Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,244,615 (GRCm39) |
Y2159* |
probably null |
Het |
Abca3 |
A |
G |
17: 24,602,901 (GRCm39) |
T499A |
probably benign |
Het |
Abcb5 |
T |
A |
12: 118,899,702 (GRCm39) |
T322S |
probably damaging |
Het |
Adamts4 |
T |
A |
1: 171,078,419 (GRCm39) |
M1K |
probably null |
Het |
Adamtsl4 |
C |
T |
3: 95,592,765 (GRCm39) |
|
probably null |
Het |
Adh4 |
A |
T |
3: 138,129,950 (GRCm39) |
I259F |
probably damaging |
Het |
Aff3 |
G |
A |
1: 38,220,505 (GRCm39) |
S1135F |
probably damaging |
Het |
Arhgef16 |
T |
C |
4: 154,370,105 (GRCm39) |
D280G |
probably benign |
Het |
Baiap3 |
T |
C |
17: 25,470,707 (GRCm39) |
E71G |
probably damaging |
Het |
Calb2 |
A |
G |
8: 110,879,332 (GRCm39) |
I91T |
possibly damaging |
Het |
Ccr5 |
A |
G |
9: 123,924,697 (GRCm39) |
N100S |
probably benign |
Het |
Cep57 |
G |
T |
9: 13,732,871 (GRCm39) |
R25S |
probably damaging |
Het |
Chadl |
A |
G |
15: 81,580,079 (GRCm39) |
L52P |
probably damaging |
Het |
Clec12b |
T |
C |
6: 129,362,438 (GRCm39) |
T6A |
probably damaging |
Het |
Cnga1 |
T |
A |
5: 72,775,593 (GRCm39) |
N43Y |
probably damaging |
Het |
Col20a1 |
A |
T |
2: 180,628,316 (GRCm39) |
|
probably null |
Het |
Csmd2 |
T |
C |
4: 128,356,682 (GRCm39) |
|
probably null |
Het |
Ctps1 |
A |
T |
4: 120,411,300 (GRCm39) |
|
probably null |
Het |
Cyp39a1 |
T |
A |
17: 43,996,099 (GRCm39) |
W224R |
possibly damaging |
Het |
Defb29 |
A |
T |
2: 152,380,848 (GRCm39) |
Y54N |
probably benign |
Het |
Dmbt1 |
A |
T |
7: 130,708,003 (GRCm39) |
D1241V |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 30,996,323 (GRCm39) |
I2671K |
probably benign |
Het |
Dnah2 |
C |
A |
11: 69,407,395 (GRCm39) |
E158* |
probably null |
Het |
Dynlt2b |
A |
G |
16: 32,238,718 (GRCm39) |
Y31C |
probably damaging |
Het |
Edar |
A |
G |
10: 58,464,463 (GRCm39) |
S59P |
possibly damaging |
Het |
Egr2 |
T |
A |
10: 67,376,596 (GRCm39) |
C339* |
probably null |
Het |
Eif5b |
G |
A |
1: 38,084,765 (GRCm39) |
V871I |
possibly damaging |
Het |
Eif5b |
G |
A |
1: 38,090,328 (GRCm39) |
G1169E |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,810,531 (GRCm39) |
Y290C |
probably damaging |
Het |
Fastkd5 |
T |
A |
2: 130,456,221 (GRCm39) |
T790S |
possibly damaging |
Het |
Fkrp |
C |
T |
7: 16,544,849 (GRCm39) |
V338M |
probably damaging |
Het |
Gabra6 |
T |
C |
11: 42,198,317 (GRCm39) |
T378A |
probably benign |
Het |
Gm4924 |
C |
A |
10: 82,214,475 (GRCm39) |
Q17K |
possibly damaging |
Het |
Gm9847 |
A |
G |
12: 14,545,000 (GRCm39) |
|
noncoding transcript |
Het |
Gpr108 |
A |
G |
17: 57,543,919 (GRCm39) |
F429S |
probably damaging |
Het |
Gpr162 |
G |
A |
6: 124,837,901 (GRCm39) |
R250* |
probably null |
Het |
Gtf2a1 |
A |
T |
12: 91,534,368 (GRCm39) |
D295E |
possibly damaging |
Het |
Gtf2h3 |
C |
T |
5: 124,722,360 (GRCm39) |
T121I |
probably benign |
Het |
Hoxb6 |
T |
A |
11: 96,191,580 (GRCm39) |
Y167* |
probably null |
Het |
Hrob |
T |
A |
11: 102,146,659 (GRCm39) |
S312T |
probably damaging |
Het |
Htt |
T |
C |
5: 35,006,419 (GRCm39) |
Y1443H |
probably damaging |
Het |
Il21r |
A |
G |
7: 125,224,470 (GRCm39) |
D28G |
probably damaging |
Het |
Impact |
T |
G |
18: 13,107,819 (GRCm39) |
V29G |
probably damaging |
Het |
Itpr3 |
A |
G |
17: 27,334,926 (GRCm39) |
T2147A |
possibly damaging |
Het |
Itsn2 |
T |
A |
12: 4,676,554 (GRCm39) |
L50Q |
probably damaging |
Het |
Jade1 |
A |
G |
3: 41,559,338 (GRCm39) |
D473G |
possibly damaging |
Het |
Kif26a |
T |
G |
12: 112,123,788 (GRCm39) |
L131R |
probably damaging |
Het |
Kif2a |
A |
T |
13: 107,130,432 (GRCm39) |
M1K |
probably null |
Het |
Lrsam1 |
C |
A |
2: 32,831,870 (GRCm39) |
Q368H |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,328,957 (GRCm39) |
Q4592R |
probably damaging |
Het |
Map3k5 |
T |
C |
10: 19,986,465 (GRCm39) |
V893A |
probably damaging |
Het |
Med13l |
G |
T |
5: 118,866,730 (GRCm39) |
V595F |
possibly damaging |
Het |
Mocs1 |
T |
A |
17: 49,761,211 (GRCm39) |
L435Q |
possibly damaging |
Het |
Mtmr4 |
T |
C |
11: 87,495,356 (GRCm39) |
L471P |
probably damaging |
Het |
Myo7a |
T |
C |
7: 97,714,023 (GRCm39) |
E1616G |
possibly damaging |
Het |
Nacad |
T |
A |
11: 6,552,136 (GRCm39) |
S352C |
probably damaging |
Het |
Nfat5 |
T |
A |
8: 108,095,767 (GRCm39) |
M817K |
possibly damaging |
Het |
Ofcc1 |
C |
A |
13: 40,248,129 (GRCm39) |
L668F |
probably damaging |
Het |
Or12j2 |
C |
A |
7: 139,915,980 (GRCm39) |
D68E |
probably damaging |
Het |
Or7e178 |
T |
C |
9: 20,225,265 (GRCm39) |
Q309R |
probably benign |
Het |
Or8j3c |
G |
A |
2: 86,253,721 (GRCm39) |
Q100* |
probably null |
Het |
Plxnb2 |
T |
C |
15: 89,048,223 (GRCm39) |
T696A |
probably benign |
Het |
Prkab2 |
T |
A |
3: 97,569,609 (GRCm39) |
F58L |
probably benign |
Het |
Prpf4 |
G |
T |
4: 62,334,206 (GRCm39) |
L220F |
probably benign |
Het |
Rad18 |
A |
T |
6: 112,658,307 (GRCm39) |
D199E |
probably benign |
Het |
Raet1e |
T |
C |
10: 22,050,304 (GRCm39) |
L29P |
probably damaging |
Het |
Ralgapb |
A |
C |
2: 158,336,630 (GRCm39) |
T1089P |
possibly damaging |
Het |
Rest |
A |
G |
5: 77,430,173 (GRCm39) |
E864G |
probably benign |
Het |
Rgsl1 |
T |
A |
1: 153,669,520 (GRCm39) |
I289F |
probably damaging |
Het |
Rint1 |
T |
C |
5: 24,015,951 (GRCm39) |
Y406H |
probably damaging |
Het |
Rmc1 |
T |
C |
18: 12,313,749 (GRCm39) |
I26T |
possibly damaging |
Het |
Rpl31 |
C |
T |
1: 39,409,108 (GRCm39) |
R41C |
probably benign |
Het |
Scn8a |
T |
C |
15: 100,872,415 (GRCm39) |
S485P |
probably damaging |
Het |
Slamf1 |
T |
A |
1: 171,615,538 (GRCm39) |
V249E |
possibly damaging |
Het |
Slc39a12 |
C |
T |
2: 14,412,414 (GRCm39) |
T362I |
possibly damaging |
Het |
Sos1 |
C |
T |
17: 80,761,319 (GRCm39) |
V126I |
possibly damaging |
Het |
Srcap |
T |
C |
7: 127,124,475 (GRCm39) |
F215S |
probably damaging |
Het |
Supt4a |
T |
A |
11: 87,634,113 (GRCm39) |
S110T |
probably benign |
Het |
Tbc1d30 |
T |
A |
10: 121,138,015 (GRCm39) |
T232S |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,732,041 (GRCm39) |
C1288R |
probably damaging |
Het |
Tespa1 |
T |
A |
10: 130,191,356 (GRCm39) |
L100* |
probably null |
Het |
Tgm1 |
C |
A |
14: 55,949,893 (GRCm39) |
R105L |
probably damaging |
Het |
Tgoln1 |
G |
A |
6: 72,593,018 (GRCm39) |
T154I |
possibly damaging |
Het |
Trp53i13 |
G |
A |
11: 77,399,552 (GRCm39) |
T259I |
probably damaging |
Het |
Tubgcp4 |
T |
A |
2: 121,015,251 (GRCm39) |
F320I |
possibly damaging |
Het |
Tut7 |
A |
T |
13: 59,936,443 (GRCm39) |
C817* |
probably null |
Het |
Vmn1r21 |
A |
C |
6: 57,821,079 (GRCm39) |
Y122D |
probably benign |
Het |
Vmn1r75 |
T |
A |
7: 11,614,407 (GRCm39) |
D46E |
probably damaging |
Het |
Vmn2r120 |
A |
T |
17: 57,852,290 (GRCm39) |
L9M |
possibly damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,696,247 (GRCm39) |
I165T |
possibly damaging |
Het |
Vmn2r76 |
A |
T |
7: 85,875,286 (GRCm39) |
Y564N |
probably damaging |
Het |
Wee1 |
G |
T |
7: 109,725,257 (GRCm39) |
E300* |
probably null |
Het |
Xdh |
T |
C |
17: 74,200,617 (GRCm39) |
D1168G |
probably damaging |
Het |
Zfp54 |
A |
G |
17: 21,653,706 (GRCm39) |
T67A |
probably damaging |
Het |
Zfp941 |
G |
T |
7: 140,392,679 (GRCm39) |
H227N |
probably benign |
Het |
Zpr1 |
T |
A |
9: 46,192,373 (GRCm39) |
V399D |
possibly damaging |
Het |
Zzz3 |
A |
G |
3: 152,161,461 (GRCm39) |
E285G |
probably damaging |
Het |
|
Other mutations in Herc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Herc1
|
APN |
9 |
66,391,248 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00159:Herc1
|
APN |
9 |
66,344,964 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00486:Herc1
|
APN |
9 |
66,383,402 (GRCm39) |
missense |
probably benign |
|
IGL00717:Herc1
|
APN |
9 |
66,392,284 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00766:Herc1
|
APN |
9 |
66,358,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00776:Herc1
|
APN |
9 |
66,328,320 (GRCm39) |
missense |
probably benign |
|
IGL00987:Herc1
|
APN |
9 |
66,315,334 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01090:Herc1
|
APN |
9 |
66,376,457 (GRCm39) |
nonsense |
probably null |
|
IGL01098:Herc1
|
APN |
9 |
66,369,204 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01106:Herc1
|
APN |
9 |
66,383,720 (GRCm39) |
splice site |
probably benign |
|
IGL01120:Herc1
|
APN |
9 |
66,336,162 (GRCm39) |
missense |
probably benign |
|
IGL01359:Herc1
|
APN |
9 |
66,346,550 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01360:Herc1
|
APN |
9 |
66,390,981 (GRCm39) |
missense |
probably benign |
|
IGL01364:Herc1
|
APN |
9 |
66,306,643 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01470:Herc1
|
APN |
9 |
66,404,918 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01670:Herc1
|
APN |
9 |
66,394,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01825:Herc1
|
APN |
9 |
66,307,089 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01903:Herc1
|
APN |
9 |
66,294,154 (GRCm39) |
nonsense |
probably null |
|
IGL01988:Herc1
|
APN |
9 |
66,395,357 (GRCm39) |
splice site |
probably benign |
|
IGL02074:Herc1
|
APN |
9 |
66,358,265 (GRCm39) |
missense |
probably benign |
|
IGL02089:Herc1
|
APN |
9 |
66,388,151 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02177:Herc1
|
APN |
9 |
66,341,793 (GRCm39) |
missense |
probably benign |
|
IGL02300:Herc1
|
APN |
9 |
66,383,645 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02304:Herc1
|
APN |
9 |
66,383,696 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02369:Herc1
|
APN |
9 |
66,399,293 (GRCm39) |
nonsense |
probably null |
|
IGL02445:Herc1
|
APN |
9 |
66,340,764 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02447:Herc1
|
APN |
9 |
66,404,610 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02549:Herc1
|
APN |
9 |
66,307,183 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02571:Herc1
|
APN |
9 |
66,341,887 (GRCm39) |
splice site |
probably benign |
|
IGL02709:Herc1
|
APN |
9 |
66,404,962 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02717:Herc1
|
APN |
9 |
66,279,203 (GRCm39) |
nonsense |
probably null |
|
IGL02726:Herc1
|
APN |
9 |
66,349,270 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02733:Herc1
|
APN |
9 |
66,358,274 (GRCm39) |
missense |
probably benign |
|
IGL02963:Herc1
|
APN |
9 |
66,296,105 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03101:Herc1
|
APN |
9 |
66,395,279 (GRCm39) |
missense |
probably benign |
|
IGL03193:Herc1
|
APN |
9 |
66,309,962 (GRCm39) |
missense |
probably benign |
|
IGL03203:Herc1
|
APN |
9 |
66,296,182 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03216:Herc1
|
APN |
9 |
66,386,228 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03282:Herc1
|
APN |
9 |
66,358,741 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03295:Herc1
|
APN |
9 |
66,303,985 (GRCm39) |
missense |
possibly damaging |
0.56 |
cradle
|
UTSW |
9 |
66,391,148 (GRCm39) |
splice site |
probably null |
|
miracles
|
UTSW |
9 |
66,370,119 (GRCm39) |
nonsense |
probably null |
|
newton
|
UTSW |
9 |
66,375,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R0907_Herc1_362
|
UTSW |
9 |
66,340,710 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4427_Herc1_231
|
UTSW |
9 |
66,403,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R5026_Herc1_363
|
UTSW |
9 |
66,393,408 (GRCm39) |
missense |
probably benign |
0.03 |
stables
|
UTSW |
9 |
66,386,735 (GRCm39) |
missense |
probably benign |
0.13 |
strangle
|
UTSW |
9 |
66,408,470 (GRCm39) |
frame shift |
probably null |
|
IGL03134:Herc1
|
UTSW |
9 |
66,341,345 (GRCm39) |
critical splice acceptor site |
probably benign |
|
PIT4243001:Herc1
|
UTSW |
9 |
66,279,489 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4486001:Herc1
|
UTSW |
9 |
66,279,671 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4696001:Herc1
|
UTSW |
9 |
66,386,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Herc1
|
UTSW |
9 |
66,355,457 (GRCm39) |
missense |
probably benign |
0.04 |
R0044:Herc1
|
UTSW |
9 |
66,355,457 (GRCm39) |
missense |
probably benign |
0.04 |
R0052:Herc1
|
UTSW |
9 |
66,307,438 (GRCm39) |
missense |
probably damaging |
0.99 |
R0114:Herc1
|
UTSW |
9 |
66,369,128 (GRCm39) |
missense |
probably damaging |
0.99 |
R0129:Herc1
|
UTSW |
9 |
66,355,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Herc1
|
UTSW |
9 |
66,388,192 (GRCm39) |
missense |
probably benign |
0.00 |
R0131:Herc1
|
UTSW |
9 |
66,388,192 (GRCm39) |
missense |
probably benign |
0.00 |
R0132:Herc1
|
UTSW |
9 |
66,388,192 (GRCm39) |
missense |
probably benign |
0.00 |
R0158:Herc1
|
UTSW |
9 |
66,403,203 (GRCm39) |
nonsense |
probably null |
|
R0333:Herc1
|
UTSW |
9 |
66,371,981 (GRCm39) |
splice site |
probably null |
|
R0384:Herc1
|
UTSW |
9 |
66,388,332 (GRCm39) |
splice site |
probably benign |
|
R0419:Herc1
|
UTSW |
9 |
66,353,356 (GRCm39) |
splice site |
probably benign |
|
R0453:Herc1
|
UTSW |
9 |
66,307,054 (GRCm39) |
missense |
probably benign |
0.20 |
R0458:Herc1
|
UTSW |
9 |
66,383,663 (GRCm39) |
missense |
probably benign |
0.12 |
R0490:Herc1
|
UTSW |
9 |
66,392,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Herc1
|
UTSW |
9 |
66,355,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R0513:Herc1
|
UTSW |
9 |
66,352,927 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0628:Herc1
|
UTSW |
9 |
66,358,163 (GRCm39) |
missense |
probably benign |
0.35 |
R0666:Herc1
|
UTSW |
9 |
66,392,170 (GRCm39) |
splice site |
probably benign |
|
R0674:Herc1
|
UTSW |
9 |
66,408,474 (GRCm39) |
missense |
probably damaging |
0.99 |
R0682:Herc1
|
UTSW |
9 |
66,389,263 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0690:Herc1
|
UTSW |
9 |
66,294,120 (GRCm39) |
nonsense |
probably null |
|
R0701:Herc1
|
UTSW |
9 |
66,395,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Herc1
|
UTSW |
9 |
66,412,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R0850:Herc1
|
UTSW |
9 |
66,373,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R0907:Herc1
|
UTSW |
9 |
66,340,710 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0972:Herc1
|
UTSW |
9 |
66,279,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R0976:Herc1
|
UTSW |
9 |
66,347,160 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1027:Herc1
|
UTSW |
9 |
66,363,250 (GRCm39) |
missense |
probably benign |
|
R1200:Herc1
|
UTSW |
9 |
66,393,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R1226:Herc1
|
UTSW |
9 |
66,323,545 (GRCm39) |
missense |
probably benign |
0.00 |
R1364:Herc1
|
UTSW |
9 |
66,307,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R1395:Herc1
|
UTSW |
9 |
66,346,463 (GRCm39) |
missense |
probably benign |
0.13 |
R1432:Herc1
|
UTSW |
9 |
66,372,751 (GRCm39) |
missense |
probably benign |
0.13 |
R1440:Herc1
|
UTSW |
9 |
66,375,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R1476:Herc1
|
UTSW |
9 |
66,415,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R1590:Herc1
|
UTSW |
9 |
66,399,235 (GRCm39) |
splice site |
probably benign |
|
R1634:Herc1
|
UTSW |
9 |
66,380,820 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1700:Herc1
|
UTSW |
9 |
66,357,960 (GRCm39) |
splice site |
probably null |
|
R1753:Herc1
|
UTSW |
9 |
66,409,366 (GRCm39) |
critical splice donor site |
probably null |
|
R1753:Herc1
|
UTSW |
9 |
66,376,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R1796:Herc1
|
UTSW |
9 |
66,296,138 (GRCm39) |
nonsense |
probably null |
|
R1830:Herc1
|
UTSW |
9 |
66,404,881 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1855:Herc1
|
UTSW |
9 |
66,298,708 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1866:Herc1
|
UTSW |
9 |
66,358,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R1894:Herc1
|
UTSW |
9 |
66,386,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R1918:Herc1
|
UTSW |
9 |
66,383,408 (GRCm39) |
splice site |
probably null |
|
R1999:Herc1
|
UTSW |
9 |
66,393,360 (GRCm39) |
missense |
probably benign |
0.07 |
R2034:Herc1
|
UTSW |
9 |
66,349,254 (GRCm39) |
missense |
probably benign |
0.01 |
R2138:Herc1
|
UTSW |
9 |
66,377,589 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2186:Herc1
|
UTSW |
9 |
66,347,183 (GRCm39) |
missense |
probably benign |
0.45 |
R2192:Herc1
|
UTSW |
9 |
66,372,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R2312:Herc1
|
UTSW |
9 |
66,415,563 (GRCm39) |
nonsense |
probably null |
|
R2338:Herc1
|
UTSW |
9 |
66,336,251 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3035:Herc1
|
UTSW |
9 |
66,391,217 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3732:Herc1
|
UTSW |
9 |
66,352,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Herc1
|
UTSW |
9 |
66,352,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R3733:Herc1
|
UTSW |
9 |
66,352,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R3917:Herc1
|
UTSW |
9 |
66,341,748 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3953:Herc1
|
UTSW |
9 |
66,341,075 (GRCm39) |
nonsense |
probably null |
|
R4073:Herc1
|
UTSW |
9 |
66,325,774 (GRCm39) |
missense |
probably benign |
0.12 |
R4075:Herc1
|
UTSW |
9 |
66,325,774 (GRCm39) |
missense |
probably benign |
0.12 |
R4241:Herc1
|
UTSW |
9 |
66,355,630 (GRCm39) |
frame shift |
probably null |
|
R4260:Herc1
|
UTSW |
9 |
66,355,630 (GRCm39) |
frame shift |
probably null |
|
R4261:Herc1
|
UTSW |
9 |
66,355,630 (GRCm39) |
frame shift |
probably null |
|
R4300:Herc1
|
UTSW |
9 |
66,396,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R4398:Herc1
|
UTSW |
9 |
66,386,735 (GRCm39) |
missense |
probably benign |
0.13 |
R4426:Herc1
|
UTSW |
9 |
66,403,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4427:Herc1
|
UTSW |
9 |
66,403,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Herc1
|
UTSW |
9 |
66,344,946 (GRCm39) |
missense |
probably damaging |
0.97 |
R4630:Herc1
|
UTSW |
9 |
66,340,996 (GRCm39) |
splice site |
probably null |
|
R4656:Herc1
|
UTSW |
9 |
66,301,993 (GRCm39) |
missense |
probably damaging |
0.97 |
R4658:Herc1
|
UTSW |
9 |
66,386,773 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4663:Herc1
|
UTSW |
9 |
66,340,660 (GRCm39) |
missense |
probably damaging |
0.98 |
R4675:Herc1
|
UTSW |
9 |
66,298,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Herc1
|
UTSW |
9 |
66,323,551 (GRCm39) |
missense |
probably benign |
0.00 |
R4754:Herc1
|
UTSW |
9 |
66,408,488 (GRCm39) |
missense |
probably benign |
0.00 |
R4766:Herc1
|
UTSW |
9 |
66,349,211 (GRCm39) |
missense |
probably benign |
0.00 |
R4792:Herc1
|
UTSW |
9 |
66,403,266 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4828:Herc1
|
UTSW |
9 |
66,404,625 (GRCm39) |
splice site |
probably null |
|
R4832:Herc1
|
UTSW |
9 |
66,403,253 (GRCm39) |
missense |
probably benign |
0.11 |
R4879:Herc1
|
UTSW |
9 |
66,370,119 (GRCm39) |
nonsense |
probably null |
|
R4948:Herc1
|
UTSW |
9 |
66,392,184 (GRCm39) |
missense |
probably benign |
|
R5021:Herc1
|
UTSW |
9 |
66,377,608 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5022:Herc1
|
UTSW |
9 |
66,377,608 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5023:Herc1
|
UTSW |
9 |
66,377,608 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5024:Herc1
|
UTSW |
9 |
66,377,608 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5025:Herc1
|
UTSW |
9 |
66,377,608 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5026:Herc1
|
UTSW |
9 |
66,393,408 (GRCm39) |
missense |
probably benign |
0.03 |
R5027:Herc1
|
UTSW |
9 |
66,380,811 (GRCm39) |
missense |
probably benign |
0.01 |
R5027:Herc1
|
UTSW |
9 |
66,411,900 (GRCm39) |
missense |
probably damaging |
0.98 |
R5038:Herc1
|
UTSW |
9 |
66,383,742 (GRCm39) |
intron |
probably benign |
|
R5041:Herc1
|
UTSW |
9 |
66,336,327 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5053:Herc1
|
UTSW |
9 |
66,377,608 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5137:Herc1
|
UTSW |
9 |
66,355,505 (GRCm39) |
missense |
probably benign |
|
R5197:Herc1
|
UTSW |
9 |
66,355,786 (GRCm39) |
missense |
probably damaging |
0.99 |
R5207:Herc1
|
UTSW |
9 |
66,307,151 (GRCm39) |
nonsense |
probably null |
|
R5247:Herc1
|
UTSW |
9 |
66,341,833 (GRCm39) |
missense |
probably benign |
0.01 |
R5267:Herc1
|
UTSW |
9 |
66,369,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R5274:Herc1
|
UTSW |
9 |
66,306,691 (GRCm39) |
missense |
probably benign |
|
R5375:Herc1
|
UTSW |
9 |
66,375,169 (GRCm39) |
missense |
probably damaging |
0.99 |
R5401:Herc1
|
UTSW |
9 |
66,409,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Herc1
|
UTSW |
9 |
66,358,401 (GRCm39) |
missense |
probably benign |
0.02 |
R5577:Herc1
|
UTSW |
9 |
66,389,263 (GRCm39) |
missense |
probably damaging |
0.99 |
R5596:Herc1
|
UTSW |
9 |
66,341,345 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R5665:Herc1
|
UTSW |
9 |
66,372,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R5744:Herc1
|
UTSW |
9 |
66,415,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R5802:Herc1
|
UTSW |
9 |
66,370,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R5822:Herc1
|
UTSW |
9 |
66,352,894 (GRCm39) |
missense |
probably benign |
0.00 |
R5954:Herc1
|
UTSW |
9 |
66,358,774 (GRCm39) |
splice site |
probably benign |
|
R5977:Herc1
|
UTSW |
9 |
66,340,604 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6022:Herc1
|
UTSW |
9 |
66,390,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R6043:Herc1
|
UTSW |
9 |
66,315,436 (GRCm39) |
missense |
probably benign |
|
R6046:Herc1
|
UTSW |
9 |
66,352,831 (GRCm39) |
missense |
probably damaging |
0.99 |
R6089:Herc1
|
UTSW |
9 |
66,352,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R6123:Herc1
|
UTSW |
9 |
66,404,532 (GRCm39) |
missense |
probably damaging |
0.97 |
R6155:Herc1
|
UTSW |
9 |
66,340,705 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6190:Herc1
|
UTSW |
9 |
66,283,663 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6220:Herc1
|
UTSW |
9 |
66,341,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Herc1
|
UTSW |
9 |
66,279,298 (GRCm39) |
missense |
probably benign |
0.05 |
R6348:Herc1
|
UTSW |
9 |
66,395,258 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6362:Herc1
|
UTSW |
9 |
66,379,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R6394:Herc1
|
UTSW |
9 |
66,302,341 (GRCm39) |
missense |
probably damaging |
0.99 |
R6434:Herc1
|
UTSW |
9 |
66,393,464 (GRCm39) |
missense |
probably damaging |
0.99 |
R6483:Herc1
|
UTSW |
9 |
66,355,811 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6607:Herc1
|
UTSW |
9 |
66,325,849 (GRCm39) |
missense |
probably benign |
0.02 |
R6633:Herc1
|
UTSW |
9 |
66,346,534 (GRCm39) |
nonsense |
probably null |
|
R6634:Herc1
|
UTSW |
9 |
66,345,026 (GRCm39) |
missense |
probably benign |
|
R6693:Herc1
|
UTSW |
9 |
66,386,258 (GRCm39) |
missense |
probably damaging |
0.99 |
R6695:Herc1
|
UTSW |
9 |
66,391,148 (GRCm39) |
splice site |
probably null |
|
R6748:Herc1
|
UTSW |
9 |
66,408,470 (GRCm39) |
frame shift |
probably null |
|
R6750:Herc1
|
UTSW |
9 |
66,408,470 (GRCm39) |
frame shift |
probably null |
|
R6751:Herc1
|
UTSW |
9 |
66,408,470 (GRCm39) |
frame shift |
probably null |
|
R6774:Herc1
|
UTSW |
9 |
66,408,470 (GRCm39) |
frame shift |
probably null |
|
R6785:Herc1
|
UTSW |
9 |
66,408,470 (GRCm39) |
frame shift |
probably null |
|
R6786:Herc1
|
UTSW |
9 |
66,408,470 (GRCm39) |
frame shift |
probably null |
|
R6856:Herc1
|
UTSW |
9 |
66,305,180 (GRCm39) |
missense |
probably benign |
0.05 |
R6966:Herc1
|
UTSW |
9 |
66,318,347 (GRCm39) |
missense |
probably benign |
0.07 |
R7020:Herc1
|
UTSW |
9 |
66,393,360 (GRCm39) |
missense |
probably benign |
0.07 |
R7109:Herc1
|
UTSW |
9 |
66,389,171 (GRCm39) |
missense |
probably benign |
0.03 |
R7122:Herc1
|
UTSW |
9 |
66,307,056 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7209:Herc1
|
UTSW |
9 |
66,292,314 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7222:Herc1
|
UTSW |
9 |
66,374,781 (GRCm39) |
missense |
probably damaging |
0.98 |
R7303:Herc1
|
UTSW |
9 |
66,358,098 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7305:Herc1
|
UTSW |
9 |
66,369,150 (GRCm39) |
missense |
|
|
R7438:Herc1
|
UTSW |
9 |
66,302,038 (GRCm39) |
missense |
probably benign |
0.00 |
R7535:Herc1
|
UTSW |
9 |
66,382,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R7585:Herc1
|
UTSW |
9 |
66,352,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R7603:Herc1
|
UTSW |
9 |
66,358,665 (GRCm39) |
nonsense |
probably null |
|
R7670:Herc1
|
UTSW |
9 |
66,323,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R7705:Herc1
|
UTSW |
9 |
66,347,116 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7723:Herc1
|
UTSW |
9 |
66,279,158 (GRCm39) |
missense |
probably benign |
0.24 |
R7730:Herc1
|
UTSW |
9 |
66,400,472 (GRCm39) |
small deletion |
probably benign |
|
R7880:Herc1
|
UTSW |
9 |
66,415,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R7958:Herc1
|
UTSW |
9 |
66,393,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R7976:Herc1
|
UTSW |
9 |
66,341,552 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8006:Herc1
|
UTSW |
9 |
66,352,842 (GRCm39) |
nonsense |
probably null |
|
R8084:Herc1
|
UTSW |
9 |
66,383,217 (GRCm39) |
missense |
probably benign |
0.45 |
R8094:Herc1
|
UTSW |
9 |
66,400,462 (GRCm39) |
missense |
probably damaging |
0.98 |
R8099:Herc1
|
UTSW |
9 |
66,279,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R8151:Herc1
|
UTSW |
9 |
66,341,073 (GRCm39) |
missense |
probably damaging |
0.98 |
R8159:Herc1
|
UTSW |
9 |
66,369,003 (GRCm39) |
missense |
probably null |
|
R8190:Herc1
|
UTSW |
9 |
66,325,733 (GRCm39) |
missense |
probably benign |
0.00 |
R8213:Herc1
|
UTSW |
9 |
66,358,170 (GRCm39) |
missense |
probably damaging |
0.99 |
R8230:Herc1
|
UTSW |
9 |
66,377,598 (GRCm39) |
missense |
probably damaging |
0.99 |
R8265:Herc1
|
UTSW |
9 |
66,293,986 (GRCm39) |
nonsense |
probably null |
|
R8270:Herc1
|
UTSW |
9 |
66,395,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Herc1
|
UTSW |
9 |
66,415,571 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8423:Herc1
|
UTSW |
9 |
66,415,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R8506:Herc1
|
UTSW |
9 |
66,380,863 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8523:Herc1
|
UTSW |
9 |
66,358,224 (GRCm39) |
missense |
probably benign |
|
R8530:Herc1
|
UTSW |
9 |
66,325,910 (GRCm39) |
missense |
probably benign |
|
R8545:Herc1
|
UTSW |
9 |
66,279,257 (GRCm39) |
nonsense |
probably null |
|
R8682:Herc1
|
UTSW |
9 |
66,370,130 (GRCm39) |
missense |
|
|
R8720:Herc1
|
UTSW |
9 |
66,389,105 (GRCm39) |
missense |
probably benign |
0.38 |
R8792:Herc1
|
UTSW |
9 |
66,372,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8915:Herc1
|
UTSW |
9 |
66,318,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R8964:Herc1
|
UTSW |
9 |
66,352,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R9056:Herc1
|
UTSW |
9 |
66,380,782 (GRCm39) |
missense |
probably benign |
0.10 |
R9158:Herc1
|
UTSW |
9 |
66,376,400 (GRCm39) |
missense |
probably benign |
0.00 |
R9167:Herc1
|
UTSW |
9 |
66,411,900 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9192:Herc1
|
UTSW |
9 |
66,321,413 (GRCm39) |
missense |
probably benign |
0.35 |
R9252:Herc1
|
UTSW |
9 |
66,309,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R9260:Herc1
|
UTSW |
9 |
66,325,691 (GRCm39) |
nonsense |
probably null |
|
R9261:Herc1
|
UTSW |
9 |
66,412,129 (GRCm39) |
missense |
probably damaging |
0.98 |
R9430:Herc1
|
UTSW |
9 |
66,325,785 (GRCm39) |
nonsense |
probably null |
|
R9519:Herc1
|
UTSW |
9 |
66,307,356 (GRCm39) |
missense |
probably damaging |
0.97 |
R9563:Herc1
|
UTSW |
9 |
66,294,193 (GRCm39) |
critical splice donor site |
probably null |
|
R9589:Herc1
|
UTSW |
9 |
66,372,840 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9600:Herc1
|
UTSW |
9 |
66,304,594 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9659:Herc1
|
UTSW |
9 |
66,307,185 (GRCm39) |
missense |
probably benign |
0.03 |
R9740:Herc1
|
UTSW |
9 |
66,355,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R9774:Herc1
|
UTSW |
9 |
66,372,032 (GRCm39) |
missense |
probably null |
|
R9781:Herc1
|
UTSW |
9 |
66,280,004 (GRCm39) |
missense |
probably benign |
|
R9788:Herc1
|
UTSW |
9 |
66,307,185 (GRCm39) |
missense |
probably benign |
0.03 |
RF023:Herc1
|
UTSW |
9 |
66,365,616 (GRCm39) |
missense |
|
|
X0011:Herc1
|
UTSW |
9 |
66,307,441 (GRCm39) |
missense |
probably benign |
0.28 |
X0067:Herc1
|
UTSW |
9 |
66,355,806 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Herc1
|
UTSW |
9 |
66,341,858 (GRCm39) |
missense |
probably benign |
|
Z1177:Herc1
|
UTSW |
9 |
66,379,193 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Herc1
|
UTSW |
9 |
66,365,707 (GRCm39) |
missense |
probably null |
|
|