Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alg6 |
A |
T |
4: 99,634,564 (GRCm39) |
D273V |
probably damaging |
Het |
Ankk1 |
T |
A |
9: 49,327,097 (GRCm39) |
H694L |
possibly damaging |
Het |
Asb7 |
G |
T |
7: 66,309,696 (GRCm39) |
N173K |
probably benign |
Het |
Atp10b |
A |
T |
11: 43,092,949 (GRCm39) |
Q428L |
probably damaging |
Het |
Bag3 |
A |
G |
7: 128,147,612 (GRCm39) |
E409G |
possibly damaging |
Het |
Bltp1 |
T |
C |
3: 37,052,416 (GRCm39) |
S3039P |
probably damaging |
Het |
Bpifb2 |
T |
A |
2: 153,733,232 (GRCm39) |
V398E |
probably damaging |
Het |
Btf3l4b |
A |
T |
13: 96,217,649 (GRCm39) |
D63E |
probably benign |
Het |
Ccr6 |
T |
C |
17: 8,474,945 (GRCm39) |
V50A |
probably benign |
Het |
Cdcp3 |
G |
T |
7: 130,898,045 (GRCm39) |
V2088L |
unknown |
Het |
Cdx1 |
T |
C |
18: 61,152,995 (GRCm39) |
N204D |
probably damaging |
Het |
Ciao1 |
T |
C |
2: 127,087,726 (GRCm39) |
D203G |
possibly damaging |
Het |
Cldn7 |
A |
T |
11: 69,856,892 (GRCm39) |
Y47F |
possibly damaging |
Het |
Col6a1 |
A |
T |
10: 76,559,305 (GRCm39) |
D110E |
possibly damaging |
Het |
Cpne6 |
C |
A |
14: 55,752,025 (GRCm39) |
Q261K |
probably benign |
Het |
Crebbp |
T |
C |
16: 3,946,389 (GRCm39) |
T497A |
probably benign |
Het |
Cyp2s1 |
A |
G |
7: 25,507,467 (GRCm39) |
|
probably null |
Het |
Ddx42 |
A |
T |
11: 106,130,887 (GRCm39) |
I454F |
possibly damaging |
Het |
Ddx5 |
G |
T |
11: 106,672,911 (GRCm39) |
A538E |
probably benign |
Het |
Dnajb1 |
T |
A |
8: 84,336,944 (GRCm39) |
V238D |
probably damaging |
Het |
Dntt |
A |
G |
19: 41,044,224 (GRCm39) |
Y463C |
probably damaging |
Het |
Eif4b |
A |
G |
15: 102,001,423 (GRCm39) |
T437A |
unknown |
Het |
Eppk1 |
T |
C |
15: 75,990,900 (GRCm39) |
T1994A |
possibly damaging |
Het |
Fbxw15 |
A |
T |
9: 109,384,658 (GRCm39) |
C381S |
probably benign |
Het |
Fosl2 |
T |
A |
5: 32,310,412 (GRCm39) |
V287D |
probably damaging |
Het |
Gdpd4 |
A |
G |
7: 97,690,077 (GRCm39) |
T590A |
probably benign |
Het |
Gm49368 |
A |
G |
7: 127,712,487 (GRCm39) |
E877G |
probably null |
Het |
Grin2b |
C |
T |
6: 135,709,497 (GRCm39) |
A1350T |
probably benign |
Het |
Gzmk |
A |
G |
13: 113,308,430 (GRCm39) |
L257P |
probably damaging |
Het |
Has2 |
T |
A |
15: 56,545,175 (GRCm39) |
K142N |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,629,411 (GRCm39) |
R949G |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,313,117 (GRCm39) |
E3442G |
probably damaging |
Het |
Irf9 |
T |
A |
14: 55,843,255 (GRCm39) |
C152* |
probably null |
Het |
Itga3 |
A |
G |
11: 94,943,290 (GRCm39) |
W936R |
probably damaging |
Het |
Klhl11 |
G |
T |
11: 100,354,740 (GRCm39) |
D360E |
probably damaging |
Het |
Lnx1 |
G |
A |
5: 74,846,060 (GRCm39) |
T130I |
probably benign |
Het |
Lrrc36 |
C |
T |
8: 106,170,396 (GRCm39) |
P82L |
probably damaging |
Het |
Map4k4 |
T |
C |
1: 40,039,694 (GRCm39) |
C29R |
|
Het |
Mki67 |
T |
C |
7: 135,296,065 (GRCm39) |
K2990E |
probably benign |
Het |
Mnt |
G |
A |
11: 74,733,799 (GRCm39) |
A477T |
unknown |
Het |
Mroh9 |
A |
G |
1: 162,890,096 (GRCm39) |
S214P |
probably benign |
Het |
Mrps18b |
C |
A |
17: 36,225,293 (GRCm39) |
R94L |
possibly damaging |
Het |
Myh6 |
T |
A |
14: 55,191,382 (GRCm39) |
I820F |
probably benign |
Het |
Nphp3 |
A |
G |
9: 103,913,050 (GRCm39) |
T943A |
probably benign |
Het |
Or51a25 |
C |
A |
7: 102,372,937 (GRCm39) |
L253F |
probably damaging |
Het |
Or52b4i |
A |
G |
7: 102,191,830 (GRCm39) |
H229R |
probably benign |
Het |
Papolb |
T |
C |
5: 142,514,353 (GRCm39) |
D430G |
probably benign |
Het |
Pdzd2 |
T |
C |
15: 12,407,458 (GRCm39) |
H334R |
probably benign |
Het |
Pkd1l2 |
T |
A |
8: 117,781,742 (GRCm39) |
M768L |
probably benign |
Het |
Pklr |
G |
T |
3: 89,052,795 (GRCm39) |
R547L |
probably benign |
Het |
Pla2g4a |
T |
C |
1: 149,716,394 (GRCm39) |
Y697C |
probably benign |
Het |
Prkcd |
T |
C |
14: 30,324,019 (GRCm39) |
T435A |
probably benign |
Het |
Rfx1 |
C |
T |
8: 84,800,657 (GRCm39) |
P86L |
probably benign |
Het |
Rnf19b |
C |
A |
4: 128,977,862 (GRCm39) |
A693D |
probably benign |
Het |
Scn9a |
A |
G |
2: 66,317,754 (GRCm39) |
I1578T |
probably damaging |
Het |
Slamf9 |
A |
G |
1: 172,303,942 (GRCm39) |
S96G |
probably benign |
Het |
Slc17a8 |
T |
C |
10: 89,412,233 (GRCm39) |
D584G |
probably benign |
Het |
Slc1a7 |
G |
A |
4: 107,869,473 (GRCm39) |
V513M |
probably benign |
Het |
Slc2a7 |
C |
A |
4: 150,252,818 (GRCm39) |
T486K |
probably damaging |
Het |
Slc6a20a |
G |
A |
9: 123,466,065 (GRCm39) |
A592V |
probably damaging |
Het |
Spz1 |
T |
C |
13: 92,711,609 (GRCm39) |
D289G |
probably benign |
Het |
Sspo |
G |
A |
6: 48,444,683 (GRCm39) |
C2226Y |
possibly damaging |
Het |
Taf4b |
T |
G |
18: 14,963,085 (GRCm39) |
D608E |
probably damaging |
Het |
Tagap1 |
A |
T |
17: 7,223,526 (GRCm39) |
I390N |
probably damaging |
Het |
Tcp11l2 |
A |
G |
10: 84,444,480 (GRCm39) |
N430D |
probably damaging |
Het |
Thsd7b |
T |
C |
1: 129,688,036 (GRCm39) |
L649P |
probably damaging |
Het |
Tmprss15 |
C |
T |
16: 78,757,473 (GRCm39) |
G956R |
probably damaging |
Het |
Tnc |
G |
T |
4: 63,935,716 (GRCm39) |
Q407K |
probably benign |
Het |
Tti1 |
C |
A |
2: 157,849,509 (GRCm39) |
E577* |
probably null |
Het |
Vmn2r79 |
A |
T |
7: 86,686,862 (GRCm39) |
M748L |
probably benign |
Het |
Zbtb37 |
C |
T |
1: 160,847,654 (GRCm39) |
R451Q |
probably damaging |
Het |
Zfp1002 |
T |
C |
2: 150,096,455 (GRCm39) |
K325E |
probably benign |
Het |
Zfp566 |
A |
T |
7: 29,777,785 (GRCm39) |
I132N |
probably benign |
Het |
Zik1 |
C |
T |
7: 10,223,930 (GRCm39) |
G389E |
probably damaging |
Het |
Zzef1 |
A |
T |
11: 72,799,295 (GRCm39) |
K2382* |
probably null |
Het |
|
Other mutations in Hectd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Hectd1
|
APN |
12 |
51,806,215 (GRCm39) |
missense |
probably benign |
|
IGL00402:Hectd1
|
APN |
12 |
51,815,891 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00419:Hectd1
|
APN |
12 |
51,810,818 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00518:Hectd1
|
APN |
12 |
51,823,272 (GRCm39) |
splice site |
probably benign |
|
IGL00565:Hectd1
|
APN |
12 |
51,837,181 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00574:Hectd1
|
APN |
12 |
51,820,787 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00576:Hectd1
|
APN |
12 |
51,806,092 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00788:Hectd1
|
APN |
12 |
51,795,571 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00978:Hectd1
|
APN |
12 |
51,838,173 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01328:Hectd1
|
APN |
12 |
51,807,904 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01337:Hectd1
|
APN |
12 |
51,849,057 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01634:Hectd1
|
APN |
12 |
51,850,562 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01731:Hectd1
|
APN |
12 |
51,849,593 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01920:Hectd1
|
APN |
12 |
51,829,337 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01951:Hectd1
|
APN |
12 |
51,841,280 (GRCm39) |
nonsense |
probably null |
|
IGL01994:Hectd1
|
APN |
12 |
51,844,725 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02140:Hectd1
|
APN |
12 |
51,820,920 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02150:Hectd1
|
APN |
12 |
51,815,974 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02156:Hectd1
|
APN |
12 |
51,800,916 (GRCm39) |
splice site |
probably benign |
|
IGL02177:Hectd1
|
APN |
12 |
51,819,103 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02502:Hectd1
|
APN |
12 |
51,844,635 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02505:Hectd1
|
APN |
12 |
51,847,496 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02519:Hectd1
|
APN |
12 |
51,815,894 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02624:Hectd1
|
APN |
12 |
51,809,233 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02833:Hectd1
|
APN |
12 |
51,810,864 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02851:Hectd1
|
APN |
12 |
51,814,423 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02866:Hectd1
|
APN |
12 |
51,837,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02981:Hectd1
|
APN |
12 |
51,815,670 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02987:Hectd1
|
APN |
12 |
51,791,550 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02999:Hectd1
|
APN |
12 |
51,874,205 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03071:Hectd1
|
APN |
12 |
51,815,957 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03078:Hectd1
|
APN |
12 |
51,849,019 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03299:Hectd1
|
APN |
12 |
51,847,671 (GRCm39) |
splice site |
probably benign |
|
3-1:Hectd1
|
UTSW |
12 |
51,800,590 (GRCm39) |
missense |
probably damaging |
0.99 |
R0039:Hectd1
|
UTSW |
12 |
51,800,608 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0238:Hectd1
|
UTSW |
12 |
51,816,101 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0238:Hectd1
|
UTSW |
12 |
51,816,101 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0239:Hectd1
|
UTSW |
12 |
51,816,101 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0239:Hectd1
|
UTSW |
12 |
51,816,101 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0268:Hectd1
|
UTSW |
12 |
51,815,891 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0268:Hectd1
|
UTSW |
12 |
51,815,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R0409:Hectd1
|
UTSW |
12 |
51,829,339 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1019:Hectd1
|
UTSW |
12 |
51,795,440 (GRCm39) |
missense |
probably damaging |
0.99 |
R1072:Hectd1
|
UTSW |
12 |
51,807,855 (GRCm39) |
missense |
probably benign |
0.11 |
R1087:Hectd1
|
UTSW |
12 |
51,823,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R1165:Hectd1
|
UTSW |
12 |
51,810,947 (GRCm39) |
splice site |
probably benign |
|
R1350:Hectd1
|
UTSW |
12 |
51,809,217 (GRCm39) |
missense |
probably benign |
|
R1553:Hectd1
|
UTSW |
12 |
51,820,661 (GRCm39) |
missense |
probably damaging |
0.98 |
R1666:Hectd1
|
UTSW |
12 |
51,800,607 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1676:Hectd1
|
UTSW |
12 |
51,791,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Hectd1
|
UTSW |
12 |
51,791,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Hectd1
|
UTSW |
12 |
51,800,590 (GRCm39) |
missense |
probably damaging |
0.99 |
R1856:Hectd1
|
UTSW |
12 |
51,791,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Hectd1
|
UTSW |
12 |
51,853,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Hectd1
|
UTSW |
12 |
51,847,738 (GRCm39) |
missense |
probably benign |
0.00 |
R1982:Hectd1
|
UTSW |
12 |
51,832,624 (GRCm39) |
missense |
probably damaging |
0.97 |
R2034:Hectd1
|
UTSW |
12 |
51,803,899 (GRCm39) |
splice site |
probably null |
|
R2061:Hectd1
|
UTSW |
12 |
51,841,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R2078:Hectd1
|
UTSW |
12 |
51,795,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R2176:Hectd1
|
UTSW |
12 |
51,792,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R2210:Hectd1
|
UTSW |
12 |
51,853,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R2248:Hectd1
|
UTSW |
12 |
51,853,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R2282:Hectd1
|
UTSW |
12 |
51,815,791 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2402:Hectd1
|
UTSW |
12 |
51,792,317 (GRCm39) |
missense |
probably benign |
0.01 |
R3876:Hectd1
|
UTSW |
12 |
51,815,513 (GRCm39) |
missense |
probably damaging |
0.98 |
R4027:Hectd1
|
UTSW |
12 |
51,849,219 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4085:Hectd1
|
UTSW |
12 |
51,821,533 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4115:Hectd1
|
UTSW |
12 |
51,815,506 (GRCm39) |
nonsense |
probably null |
|
R4116:Hectd1
|
UTSW |
12 |
51,815,506 (GRCm39) |
nonsense |
probably null |
|
R4169:Hectd1
|
UTSW |
12 |
51,837,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R4434:Hectd1
|
UTSW |
12 |
51,798,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R4507:Hectd1
|
UTSW |
12 |
51,837,276 (GRCm39) |
missense |
probably damaging |
0.97 |
R4578:Hectd1
|
UTSW |
12 |
51,798,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Hectd1
|
UTSW |
12 |
51,791,356 (GRCm39) |
missense |
probably damaging |
0.97 |
R4709:Hectd1
|
UTSW |
12 |
51,834,695 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4812:Hectd1
|
UTSW |
12 |
51,874,134 (GRCm39) |
critical splice donor site |
probably null |
|
R4883:Hectd1
|
UTSW |
12 |
51,831,030 (GRCm39) |
nonsense |
probably null |
|
R4885:Hectd1
|
UTSW |
12 |
51,847,505 (GRCm39) |
missense |
probably damaging |
0.97 |
R4975:Hectd1
|
UTSW |
12 |
51,809,280 (GRCm39) |
missense |
probably benign |
0.02 |
R4983:Hectd1
|
UTSW |
12 |
51,831,045 (GRCm39) |
missense |
probably benign |
0.01 |
R5007:Hectd1
|
UTSW |
12 |
51,849,443 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5046:Hectd1
|
UTSW |
12 |
51,797,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R5062:Hectd1
|
UTSW |
12 |
51,791,662 (GRCm39) |
missense |
probably damaging |
0.98 |
R5164:Hectd1
|
UTSW |
12 |
51,874,272 (GRCm39) |
start codon destroyed |
probably null |
0.60 |
R5213:Hectd1
|
UTSW |
12 |
51,849,316 (GRCm39) |
critical splice donor site |
probably null |
|
R5535:Hectd1
|
UTSW |
12 |
51,849,109 (GRCm39) |
missense |
probably damaging |
0.98 |
R5776:Hectd1
|
UTSW |
12 |
51,810,897 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5846:Hectd1
|
UTSW |
12 |
51,820,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R5907:Hectd1
|
UTSW |
12 |
51,845,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R5911:Hectd1
|
UTSW |
12 |
51,849,035 (GRCm39) |
missense |
probably damaging |
0.99 |
R5919:Hectd1
|
UTSW |
12 |
51,815,855 (GRCm39) |
missense |
probably damaging |
0.98 |
R6051:Hectd1
|
UTSW |
12 |
51,800,887 (GRCm39) |
missense |
probably benign |
|
R6141:Hectd1
|
UTSW |
12 |
51,792,875 (GRCm39) |
critical splice donor site |
probably null |
|
R6172:Hectd1
|
UTSW |
12 |
51,816,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6194:Hectd1
|
UTSW |
12 |
51,795,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R6356:Hectd1
|
UTSW |
12 |
51,791,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R6795:Hectd1
|
UTSW |
12 |
51,841,270 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6909:Hectd1
|
UTSW |
12 |
51,810,945 (GRCm39) |
splice site |
probably null |
|
R6971:Hectd1
|
UTSW |
12 |
51,795,526 (GRCm39) |
nonsense |
probably null |
|
R7079:Hectd1
|
UTSW |
12 |
51,834,638 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7104:Hectd1
|
UTSW |
12 |
51,874,134 (GRCm39) |
critical splice donor site |
probably null |
|
R7171:Hectd1
|
UTSW |
12 |
51,806,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R7296:Hectd1
|
UTSW |
12 |
51,832,635 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7346:Hectd1
|
UTSW |
12 |
51,797,104 (GRCm39) |
missense |
probably benign |
|
R7355:Hectd1
|
UTSW |
12 |
51,838,081 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7468:Hectd1
|
UTSW |
12 |
51,791,588 (GRCm39) |
splice site |
probably null |
|
R7531:Hectd1
|
UTSW |
12 |
51,853,150 (GRCm39) |
missense |
probably benign |
0.33 |
R7532:Hectd1
|
UTSW |
12 |
51,837,233 (GRCm39) |
missense |
probably damaging |
0.98 |
R7755:Hectd1
|
UTSW |
12 |
51,849,003 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7807:Hectd1
|
UTSW |
12 |
51,792,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Hectd1
|
UTSW |
12 |
51,819,343 (GRCm39) |
missense |
probably damaging |
0.99 |
R7922:Hectd1
|
UTSW |
12 |
51,836,978 (GRCm39) |
nonsense |
probably null |
|
R8059:Hectd1
|
UTSW |
12 |
51,837,161 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8085:Hectd1
|
UTSW |
12 |
51,795,679 (GRCm39) |
missense |
probably damaging |
0.97 |
R8157:Hectd1
|
UTSW |
12 |
51,838,073 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8405:Hectd1
|
UTSW |
12 |
51,874,178 (GRCm39) |
missense |
probably benign |
0.01 |
R8505:Hectd1
|
UTSW |
12 |
51,797,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Hectd1
|
UTSW |
12 |
51,834,654 (GRCm39) |
missense |
probably benign |
0.01 |
R8697:Hectd1
|
UTSW |
12 |
51,819,320 (GRCm39) |
critical splice donor site |
probably benign |
|
R8725:Hectd1
|
UTSW |
12 |
51,849,000 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8727:Hectd1
|
UTSW |
12 |
51,849,000 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8911:Hectd1
|
UTSW |
12 |
51,795,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R8983:Hectd1
|
UTSW |
12 |
51,791,410 (GRCm39) |
missense |
probably damaging |
0.97 |
R9037:Hectd1
|
UTSW |
12 |
51,832,665 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9219:Hectd1
|
UTSW |
12 |
51,800,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R9413:Hectd1
|
UTSW |
12 |
51,792,880 (GRCm39) |
nonsense |
probably null |
|
R9456:Hectd1
|
UTSW |
12 |
51,832,584 (GRCm39) |
missense |
probably benign |
|
R9513:Hectd1
|
UTSW |
12 |
51,816,079 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9640:Hectd1
|
UTSW |
12 |
51,795,197 (GRCm39) |
nonsense |
probably null |
|
R9641:Hectd1
|
UTSW |
12 |
51,816,047 (GRCm39) |
missense |
probably benign |
0.00 |
R9713:Hectd1
|
UTSW |
12 |
51,823,328 (GRCm39) |
missense |
probably benign |
0.02 |
|