Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700061I17Rik |
G |
T |
3: 116,861,385 (GRCm39) |
|
noncoding transcript |
Het |
2300003K06Rik |
G |
T |
11: 99,728,793 (GRCm39) |
Q17K |
probably benign |
Het |
Abca16 |
T |
C |
7: 120,119,256 (GRCm39) |
V999A |
probably benign |
Het |
Actn3 |
C |
T |
19: 4,915,483 (GRCm39) |
|
probably benign |
Het |
Agap2 |
T |
A |
10: 126,926,981 (GRCm39) |
|
probably benign |
Het |
Ago3 |
C |
A |
4: 126,265,580 (GRCm39) |
R278L |
probably benign |
Het |
Aldh1a2 |
T |
C |
9: 71,192,492 (GRCm39) |
V449A |
possibly damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Aplnr |
A |
G |
2: 84,967,353 (GRCm39) |
Y126C |
probably damaging |
Het |
Apob |
T |
C |
12: 8,066,084 (GRCm39) |
I4351T |
possibly damaging |
Het |
Ash1l |
T |
C |
3: 88,914,659 (GRCm39) |
L1763P |
probably benign |
Het |
Aspn |
T |
C |
13: 49,710,849 (GRCm39) |
S165P |
possibly damaging |
Het |
Atg13 |
A |
T |
2: 91,510,335 (GRCm39) |
V349E |
probably damaging |
Het |
Atp1b2 |
T |
A |
11: 69,493,309 (GRCm39) |
|
probably null |
Het |
B3glct |
A |
T |
5: 149,677,604 (GRCm39) |
D411V |
probably damaging |
Het |
Bcar3 |
A |
T |
3: 122,316,840 (GRCm39) |
I255F |
probably damaging |
Het |
Cacna1b |
G |
A |
2: 24,608,148 (GRCm39) |
|
probably benign |
Het |
Cep164 |
T |
G |
9: 45,690,198 (GRCm39) |
E675A |
possibly damaging |
Het |
Chd1l |
C |
T |
3: 97,490,047 (GRCm39) |
E503K |
probably benign |
Het |
Chst8 |
C |
A |
7: 34,447,593 (GRCm39) |
M8I |
possibly damaging |
Het |
Clec4n |
A |
G |
6: 123,212,475 (GRCm39) |
E67G |
probably benign |
Het |
Cobll1 |
A |
T |
2: 64,929,480 (GRCm39) |
D653E |
probably damaging |
Het |
Col9a1 |
T |
C |
1: 24,276,579 (GRCm39) |
|
probably null |
Het |
Crip2 |
T |
C |
12: 113,107,124 (GRCm39) |
L30P |
probably damaging |
Het |
Ctbp1 |
C |
T |
5: 33,418,407 (GRCm39) |
V22I |
probably benign |
Het |
Cwc22 |
T |
C |
2: 77,747,521 (GRCm39) |
|
probably benign |
Het |
Cyp4a32 |
C |
A |
4: 115,460,147 (GRCm39) |
Y119* |
probably null |
Het |
Dido1 |
G |
T |
2: 180,313,263 (GRCm39) |
A463E |
possibly damaging |
Het |
Dnah7a |
G |
A |
1: 53,567,956 (GRCm39) |
P1880L |
probably benign |
Het |
Dock2 |
T |
A |
11: 34,189,705 (GRCm39) |
T1489S |
probably benign |
Het |
Dsp |
A |
G |
13: 38,375,907 (GRCm39) |
T1231A |
probably damaging |
Het |
Eif2ak1 |
G |
T |
5: 143,810,717 (GRCm39) |
|
probably benign |
Het |
Entrep1 |
G |
A |
19: 23,998,998 (GRCm39) |
T140M |
probably damaging |
Het |
Epc1 |
A |
T |
18: 6,452,360 (GRCm39) |
M233K |
probably damaging |
Het |
Gigyf2 |
A |
G |
1: 87,371,360 (GRCm39) |
|
probably benign |
Het |
Greb1 |
T |
G |
12: 16,757,852 (GRCm39) |
H58P |
probably damaging |
Het |
Gtpbp1 |
T |
C |
15: 79,597,649 (GRCm39) |
I348T |
possibly damaging |
Het |
Hck |
A |
T |
2: 152,970,192 (GRCm39) |
N64Y |
probably benign |
Het |
Inpp4b |
T |
A |
8: 82,679,463 (GRCm39) |
|
probably null |
Het |
Kcnq5 |
A |
C |
1: 21,475,248 (GRCm39) |
S473A |
probably benign |
Het |
Lrat |
T |
G |
3: 82,810,676 (GRCm39) |
D115A |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,814,639 (GRCm39) |
I1131M |
possibly damaging |
Het |
Man2a2 |
T |
C |
7: 80,018,310 (GRCm39) |
D160G |
probably benign |
Het |
Marf1 |
C |
T |
16: 13,933,688 (GRCm39) |
D1567N |
probably benign |
Het |
Mars1 |
T |
C |
10: 127,133,857 (GRCm39) |
D680G |
possibly damaging |
Het |
Mat1a |
T |
C |
14: 40,843,797 (GRCm39) |
S339P |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,042,081 (GRCm39) |
S1300P |
probably damaging |
Het |
Mga |
T |
C |
2: 119,733,179 (GRCm39) |
L9S |
probably damaging |
Het |
Mllt6 |
T |
C |
11: 97,563,277 (GRCm39) |
|
probably benign |
Het |
Mrpl37 |
A |
G |
4: 106,921,692 (GRCm39) |
L179P |
probably benign |
Het |
Mtnr1a |
G |
T |
8: 45,540,782 (GRCm39) |
V248L |
probably benign |
Het |
Mylk |
T |
C |
16: 34,635,835 (GRCm39) |
S19P |
possibly damaging |
Het |
Or11g1 |
A |
G |
14: 50,651,858 (GRCm39) |
T286A |
probably damaging |
Het |
Pacc1 |
A |
G |
1: 191,080,559 (GRCm39) |
|
probably benign |
Het |
Parp8 |
A |
T |
13: 117,161,886 (GRCm39) |
|
probably null |
Het |
Pcnx2 |
T |
C |
8: 126,479,023 (GRCm39) |
D2075G |
probably damaging |
Het |
Pigo |
A |
T |
4: 43,021,460 (GRCm39) |
I494K |
probably benign |
Het |
Pkd1l1 |
A |
T |
11: 8,820,313 (GRCm39) |
D1217E |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,369,040 (GRCm39) |
V895A |
probably benign |
Het |
Plcb4 |
A |
T |
2: 135,842,109 (GRCm39) |
H1031L |
possibly damaging |
Het |
Plxnb1 |
A |
G |
9: 108,937,989 (GRCm39) |
K1245R |
probably null |
Het |
Pold1 |
C |
T |
7: 44,192,181 (GRCm39) |
|
probably benign |
Het |
Ptprq |
T |
C |
10: 107,498,423 (GRCm39) |
I885V |
probably damaging |
Het |
Ptprz1 |
A |
G |
6: 23,050,473 (GRCm39) |
D1398G |
probably damaging |
Het |
Pygm |
G |
A |
19: 6,439,917 (GRCm39) |
A364T |
probably benign |
Het |
Rbl1 |
T |
C |
2: 157,035,018 (GRCm39) |
N354S |
probably benign |
Het |
Scgb2b19 |
C |
T |
7: 32,979,037 (GRCm39) |
|
probably null |
Het |
Slc26a8 |
C |
T |
17: 28,867,187 (GRCm39) |
V545M |
possibly damaging |
Het |
Slc27a1 |
T |
A |
8: 72,036,757 (GRCm39) |
|
probably null |
Het |
Smpd1 |
A |
G |
7: 105,205,881 (GRCm39) |
D416G |
possibly damaging |
Het |
Sorbs3 |
A |
G |
14: 70,431,095 (GRCm39) |
V284A |
probably benign |
Het |
Stfa2l1 |
T |
C |
16: 35,982,154 (GRCm39) |
V75A |
probably damaging |
Het |
Syndig1 |
A |
G |
2: 149,772,841 (GRCm39) |
D166G |
probably damaging |
Het |
Tcp10a |
G |
A |
17: 7,593,406 (GRCm39) |
|
probably null |
Het |
Themis2 |
T |
A |
4: 132,510,212 (GRCm39) |
I663F |
possibly damaging |
Het |
Thrap3 |
T |
C |
4: 126,070,129 (GRCm39) |
Q586R |
probably damaging |
Het |
Tinag |
C |
A |
9: 76,952,798 (GRCm39) |
C62F |
probably damaging |
Het |
Tmod1 |
T |
C |
4: 46,090,884 (GRCm39) |
Y146H |
probably damaging |
Het |
Tmprss4 |
T |
A |
9: 45,095,683 (GRCm39) |
I54F |
possibly damaging |
Het |
Tnks |
A |
C |
8: 35,301,757 (GRCm39) |
|
probably benign |
Het |
Trim43a |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
9: 88,465,042 (GRCm39) |
|
probably benign |
Het |
Trpc6 |
A |
G |
9: 8,680,538 (GRCm39) |
E844G |
probably benign |
Het |
Ubtd2 |
C |
T |
11: 32,466,125 (GRCm39) |
R115W |
probably damaging |
Het |
Ubxn6 |
T |
C |
17: 56,376,042 (GRCm39) |
D373G |
probably benign |
Het |
Upf1 |
T |
A |
8: 70,794,174 (GRCm39) |
Q244L |
probably benign |
Het |
Usp33 |
A |
G |
3: 152,074,271 (GRCm39) |
I372M |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,301,629 (GRCm39) |
E351G |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,554,318 (GRCm39) |
|
probably benign |
Het |
Vmn1r78 |
A |
G |
7: 11,886,508 (GRCm39) |
K40E |
possibly damaging |
Het |
Vmn2r7 |
T |
A |
3: 64,632,223 (GRCm39) |
M80L |
probably benign |
Het |
Vps13a |
G |
T |
19: 16,678,602 (GRCm39) |
Y1126* |
probably null |
Het |
Wfdc11 |
T |
C |
2: 164,506,366 (GRCm39) |
N60S |
probably benign |
Het |
Wnk2 |
C |
T |
13: 49,224,586 (GRCm39) |
D992N |
probably damaging |
Het |
Zpbp2 |
C |
A |
11: 98,444,670 (GRCm39) |
T66K |
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 |
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 |
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 |
|