Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
T |
G |
1: 156,450,104 (GRCm39) |
N90K |
possibly damaging |
Het |
Acox1 |
T |
C |
11: 116,069,001 (GRCm39) |
T415A |
possibly damaging |
Het |
Acy1 |
T |
C |
9: 106,314,921 (GRCm39) |
M1V |
probably null |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Alpk3 |
C |
A |
7: 80,750,746 (GRCm39) |
Y1505* |
probably null |
Het |
Ankrd17 |
T |
C |
5: 90,390,902 (GRCm39) |
N2256S |
probably benign |
Het |
Ankrd22 |
C |
A |
19: 34,126,692 (GRCm39) |
C46F |
possibly damaging |
Het |
Arhgef5 |
A |
T |
6: 43,257,605 (GRCm39) |
K1291* |
probably null |
Het |
Arl9 |
T |
A |
5: 77,158,276 (GRCm39) |
Y119* |
probably null |
Het |
Asb14 |
T |
C |
14: 26,622,805 (GRCm39) |
V89A |
probably benign |
Het |
Banp |
T |
G |
8: 122,676,588 (GRCm39) |
|
probably null |
Het |
Btn2a2 |
T |
C |
13: 23,666,933 (GRCm39) |
N224S |
probably benign |
Het |
C1ra |
C |
T |
6: 124,499,403 (GRCm39) |
Q530* |
probably null |
Het |
C2cd6 |
A |
C |
1: 59,107,844 (GRCm39) |
S273A |
probably benign |
Het |
Cd1d2 |
A |
T |
3: 86,895,583 (GRCm39) |
|
probably null |
Het |
Cdc42bpb |
T |
C |
12: 111,306,307 (GRCm39) |
D132G |
probably damaging |
Het |
Cfap45 |
C |
A |
1: 172,362,877 (GRCm39) |
Y289* |
probably null |
Het |
Chrdl2 |
T |
C |
7: 99,659,332 (GRCm39) |
|
probably null |
Het |
Cilk1 |
A |
G |
9: 78,065,221 (GRCm39) |
K377R |
probably benign |
Het |
Cst5 |
C |
T |
2: 149,247,496 (GRCm39) |
L71F |
probably benign |
Het |
Dcaf11 |
T |
C |
14: 55,802,966 (GRCm39) |
F292L |
possibly damaging |
Het |
Dgcr8 |
A |
G |
16: 18,077,487 (GRCm39) |
F641S |
probably damaging |
Het |
Dnm3 |
G |
A |
1: 162,149,198 (GRCm39) |
|
probably null |
Het |
Efcab3 |
G |
T |
11: 104,640,526 (GRCm39) |
S1088I |
probably benign |
Het |
Eral1 |
T |
C |
11: 77,966,219 (GRCm39) |
K320E |
probably damaging |
Het |
Eva1a |
A |
G |
6: 82,069,002 (GRCm39) |
T110A |
possibly damaging |
Het |
Fbxo42 |
A |
G |
4: 140,926,917 (GRCm39) |
D399G |
possibly damaging |
Het |
Frs2 |
T |
C |
10: 116,910,007 (GRCm39) |
T452A |
possibly damaging |
Het |
Git2 |
T |
A |
5: 114,871,958 (GRCm39) |
D542V |
probably damaging |
Het |
Grk2 |
T |
A |
19: 4,356,063 (GRCm39) |
|
probably benign |
Het |
Gsg1l2 |
A |
G |
11: 67,676,110 (GRCm39) |
N158S |
possibly damaging |
Het |
Hc |
T |
C |
2: 34,918,063 (GRCm39) |
N740S |
probably benign |
Het |
Hemk1 |
A |
G |
9: 107,208,288 (GRCm39) |
|
probably null |
Het |
Hormad2 |
G |
T |
11: 4,362,245 (GRCm39) |
Y126* |
probably null |
Het |
Hr |
A |
G |
14: 70,795,652 (GRCm39) |
E399G |
possibly damaging |
Het |
Ilf3 |
C |
A |
9: 21,314,707 (GRCm39) |
H780N |
unknown |
Het |
Inpp5e |
A |
T |
2: 26,298,161 (GRCm39) |
S147T |
probably benign |
Het |
Irag2 |
C |
A |
6: 145,119,427 (GRCm39) |
|
probably null |
Het |
Jmjd6 |
T |
C |
11: 116,733,275 (GRCm39) |
D134G |
probably damaging |
Het |
Kif23 |
G |
T |
9: 61,844,457 (GRCm39) |
Y120* |
probably null |
Het |
Klk12 |
T |
A |
7: 43,422,780 (GRCm39) |
Y236N |
probably damaging |
Het |
Kmt5b |
C |
A |
19: 3,852,799 (GRCm39) |
Y186* |
probably null |
Het |
Krtap9-5 |
A |
G |
11: 99,840,132 (GRCm39) |
T278A |
unknown |
Het |
Lca5 |
T |
A |
9: 83,305,509 (GRCm39) |
D99V |
probably damaging |
Het |
Leng9 |
A |
G |
7: 4,151,800 (GRCm39) |
V292A |
probably benign |
Het |
Lime1 |
A |
G |
2: 181,025,135 (GRCm39) |
R231G |
probably benign |
Het |
Mctp2 |
T |
A |
7: 71,861,438 (GRCm39) |
E402D |
probably damaging |
Het |
Mrpl28 |
T |
A |
17: 26,343,589 (GRCm39) |
S116R |
probably damaging |
Het |
Muc15 |
A |
T |
2: 110,561,862 (GRCm39) |
R99S |
probably benign |
Het |
Myh2 |
G |
A |
11: 67,083,368 (GRCm39) |
A1444T |
probably benign |
Het |
Mynn |
T |
A |
3: 30,657,825 (GRCm39) |
Y48N |
probably damaging |
Het |
Myo1b |
A |
T |
1: 51,836,639 (GRCm39) |
V274E |
possibly damaging |
Het |
Nemp1 |
T |
A |
10: 127,528,923 (GRCm39) |
M209K |
possibly damaging |
Het |
Nlrc4 |
G |
T |
17: 74,752,507 (GRCm39) |
D625E |
probably benign |
Het |
Or10al6 |
C |
T |
17: 38,082,910 (GRCm39) |
A122V |
probably damaging |
Het |
Or11a4 |
T |
C |
17: 37,536,276 (GRCm39) |
F87L |
probably benign |
Het |
Or4p4 |
T |
C |
2: 88,482,622 (GRCm39) |
L42P |
probably damaging |
Het |
Otog |
T |
C |
7: 45,913,543 (GRCm39) |
V792A |
probably benign |
Het |
Paqr8 |
T |
C |
1: 21,005,442 (GRCm39) |
Y199H |
probably damaging |
Het |
Popdc3 |
A |
G |
10: 45,191,117 (GRCm39) |
D76G |
probably damaging |
Het |
Ppme1 |
T |
C |
7: 99,991,069 (GRCm39) |
N210D |
probably benign |
Het |
Prdm15 |
A |
C |
16: 97,636,842 (GRCm39) |
Y158* |
probably null |
Het |
Prrg2 |
A |
T |
7: 44,709,687 (GRCm39) |
L70Q |
probably benign |
Het |
Psmg4 |
C |
T |
13: 34,361,966 (GRCm39) |
R85W |
probably damaging |
Het |
Rab11fip4 |
A |
T |
11: 79,580,478 (GRCm39) |
T437S |
probably benign |
Het |
Rap2a |
T |
A |
14: 120,716,338 (GRCm39) |
M67K |
probably damaging |
Het |
Rnf123 |
A |
T |
9: 107,946,208 (GRCm39) |
H322Q |
probably benign |
Het |
Rxfp2 |
A |
T |
5: 149,990,801 (GRCm39) |
T521S |
possibly damaging |
Het |
Scrn2 |
T |
G |
11: 96,923,992 (GRCm39) |
V292G |
possibly damaging |
Het |
Serpina3n |
C |
A |
12: 104,377,656 (GRCm39) |
P303H |
probably benign |
Het |
Spop |
C |
T |
11: 95,376,727 (GRCm39) |
T260M |
probably damaging |
Het |
Surf2 |
G |
A |
2: 26,809,354 (GRCm39) |
G224D |
probably benign |
Het |
Synm |
T |
G |
7: 67,382,971 (GRCm39) |
N669T |
unknown |
Het |
Tmprss13 |
T |
C |
9: 45,239,721 (GRCm39) |
S10P |
unknown |
Het |
Trav9d-1 |
T |
A |
14: 53,029,970 (GRCm39) |
S25T |
probably benign |
Het |
Trpc3 |
A |
T |
3: 36,678,565 (GRCm39) |
I840K |
probably damaging |
Het |
Tsbp1 |
T |
A |
17: 34,636,539 (GRCm39) |
|
probably null |
Het |
Tssc4 |
C |
A |
7: 142,622,999 (GRCm39) |
|
probably benign |
Het |
Ttc39d |
G |
T |
17: 80,523,579 (GRCm39) |
R79S |
possibly damaging |
Het |
Txlnb |
T |
A |
10: 17,675,082 (GRCm39) |
S78R |
probably damaging |
Het |
Vmn1r142 |
T |
A |
7: 21,862,784 (GRCm39) |
Q226L |
possibly damaging |
Het |
Vmn1r230 |
T |
C |
17: 21,067,146 (GRCm39) |
S112P |
probably damaging |
Het |
Wrnip1 |
T |
C |
13: 33,000,360 (GRCm39) |
F456L |
possibly damaging |
Het |
Zc3h8 |
G |
T |
2: 128,775,215 (GRCm39) |
H148Q |
probably benign |
Het |
Zcchc3 |
A |
G |
2: 152,256,615 (GRCm39) |
V28A |
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,346,669 (GRCm39) |
C1683S |
probably benign |
Het |
Zfp874a |
T |
C |
13: 67,573,723 (GRCm39) |
|
probably null |
Het |
Zmym4 |
A |
G |
4: 126,776,029 (GRCm39) |
S1260P |
probably benign |
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 |
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 |
R8145:Hectd1
|
UTSW |
12 |
51,831,016 (GRCm39) |
missense |
possibly damaging |
0.72 |
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 |
|