540 (GRCm39) |
R176W |
probably damaging |
Het |
Ska2 |
A |
G |
11: 87,006,990 (GRCm39) |
T32A |
probably benign |
Het |
Slc6a18 |
G |
T |
13: 73,826,042 (GRCm39) |
Q3K |
probably benign |
Het |
Slc7a14 |
T |
C |
3: 31,292,919 (GRCm39) |
Y122C |
probably damaging |
Het |
Svep1 |
T |
A |
4: 58,070,308 (GRCm39) |
K2493* |
probably null |
Het |
Trpm6 |
T |
A |
19: 18,790,850 (GRCm39) |
N628K |
probably benign |
Het |
Ttc17 |
T |
A |
2: 94,205,566 (GRCm39) |
N260I |
probably damaging |
Het |
Ttc7b |
T |
C |
12: 100,291,994 (GRCm39) |
I193V |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,542,583 (GRCm39) |
T25141S |
possibly damaging |
Het |
Zfhx4 |
A |
C |
3: 5,476,910 (GRCm39) |
Q3150P |
probably damaging |
Het |
|
Other mutations in Hc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00694:Hc
|
APN |
2 |
34,881,641 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00922:Hc
|
APN |
2 |
34,881,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01523:Hc
|
APN |
2 |
34,929,250 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01746:Hc
|
APN |
2 |
34,947,338 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01793:Hc
|
APN |
2 |
34,918,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01972:Hc
|
APN |
2 |
34,873,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:Hc
|
APN |
2 |
34,903,531 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02048:Hc
|
APN |
2 |
34,886,039 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02227:Hc
|
APN |
2 |
34,899,923 (GRCm39) |
intron |
probably benign |
|
IGL02230:Hc
|
APN |
2 |
34,903,682 (GRCm39) |
missense |
probably benign |
|
IGL02254:Hc
|
APN |
2 |
34,874,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02363:Hc
|
APN |
2 |
34,890,847 (GRCm39) |
missense |
probably benign |
|
IGL02650:Hc
|
APN |
2 |
34,890,886 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03053:Hc
|
APN |
2 |
34,914,210 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03168:Hc
|
APN |
2 |
34,914,210 (GRCm39) |
missense |
probably benign |
0.07 |
PIT4142001:Hc
|
UTSW |
2 |
34,921,833 (GRCm39) |
splice site |
probably benign |
|
PIT4378001:Hc
|
UTSW |
2 |
34,921,876 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4508001:Hc
|
UTSW |
2 |
34,874,816 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4812001:Hc
|
UTSW |
2 |
34,919,464 (GRCm39) |
missense |
probably benign |
0.16 |
R0025:Hc
|
UTSW |
2 |
34,876,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Hc
|
UTSW |
2 |
34,947,287 (GRCm39) |
missense |
probably benign |
0.32 |
R0197:Hc
|
UTSW |
2 |
34,874,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0218:Hc
|
UTSW |
2 |
34,918,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Hc
|
UTSW |
2 |
34,926,166 (GRCm39) |
splice site |
probably benign |
|
R0496:Hc
|
UTSW |
2 |
34,903,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1205:Hc
|
UTSW |
2 |
34,893,536 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1468:Hc
|
UTSW |
2 |
34,873,819 (GRCm39) |
nonsense |
probably null |
|
R1468:Hc
|
UTSW |
2 |
34,873,819 (GRCm39) |
nonsense |
probably null |
|
R1574:Hc
|
UTSW |
2 |
34,890,777 (GRCm39) |
intron |
probably benign |
|
R1610:Hc
|
UTSW |
2 |
34,896,173 (GRCm39) |
missense |
probably benign |
0.44 |
R1640:Hc
|
UTSW |
2 |
34,947,336 (GRCm39) |
nonsense |
probably null |
|
R1887:Hc
|
UTSW |
2 |
34,924,623 (GRCm39) |
missense |
probably benign |
|
R1920:Hc
|
UTSW |
2 |
34,919,407 (GRCm39) |
splice site |
probably benign |
|
R2018:Hc
|
UTSW |
2 |
34,903,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Hc
|
UTSW |
2 |
34,903,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Hc
|
UTSW |
2 |
34,881,115 (GRCm39) |
intron |
probably benign |
|
R2366:Hc
|
UTSW |
2 |
34,903,648 (GRCm39) |
missense |
probably benign |
|
R4093:Hc
|
UTSW |
2 |
34,873,819 (GRCm39) |
nonsense |
probably null |
|
R4288:Hc
|
UTSW |
2 |
34,920,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R4501:Hc
|
UTSW |
2 |
34,887,488 (GRCm39) |
splice site |
probably null |
|
R4502:Hc
|
UTSW |
2 |
34,896,264 (GRCm39) |
missense |
probably benign |
0.00 |
R4508:Hc
|
UTSW |
2 |
34,903,077 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4583:Hc
|
UTSW |
2 |
34,918,189 (GRCm39) |
missense |
probably benign |
0.00 |
R4686:Hc
|
UTSW |
2 |
34,929,260 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4776:Hc
|
UTSW |
2 |
34,929,746 (GRCm39) |
missense |
probably benign |
0.12 |
R4846:Hc
|
UTSW |
2 |
34,909,682 (GRCm39) |
missense |
probably benign |
0.00 |
R5032:Hc
|
UTSW |
2 |
34,903,544 (GRCm39) |
missense |
probably benign |
0.07 |
R5089:Hc
|
UTSW |
2 |
34,914,902 (GRCm39) |
missense |
probably benign |
0.01 |
R5289:Hc
|
UTSW |
2 |
34,886,026 (GRCm39) |
critical splice donor site |
probably null |
|
R5347:Hc
|
UTSW |
2 |
34,927,636 (GRCm39) |
missense |
probably benign |
0.04 |
R5356:Hc
|
UTSW |
2 |
34,885,007 (GRCm39) |
missense |
probably benign |
0.00 |
R5379:Hc
|
UTSW |
2 |
34,881,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R5403:Hc
|
UTSW |
2 |
34,947,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R5418:Hc
|
UTSW |
2 |
34,898,195 (GRCm39) |
critical splice donor site |
probably null |
|
R5450:Hc
|
UTSW |
2 |
34,903,050 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5494:Hc
|
UTSW |
2 |
34,893,551 (GRCm39) |
splice site |
probably null |
|
R5713:Hc
|
UTSW |
2 |
34,903,543 (GRCm39) |
missense |
probably damaging |
0.99 |
R5898:Hc
|
UTSW |
2 |
34,887,449 (GRCm39) |
missense |
probably benign |
0.06 |
R5925:Hc
|
UTSW |
2 |
34,920,462 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5942:Hc
|
UTSW |
2 |
34,918,137 (GRCm39) |
nonsense |
probably null |
|
R5991:Hc
|
UTSW |
2 |
34,896,117 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6036:Hc
|
UTSW |
2 |
34,929,696 (GRCm39) |
missense |
probably benign |
0.00 |
R6036:Hc
|
UTSW |
2 |
34,929,696 (GRCm39) |
missense |
probably benign |
0.00 |
R6115:Hc
|
UTSW |
2 |
34,903,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R6234:Hc
|
UTSW |
2 |
34,918,058 (GRCm39) |
missense |
probably benign |
|
R6264:Hc
|
UTSW |
2 |
34,896,285 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6313:Hc
|
UTSW |
2 |
34,879,851 (GRCm39) |
splice site |
probably null |
|
R6525:Hc
|
UTSW |
2 |
34,881,236 (GRCm39) |
missense |
probably benign |
0.06 |
R6577:Hc
|
UTSW |
2 |
34,922,138 (GRCm39) |
missense |
probably benign |
0.00 |
R6601:Hc
|
UTSW |
2 |
34,935,906 (GRCm39) |
missense |
probably benign |
0.03 |
R6916:Hc
|
UTSW |
2 |
34,900,044 (GRCm39) |
nonsense |
probably null |
|
R7108:Hc
|
UTSW |
2 |
34,929,706 (GRCm39) |
missense |
probably benign |
0.03 |
R7143:Hc
|
UTSW |
2 |
34,940,450 (GRCm39) |
missense |
probably benign |
0.00 |
R7388:Hc
|
UTSW |
2 |
34,874,859 (GRCm39) |
splice site |
probably null |
|
R7468:Hc
|
UTSW |
2 |
34,918,063 (GRCm39) |
missense |
probably benign |
0.00 |
R7504:Hc
|
UTSW |
2 |
34,951,331 (GRCm39) |
missense |
not run |
|
R7521:Hc
|
UTSW |
2 |
34,935,344 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7582:Hc
|
UTSW |
2 |
34,881,278 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7596:Hc
|
UTSW |
2 |
34,890,859 (GRCm39) |
missense |
probably damaging |
0.96 |
R7599:Hc
|
UTSW |
2 |
34,940,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R7692:Hc
|
UTSW |
2 |
34,914,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R7853:Hc
|
UTSW |
2 |
34,900,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:Hc
|
UTSW |
2 |
34,887,411 (GRCm39) |
nonsense |
probably null |
|
R8329:Hc
|
UTSW |
2 |
34,902,910 (GRCm39) |
splice site |
probably null |
|
R8375:Hc
|
UTSW |
2 |
34,873,731 (GRCm39) |
missense |
probably benign |
0.32 |
R8477:Hc
|
UTSW |
2 |
34,879,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Hc
|
UTSW |
2 |
34,909,535 (GRCm39) |
missense |
probably benign |
0.06 |
R8888:Hc
|
UTSW |
2 |
34,890,861 (GRCm39) |
missense |
probably benign |
0.00 |
R8895:Hc
|
UTSW |
2 |
34,890,861 (GRCm39) |
missense |
probably benign |
0.00 |
R8968:Hc
|
UTSW |
2 |
34,922,317 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8969:Hc
|
UTSW |
2 |
34,909,475 (GRCm39) |
critical splice donor site |
probably null |
|
R9146:Hc
|
UTSW |
2 |
34,924,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R9218:Hc
|
UTSW |
2 |
34,922,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9340:Hc
|
UTSW |
2 |
34,876,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R9396:Hc
|
UTSW |
2 |
34,927,615 (GRCm39) |
nonsense |
probably null |
|
R9569:Hc
|
UTSW |
2 |
34,926,359 (GRCm39) |
missense |
probably benign |
0.00 |
R9576:Hc
|
UTSW |
2 |
34,873,767 (GRCm39) |
missense |
probably benign |
0.01 |
R9706:Hc
|
UTSW |
2 |
34,914,196 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Hc
|
UTSW |
2 |
34,873,723 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Hc
|
UTSW |
2 |
34,919,482 (GRCm39) |
missense |
probably benign |
0.02 |
Z1088:Hc
|
UTSW |
2 |
34,898,261 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Hc
|
UTSW |
2 |
34,896,285 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Hc
|
UTSW |
2 |
34,903,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|