Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
A |
T |
6: 23,092,561 (GRCm39) |
Y146* |
probably null |
Het |
Adcy2 |
A |
G |
13: 68,944,722 (GRCm39) |
L220P |
probably damaging |
Het |
Agl |
T |
C |
3: 116,574,914 (GRCm39) |
Y660C |
probably damaging |
Het |
Ak1 |
A |
G |
2: 32,519,622 (GRCm39) |
T17A |
probably benign |
Het |
Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
Ankrd11 |
A |
T |
8: 123,629,161 (GRCm39) |
|
probably null |
Het |
Ap5b1 |
T |
C |
19: 5,620,502 (GRCm39) |
S641P |
possibly damaging |
Het |
Apoc4 |
A |
G |
7: 19,415,304 (GRCm39) |
M1T |
probably null |
Het |
Arhgap5 |
T |
C |
12: 52,564,817 (GRCm39) |
V596A |
probably benign |
Het |
Ascc3 |
A |
G |
10: 50,493,838 (GRCm39) |
E91G |
probably damaging |
Het |
Bach2 |
T |
A |
4: 32,580,055 (GRCm39) |
V637E |
probably benign |
Het |
Bicd2 |
T |
G |
13: 49,532,881 (GRCm39) |
L489R |
possibly damaging |
Het |
Bltp1 |
C |
T |
3: 36,949,527 (GRCm39) |
T2I |
possibly damaging |
Het |
Boc |
A |
T |
16: 44,322,007 (GRCm39) |
|
probably null |
Het |
Cbln2 |
T |
A |
18: 86,734,791 (GRCm39) |
V188D |
probably damaging |
Het |
Ccl11 |
A |
C |
11: 81,953,123 (GRCm39) |
T94P |
probably damaging |
Het |
Cd109 |
A |
T |
9: 78,611,044 (GRCm39) |
H1220L |
probably benign |
Het |
Cd226 |
A |
G |
18: 89,265,435 (GRCm39) |
I125V |
probably benign |
Het |
Cep135 |
T |
A |
5: 76,780,176 (GRCm39) |
|
probably null |
Het |
Cgnl1 |
T |
G |
9: 71,537,821 (GRCm39) |
E1233A |
probably damaging |
Het |
Ckap5 |
T |
A |
2: 91,437,891 (GRCm39) |
D1597E |
possibly damaging |
Het |
Clptm1 |
A |
G |
7: 19,380,762 (GRCm39) |
I63T |
possibly damaging |
Het |
Cpsf7 |
C |
T |
19: 10,518,073 (GRCm39) |
P428S |
probably damaging |
Het |
Cuedc1 |
C |
T |
11: 88,068,216 (GRCm39) |
P155S |
probably damaging |
Het |
Dgkb |
T |
C |
12: 38,134,228 (GRCm39) |
Y45H |
probably damaging |
Het |
Dglucy |
T |
C |
12: 100,823,181 (GRCm39) |
F459L |
probably damaging |
Het |
Dmp1 |
T |
A |
5: 104,359,790 (GRCm39) |
D155E |
possibly damaging |
Het |
Dnah1 |
T |
A |
14: 31,023,813 (GRCm39) |
I960F |
possibly damaging |
Het |
Drosha |
G |
T |
15: 12,915,467 (GRCm39) |
M795I |
probably damaging |
Het |
Dsg1b |
A |
G |
18: 20,529,532 (GRCm39) |
T326A |
probably damaging |
Het |
Dusp16 |
T |
G |
6: 134,695,802 (GRCm39) |
N343T |
probably benign |
Het |
Faim2 |
T |
C |
15: 99,398,127 (GRCm39) |
S274G |
possibly damaging |
Het |
Fhip2a |
G |
T |
19: 57,370,324 (GRCm39) |
V523L |
probably benign |
Het |
Fndc1 |
T |
C |
17: 8,023,761 (GRCm39) |
R65G |
probably damaging |
Het |
Fnip2 |
A |
T |
3: 79,419,632 (GRCm39) |
|
probably benign |
Het |
Grm3 |
T |
C |
5: 9,639,793 (GRCm39) |
Y84C |
possibly damaging |
Het |
Hivep1 |
C |
T |
13: 42,313,625 (GRCm39) |
T1955I |
possibly damaging |
Het |
Ift20 |
T |
C |
11: 78,431,797 (GRCm39) |
I97T |
probably damaging |
Het |
Il36rn |
T |
C |
2: 24,171,376 (GRCm39) |
C155R |
probably damaging |
Het |
Lca5l |
T |
A |
16: 95,963,849 (GRCm39) |
K358N |
probably damaging |
Het |
Lca5l |
T |
C |
16: 95,977,218 (GRCm39) |
N196S |
possibly damaging |
Het |
Maf1 |
G |
A |
15: 76,237,563 (GRCm39) |
D175N |
probably damaging |
Het |
Mical3 |
T |
C |
6: 120,928,283 (GRCm39) |
K996E |
probably damaging |
Het |
Midn |
A |
G |
10: 79,990,983 (GRCm39) |
N331S |
probably benign |
Het |
Mki67 |
T |
A |
7: 135,300,238 (GRCm39) |
K1599* |
probably null |
Het |
Mlx |
A |
G |
11: 100,979,805 (GRCm39) |
Q162R |
possibly damaging |
Het |
Nalf1 |
A |
G |
8: 9,820,607 (GRCm39) |
S138P |
probably benign |
Het |
Ngp |
T |
C |
9: 110,249,929 (GRCm39) |
C76R |
probably damaging |
Het |
Nin |
C |
T |
12: 70,072,251 (GRCm39) |
G1210D |
probably benign |
Het |
Nlgn1 |
A |
G |
3: 25,488,034 (GRCm39) |
I738T |
probably benign |
Het |
Nop53 |
A |
C |
7: 15,672,153 (GRCm39) |
F465C |
probably damaging |
Het |
Npas3 |
A |
G |
12: 54,114,680 (GRCm39) |
D503G |
possibly damaging |
Het |
Npbwr1 |
T |
A |
1: 5,986,570 (GRCm39) |
S315C |
probably damaging |
Het |
Nup42 |
G |
T |
5: 24,386,989 (GRCm39) |
G260* |
probably null |
Het |
Ogdh |
G |
C |
11: 6,284,626 (GRCm39) |
R200P |
possibly damaging |
Het |
Or4b13 |
T |
A |
2: 90,083,036 (GRCm39) |
I99L |
probably benign |
Het |
Or52n20 |
A |
G |
7: 104,320,808 (GRCm39) |
T300A |
possibly damaging |
Het |
Or5m13b |
T |
G |
2: 85,753,939 (GRCm39) |
|
probably null |
Het |
Or6ae1 |
C |
T |
7: 139,742,729 (GRCm39) |
V45I |
probably damaging |
Het |
Or7g16 |
G |
A |
9: 18,726,801 (GRCm39) |
S263L |
probably benign |
Het |
Or7g33 |
A |
T |
9: 19,448,688 (GRCm39) |
C179* |
probably null |
Het |
Ovgp1 |
T |
A |
3: 105,894,309 (GRCm39) |
|
probably benign |
Het |
Papln |
T |
A |
12: 83,819,992 (GRCm39) |
C150S |
probably damaging |
Het |
Pde1c |
A |
T |
6: 56,135,996 (GRCm39) |
L316Q |
probably damaging |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Piezo2 |
G |
T |
18: 63,277,997 (GRCm39) |
D302E |
probably damaging |
Het |
Pirb |
A |
T |
7: 3,720,637 (GRCm39) |
L287Q |
probably benign |
Het |
Plin1 |
A |
G |
7: 79,375,378 (GRCm39) |
|
probably benign |
Het |
Plxnc1 |
A |
G |
10: 94,688,484 (GRCm39) |
I698T |
probably damaging |
Het |
Ppp1r12c |
G |
T |
7: 4,485,974 (GRCm39) |
C572* |
probably null |
Het |
Ptgis |
T |
C |
2: 167,056,769 (GRCm39) |
M273V |
possibly damaging |
Het |
Samd14 |
C |
A |
11: 94,914,110 (GRCm39) |
T283K |
probably damaging |
Het |
Scnn1g |
A |
T |
7: 121,337,411 (GRCm39) |
K91* |
probably null |
Het |
Slc24a4 |
A |
G |
12: 102,180,166 (GRCm39) |
Q95R |
probably damaging |
Het |
Slfn9 |
T |
G |
11: 82,879,027 (GRCm39) |
D34A |
probably benign |
Het |
Smarca4 |
A |
T |
9: 21,588,776 (GRCm39) |
I1193F |
probably damaging |
Het |
Spata31e5 |
A |
G |
1: 28,816,260 (GRCm39) |
W591R |
probably damaging |
Het |
Sphkap |
T |
C |
1: 83,255,632 (GRCm39) |
M706V |
probably benign |
Het |
Stard9 |
C |
A |
2: 120,504,117 (GRCm39) |
S221R |
probably damaging |
Het |
Stxbp1 |
T |
C |
2: 32,688,201 (GRCm39) |
D488G |
probably damaging |
Het |
Sugp2 |
C |
T |
8: 70,695,306 (GRCm39) |
|
probably null |
Het |
Tekt5 |
T |
C |
16: 10,213,070 (GRCm39) |
I72V |
probably benign |
Het |
Themis |
T |
A |
10: 28,658,720 (GRCm39) |
N582K |
probably benign |
Het |
Tmed11 |
C |
A |
5: 108,934,000 (GRCm39) |
M65I |
possibly damaging |
Het |
Top3a |
G |
T |
11: 60,633,315 (GRCm39) |
P927Q |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,976,207 (GRCm39) |
N165K |
possibly damaging |
Het |
Tsfm |
A |
G |
10: 126,866,663 (GRCm39) |
S2P |
probably damaging |
Het |
Wdr47 |
C |
A |
3: 108,534,758 (GRCm39) |
S559* |
probably null |
Het |
Wnt2b |
T |
C |
3: 104,860,331 (GRCm39) |
Y192C |
probably damaging |
Het |
Zfp280b |
A |
G |
10: 75,874,370 (GRCm39) |
D83G |
probably benign |
Het |
Zfp345 |
T |
C |
2: 150,314,038 (GRCm39) |
T500A |
possibly damaging |
Het |
Zfp78 |
T |
A |
7: 6,382,074 (GRCm39) |
C343S |
probably damaging |
Het |
|
Other mutations in Herc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00329:Herc2
|
APN |
7 |
55,774,047 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00529:Herc2
|
APN |
7 |
55,807,501 (GRCm39) |
missense |
probably benign |
|
IGL00548:Herc2
|
APN |
7 |
55,856,313 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00970:Herc2
|
APN |
7 |
55,830,812 (GRCm39) |
splice site |
probably benign |
|
IGL01141:Herc2
|
APN |
7 |
55,862,589 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL01147:Herc2
|
APN |
7 |
55,806,697 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01150:Herc2
|
APN |
7 |
55,830,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01519:Herc2
|
APN |
7 |
55,753,698 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01576:Herc2
|
APN |
7 |
55,876,409 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01626:Herc2
|
APN |
7 |
55,734,890 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01658:Herc2
|
APN |
7 |
55,809,200 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01707:Herc2
|
APN |
7 |
55,814,935 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01727:Herc2
|
APN |
7 |
55,787,554 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01935:Herc2
|
APN |
7 |
55,803,541 (GRCm39) |
missense |
probably benign |
|
IGL01969:Herc2
|
APN |
7 |
55,835,579 (GRCm39) |
splice site |
probably benign |
|
IGL02074:Herc2
|
APN |
7 |
55,737,192 (GRCm39) |
splice site |
probably benign |
|
IGL02261:Herc2
|
APN |
7 |
55,856,492 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02339:Herc2
|
APN |
7 |
55,771,470 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02353:Herc2
|
APN |
7 |
55,764,560 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02360:Herc2
|
APN |
7 |
55,764,560 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02409:Herc2
|
APN |
7 |
55,870,217 (GRCm39) |
splice site |
probably null |
|
IGL02528:Herc2
|
APN |
7 |
55,758,641 (GRCm39) |
splice site |
probably benign |
|
IGL02571:Herc2
|
APN |
7 |
55,803,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02578:Herc2
|
APN |
7 |
55,756,283 (GRCm39) |
splice site |
probably null |
|
IGL02661:Herc2
|
APN |
7 |
55,762,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Herc2
|
APN |
7 |
55,785,426 (GRCm39) |
nonsense |
probably null |
|
IGL02675:Herc2
|
APN |
7 |
55,813,849 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02689:Herc2
|
APN |
7 |
55,815,031 (GRCm39) |
splice site |
probably benign |
|
IGL02710:Herc2
|
APN |
7 |
55,787,562 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02750:Herc2
|
APN |
7 |
55,854,127 (GRCm39) |
splice site |
probably benign |
|
IGL02754:Herc2
|
APN |
7 |
55,747,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03029:Herc2
|
APN |
7 |
55,818,715 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03039:Herc2
|
APN |
7 |
55,818,769 (GRCm39) |
splice site |
probably benign |
|
IGL03082:Herc2
|
APN |
7 |
55,835,671 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03090:Herc2
|
APN |
7 |
55,854,221 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03154:Herc2
|
APN |
7 |
55,851,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03165:Herc2
|
APN |
7 |
55,841,660 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03201:Herc2
|
APN |
7 |
55,869,516 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03234:Herc2
|
APN |
7 |
55,753,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03293:Herc2
|
APN |
7 |
55,804,878 (GRCm39) |
missense |
probably benign |
0.43 |
IGL03331:Herc2
|
APN |
7 |
55,785,015 (GRCm39) |
splice site |
probably benign |
|
IGL03340:Herc2
|
APN |
7 |
55,740,668 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03409:Herc2
|
APN |
7 |
55,878,317 (GRCm39) |
missense |
probably damaging |
1.00 |
alarmed
|
UTSW |
7 |
55,879,410 (GRCm39) |
missense |
possibly damaging |
0.92 |
hyper
|
UTSW |
7 |
55,809,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R0798_herc2_487
|
UTSW |
7 |
55,785,431 (GRCm39) |
critical splice donor site |
probably null |
|
R1370_Herc2_948
|
UTSW |
7 |
55,818,621 (GRCm39) |
missense |
probably benign |
0.01 |
R2030_Herc2_144
|
UTSW |
7 |
55,834,121 (GRCm39) |
missense |
probably damaging |
0.99 |
uptight
|
UTSW |
7 |
55,762,958 (GRCm39) |
missense |
probably damaging |
1.00 |
I0000:Herc2
|
UTSW |
7 |
55,786,477 (GRCm39) |
splice site |
probably benign |
|
PIT1430001:Herc2
|
UTSW |
7 |
55,876,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Herc2
|
UTSW |
7 |
55,857,560 (GRCm39) |
missense |
probably benign |
0.03 |
R0009:Herc2
|
UTSW |
7 |
55,857,560 (GRCm39) |
missense |
probably benign |
0.03 |
R0058:Herc2
|
UTSW |
7 |
55,820,231 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0114:Herc2
|
UTSW |
7 |
55,803,522 (GRCm39) |
splice site |
probably benign |
|
R0117:Herc2
|
UTSW |
7 |
55,863,359 (GRCm39) |
splice site |
probably benign |
|
R0141:Herc2
|
UTSW |
7 |
55,771,309 (GRCm39) |
missense |
probably benign |
0.17 |
R0266:Herc2
|
UTSW |
7 |
55,856,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R0401:Herc2
|
UTSW |
7 |
55,807,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R0403:Herc2
|
UTSW |
7 |
55,809,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Herc2
|
UTSW |
7 |
55,869,563 (GRCm39) |
nonsense |
probably null |
|
R0491:Herc2
|
UTSW |
7 |
55,772,114 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0499:Herc2
|
UTSW |
7 |
55,834,117 (GRCm39) |
nonsense |
probably null |
|
R0580:Herc2
|
UTSW |
7 |
55,788,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Herc2
|
UTSW |
7 |
55,762,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Herc2
|
UTSW |
7 |
55,855,784 (GRCm39) |
splice site |
probably benign |
|
R0798:Herc2
|
UTSW |
7 |
55,785,431 (GRCm39) |
critical splice donor site |
probably null |
|
R0842:Herc2
|
UTSW |
7 |
55,771,453 (GRCm39) |
missense |
probably benign |
|
R0849:Herc2
|
UTSW |
7 |
55,856,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R0850:Herc2
|
UTSW |
7 |
55,854,231 (GRCm39) |
missense |
probably benign |
0.09 |
R0926:Herc2
|
UTSW |
7 |
55,782,296 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1146:Herc2
|
UTSW |
7 |
55,796,444 (GRCm39) |
missense |
probably benign |
|
R1146:Herc2
|
UTSW |
7 |
55,796,444 (GRCm39) |
missense |
probably benign |
|
R1292:Herc2
|
UTSW |
7 |
55,846,951 (GRCm39) |
missense |
probably benign |
0.05 |
R1370:Herc2
|
UTSW |
7 |
55,818,621 (GRCm39) |
missense |
probably benign |
0.01 |
R1443:Herc2
|
UTSW |
7 |
55,854,481 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1445:Herc2
|
UTSW |
7 |
55,818,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R1541:Herc2
|
UTSW |
7 |
55,785,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R1550:Herc2
|
UTSW |
7 |
55,785,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R1551:Herc2
|
UTSW |
7 |
55,796,417 (GRCm39) |
missense |
probably benign |
0.01 |
R1633:Herc2
|
UTSW |
7 |
55,879,117 (GRCm39) |
missense |
probably null |
1.00 |
R1635:Herc2
|
UTSW |
7 |
55,786,415 (GRCm39) |
missense |
probably benign |
0.00 |
R1659:Herc2
|
UTSW |
7 |
55,784,853 (GRCm39) |
missense |
probably benign |
0.00 |
R1682:Herc2
|
UTSW |
7 |
55,738,148 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1697:Herc2
|
UTSW |
7 |
55,803,653 (GRCm39) |
missense |
probably benign |
0.43 |
R1748:Herc2
|
UTSW |
7 |
55,798,571 (GRCm39) |
critical splice donor site |
probably null |
|
R1802:Herc2
|
UTSW |
7 |
55,834,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Herc2
|
UTSW |
7 |
55,856,513 (GRCm39) |
nonsense |
probably null |
|
R1836:Herc2
|
UTSW |
7 |
55,804,853 (GRCm39) |
nonsense |
probably null |
|
R1872:Herc2
|
UTSW |
7 |
55,807,257 (GRCm39) |
missense |
probably benign |
0.18 |
R1889:Herc2
|
UTSW |
7 |
55,839,561 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1906:Herc2
|
UTSW |
7 |
55,764,612 (GRCm39) |
missense |
probably benign |
0.01 |
R2030:Herc2
|
UTSW |
7 |
55,834,121 (GRCm39) |
missense |
probably damaging |
0.99 |
R2037:Herc2
|
UTSW |
7 |
55,855,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R2059:Herc2
|
UTSW |
7 |
55,813,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R2068:Herc2
|
UTSW |
7 |
55,782,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Herc2
|
UTSW |
7 |
55,876,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R2085:Herc2
|
UTSW |
7 |
55,862,713 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2115:Herc2
|
UTSW |
7 |
55,835,576 (GRCm39) |
splice site |
probably benign |
|
R2160:Herc2
|
UTSW |
7 |
55,862,670 (GRCm39) |
missense |
probably benign |
0.00 |
R2173:Herc2
|
UTSW |
7 |
55,835,699 (GRCm39) |
missense |
probably benign |
0.27 |
R2221:Herc2
|
UTSW |
7 |
55,818,766 (GRCm39) |
critical splice donor site |
probably null |
|
R2280:Herc2
|
UTSW |
7 |
55,787,019 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3078:Herc2
|
UTSW |
7 |
55,786,991 (GRCm39) |
missense |
probably benign |
|
R3104:Herc2
|
UTSW |
7 |
55,785,103 (GRCm39) |
missense |
probably benign |
0.23 |
R3177:Herc2
|
UTSW |
7 |
55,803,176 (GRCm39) |
missense |
probably benign |
0.00 |
R3277:Herc2
|
UTSW |
7 |
55,803,176 (GRCm39) |
missense |
probably benign |
0.00 |
R3766:Herc2
|
UTSW |
7 |
55,813,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R3770:Herc2
|
UTSW |
7 |
55,814,755 (GRCm39) |
missense |
probably benign |
|
R3807:Herc2
|
UTSW |
7 |
55,857,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R3912:Herc2
|
UTSW |
7 |
55,748,185 (GRCm39) |
missense |
probably damaging |
0.98 |
R4004:Herc2
|
UTSW |
7 |
55,756,213 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4039:Herc2
|
UTSW |
7 |
55,806,159 (GRCm39) |
missense |
probably damaging |
0.98 |
R4190:Herc2
|
UTSW |
7 |
55,772,196 (GRCm39) |
missense |
probably benign |
0.03 |
R4225:Herc2
|
UTSW |
7 |
55,814,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R4334:Herc2
|
UTSW |
7 |
55,876,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R4405:Herc2
|
UTSW |
7 |
55,820,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R4448:Herc2
|
UTSW |
7 |
55,877,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R4450:Herc2
|
UTSW |
7 |
55,877,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R4565:Herc2
|
UTSW |
7 |
55,803,586 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4667:Herc2
|
UTSW |
7 |
55,781,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R4747:Herc2
|
UTSW |
7 |
55,756,141 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4762:Herc2
|
UTSW |
7 |
55,820,388 (GRCm39) |
missense |
probably benign |
0.19 |
R4829:Herc2
|
UTSW |
7 |
55,756,240 (GRCm39) |
missense |
probably benign |
0.39 |
R4832:Herc2
|
UTSW |
7 |
55,748,165 (GRCm39) |
nonsense |
probably null |
|
R4895:Herc2
|
UTSW |
7 |
55,872,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R4904:Herc2
|
UTSW |
7 |
55,807,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R4908:Herc2
|
UTSW |
7 |
55,827,660 (GRCm39) |
missense |
probably benign |
0.01 |
R4911:Herc2
|
UTSW |
7 |
55,877,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Herc2
|
UTSW |
7 |
55,879,438 (GRCm39) |
missense |
probably benign |
0.04 |
R4939:Herc2
|
UTSW |
7 |
55,856,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R5155:Herc2
|
UTSW |
7 |
55,877,574 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5184:Herc2
|
UTSW |
7 |
55,772,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5269:Herc2
|
UTSW |
7 |
55,818,618 (GRCm39) |
nonsense |
probably null |
|
R5306:Herc2
|
UTSW |
7 |
55,834,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R5314:Herc2
|
UTSW |
7 |
55,869,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R5369:Herc2
|
UTSW |
7 |
55,832,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R5418:Herc2
|
UTSW |
7 |
55,787,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R5420:Herc2
|
UTSW |
7 |
55,853,578 (GRCm39) |
missense |
probably damaging |
0.96 |
R5463:Herc2
|
UTSW |
7 |
55,844,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R5510:Herc2
|
UTSW |
7 |
55,856,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R5634:Herc2
|
UTSW |
7 |
55,856,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R5638:Herc2
|
UTSW |
7 |
55,854,164 (GRCm39) |
missense |
probably benign |
0.01 |
R5690:Herc2
|
UTSW |
7 |
55,807,453 (GRCm39) |
missense |
probably benign |
|
R5762:Herc2
|
UTSW |
7 |
55,846,938 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5807:Herc2
|
UTSW |
7 |
55,880,667 (GRCm39) |
missense |
probably damaging |
0.99 |
R5878:Herc2
|
UTSW |
7 |
55,773,996 (GRCm39) |
missense |
probably benign |
|
R6036:Herc2
|
UTSW |
7 |
55,717,801 (GRCm39) |
missense |
probably benign |
0.01 |
R6036:Herc2
|
UTSW |
7 |
55,717,801 (GRCm39) |
missense |
probably benign |
0.01 |
R6083:Herc2
|
UTSW |
7 |
55,878,253 (GRCm39) |
missense |
probably benign |
0.00 |
R6192:Herc2
|
UTSW |
7 |
55,857,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R6193:Herc2
|
UTSW |
7 |
55,806,649 (GRCm39) |
missense |
probably damaging |
0.98 |
R6261:Herc2
|
UTSW |
7 |
55,846,820 (GRCm39) |
nonsense |
probably null |
|
R6267:Herc2
|
UTSW |
7 |
55,802,914 (GRCm39) |
nonsense |
probably null |
|
R6267:Herc2
|
UTSW |
7 |
55,854,466 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6298:Herc2
|
UTSW |
7 |
55,841,013 (GRCm39) |
missense |
probably benign |
|
R6299:Herc2
|
UTSW |
7 |
55,784,803 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6326:Herc2
|
UTSW |
7 |
55,872,682 (GRCm39) |
missense |
probably damaging |
0.98 |
R6347:Herc2
|
UTSW |
7 |
55,844,151 (GRCm39) |
critical splice donor site |
probably null |
|
R6394:Herc2
|
UTSW |
7 |
55,865,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R6500:Herc2
|
UTSW |
7 |
55,796,393 (GRCm39) |
nonsense |
probably null |
|
R6526:Herc2
|
UTSW |
7 |
55,807,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R6592:Herc2
|
UTSW |
7 |
55,857,438 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6619:Herc2
|
UTSW |
7 |
55,717,840 (GRCm39) |
nonsense |
probably null |
|
R6719:Herc2
|
UTSW |
7 |
55,862,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Herc2
|
UTSW |
7 |
55,747,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R6807:Herc2
|
UTSW |
7 |
55,814,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R6811:Herc2
|
UTSW |
7 |
55,763,181 (GRCm39) |
nonsense |
probably null |
|
R6837:Herc2
|
UTSW |
7 |
55,839,589 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6838:Herc2
|
UTSW |
7 |
55,758,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R6902:Herc2
|
UTSW |
7 |
55,785,234 (GRCm39) |
missense |
probably benign |
0.37 |
R6983:Herc2
|
UTSW |
7 |
55,756,201 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6985:Herc2
|
UTSW |
7 |
55,782,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R6985:Herc2
|
UTSW |
7 |
55,756,201 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6986:Herc2
|
UTSW |
7 |
55,756,201 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6987:Herc2
|
UTSW |
7 |
55,756,201 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7113:Herc2
|
UTSW |
7 |
55,853,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R7173:Herc2
|
UTSW |
7 |
55,853,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R7202:Herc2
|
UTSW |
7 |
55,781,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R7205:Herc2
|
UTSW |
7 |
55,832,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Herc2
|
UTSW |
7 |
55,734,828 (GRCm39) |
missense |
probably benign |
0.29 |
R7297:Herc2
|
UTSW |
7 |
55,786,406 (GRCm39) |
missense |
probably benign |
0.00 |
R7358:Herc2
|
UTSW |
7 |
55,832,423 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7438:Herc2
|
UTSW |
7 |
55,753,466 (GRCm39) |
splice site |
probably null |
|
R7537:Herc2
|
UTSW |
7 |
55,869,527 (GRCm39) |
nonsense |
probably null |
|
R7578:Herc2
|
UTSW |
7 |
55,784,548 (GRCm39) |
missense |
probably benign |
0.07 |
R7614:Herc2
|
UTSW |
7 |
55,803,023 (GRCm39) |
nonsense |
probably null |
|
R7638:Herc2
|
UTSW |
7 |
55,807,186 (GRCm39) |
missense |
probably benign |
0.26 |
R7638:Herc2
|
UTSW |
7 |
55,870,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R7646:Herc2
|
UTSW |
7 |
55,784,361 (GRCm39) |
missense |
probably benign |
|
R7663:Herc2
|
UTSW |
7 |
55,786,433 (GRCm39) |
missense |
probably benign |
|
R7665:Herc2
|
UTSW |
7 |
55,802,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R7691:Herc2
|
UTSW |
7 |
55,841,593 (GRCm39) |
missense |
probably benign |
|
R7733:Herc2
|
UTSW |
7 |
55,838,412 (GRCm39) |
missense |
probably damaging |
0.99 |
R7767:Herc2
|
UTSW |
7 |
55,878,275 (GRCm39) |
missense |
probably benign |
0.39 |
R7802:Herc2
|
UTSW |
7 |
55,813,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R7847:Herc2
|
UTSW |
7 |
55,807,308 (GRCm39) |
critical splice donor site |
probably null |
|
R7956:Herc2
|
UTSW |
7 |
55,763,148 (GRCm39) |
missense |
probably damaging |
0.97 |
R7985:Herc2
|
UTSW |
7 |
55,814,992 (GRCm39) |
missense |
probably benign |
|
R8003:Herc2
|
UTSW |
7 |
55,818,652 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8045:Herc2
|
UTSW |
7 |
55,834,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Herc2
|
UTSW |
7 |
55,879,427 (GRCm39) |
missense |
probably benign |
0.01 |
R8134:Herc2
|
UTSW |
7 |
55,734,884 (GRCm39) |
missense |
probably benign |
0.10 |
R8259:Herc2
|
UTSW |
7 |
55,855,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R8286:Herc2
|
UTSW |
7 |
55,879,410 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8304:Herc2
|
UTSW |
7 |
55,809,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R8321:Herc2
|
UTSW |
7 |
55,879,096 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8332:Herc2
|
UTSW |
7 |
55,796,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R8432:Herc2
|
UTSW |
7 |
55,804,860 (GRCm39) |
missense |
probably benign |
0.14 |
R8516:Herc2
|
UTSW |
7 |
55,856,318 (GRCm39) |
missense |
probably benign |
0.05 |
R8676:Herc2
|
UTSW |
7 |
55,838,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R8738:Herc2
|
UTSW |
7 |
55,798,402 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8742:Herc2
|
UTSW |
7 |
55,744,143 (GRCm39) |
missense |
probably benign |
0.12 |
R8796:Herc2
|
UTSW |
7 |
55,785,123 (GRCm39) |
missense |
probably benign |
0.01 |
R8825:Herc2
|
UTSW |
7 |
55,700,626 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R8826:Herc2
|
UTSW |
7 |
55,756,144 (GRCm39) |
missense |
probably benign |
0.12 |
R8842:Herc2
|
UTSW |
7 |
55,738,059 (GRCm39) |
missense |
probably damaging |
0.99 |
R9103:Herc2
|
UTSW |
7 |
55,784,803 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9124:Herc2
|
UTSW |
7 |
55,834,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R9134:Herc2
|
UTSW |
7 |
55,832,177 (GRCm39) |
missense |
probably damaging |
0.99 |
R9168:Herc2
|
UTSW |
7 |
55,802,208 (GRCm39) |
missense |
probably damaging |
0.99 |
R9173:Herc2
|
UTSW |
7 |
55,856,350 (GRCm39) |
missense |
probably damaging |
0.97 |
R9238:Herc2
|
UTSW |
7 |
55,813,508 (GRCm39) |
missense |
probably damaging |
0.98 |
R9249:Herc2
|
UTSW |
7 |
55,762,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R9344:Herc2
|
UTSW |
7 |
55,772,112 (GRCm39) |
missense |
probably benign |
0.07 |
R9432:Herc2
|
UTSW |
7 |
55,780,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R9472:Herc2
|
UTSW |
7 |
55,813,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9513:Herc2
|
UTSW |
7 |
55,762,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R9579:Herc2
|
UTSW |
7 |
55,758,500 (GRCm39) |
missense |
probably damaging |
0.99 |
R9596:Herc2
|
UTSW |
7 |
55,834,595 (GRCm39) |
missense |
|
|
R9664:Herc2
|
UTSW |
7 |
55,820,338 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9760:Herc2
|
UTSW |
7 |
55,813,659 (GRCm39) |
critical splice donor site |
probably null |
|
R9781:Herc2
|
UTSW |
7 |
55,750,096 (GRCm39) |
missense |
possibly damaging |
0.53 |
RF024:Herc2
|
UTSW |
7 |
55,876,273 (GRCm39) |
missense |
probably damaging |
1.00 |
X0011:Herc2
|
UTSW |
7 |
55,781,040 (GRCm39) |
missense |
probably benign |
|
X0023:Herc2
|
UTSW |
7 |
55,740,666 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0057:Herc2
|
UTSW |
7 |
55,879,438 (GRCm39) |
missense |
probably benign |
0.04 |
X0064:Herc2
|
UTSW |
7 |
55,841,006 (GRCm39) |
missense |
probably benign |
|
X0064:Herc2
|
UTSW |
7 |
55,840,959 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Herc2
|
UTSW |
7 |
55,781,040 (GRCm39) |
missense |
probably benign |
|
Z1088:Herc2
|
UTSW |
7 |
55,737,089 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Herc2
|
UTSW |
7 |
55,876,337 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Herc2
|
UTSW |
7 |
55,865,180 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Herc2
|
UTSW |
7 |
55,865,129 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Herc2
|
UTSW |
7 |
55,781,040 (GRCm39) |
missense |
probably benign |
|
Z1176:Herc2
|
UTSW |
7 |
55,747,281 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Herc2
|
UTSW |
7 |
55,782,246 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Herc2
|
UTSW |
7 |
55,781,040 (GRCm39) |
missense |
probably benign |
|
Z1177:Herc2
|
UTSW |
7 |
55,771,337 (GRCm39) |
missense |
possibly damaging |
0.55 |
|