Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
A |
G |
1: 156,464,429 (GRCm39) |
T535A |
possibly damaging |
Het |
Adcy9 |
A |
T |
16: 4,236,088 (GRCm39) |
L441Q |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,668,780 (GRCm39) |
V2592E |
probably damaging |
Het |
Ahdc1 |
A |
G |
4: 132,790,825 (GRCm39) |
S689G |
probably benign |
Het |
Ankrd24 |
G |
A |
10: 81,474,523 (GRCm39) |
G229E |
unknown |
Het |
Ankrd34c |
T |
A |
9: 89,610,914 (GRCm39) |
I476F |
probably damaging |
Het |
Arhgef19 |
A |
G |
4: 140,984,090 (GRCm39) |
H770R |
possibly damaging |
Het |
Arhgef4 |
T |
G |
1: 34,771,316 (GRCm39) |
S1208A |
possibly damaging |
Het |
Arid1a |
A |
T |
4: 133,418,466 (GRCm39) |
M654K |
unknown |
Het |
Atp11b |
T |
A |
3: 35,864,259 (GRCm39) |
|
probably null |
Het |
Cadps |
A |
G |
14: 12,454,260 (GRCm38) |
I1086T |
probably damaging |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Cfap276 |
T |
A |
3: 108,449,848 (GRCm39) |
D42E |
probably benign |
Het |
Cntn3 |
T |
C |
6: 102,142,337 (GRCm39) |
H1010R |
probably benign |
Het |
Cyp2c66 |
T |
A |
19: 39,159,472 (GRCm39) |
Y308N |
probably damaging |
Het |
Dok6 |
T |
A |
18: 89,492,067 (GRCm39) |
H170L |
probably damaging |
Het |
Eefsec |
C |
T |
6: 88,258,576 (GRCm39) |
D506N |
possibly damaging |
Het |
Fam181a |
C |
T |
12: 103,282,805 (GRCm39) |
P237S |
probably damaging |
Het |
Fam186b |
T |
C |
15: 99,184,867 (GRCm39) |
I19V |
probably damaging |
Het |
Gm3285 |
A |
T |
10: 77,697,865 (GRCm39) |
T5S |
unknown |
Het |
Heg1 |
A |
G |
16: 33,547,733 (GRCm39) |
E864G |
probably benign |
Het |
Hexa |
T |
C |
9: 59,469,230 (GRCm39) |
S331P |
probably damaging |
Het |
Hspb1 |
A |
T |
5: 135,917,223 (GRCm39) |
D104V |
probably damaging |
Het |
Ikzf1 |
A |
T |
11: 11,719,019 (GRCm39) |
Q329L |
probably damaging |
Het |
Kcnf1 |
C |
A |
12: 17,224,787 (GRCm39) |
R478L |
probably benign |
Het |
Kdm3a |
T |
C |
6: 71,568,937 (GRCm39) |
T1161A |
possibly damaging |
Het |
Krtap31-2 |
T |
C |
11: 99,827,429 (GRCm39) |
I87T |
possibly damaging |
Het |
Lars2 |
T |
C |
9: 123,224,176 (GRCm39) |
S116P |
|
Het |
Lrrk2 |
A |
G |
15: 91,657,061 (GRCm39) |
D1785G |
probably damaging |
Het |
Myo10 |
A |
G |
15: 25,701,709 (GRCm39) |
H61R |
probably benign |
Het |
Or10x4 |
T |
G |
1: 174,219,220 (GRCm39) |
F195C |
probably damaging |
Het |
Or9s13 |
A |
G |
1: 92,548,183 (GRCm39) |
Y185C |
probably damaging |
Het |
Pcdhb4 |
C |
A |
18: 37,442,602 (GRCm39) |
H637Q |
probably benign |
Het |
Pcsk9 |
T |
A |
4: 106,304,763 (GRCm39) |
D435V |
probably benign |
Het |
Prickle2 |
T |
A |
6: 92,402,631 (GRCm39) |
Y119F |
possibly damaging |
Het |
Prr5 |
A |
G |
15: 84,641,276 (GRCm39) |
T181A |
probably benign |
Het |
Psd |
T |
A |
19: 46,301,877 (GRCm39) |
Q903L |
probably damaging |
Het |
Ptpn13 |
T |
A |
5: 103,649,331 (GRCm39) |
S245T |
probably benign |
Het |
Resp18 |
T |
C |
1: 75,254,882 (GRCm39) |
S24G |
probably damaging |
Het |
Slc17a4 |
T |
C |
13: 24,090,580 (GRCm39) |
T89A |
probably benign |
Het |
Slc9a9 |
A |
G |
9: 94,737,792 (GRCm39) |
Y233C |
probably damaging |
Het |
Slit1 |
T |
A |
19: 41,622,639 (GRCm39) |
I707F |
probably damaging |
Het |
Sp4 |
T |
C |
12: 118,218,174 (GRCm39) |
E691G |
possibly damaging |
Het |
Sun2 |
G |
T |
15: 79,623,225 (GRCm39) |
|
probably null |
Het |
Syne3 |
T |
C |
12: 104,912,901 (GRCm39) |
T723A |
not run |
Het |
Tcp1 |
T |
A |
17: 13,141,540 (GRCm39) |
F340I |
possibly damaging |
Het |
Tmem39b |
A |
T |
4: 129,587,694 (GRCm39) |
V39D |
probably damaging |
Het |
Tmtc3 |
A |
T |
10: 100,286,214 (GRCm39) |
Y536* |
probably null |
Het |
Tnfrsf11a |
A |
T |
1: 105,755,094 (GRCm39) |
T389S |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,598,873 (GRCm39) |
T19347A |
possibly damaging |
Het |
Vmn1r68 |
A |
G |
7: 10,261,553 (GRCm39) |
S182P |
probably benign |
Het |
Vmn2r95 |
A |
G |
17: 18,660,352 (GRCm39) |
T255A |
probably benign |
Het |
Wdr59 |
T |
C |
8: 112,219,394 (GRCm39) |
Y221C |
|
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 |
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 |
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 |
|