Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26a |
T |
A |
8: 44,023,190 (GRCm39) |
H100L |
probably benign |
Het |
Adgrf2 |
T |
C |
17: 43,022,263 (GRCm39) |
N187S |
probably damaging |
Het |
Adipoq |
T |
A |
16: 22,976,332 (GRCm39) |
H244Q |
probably damaging |
Het |
Arhgap40 |
T |
A |
2: 158,373,845 (GRCm39) |
S209T |
probably benign |
Het |
Arrdc3 |
C |
T |
13: 81,037,212 (GRCm39) |
L123F |
probably damaging |
Het |
Aspscr1 |
A |
G |
11: 120,579,865 (GRCm39) |
N212D |
probably benign |
Het |
Ccr9 |
A |
T |
9: 123,608,371 (GRCm39) |
S18C |
probably damaging |
Het |
Cdc42bpa |
T |
A |
1: 179,892,646 (GRCm39) |
V270D |
probably damaging |
Het |
Clic4 |
A |
G |
4: 134,944,516 (GRCm39) |
Y220H |
probably damaging |
Het |
Cntln |
A |
C |
4: 84,897,577 (GRCm39) |
H388P |
possibly damaging |
Het |
Col12a1 |
A |
G |
9: 79,538,925 (GRCm39) |
V2457A |
probably damaging |
Het |
Ctsk |
A |
G |
3: 95,408,925 (GRCm39) |
N103D |
probably benign |
Het |
Ddx60 |
T |
C |
8: 62,428,826 (GRCm39) |
S779P |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,246,378 (GRCm39) |
|
probably null |
Het |
Dnah7b |
T |
A |
1: 46,148,462 (GRCm39) |
D279E |
probably benign |
Het |
Eif1ad10 |
T |
C |
12: 88,216,524 (GRCm39) |
N116S |
probably benign |
Het |
Fam117a |
A |
G |
11: 95,269,660 (GRCm39) |
N308S |
probably benign |
Het |
Fasn |
A |
G |
11: 120,704,245 (GRCm39) |
V1419A |
probably damaging |
Het |
Fhad1 |
A |
G |
4: 141,678,802 (GRCm39) |
S625P |
probably benign |
Het |
Gemin5 |
A |
G |
11: 58,038,754 (GRCm39) |
V585A |
probably benign |
Het |
Gm5145 |
C |
A |
17: 20,790,646 (GRCm39) |
P8Q |
probably benign |
Het |
Herc6 |
T |
C |
6: 57,637,107 (GRCm39) |
I824T |
probably damaging |
Het |
Klrb1 |
C |
T |
6: 128,687,050 (GRCm39) |
V161I |
probably benign |
Het |
Krtap31-1 |
A |
G |
11: 99,799,258 (GRCm39) |
N154D |
not run |
Het |
Lcp1 |
A |
T |
14: 75,437,871 (GRCm39) |
I94F |
probably benign |
Het |
Lin7a |
A |
T |
10: 107,218,552 (GRCm39) |
Q154L |
possibly damaging |
Het |
Lnx1 |
T |
C |
5: 74,846,351 (GRCm39) |
Y33C |
probably damaging |
Het |
Myo5b |
T |
C |
18: 74,834,517 (GRCm39) |
V859A |
probably benign |
Het |
Ncbp1 |
A |
G |
4: 46,170,015 (GRCm39) |
Q696R |
probably damaging |
Het |
Neurl1b |
C |
G |
17: 26,657,720 (GRCm39) |
H219Q |
probably benign |
Het |
Nme8 |
T |
C |
13: 19,842,999 (GRCm39) |
E392G |
probably benign |
Het |
Nufip1 |
CAAAACAGAAAACAGAAAAC |
CAAAACAGAAAACAGAAAACAGAAAAC |
14: 76,349,414 (GRCm39) |
|
probably null |
Het |
Nuggc |
A |
G |
14: 65,850,975 (GRCm39) |
I298V |
probably damaging |
Het |
Nup155 |
A |
C |
15: 8,183,180 (GRCm39) |
K1247Q |
probably damaging |
Het |
Or1a1 |
A |
G |
11: 74,087,033 (GRCm39) |
K235E |
probably damaging |
Het |
Or5c1 |
A |
T |
2: 37,221,771 (GRCm39) |
E4V |
probably benign |
Het |
Otud4 |
T |
A |
8: 80,382,493 (GRCm39) |
|
probably null |
Het |
Pacc1 |
A |
G |
1: 191,073,065 (GRCm39) |
N162S |
probably benign |
Het |
Pcdhb18 |
T |
C |
18: 37,624,749 (GRCm39) |
V693A |
probably damaging |
Het |
Pcnx3 |
A |
G |
19: 5,727,210 (GRCm39) |
F1108L |
probably benign |
Het |
Prkca |
A |
T |
11: 107,905,170 (GRCm39) |
N189K |
probably damaging |
Het |
Rbm24 |
A |
G |
13: 46,582,683 (GRCm39) |
I201V |
probably benign |
Het |
Reep6 |
T |
C |
10: 80,169,627 (GRCm39) |
L105P |
probably damaging |
Het |
Retreg1 |
T |
C |
15: 25,941,126 (GRCm39) |
|
probably benign |
Het |
Rev3l |
C |
T |
10: 39,712,718 (GRCm39) |
T2382I |
probably benign |
Het |
Rnf31 |
A |
G |
14: 55,831,818 (GRCm39) |
N230S |
probably benign |
Het |
Rreb1 |
T |
C |
13: 38,115,548 (GRCm39) |
L969P |
probably benign |
Het |
Rsph4a |
T |
A |
10: 33,785,029 (GRCm39) |
N313K |
probably damaging |
Het |
Serpina3f |
T |
A |
12: 104,183,525 (GRCm39) |
L129Q |
probably damaging |
Het |
Slc9a2 |
T |
A |
1: 40,758,157 (GRCm39) |
V232D |
probably damaging |
Het |
Stmn2 |
T |
C |
3: 8,619,925 (GRCm39) |
L121P |
probably damaging |
Het |
Svep1 |
C |
T |
4: 58,097,424 (GRCm39) |
G1373D |
probably damaging |
Het |
Tex55 |
C |
T |
16: 38,648,453 (GRCm39) |
D219N |
possibly damaging |
Het |
Tns1 |
C |
A |
1: 73,991,636 (GRCm39) |
R1014L |
possibly damaging |
Het |
Top2b |
T |
C |
14: 16,416,620 (GRCm38) |
S1127P |
possibly damaging |
Het |
Txndc16 |
A |
T |
14: 45,373,324 (GRCm39) |
C768* |
probably null |
Het |
Ubl7 |
A |
T |
9: 57,837,052 (GRCm39) |
E354D |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,516,905 (GRCm39) |
L3205P |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,340,917 (GRCm39) |
T1053A |
possibly damaging |
Het |
Zbtb21 |
A |
G |
16: 97,753,077 (GRCm39) |
L402P |
probably damaging |
Het |
Zfp27 |
T |
A |
7: 29,594,221 (GRCm39) |
K581N |
possibly damaging |
Het |
Zfp62 |
A |
T |
11: 49,105,903 (GRCm39) |
|
probably benign |
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 |
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 |
|
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 |
|
|