Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003H04Rik |
C |
T |
3: 124,350,493 (GRCm39) |
C133Y |
unknown |
Het |
Abce1 |
A |
G |
8: 80,416,880 (GRCm39) |
M377T |
possibly damaging |
Het |
Adam25 |
A |
T |
8: 41,208,263 (GRCm39) |
R510* |
probably null |
Het |
Adamts12 |
G |
T |
15: 11,217,966 (GRCm39) |
E308* |
probably null |
Het |
Adgrg3 |
C |
A |
8: 95,760,070 (GRCm39) |
N96K |
possibly damaging |
Het |
Afdn |
T |
C |
17: 14,101,578 (GRCm39) |
V1022A |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,051,406 (GRCm39) |
V1391A |
probably damaging |
Het |
Akip1 |
A |
G |
7: 109,310,982 (GRCm39) |
Y174C |
probably damaging |
Het |
Aoc1l1 |
A |
G |
6: 48,952,554 (GRCm39) |
I160V |
probably benign |
Het |
Ap3b2 |
T |
C |
7: 81,113,898 (GRCm39) |
T830A |
unknown |
Het |
Aph1a |
A |
G |
3: 95,802,876 (GRCm39) |
T159A |
probably damaging |
Het |
Ccdc146 |
T |
C |
5: 21,506,288 (GRCm39) |
T718A |
probably benign |
Het |
Cdk5r2 |
T |
C |
1: 74,894,981 (GRCm39) |
L242P |
probably damaging |
Het |
Cep97 |
T |
A |
16: 55,748,229 (GRCm39) |
N67I |
probably damaging |
Het |
Cgas |
T |
C |
9: 78,340,484 (GRCm39) |
D416G |
probably benign |
Het |
Chic2 |
A |
T |
5: 75,172,140 (GRCm39) |
W121R |
possibly damaging |
Het |
Clock |
A |
G |
5: 76,396,309 (GRCm39) |
S147P |
possibly damaging |
Het |
Cntnap5a |
T |
G |
1: 116,016,940 (GRCm39) |
S178A |
probably benign |
Het |
Col11a2 |
C |
A |
17: 34,281,529 (GRCm39) |
|
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,757,936 (GRCm39) |
H6L |
probably damaging |
Het |
Cpne5 |
T |
C |
17: 29,423,667 (GRCm39) |
N154D |
probably benign |
Het |
Ctsz |
T |
G |
2: 174,269,769 (GRCm39) |
K273Q |
probably benign |
Het |
Cybrd1 |
G |
A |
2: 70,960,104 (GRCm39) |
V101M |
probably benign |
Het |
Cyp2c23 |
T |
A |
19: 43,993,990 (GRCm39) |
K459* |
probably null |
Het |
Cyp4a31 |
A |
T |
4: 115,431,933 (GRCm39) |
H419L |
probably damaging |
Het |
D930020B18Rik |
G |
A |
10: 121,477,879 (GRCm39) |
V35M |
probably damaging |
Het |
Depp1 |
G |
A |
6: 116,628,683 (GRCm39) |
V9M |
possibly damaging |
Het |
Dnah9 |
C |
T |
11: 65,928,316 (GRCm39) |
V2118M |
probably benign |
Het |
Dtna |
T |
C |
18: 23,730,617 (GRCm39) |
|
probably null |
Het |
Ednra |
C |
T |
8: 78,447,025 (GRCm39) |
V18I |
possibly damaging |
Het |
Elac1 |
T |
C |
18: 73,875,717 (GRCm39) |
R105G |
probably benign |
Het |
Exoc2 |
A |
G |
13: 31,006,644 (GRCm39) |
S844P |
probably benign |
Het |
Fam185a |
A |
T |
5: 21,685,328 (GRCm39) |
|
probably null |
Het |
Fam204a |
A |
G |
19: 60,187,881 (GRCm39) |
M233T |
possibly damaging |
Het |
Fat1 |
C |
A |
8: 45,406,341 (GRCm39) |
H1031N |
probably benign |
Het |
Fat1 |
T |
A |
8: 45,491,386 (GRCm39) |
Y3816N |
probably damaging |
Het |
Fbxo38 |
C |
T |
18: 62,650,094 (GRCm39) |
R621Q |
probably benign |
Het |
Fhod3 |
C |
A |
18: 25,263,667 (GRCm39) |
R1524S |
probably damaging |
Het |
Fnip1 |
A |
T |
11: 54,378,561 (GRCm39) |
R192W |
probably damaging |
Het |
Frem3 |
T |
A |
8: 81,339,205 (GRCm39) |
H499Q |
probably damaging |
Het |
Gab2 |
C |
T |
7: 96,948,250 (GRCm39) |
T280I |
probably damaging |
Het |
Gdpgp1 |
A |
G |
7: 79,888,172 (GRCm39) |
R68G |
probably benign |
Het |
Gm10382 |
C |
T |
5: 125,466,624 (GRCm39) |
|
probably benign |
Het |
Gmps |
A |
G |
3: 63,908,938 (GRCm39) |
H480R |
probably benign |
Het |
Hecw1 |
G |
A |
13: 14,455,034 (GRCm39) |
R674* |
probably null |
Het |
Homer2 |
C |
T |
7: 81,286,150 (GRCm39) |
V21M |
probably damaging |
Het |
Ifna9 |
A |
G |
4: 88,510,492 (GRCm39) |
M44T |
probably damaging |
Het |
Igfl3 |
A |
G |
7: 17,913,821 (GRCm39) |
D57G |
possibly damaging |
Het |
Jcad |
T |
C |
18: 4,673,048 (GRCm39) |
M270T |
probably benign |
Het |
Kdm5b |
T |
C |
1: 134,552,732 (GRCm39) |
L1236P |
probably damaging |
Het |
Kif14 |
T |
A |
1: 136,414,096 (GRCm39) |
L724Q |
probably damaging |
Het |
Lhb |
T |
C |
7: 45,070,757 (GRCm39) |
V45A |
probably damaging |
Het |
Lhpp |
A |
G |
7: 132,235,816 (GRCm39) |
N134D |
probably benign |
Het |
Mas1 |
T |
C |
17: 13,061,078 (GRCm39) |
Y115C |
probably damaging |
Het |
Mgam |
A |
T |
6: 40,638,234 (GRCm39) |
K395* |
probably null |
Het |
Mms22l |
A |
G |
4: 24,598,807 (GRCm39) |
N1134S |
probably damaging |
Het |
Mrc1 |
A |
G |
2: 14,330,192 (GRCm39) |
|
probably null |
Het |
Mrgprg |
G |
A |
7: 143,318,281 (GRCm39) |
S277L |
probably damaging |
Het |
Mrpl49 |
G |
T |
19: 6,107,010 (GRCm39) |
P60T |
possibly damaging |
Het |
Mrps10 |
G |
A |
17: 47,683,377 (GRCm39) |
G104D |
possibly damaging |
Het |
Msantd3 |
A |
G |
4: 48,552,771 (GRCm39) |
Y120C |
probably damaging |
Het |
Mtcl2 |
A |
G |
2: 156,882,181 (GRCm39) |
C624R |
possibly damaging |
Het |
N4bp2 |
C |
T |
5: 65,951,861 (GRCm39) |
|
probably benign |
Het |
Nbea |
A |
G |
3: 55,550,310 (GRCm39) |
V2706A |
probably benign |
Het |
Nfic |
T |
A |
10: 81,256,518 (GRCm39) |
M71L |
possibly damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Or12e1 |
A |
G |
2: 87,022,222 (GRCm39) |
T64A |
possibly damaging |
Het |
Or14j4 |
G |
T |
17: 37,920,803 (GRCm39) |
P280T |
probably damaging |
Het |
Or4a15 |
A |
G |
2: 89,192,933 (GRCm39) |
L280P |
probably damaging |
Het |
Or4c105 |
T |
A |
2: 88,648,280 (GRCm39) |
V255E |
probably benign |
Het |
Pak5 |
T |
C |
2: 135,927,508 (GRCm39) |
I655V |
possibly damaging |
Het |
Pip5k1c |
A |
G |
10: 81,142,153 (GRCm39) |
N121S |
probably damaging |
Het |
Plce1 |
A |
T |
19: 38,748,521 (GRCm39) |
I1737F |
probably damaging |
Het |
Prrt1 |
T |
C |
17: 34,849,925 (GRCm39) |
L113P |
probably damaging |
Het |
Ptprq |
T |
A |
10: 107,479,860 (GRCm39) |
T1137S |
probably benign |
Het |
Recql5 |
T |
C |
11: 115,814,135 (GRCm39) |
I223V |
probably benign |
Het |
Reg3g |
A |
T |
6: 78,444,836 (GRCm39) |
Y47* |
probably null |
Het |
Rgs12 |
T |
G |
5: 35,123,165 (GRCm39) |
M316R |
probably damaging |
Het |
Ric1 |
T |
C |
19: 29,580,068 (GRCm39) |
S1290P |
probably benign |
Het |
Rpl36al |
A |
G |
12: 69,229,697 (GRCm39) |
C72R |
probably damaging |
Het |
Rplp0 |
T |
A |
5: 115,701,374 (GRCm39) |
F275L |
possibly damaging |
Het |
Rpp30 |
G |
A |
19: 36,064,793 (GRCm39) |
V89I |
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,539,482 (GRCm39) |
F3253L |
possibly damaging |
Het |
Serpina3n |
A |
T |
12: 104,375,203 (GRCm39) |
N92Y |
probably benign |
Het |
Setd7 |
G |
T |
3: 51,450,252 (GRCm39) |
T58N |
probably benign |
Het |
Sh3tc2 |
T |
A |
18: 62,144,954 (GRCm39) |
L1136Q |
probably damaging |
Het |
Slc35b4 |
G |
A |
6: 34,135,440 (GRCm39) |
Q291* |
probably null |
Het |
Sort1 |
A |
G |
3: 108,248,011 (GRCm39) |
N452S |
probably benign |
Het |
Sympk |
A |
G |
7: 18,763,070 (GRCm39) |
I46V |
probably benign |
Het |
Syngr2 |
T |
C |
11: 117,703,364 (GRCm39) |
V60A |
probably damaging |
Het |
Syt17 |
A |
T |
7: 118,007,341 (GRCm39) |
F318I |
probably benign |
Het |
Tdpoz8 |
T |
A |
3: 92,981,729 (GRCm39) |
L249H |
probably damaging |
Het |
Tgfb1 |
T |
A |
7: 25,391,891 (GRCm39) |
L149M |
probably damaging |
Het |
Ticam1 |
A |
T |
17: 56,578,897 (GRCm39) |
M66K |
probably benign |
Het |
Tmem131 |
G |
T |
1: 36,847,008 (GRCm39) |
D1363E |
probably benign |
Het |
Tns4 |
A |
C |
11: 98,970,926 (GRCm39) |
D261E |
probably damaging |
Het |
Trim30a |
T |
C |
7: 104,078,417 (GRCm39) |
N220D |
probably benign |
Het |
Trmt10a |
T |
C |
3: 137,862,481 (GRCm39) |
L257P |
probably damaging |
Het |
Troap |
G |
T |
15: 98,973,233 (GRCm39) |
|
probably benign |
Het |
Ttc6 |
T |
C |
12: 57,751,338 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Vav1 |
A |
C |
17: 57,631,750 (GRCm39) |
K775T |
probably damaging |
Het |
Vmn1r236 |
A |
G |
17: 21,507,673 (GRCm39) |
K264E |
possibly damaging |
Het |
Vmn1r84 |
A |
G |
7: 12,096,555 (GRCm39) |
V46A |
probably benign |
Het |
Wdr59 |
A |
T |
8: 112,185,649 (GRCm39) |
W835R |
probably damaging |
Het |
Zfp513 |
T |
G |
5: 31,357,767 (GRCm39) |
K202T |
probably damaging |
Het |
Zfp7 |
T |
G |
15: 76,775,977 (GRCm39) |
I673S |
probably benign |
Het |
Zmynd11 |
A |
G |
13: 9,748,737 (GRCm39) |
I108T |
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 |
|
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 |
|