Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap6 |
T |
A |
12: 52,958,591 (GRCm39) |
V782E |
probably damaging |
Het |
Atg9a |
A |
G |
1: 75,161,734 (GRCm39) |
L604P |
probably damaging |
Het |
Atp1a3 |
T |
C |
7: 24,689,974 (GRCm39) |
I482V |
probably benign |
Het |
Bltp2 |
T |
G |
11: 78,178,813 (GRCm39) |
M2026R |
probably damaging |
Het |
Bltp2 |
T |
A |
11: 78,168,038 (GRCm39) |
L1491* |
probably null |
Het |
Ccdc18 |
T |
G |
5: 108,311,530 (GRCm39) |
V412G |
probably benign |
Het |
Ccn6 |
T |
C |
10: 39,027,285 (GRCm39) |
R316G |
probably benign |
Het |
Cct6a |
A |
G |
5: 129,871,449 (GRCm39) |
|
noncoding transcript |
Het |
Clpx |
A |
G |
9: 65,217,507 (GRCm39) |
N25S |
probably damaging |
Het |
Cnpy2 |
T |
A |
10: 128,162,894 (GRCm39) |
C171* |
probably null |
Het |
Cntnap3 |
C |
T |
13: 64,905,211 (GRCm39) |
D857N |
probably damaging |
Het |
Col5a1 |
A |
G |
2: 27,922,697 (GRCm39) |
Y255C |
probably damaging |
Het |
Coro7 |
A |
T |
16: 4,449,775 (GRCm39) |
F638Y |
possibly damaging |
Het |
Cpd |
A |
G |
11: 76,673,153 (GRCm39) |
F1331L |
probably damaging |
Het |
Csmd1 |
A |
T |
8: 16,119,063 (GRCm39) |
I1842N |
possibly damaging |
Het |
Dgkg |
T |
A |
16: 22,381,480 (GRCm39) |
D490V |
probably damaging |
Het |
Dnah9 |
A |
T |
11: 65,976,284 (GRCm39) |
M1255K |
probably benign |
Het |
E2f1 |
A |
G |
2: 154,402,849 (GRCm39) |
V306A |
probably benign |
Het |
Entpd1 |
A |
G |
19: 40,648,350 (GRCm39) |
|
probably benign |
Het |
Esrrb |
T |
A |
12: 86,552,676 (GRCm39) |
I222N |
probably benign |
Het |
Flt4 |
G |
T |
11: 49,516,274 (GRCm39) |
A126S |
possibly damaging |
Het |
Galnt11 |
C |
T |
5: 25,457,145 (GRCm39) |
T237I |
possibly damaging |
Het |
Galnt2l |
A |
T |
8: 122,997,727 (GRCm39) |
|
probably benign |
Het |
Gbf1 |
A |
G |
19: 46,250,983 (GRCm39) |
|
probably benign |
Het |
H2-T9 |
T |
C |
17: 36,438,726 (GRCm39) |
T222A |
possibly damaging |
Het |
Hsph1 |
T |
C |
5: 149,554,967 (GRCm39) |
Y105C |
probably damaging |
Het |
Il23r |
T |
C |
6: 67,411,664 (GRCm39) |
T358A |
probably benign |
Het |
Il2ra |
C |
T |
2: 11,647,884 (GRCm39) |
|
probably benign |
Het |
Kbtbd4 |
G |
T |
2: 90,744,459 (GRCm39) |
|
probably benign |
Het |
Kcnt1 |
A |
G |
2: 25,781,255 (GRCm39) |
|
probably benign |
Het |
Kng2 |
A |
G |
16: 22,815,872 (GRCm39) |
|
probably benign |
Het |
Lap3 |
C |
T |
5: 45,669,270 (GRCm39) |
T473I |
possibly damaging |
Het |
Lrrk2 |
T |
C |
15: 91,641,273 (GRCm39) |
|
probably null |
Het |
Map1s |
A |
G |
8: 71,366,696 (GRCm39) |
N534D |
possibly damaging |
Het |
Mtg1 |
G |
A |
7: 139,724,257 (GRCm39) |
V122I |
probably benign |
Het |
Myadm |
T |
A |
7: 3,345,865 (GRCm39) |
I209K |
probably damaging |
Het |
Ntsr2 |
G |
A |
12: 16,703,981 (GRCm39) |
V75I |
probably benign |
Het |
Or4b1b |
A |
T |
2: 90,112,212 (GRCm39) |
S236T |
probably damaging |
Het |
Or8u10 |
G |
A |
2: 85,915,557 (GRCm39) |
A188V |
probably benign |
Het |
Pfn1 |
T |
C |
11: 70,545,192 (GRCm39) |
T39A |
probably benign |
Het |
Pipox |
T |
A |
11: 77,774,651 (GRCm39) |
K144M |
probably benign |
Het |
Plekhh1 |
G |
A |
12: 79,115,889 (GRCm39) |
E811K |
probably damaging |
Het |
Pnpla3 |
T |
A |
15: 84,063,506 (GRCm39) |
W295R |
probably benign |
Het |
Prkacb |
T |
A |
3: 146,457,273 (GRCm39) |
T136S |
probably damaging |
Het |
Ralbp1 |
T |
A |
17: 66,161,124 (GRCm39) |
N473I |
probably benign |
Het |
Rbp4 |
G |
A |
19: 38,106,908 (GRCm39) |
T127M |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rps3a1 |
G |
A |
3: 86,045,424 (GRCm39) |
|
probably benign |
Het |
Scg3 |
G |
T |
9: 75,551,222 (GRCm39) |
Y429* |
probably null |
Het |
Shisal2b |
G |
T |
13: 104,994,862 (GRCm39) |
T95K |
possibly damaging |
Het |
Spag5 |
T |
C |
11: 78,204,222 (GRCm39) |
S492P |
probably damaging |
Het |
St7 |
T |
A |
6: 17,934,238 (GRCm39) |
M540K |
probably damaging |
Het |
Stxbp3 |
C |
A |
3: 108,712,618 (GRCm39) |
V281F |
possibly damaging |
Het |
Sun5 |
A |
G |
2: 153,700,968 (GRCm39) |
V242A |
possibly damaging |
Het |
Susd5 |
G |
T |
9: 113,924,852 (GRCm39) |
R245L |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 75,969,787 (GRCm39) |
E954G |
probably damaging |
Het |
Synpo2 |
A |
T |
3: 122,907,708 (GRCm39) |
V536E |
probably damaging |
Het |
Tas2r140 |
T |
C |
6: 133,032,405 (GRCm39) |
I118V |
probably benign |
Het |
Tbx18 |
C |
A |
9: 87,606,462 (GRCm39) |
V228L |
probably benign |
Het |
Tdrd9 |
T |
A |
12: 111,974,014 (GRCm39) |
|
probably benign |
Het |
Tektl1 |
C |
A |
10: 78,586,381 (GRCm39) |
L223F |
probably benign |
Het |
Tg |
T |
C |
15: 66,609,370 (GRCm39) |
M310T |
probably benign |
Het |
Ticam2 |
T |
A |
18: 46,693,718 (GRCm39) |
D123V |
probably damaging |
Het |
Timm23 |
A |
G |
14: 31,920,993 (GRCm39) |
|
probably benign |
Het |
Tinag |
C |
T |
9: 76,912,969 (GRCm39) |
R280H |
probably benign |
Het |
Topbp1 |
G |
A |
9: 103,186,011 (GRCm39) |
R51K |
probably benign |
Het |
Tor1b |
A |
G |
2: 30,843,925 (GRCm39) |
I121V |
probably damaging |
Het |
Tpmt |
C |
A |
13: 47,185,930 (GRCm39) |
G148V |
probably damaging |
Het |
Tubb1 |
A |
G |
2: 174,299,548 (GRCm39) |
E410G |
probably damaging |
Het |
Ubash3b |
C |
A |
9: 40,958,360 (GRCm39) |
V7L |
possibly damaging |
Het |
Ube2o |
C |
T |
11: 116,433,661 (GRCm39) |
E686K |
probably damaging |
Het |
Unc13d |
T |
A |
11: 115,960,318 (GRCm39) |
|
probably benign |
Het |
Vmn1r183 |
A |
T |
7: 23,754,601 (GRCm39) |
M135L |
probably benign |
Het |
Xkr8 |
T |
C |
4: 132,459,649 (GRCm39) |
Y43C |
probably damaging |
Het |
Zc3h4 |
T |
A |
7: 16,168,697 (GRCm39) |
N935K |
unknown |
Het |
Zc3h7a |
G |
A |
16: 10,974,167 (GRCm39) |
|
probably benign |
Het |
Zfp84 |
C |
T |
7: 29,476,276 (GRCm39) |
H323Y |
probably damaging |
Het |
Zfp873 |
G |
T |
10: 81,896,595 (GRCm39) |
S442I |
possibly damaging |
Het |
Zfp938 |
A |
G |
10: 82,061,606 (GRCm39) |
L338P |
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 |
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 |
R5566:Herc1
|
UTSW |
9 |
66,372,819 (GRCm39) |
missense |
possibly damaging |
0.95 |
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 |
|
|