Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl4 |
A |
G |
3: 151,205,755 (GRCm39) |
M156V |
probably benign |
Het |
Aire |
A |
T |
10: 77,866,089 (GRCm39) |
F546I |
probably damaging |
Het |
Ankk1 |
T |
C |
9: 49,331,320 (GRCm39) |
E230G |
probably benign |
Het |
Anp32a |
A |
T |
9: 62,279,397 (GRCm39) |
K86N |
possibly damaging |
Het |
Aqp4 |
T |
C |
18: 15,532,953 (GRCm39) |
I47V |
possibly damaging |
Het |
Arap3 |
A |
G |
18: 38,112,916 (GRCm39) |
V1098A |
possibly damaging |
Het |
Ascc3 |
T |
A |
10: 50,625,158 (GRCm39) |
W1652R |
probably damaging |
Het |
Atad2 |
T |
A |
15: 57,970,209 (GRCm39) |
H464L |
probably damaging |
Het |
Brca2 |
C |
A |
5: 150,463,673 (GRCm39) |
H1146N |
possibly damaging |
Het |
Capn9 |
G |
A |
8: 125,324,308 (GRCm39) |
V203M |
probably damaging |
Het |
Ccr6 |
T |
A |
17: 8,474,881 (GRCm39) |
S29T |
probably benign |
Het |
Cfap99 |
G |
T |
5: 34,467,561 (GRCm39) |
|
probably null |
Het |
Cpt1c |
C |
T |
7: 44,609,342 (GRCm39) |
G716S |
probably damaging |
Het |
Dhx29 |
A |
T |
13: 113,089,395 (GRCm39) |
Q722L |
probably benign |
Het |
Dmxl1 |
C |
T |
18: 49,985,355 (GRCm39) |
R201* |
probably null |
Het |
Dsg2 |
G |
A |
18: 20,734,859 (GRCm39) |
G946S |
probably damaging |
Het |
Erg |
C |
A |
16: 95,169,510 (GRCm39) |
|
probably null |
Het |
Fbxo32 |
G |
A |
15: 58,078,037 (GRCm39) |
|
probably benign |
Het |
Gask1b |
G |
T |
3: 79,793,448 (GRCm39) |
|
probably benign |
Het |
Glis1 |
T |
G |
4: 107,293,076 (GRCm39) |
D66E |
probably damaging |
Het |
Grm6 |
A |
T |
11: 50,750,652 (GRCm39) |
N605I |
probably damaging |
Het |
Gtf3c6 |
T |
C |
10: 40,125,668 (GRCm39) |
E183G |
probably benign |
Het |
Igkv12-41 |
A |
T |
6: 69,835,513 (GRCm39) |
S80T |
probably damaging |
Het |
Itprid2 |
C |
T |
2: 79,488,049 (GRCm39) |
R711C |
probably damaging |
Het |
Kcnt2 |
T |
C |
1: 140,523,742 (GRCm39) |
S1057P |
probably damaging |
Het |
Krt36 |
T |
G |
11: 99,994,216 (GRCm39) |
Q287P |
probably damaging |
Het |
Ldhd |
A |
G |
8: 112,356,906 (GRCm39) |
S13P |
probably benign |
Het |
Lmtk3 |
T |
A |
7: 45,443,721 (GRCm39) |
|
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,343,612 (GRCm39) |
F916I |
probably damaging |
Het |
Map4k1 |
A |
T |
7: 28,686,259 (GRCm39) |
I92F |
probably damaging |
Het |
Naa25 |
A |
T |
5: 121,576,867 (GRCm39) |
K872M |
probably damaging |
Het |
Nek3 |
C |
A |
8: 22,619,463 (GRCm39) |
G443V |
probably damaging |
Het |
Noxred1 |
T |
C |
12: 87,273,810 (GRCm39) |
E77G |
probably benign |
Het |
Nup210 |
G |
A |
6: 91,064,895 (GRCm39) |
Q202* |
probably null |
Het |
Or52d1 |
A |
T |
7: 103,755,998 (GRCm39) |
M171L |
probably benign |
Het |
Or8k27 |
G |
T |
2: 86,276,251 (GRCm39) |
S25Y |
probably benign |
Het |
Pax3 |
A |
G |
1: 78,109,056 (GRCm39) |
S201P |
probably damaging |
Het |
Pcdhgb5 |
T |
A |
18: 37,866,457 (GRCm39) |
Y751N |
probably benign |
Het |
Pign |
A |
T |
1: 105,481,620 (GRCm39) |
L792* |
probably null |
Het |
Pkd1 |
T |
C |
17: 24,792,467 (GRCm39) |
F1385L |
probably benign |
Het |
Plxnb2 |
A |
C |
15: 89,048,523 (GRCm39) |
C629G |
probably benign |
Het |
Prpsap2 |
A |
T |
11: 61,621,097 (GRCm39) |
I328N |
probably benign |
Het |
Prrc2c |
A |
G |
1: 162,509,940 (GRCm39) |
L2317P |
probably damaging |
Het |
Ptgfrn |
T |
C |
3: 100,952,762 (GRCm39) |
D824G |
probably damaging |
Het |
Ptpra |
G |
A |
2: 130,361,301 (GRCm39) |
S204N |
probably damaging |
Het |
Pygm |
G |
T |
19: 6,443,787 (GRCm39) |
G583C |
probably damaging |
Het |
Rap1a |
A |
G |
3: 105,639,384 (GRCm39) |
F92L |
probably damaging |
Het |
Slmap |
A |
T |
14: 26,151,247 (GRCm39) |
|
probably null |
Het |
Spdye4c |
A |
G |
2: 128,438,050 (GRCm39) |
|
probably null |
Het |
Speer4a3 |
A |
G |
5: 26,155,843 (GRCm39) |
I167T |
probably benign |
Het |
Stk11 |
C |
A |
10: 79,963,924 (GRCm39) |
F97L |
probably benign |
Het |
Tbc1d9b |
G |
A |
11: 50,059,573 (GRCm39) |
A992T |
probably benign |
Het |
Tmem232 |
G |
A |
17: 65,757,305 (GRCm39) |
T296M |
possibly damaging |
Het |
Trim33 |
C |
T |
3: 103,259,365 (GRCm39) |
T1018M |
probably damaging |
Het |
Trpv2 |
A |
C |
11: 62,475,441 (GRCm39) |
I285L |
probably benign |
Het |
Usp46 |
A |
G |
5: 74,189,595 (GRCm39) |
|
probably benign |
Het |
Vmn1r27 |
T |
A |
6: 58,192,432 (GRCm39) |
M191L |
possibly damaging |
Het |
Vwf |
G |
T |
6: 125,619,113 (GRCm39) |
E1264* |
probably null |
Het |
Zfp109 |
A |
T |
7: 23,928,823 (GRCm39) |
N195K |
probably benign |
Het |
Zfp385b |
T |
A |
2: 77,246,138 (GRCm39) |
L208F |
probably damaging |
Het |
Zfp839 |
T |
A |
12: 110,833,195 (GRCm39) |
Y515* |
probably null |
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 |
|
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 |
|
|