Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts6 |
T |
C |
13: 104,449,267 (GRCm39) |
S226P |
probably benign |
Het |
Adarb2 |
T |
C |
13: 8,781,881 (GRCm39) |
Y586H |
probably damaging |
Het |
Ano7 |
A |
T |
1: 93,313,342 (GRCm39) |
E160V |
probably benign |
Het |
Apob |
G |
C |
12: 8,045,539 (GRCm39) |
A895P |
probably damaging |
Het |
Ccdc157 |
T |
C |
11: 4,098,889 (GRCm39) |
T206A |
possibly damaging |
Het |
Ceacam18 |
A |
G |
7: 43,291,400 (GRCm39) |
N281D |
probably benign |
Het |
Chil4 |
T |
C |
3: 106,110,083 (GRCm39) |
D337G |
probably damaging |
Het |
Chil4 |
T |
G |
3: 106,121,664 (GRCm39) |
K62Q |
probably benign |
Het |
Cic |
A |
T |
7: 24,972,869 (GRCm39) |
I867F |
probably benign |
Het |
Cntln |
A |
G |
4: 84,968,064 (GRCm39) |
E761G |
probably damaging |
Het |
Cyp2d26 |
T |
A |
15: 82,674,403 (GRCm39) |
Y493F |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,075,788 (GRCm39) |
F3026L |
probably benign |
Het |
Ehd3 |
T |
A |
17: 74,137,179 (GRCm39) |
D449E |
probably benign |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Hivep3 |
T |
A |
4: 119,955,566 (GRCm39) |
I1294N |
probably damaging |
Het |
Il19 |
T |
C |
1: 130,862,732 (GRCm39) |
I139V |
probably benign |
Het |
Jmjd1c |
T |
A |
10: 66,993,780 (GRCm39) |
I87N |
probably damaging |
Het |
Kcnma1 |
A |
G |
14: 23,513,224 (GRCm39) |
Y392H |
probably damaging |
Het |
Kcnv2 |
T |
C |
19: 27,301,448 (GRCm39) |
L433P |
probably damaging |
Het |
Kif9 |
A |
T |
9: 110,335,732 (GRCm39) |
N378Y |
probably damaging |
Het |
Lonrf1 |
A |
T |
8: 36,697,664 (GRCm39) |
V440E |
probably benign |
Het |
Lrrc37 |
A |
G |
11: 103,509,625 (GRCm39) |
I781T |
unknown |
Het |
Manea |
A |
T |
4: 26,336,718 (GRCm39) |
L186Q |
probably damaging |
Het |
Mas1 |
A |
G |
17: 13,061,324 (GRCm39) |
I33T |
probably benign |
Het |
Med13l |
A |
G |
5: 118,864,330 (GRCm39) |
S389G |
probably benign |
Het |
Nxph3 |
T |
C |
11: 95,401,892 (GRCm39) |
N174S |
possibly damaging |
Het |
Or1l4 |
T |
A |
2: 37,091,568 (GRCm39) |
F105Y |
possibly damaging |
Het |
Or8g52 |
G |
C |
9: 39,630,973 (GRCm39) |
C150S |
probably benign |
Het |
Pcdha5 |
A |
G |
18: 37,094,757 (GRCm39) |
D422G |
probably benign |
Het |
Pias4 |
A |
C |
10: 80,990,287 (GRCm39) |
V416G |
possibly damaging |
Het |
Pik3cg |
T |
A |
12: 32,255,666 (GRCm39) |
Y107F |
probably damaging |
Het |
Plcg1 |
T |
A |
2: 160,590,203 (GRCm39) |
W156R |
possibly damaging |
Het |
Plcl2 |
A |
G |
17: 50,913,492 (GRCm39) |
D167G |
probably damaging |
Het |
Podxl |
T |
A |
6: 31,501,668 (GRCm39) |
|
probably null |
Het |
Ppp1r2 |
T |
C |
16: 31,073,536 (GRCm39) |
D197G |
probably benign |
Het |
Ptprs |
C |
G |
17: 56,758,697 (GRCm39) |
V175L |
probably benign |
Het |
Rad17 |
A |
T |
13: 100,766,025 (GRCm39) |
S368T |
probably benign |
Het |
Rdh8 |
G |
T |
9: 20,736,623 (GRCm39) |
R230L |
probably benign |
Het |
Rpl35 |
A |
C |
2: 38,894,168 (GRCm39) |
L58R |
probably damaging |
Het |
Rtp3 |
A |
C |
9: 110,815,767 (GRCm39) |
C199W |
probably damaging |
Het |
S100pbp |
G |
A |
4: 129,075,896 (GRCm39) |
T143I |
probably damaging |
Het |
Scarf1 |
A |
G |
11: 75,416,904 (GRCm39) |
E782G |
probably damaging |
Het |
Slc30a9 |
T |
C |
5: 67,484,205 (GRCm39) |
V114A |
probably benign |
Het |
Speer1c |
G |
A |
5: 10,292,977 (GRCm39) |
P189S |
|
Het |
Stpg2 |
G |
A |
3: 139,407,535 (GRCm39) |
|
probably null |
Het |
Tdpoz1 |
T |
C |
3: 93,578,113 (GRCm39) |
S224G |
possibly damaging |
Het |
Triml2 |
T |
A |
8: 43,636,370 (GRCm39) |
Y52N |
probably benign |
Het |
Trpm2 |
A |
T |
10: 77,783,765 (GRCm39) |
I236N |
probably damaging |
Het |
Unc5c |
A |
G |
3: 141,507,054 (GRCm39) |
D602G |
probably benign |
Het |
Upk1a |
A |
G |
7: 30,309,236 (GRCm39) |
S29P |
probably damaging |
Het |
Vmn2r54 |
A |
G |
7: 12,350,001 (GRCm39) |
L527P |
probably damaging |
Het |
Vmn2r72 |
A |
T |
7: 85,399,011 (GRCm39) |
|
probably null |
Het |
Vstm2l |
G |
T |
2: 157,756,649 (GRCm39) |
|
probably benign |
Het |
Vwf |
G |
T |
6: 125,632,007 (GRCm39) |
G1952V |
|
Het |
Zfand6 |
A |
C |
7: 84,265,077 (GRCm39) |
I208S |
probably damaging |
Het |
Zfp236 |
A |
G |
18: 82,638,462 (GRCm39) |
I1386T |
possibly 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 |
R2004:Herc2
|
UTSW |
7 |
55,787,607 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|