Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,775,433 (GRCm39) |
T1541A |
probably benign |
Het |
9530002B09Rik |
T |
C |
4: 122,594,285 (GRCm39) |
M59T |
probably benign |
Het |
Adam18 |
C |
T |
8: 25,131,827 (GRCm39) |
C428Y |
probably damaging |
Het |
Adcy5 |
A |
G |
16: 35,098,872 (GRCm39) |
E700G |
possibly damaging |
Het |
Adprh |
G |
T |
16: 38,266,142 (GRCm39) |
Y333* |
probably null |
Het |
Agfg2 |
C |
A |
5: 137,665,439 (GRCm39) |
|
probably null |
Het |
Akip1 |
A |
T |
7: 109,310,961 (GRCm39) |
E167V |
probably damaging |
Het |
Akr1c21 |
A |
T |
13: 4,630,304 (GRCm39) |
Q199L |
probably damaging |
Het |
Aldh9a1 |
C |
A |
1: 167,193,358 (GRCm39) |
A455E |
probably damaging |
Het |
Amph |
G |
A |
13: 19,321,869 (GRCm39) |
S520N |
probably benign |
Het |
Ankrd52 |
A |
G |
10: 128,226,376 (GRCm39) |
D1006G |
probably benign |
Het |
Ap5z1 |
A |
C |
5: 142,453,431 (GRCm39) |
Q133P |
probably damaging |
Het |
Babam1 |
C |
T |
8: 71,857,032 (GRCm39) |
A331V |
possibly damaging |
Het |
Btc |
T |
C |
5: 91,510,160 (GRCm39) |
|
probably null |
Het |
Cacna2d3 |
A |
G |
14: 28,704,289 (GRCm39) |
F831L |
probably benign |
Het |
Cadm3 |
G |
A |
1: 173,164,664 (GRCm39) |
P372L |
probably damaging |
Het |
Capn5 |
A |
T |
7: 97,775,624 (GRCm39) |
M439K |
probably damaging |
Het |
Carf |
T |
C |
1: 60,189,796 (GRCm39) |
S639P |
probably damaging |
Het |
Casp12 |
C |
T |
9: 5,352,250 (GRCm39) |
R81C |
probably benign |
Het |
Ces2e |
G |
T |
8: 105,660,330 (GRCm39) |
R555M |
probably benign |
Het |
Cfap54 |
T |
A |
10: 92,902,661 (GRCm39) |
I164F |
probably benign |
Het |
Cltc |
C |
T |
11: 86,598,327 (GRCm39) |
V1012I |
probably damaging |
Het |
Cmya5 |
G |
A |
13: 93,232,295 (GRCm39) |
T931I |
possibly damaging |
Het |
Cntn6 |
A |
G |
6: 104,751,435 (GRCm39) |
I364V |
probably damaging |
Het |
Cntnap1 |
A |
T |
11: 101,068,251 (GRCm39) |
I59F |
possibly damaging |
Het |
Cop1 |
T |
C |
1: 159,067,167 (GRCm39) |
M80T |
probably damaging |
Het |
Cplx2 |
A |
G |
13: 54,527,460 (GRCm39) |
S115G |
possibly damaging |
Het |
Crtac1 |
A |
G |
19: 42,307,179 (GRCm39) |
Y195H |
probably damaging |
Het |
Csn1s2a |
A |
C |
5: 87,929,697 (GRCm39) |
S99R |
possibly damaging |
Het |
Csn1s2b |
T |
A |
5: 87,961,820 (GRCm39) |
D41E |
possibly damaging |
Het |
Cul9 |
C |
T |
17: 46,849,451 (GRCm39) |
D565N |
probably damaging |
Het |
Cux1 |
A |
T |
5: 136,340,410 (GRCm39) |
N625K |
possibly damaging |
Het |
Cyp2c37 |
A |
T |
19: 40,000,206 (GRCm39) |
M443L |
possibly damaging |
Het |
Cyp2s1 |
G |
A |
7: 25,508,710 (GRCm39) |
T244I |
possibly damaging |
Het |
Dgkh |
C |
T |
14: 78,861,861 (GRCm39) |
V135M |
probably damaging |
Het |
Dtl |
T |
C |
1: 191,278,677 (GRCm39) |
E395G |
possibly damaging |
Het |
Dyrk1a |
G |
T |
16: 94,492,854 (GRCm39) |
G658* |
probably null |
Het |
Erlin2 |
T |
C |
8: 27,519,623 (GRCm39) |
F117S |
probably damaging |
Het |
Fkbp8 |
A |
G |
8: 70,984,173 (GRCm39) |
|
probably null |
Het |
Fras1 |
T |
C |
5: 96,874,439 (GRCm39) |
F2288S |
possibly damaging |
Het |
Frmd3 |
A |
G |
4: 74,071,837 (GRCm39) |
T240A |
probably damaging |
Het |
H2-D1 |
A |
G |
17: 35,482,881 (GRCm39) |
Y137C |
probably damaging |
Het |
Helz2 |
A |
G |
2: 180,882,709 (GRCm39) |
V28A |
possibly damaging |
Het |
Il6 |
A |
T |
5: 30,218,491 (GRCm39) |
Y29F |
possibly damaging |
Het |
Ildr2 |
A |
G |
1: 166,135,409 (GRCm39) |
D368G |
probably damaging |
Het |
Junb |
T |
A |
8: 85,704,788 (GRCm39) |
I91F |
probably damaging |
Het |
Kat2a |
C |
A |
11: 100,603,029 (GRCm39) |
|
probably benign |
Het |
Kat2a |
A |
T |
11: 100,603,030 (GRCm39) |
|
probably benign |
Het |
Kcnh5 |
T |
A |
12: 75,011,925 (GRCm39) |
T665S |
probably benign |
Het |
Kdm1b |
A |
T |
13: 47,227,843 (GRCm39) |
D608V |
probably damaging |
Het |
Krcc1 |
A |
G |
6: 71,261,621 (GRCm39) |
K218E |
probably damaging |
Het |
Krt8 |
C |
T |
15: 101,905,386 (GRCm39) |
V488M |
probably benign |
Het |
Lzts1 |
C |
T |
8: 69,591,414 (GRCm39) |
A245T |
probably benign |
Het |
Mcm6 |
T |
A |
1: 128,287,223 (GRCm39) |
Q27L |
probably damaging |
Het |
Mfsd4b3-ps |
G |
T |
10: 39,823,686 (GRCm39) |
Y191* |
probably null |
Het |
Mgme1 |
C |
T |
2: 144,118,324 (GRCm39) |
Q199* |
probably null |
Het |
Mgme1 |
T |
C |
2: 144,121,540 (GRCm39) |
L332P |
probably benign |
Het |
Morc3 |
G |
T |
16: 93,657,475 (GRCm39) |
E25* |
probably null |
Het |
Mroh7 |
G |
A |
4: 106,548,184 (GRCm39) |
A1098V |
possibly damaging |
Het |
Mtrf1 |
G |
A |
14: 79,644,027 (GRCm39) |
R174H |
probably benign |
Het |
Mybpc3 |
G |
A |
2: 90,949,592 (GRCm39) |
G45D |
possibly damaging |
Het |
Mycbpap |
A |
T |
11: 94,395,764 (GRCm39) |
N733K |
probably damaging |
Het |
N4bp1 |
T |
C |
8: 87,578,314 (GRCm39) |
I684V |
possibly damaging |
Het |
Nav2 |
A |
T |
7: 49,202,625 (GRCm39) |
R1470* |
probably null |
Het |
Ndufa9 |
A |
T |
6: 126,799,026 (GRCm39) |
S364T |
probably benign |
Het |
Nipal4 |
C |
A |
11: 46,052,837 (GRCm39) |
A43S |
possibly damaging |
Het |
Nlrp1a |
T |
A |
11: 70,983,141 (GRCm39) |
Y1275F |
possibly damaging |
Het |
Nova1 |
A |
T |
12: 46,767,618 (GRCm39) |
L8* |
probably null |
Het |
Odam |
G |
T |
5: 88,037,967 (GRCm39) |
G181* |
probably null |
Het |
Optn |
T |
A |
2: 5,026,190 (GRCm39) |
Q576L |
probably benign |
Het |
Or2c1 |
T |
C |
16: 3,657,434 (GRCm39) |
L199P |
probably damaging |
Het |
Or4k47 |
T |
C |
2: 111,451,879 (GRCm39) |
D180G |
probably damaging |
Het |
Or4l1 |
C |
T |
14: 50,166,354 (GRCm39) |
V216I |
probably benign |
Het |
Or51a39 |
A |
T |
7: 102,362,702 (GRCm39) |
I306N |
probably damaging |
Het |
Or5as1 |
T |
A |
2: 86,981,003 (GRCm39) |
M1L |
possibly damaging |
Het |
Or5h18 |
A |
T |
16: 58,847,696 (GRCm39) |
D191E |
probably damaging |
Het |
Or8s2 |
T |
C |
15: 98,277,030 (GRCm39) |
|
probably benign |
Het |
Patl2 |
G |
T |
2: 121,959,329 (GRCm39) |
S45* |
probably null |
Het |
Pde2a |
G |
A |
7: 101,152,140 (GRCm39) |
G349E |
probably benign |
Het |
Pdlim2 |
T |
A |
14: 70,405,464 (GRCm39) |
|
probably benign |
Het |
Per1 |
T |
C |
11: 68,995,227 (GRCm39) |
V653A |
probably benign |
Het |
Phlda2 |
A |
G |
7: 143,056,005 (GRCm39) |
S75P |
probably damaging |
Het |
Poldip3 |
A |
T |
15: 83,021,706 (GRCm39) |
M167K |
possibly damaging |
Het |
Potegl |
C |
A |
2: 23,135,127 (GRCm39) |
T312K |
probably benign |
Het |
Prpf38a |
T |
C |
4: 108,436,278 (GRCm39) |
I12V |
probably benign |
Het |
Prrc1 |
G |
A |
18: 57,507,622 (GRCm39) |
V259I |
possibly damaging |
Het |
Ptges3l |
A |
T |
11: 101,315,448 (GRCm39) |
M1K |
probably null |
Het |
Rdh5 |
A |
G |
10: 128,749,653 (GRCm39) |
Y296H |
probably damaging |
Het |
Resf1 |
G |
T |
6: 149,229,896 (GRCm39) |
G981* |
probably null |
Het |
Rnf2 |
T |
A |
1: 151,348,968 (GRCm39) |
K51* |
probably null |
Het |
Rpusd3 |
C |
A |
6: 113,393,809 (GRCm39) |
R215L |
probably benign |
Het |
Rsph4a |
A |
T |
10: 33,785,236 (GRCm39) |
E382D |
probably damaging |
Het |
S1pr2 |
G |
A |
9: 20,879,745 (GRCm39) |
Q28* |
probably null |
Het |
Sesn1 |
A |
T |
10: 41,771,005 (GRCm39) |
I179F |
probably damaging |
Het |
Setd3 |
T |
A |
12: 108,079,630 (GRCm39) |
E291V |
probably benign |
Het |
Shc1 |
G |
T |
3: 89,334,303 (GRCm39) |
R323L |
probably damaging |
Het |
Slc22a5 |
T |
C |
11: 53,782,352 (GRCm39) |
D5G |
possibly damaging |
Het |
Slc6a19 |
T |
C |
13: 73,848,677 (GRCm39) |
K26E |
probably benign |
Het |
Slc9a3 |
A |
G |
13: 74,312,412 (GRCm39) |
N670D |
possibly damaging |
Het |
Spata19 |
A |
T |
9: 27,311,761 (GRCm39) |
I127L |
probably benign |
Het |
Speg |
G |
T |
1: 75,404,347 (GRCm39) |
V2751L |
probably damaging |
Het |
Sptbn2 |
A |
G |
19: 4,779,337 (GRCm39) |
D298G |
probably benign |
Het |
Srm |
T |
C |
4: 148,678,640 (GRCm39) |
V289A |
possibly damaging |
Het |
Stip1 |
C |
T |
19: 7,012,938 (GRCm39) |
A49T |
probably benign |
Het |
Tas2r118 |
C |
A |
6: 23,969,627 (GRCm39) |
V145F |
probably benign |
Het |
Tbc1d12 |
A |
T |
19: 38,854,169 (GRCm39) |
K284* |
probably null |
Het |
Tfcp2 |
T |
C |
15: 100,423,531 (GRCm39) |
H125R |
probably damaging |
Het |
Tfdp1 |
T |
C |
8: 13,423,073 (GRCm39) |
V206A |
probably damaging |
Het |
Tgtp2 |
A |
G |
11: 48,950,237 (GRCm39) |
W112R |
probably damaging |
Het |
Tmem71 |
T |
G |
15: 66,410,710 (GRCm39) |
M221L |
probably benign |
Het |
Tpcn1 |
T |
C |
5: 120,685,552 (GRCm39) |
N436S |
possibly damaging |
Het |
Usp4 |
C |
T |
9: 108,239,819 (GRCm39) |
L183F |
probably damaging |
Het |
Vmn2r55 |
A |
T |
7: 12,404,478 (GRCm39) |
N308K |
possibly damaging |
Het |
Zfp106 |
T |
A |
2: 120,364,400 (GRCm39) |
D669V |
probably damaging |
Het |
Zfp108 |
A |
T |
7: 23,959,573 (GRCm39) |
I55L |
probably benign |
Het |
Zfp512b |
A |
T |
2: 181,228,131 (GRCm39) |
S8R |
probably damaging |
Het |
Zfp827 |
T |
C |
8: 79,787,910 (GRCm39) |
S359P |
probably benign |
Het |
|
Other mutations in Hydin |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00338:Hydin
|
APN |
8 |
111,296,434 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL00432:Hydin
|
APN |
8 |
111,327,884 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01025:Hydin
|
APN |
8 |
111,053,033 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01140:Hydin
|
APN |
8 |
111,124,694 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01317:Hydin
|
APN |
8 |
111,053,078 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01473:Hydin
|
APN |
8 |
111,038,792 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01473:Hydin
|
APN |
8 |
111,081,585 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01610:Hydin
|
APN |
8 |
111,284,345 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01685:Hydin
|
APN |
8 |
111,081,665 (GRCm39) |
nonsense |
probably null |
|
IGL01734:Hydin
|
APN |
8 |
111,217,421 (GRCm39) |
nonsense |
probably null |
|
IGL01743:Hydin
|
APN |
8 |
111,319,408 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01829:Hydin
|
APN |
8 |
111,316,154 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01919:Hydin
|
APN |
8 |
111,245,806 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01946:Hydin
|
APN |
8 |
111,217,350 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01983:Hydin
|
APN |
8 |
111,241,527 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02122:Hydin
|
APN |
8 |
111,221,047 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02140:Hydin
|
APN |
8 |
111,293,570 (GRCm39) |
missense |
probably benign |
|
IGL02158:Hydin
|
APN |
8 |
111,336,598 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02167:Hydin
|
APN |
8 |
111,145,055 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02171:Hydin
|
APN |
8 |
111,178,590 (GRCm39) |
nonsense |
probably null |
|
IGL02185:Hydin
|
APN |
8 |
111,233,108 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02517:Hydin
|
APN |
8 |
111,293,604 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02639:Hydin
|
APN |
8 |
111,265,081 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02644:Hydin
|
APN |
8 |
111,265,100 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02652:Hydin
|
APN |
8 |
111,316,154 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02658:Hydin
|
APN |
8 |
111,139,908 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02706:Hydin
|
APN |
8 |
111,137,198 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02892:Hydin
|
APN |
8 |
111,325,591 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02947:Hydin
|
APN |
8 |
111,145,094 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03136:Hydin
|
APN |
8 |
111,145,156 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03248:Hydin
|
APN |
8 |
111,321,921 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03251:Hydin
|
APN |
8 |
111,217,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03350:Hydin
|
APN |
8 |
111,038,856 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03366:Hydin
|
APN |
8 |
110,993,995 (GRCm39) |
missense |
unknown |
|
IGL03404:Hydin
|
APN |
8 |
111,296,409 (GRCm39) |
missense |
probably benign |
0.06 |
Franz_joseph
|
UTSW |
8 |
111,327,950 (GRCm39) |
missense |
probably damaging |
1.00 |
jahreszeiten
|
UTSW |
8 |
111,295,991 (GRCm39) |
missense |
probably damaging |
1.00 |
maria
|
UTSW |
8 |
111,235,759 (GRCm39) |
splice site |
probably benign |
|
schoepfung
|
UTSW |
8 |
111,326,877 (GRCm39) |
missense |
possibly damaging |
0.68 |
surprise
|
UTSW |
8 |
111,254,648 (GRCm39) |
missense |
probably benign |
|
teresa
|
UTSW |
8 |
111,336,303 (GRCm39) |
missense |
possibly damaging |
0.79 |
BB001:Hydin
|
UTSW |
8 |
111,145,103 (GRCm39) |
missense |
possibly damaging |
0.93 |
BB004:Hydin
|
UTSW |
8 |
111,307,476 (GRCm39) |
missense |
possibly damaging |
0.89 |
BB011:Hydin
|
UTSW |
8 |
111,145,103 (GRCm39) |
missense |
possibly damaging |
0.93 |
BB014:Hydin
|
UTSW |
8 |
111,307,476 (GRCm39) |
missense |
possibly damaging |
0.89 |
P0005:Hydin
|
UTSW |
8 |
111,220,921 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0099:Hydin
|
UTSW |
8 |
111,316,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Hydin
|
UTSW |
8 |
111,189,163 (GRCm39) |
missense |
probably benign |
0.12 |
R0157:Hydin
|
UTSW |
8 |
111,026,642 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0241:Hydin
|
UTSW |
8 |
111,124,655 (GRCm39) |
missense |
probably benign |
0.04 |
R0241:Hydin
|
UTSW |
8 |
111,124,655 (GRCm39) |
missense |
probably benign |
0.04 |
R0255:Hydin
|
UTSW |
8 |
111,291,650 (GRCm39) |
missense |
probably benign |
0.00 |
R0352:Hydin
|
UTSW |
8 |
111,296,533 (GRCm39) |
critical splice donor site |
probably null |
|
R0379:Hydin
|
UTSW |
8 |
111,235,759 (GRCm39) |
splice site |
probably benign |
|
R0468:Hydin
|
UTSW |
8 |
111,139,855 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0477:Hydin
|
UTSW |
8 |
111,145,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0479:Hydin
|
UTSW |
8 |
111,325,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R0539:Hydin
|
UTSW |
8 |
111,249,704 (GRCm39) |
missense |
probably benign |
|
R0550:Hydin
|
UTSW |
8 |
111,314,407 (GRCm39) |
missense |
probably benign |
0.01 |
R0571:Hydin
|
UTSW |
8 |
111,240,735 (GRCm39) |
splice site |
probably null |
|
R0606:Hydin
|
UTSW |
8 |
111,276,430 (GRCm39) |
splice site |
probably benign |
|
R0789:Hydin
|
UTSW |
8 |
111,293,603 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0849:Hydin
|
UTSW |
8 |
111,325,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0946:Hydin
|
UTSW |
8 |
111,257,685 (GRCm39) |
missense |
probably benign |
0.25 |
R1201:Hydin
|
UTSW |
8 |
111,296,487 (GRCm39) |
missense |
probably benign |
0.01 |
R1375:Hydin
|
UTSW |
8 |
111,232,854 (GRCm39) |
critical splice donor site |
probably null |
|
R1385:Hydin
|
UTSW |
8 |
111,249,836 (GRCm39) |
missense |
probably benign |
0.40 |
R1411:Hydin
|
UTSW |
8 |
111,301,663 (GRCm39) |
missense |
probably benign |
0.04 |
R1437:Hydin
|
UTSW |
8 |
111,308,617 (GRCm39) |
nonsense |
probably null |
|
R1447:Hydin
|
UTSW |
8 |
111,249,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Hydin
|
UTSW |
8 |
111,173,217 (GRCm39) |
missense |
probably benign |
0.27 |
R1466:Hydin
|
UTSW |
8 |
111,259,585 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1466:Hydin
|
UTSW |
8 |
111,259,585 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1523:Hydin
|
UTSW |
8 |
111,259,903 (GRCm39) |
missense |
probably benign |
0.05 |
R1544:Hydin
|
UTSW |
8 |
111,301,486 (GRCm39) |
missense |
probably benign |
0.30 |
R1581:Hydin
|
UTSW |
8 |
111,137,092 (GRCm39) |
missense |
probably benign |
|
R1584:Hydin
|
UTSW |
8 |
111,307,447 (GRCm39) |
missense |
probably benign |
0.27 |
R1598:Hydin
|
UTSW |
8 |
111,137,306 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1633:Hydin
|
UTSW |
8 |
111,233,614 (GRCm39) |
missense |
probably benign |
0.10 |
R1777:Hydin
|
UTSW |
8 |
111,316,203 (GRCm39) |
missense |
probably benign |
0.14 |
R1817:Hydin
|
UTSW |
8 |
111,259,459 (GRCm39) |
missense |
probably benign |
0.00 |
R1828:Hydin
|
UTSW |
8 |
111,237,526 (GRCm39) |
missense |
probably benign |
0.03 |
R1837:Hydin
|
UTSW |
8 |
111,296,257 (GRCm39) |
missense |
probably benign |
0.20 |
R1848:Hydin
|
UTSW |
8 |
111,296,440 (GRCm39) |
missense |
probably benign |
0.19 |
R1869:Hydin
|
UTSW |
8 |
111,227,337 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1909:Hydin
|
UTSW |
8 |
111,314,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Hydin
|
UTSW |
8 |
111,229,579 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1950:Hydin
|
UTSW |
8 |
111,336,619 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2095:Hydin
|
UTSW |
8 |
111,189,289 (GRCm39) |
missense |
probably damaging |
0.96 |
R2172:Hydin
|
UTSW |
8 |
111,308,681 (GRCm39) |
missense |
probably benign |
0.42 |
R2217:Hydin
|
UTSW |
8 |
111,145,138 (GRCm39) |
missense |
probably benign |
|
R2248:Hydin
|
UTSW |
8 |
111,304,835 (GRCm39) |
missense |
probably benign |
0.09 |
R2272:Hydin
|
UTSW |
8 |
111,035,764 (GRCm39) |
missense |
probably benign |
0.01 |
R2294:Hydin
|
UTSW |
8 |
111,026,591 (GRCm39) |
missense |
probably damaging |
0.99 |
R2315:Hydin
|
UTSW |
8 |
111,124,676 (GRCm39) |
missense |
probably benign |
0.01 |
R2330:Hydin
|
UTSW |
8 |
111,291,641 (GRCm39) |
missense |
probably benign |
0.01 |
R2374:Hydin
|
UTSW |
8 |
111,291,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R2446:Hydin
|
UTSW |
8 |
111,314,347 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2484:Hydin
|
UTSW |
8 |
111,239,747 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2698:Hydin
|
UTSW |
8 |
111,336,561 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2843:Hydin
|
UTSW |
8 |
111,245,746 (GRCm39) |
missense |
probably benign |
|
R2844:Hydin
|
UTSW |
8 |
111,245,746 (GRCm39) |
missense |
probably benign |
|
R2846:Hydin
|
UTSW |
8 |
111,245,746 (GRCm39) |
missense |
probably benign |
|
R2882:Hydin
|
UTSW |
8 |
111,293,555 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2937:Hydin
|
UTSW |
8 |
111,130,927 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3031:Hydin
|
UTSW |
8 |
111,329,848 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3038:Hydin
|
UTSW |
8 |
111,309,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R3121:Hydin
|
UTSW |
8 |
111,233,138 (GRCm39) |
missense |
probably benign |
|
R3157:Hydin
|
UTSW |
8 |
110,994,005 (GRCm39) |
missense |
unknown |
|
R3547:Hydin
|
UTSW |
8 |
111,308,699 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3696:Hydin
|
UTSW |
8 |
111,329,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R3850:Hydin
|
UTSW |
8 |
111,290,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R3896:Hydin
|
UTSW |
8 |
111,235,711 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3983:Hydin
|
UTSW |
8 |
111,118,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R4031:Hydin
|
UTSW |
8 |
111,336,679 (GRCm39) |
missense |
probably benign |
0.30 |
R4072:Hydin
|
UTSW |
8 |
111,231,888 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4095:Hydin
|
UTSW |
8 |
111,268,179 (GRCm39) |
missense |
probably damaging |
0.98 |
R4176:Hydin
|
UTSW |
8 |
111,320,452 (GRCm39) |
missense |
probably benign |
0.00 |
R4213:Hydin
|
UTSW |
8 |
111,183,139 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4412:Hydin
|
UTSW |
8 |
111,142,368 (GRCm39) |
missense |
probably damaging |
0.99 |
R4471:Hydin
|
UTSW |
8 |
111,313,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R4474:Hydin
|
UTSW |
8 |
111,290,497 (GRCm39) |
missense |
probably benign |
0.11 |
R4495:Hydin
|
UTSW |
8 |
111,322,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R4508:Hydin
|
UTSW |
8 |
111,245,886 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4578:Hydin
|
UTSW |
8 |
110,993,971 (GRCm39) |
missense |
unknown |
|
R4583:Hydin
|
UTSW |
8 |
111,321,857 (GRCm39) |
missense |
probably benign |
0.36 |
R4600:Hydin
|
UTSW |
8 |
111,293,582 (GRCm39) |
missense |
probably benign |
0.04 |
R4681:Hydin
|
UTSW |
8 |
111,233,103 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4685:Hydin
|
UTSW |
8 |
111,189,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R4689:Hydin
|
UTSW |
8 |
111,322,046 (GRCm39) |
missense |
probably benign |
0.18 |
R4735:Hydin
|
UTSW |
8 |
111,282,264 (GRCm39) |
critical splice donor site |
probably null |
|
R4736:Hydin
|
UTSW |
8 |
111,249,840 (GRCm39) |
missense |
probably benign |
0.02 |
R4740:Hydin
|
UTSW |
8 |
111,173,071 (GRCm39) |
missense |
probably benign |
0.06 |
R4771:Hydin
|
UTSW |
8 |
111,259,515 (GRCm39) |
missense |
probably benign |
|
R4777:Hydin
|
UTSW |
8 |
111,137,096 (GRCm39) |
missense |
probably damaging |
0.98 |
R4859:Hydin
|
UTSW |
8 |
111,233,126 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4911:Hydin
|
UTSW |
8 |
111,322,070 (GRCm39) |
missense |
probably benign |
0.01 |
R4964:Hydin
|
UTSW |
8 |
111,217,305 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4989:Hydin
|
UTSW |
8 |
111,290,554 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4995:Hydin
|
UTSW |
8 |
111,296,274 (GRCm39) |
missense |
probably damaging |
0.97 |
R5059:Hydin
|
UTSW |
8 |
111,232,401 (GRCm39) |
missense |
probably damaging |
0.96 |
R5071:Hydin
|
UTSW |
8 |
111,265,105 (GRCm39) |
missense |
probably benign |
0.03 |
R5073:Hydin
|
UTSW |
8 |
111,265,105 (GRCm39) |
missense |
probably benign |
0.03 |
R5092:Hydin
|
UTSW |
8 |
111,309,300 (GRCm39) |
missense |
probably benign |
0.16 |
R5156:Hydin
|
UTSW |
8 |
111,336,333 (GRCm39) |
missense |
probably benign |
0.00 |
R5166:Hydin
|
UTSW |
8 |
111,249,774 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5189:Hydin
|
UTSW |
8 |
111,139,843 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5243:Hydin
|
UTSW |
8 |
111,232,380 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5244:Hydin
|
UTSW |
8 |
111,259,451 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5256:Hydin
|
UTSW |
8 |
111,313,855 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5266:Hydin
|
UTSW |
8 |
111,061,416 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5283:Hydin
|
UTSW |
8 |
111,178,612 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5343:Hydin
|
UTSW |
8 |
111,212,051 (GRCm39) |
missense |
probably benign |
0.40 |
R5359:Hydin
|
UTSW |
8 |
111,265,004 (GRCm39) |
missense |
probably benign |
0.00 |
R5390:Hydin
|
UTSW |
8 |
111,322,099 (GRCm39) |
missense |
probably benign |
|
R5394:Hydin
|
UTSW |
8 |
111,266,474 (GRCm39) |
splice site |
probably null |
|
R5441:Hydin
|
UTSW |
8 |
111,291,741 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5461:Hydin
|
UTSW |
8 |
111,245,863 (GRCm39) |
missense |
probably damaging |
0.96 |
R5662:Hydin
|
UTSW |
8 |
111,307,341 (GRCm39) |
missense |
probably benign |
0.02 |
R5695:Hydin
|
UTSW |
8 |
111,261,915 (GRCm39) |
missense |
probably benign |
0.35 |
R5732:Hydin
|
UTSW |
8 |
111,178,690 (GRCm39) |
missense |
probably benign |
0.03 |
R5774:Hydin
|
UTSW |
8 |
111,298,547 (GRCm39) |
nonsense |
probably null |
|
R5780:Hydin
|
UTSW |
8 |
111,312,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R5787:Hydin
|
UTSW |
8 |
111,052,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R5802:Hydin
|
UTSW |
8 |
111,178,692 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5841:Hydin
|
UTSW |
8 |
111,259,846 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5856:Hydin
|
UTSW |
8 |
111,268,474 (GRCm39) |
missense |
probably damaging |
0.99 |
R5893:Hydin
|
UTSW |
8 |
111,217,308 (GRCm39) |
missense |
probably benign |
0.12 |
R5963:Hydin
|
UTSW |
8 |
111,220,926 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6008:Hydin
|
UTSW |
8 |
111,325,717 (GRCm39) |
missense |
probably benign |
0.02 |
R6019:Hydin
|
UTSW |
8 |
111,293,252 (GRCm39) |
missense |
probably benign |
|
R6038:Hydin
|
UTSW |
8 |
111,325,663 (GRCm39) |
missense |
probably benign |
0.16 |
R6038:Hydin
|
UTSW |
8 |
111,325,663 (GRCm39) |
missense |
probably benign |
0.16 |
R6133:Hydin
|
UTSW |
8 |
111,327,908 (GRCm39) |
missense |
probably benign |
0.00 |
R6135:Hydin
|
UTSW |
8 |
111,189,292 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6157:Hydin
|
UTSW |
8 |
111,254,648 (GRCm39) |
missense |
probably benign |
|
R6209:Hydin
|
UTSW |
8 |
111,320,434 (GRCm39) |
missense |
probably benign |
0.05 |
R6238:Hydin
|
UTSW |
8 |
111,118,743 (GRCm39) |
splice site |
probably null |
|
R6293:Hydin
|
UTSW |
8 |
111,324,543 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6340:Hydin
|
UTSW |
8 |
111,081,574 (GRCm39) |
splice site |
probably null |
|
R6349:Hydin
|
UTSW |
8 |
111,145,091 (GRCm39) |
nonsense |
probably null |
|
R6357:Hydin
|
UTSW |
8 |
111,268,289 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6385:Hydin
|
UTSW |
8 |
111,038,856 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6396:Hydin
|
UTSW |
8 |
111,233,521 (GRCm39) |
missense |
probably damaging |
0.96 |
R6466:Hydin
|
UTSW |
8 |
111,233,600 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6648:Hydin
|
UTSW |
8 |
111,252,299 (GRCm39) |
splice site |
probably null |
|
R6671:Hydin
|
UTSW |
8 |
111,327,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R6695:Hydin
|
UTSW |
8 |
111,053,092 (GRCm39) |
missense |
probably benign |
0.05 |
R6800:Hydin
|
UTSW |
8 |
111,324,603 (GRCm39) |
missense |
probably benign |
0.09 |
R6841:Hydin
|
UTSW |
8 |
111,265,007 (GRCm39) |
missense |
probably benign |
0.09 |
R6867:Hydin
|
UTSW |
8 |
111,266,434 (GRCm39) |
missense |
probably benign |
0.08 |
R6889:Hydin
|
UTSW |
8 |
111,259,488 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6895:Hydin
|
UTSW |
8 |
111,038,883 (GRCm39) |
missense |
probably benign |
0.00 |
R6940:Hydin
|
UTSW |
8 |
111,217,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R6951:Hydin
|
UTSW |
8 |
111,124,757 (GRCm39) |
missense |
probably benign |
|
R6980:Hydin
|
UTSW |
8 |
111,139,916 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6981:Hydin
|
UTSW |
8 |
111,257,704 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7061:Hydin
|
UTSW |
8 |
111,329,920 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7085:Hydin
|
UTSW |
8 |
111,329,962 (GRCm39) |
missense |
probably benign |
0.03 |
R7086:Hydin
|
UTSW |
8 |
111,326,877 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7110:Hydin
|
UTSW |
8 |
111,081,583 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7158:Hydin
|
UTSW |
8 |
111,336,303 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7163:Hydin
|
UTSW |
8 |
111,329,968 (GRCm39) |
missense |
probably benign |
0.25 |
R7209:Hydin
|
UTSW |
8 |
111,216,424 (GRCm39) |
nonsense |
probably null |
|
R7244:Hydin
|
UTSW |
8 |
111,276,307 (GRCm39) |
missense |
probably damaging |
0.98 |
R7347:Hydin
|
UTSW |
8 |
111,326,994 (GRCm39) |
missense |
probably benign |
0.06 |
R7349:Hydin
|
UTSW |
8 |
111,124,803 (GRCm39) |
splice site |
probably null |
|
R7359:Hydin
|
UTSW |
8 |
111,232,733 (GRCm39) |
missense |
probably damaging |
0.98 |
R7365:Hydin
|
UTSW |
8 |
111,327,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R7365:Hydin
|
UTSW |
8 |
111,284,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R7436:Hydin
|
UTSW |
8 |
111,310,546 (GRCm39) |
missense |
probably damaging |
0.96 |
R7528:Hydin
|
UTSW |
8 |
111,107,204 (GRCm39) |
nonsense |
probably null |
|
R7544:Hydin
|
UTSW |
8 |
111,316,157 (GRCm39) |
missense |
probably benign |
0.35 |
R7625:Hydin
|
UTSW |
8 |
111,268,476 (GRCm39) |
missense |
probably benign |
0.01 |
R7713:Hydin
|
UTSW |
8 |
111,320,444 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7763:Hydin
|
UTSW |
8 |
111,232,475 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7771:Hydin
|
UTSW |
8 |
111,291,717 (GRCm39) |
missense |
probably damaging |
0.97 |
R7794:Hydin
|
UTSW |
8 |
111,235,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R7833:Hydin
|
UTSW |
8 |
111,316,092 (GRCm39) |
missense |
probably damaging |
0.99 |
R7894:Hydin
|
UTSW |
8 |
111,239,642 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7899:Hydin
|
UTSW |
8 |
111,314,380 (GRCm39) |
missense |
probably benign |
0.00 |
R7908:Hydin
|
UTSW |
8 |
111,237,499 (GRCm39) |
missense |
probably benign |
0.01 |
R7912:Hydin
|
UTSW |
8 |
111,282,239 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7919:Hydin
|
UTSW |
8 |
110,993,971 (GRCm39) |
missense |
unknown |
|
R7924:Hydin
|
UTSW |
8 |
111,145,103 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7927:Hydin
|
UTSW |
8 |
111,307,476 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7970:Hydin
|
UTSW |
8 |
111,035,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R7993:Hydin
|
UTSW |
8 |
111,306,264 (GRCm39) |
missense |
probably benign |
|
R8011:Hydin
|
UTSW |
8 |
111,310,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R8041:Hydin
|
UTSW |
8 |
111,301,626 (GRCm39) |
missense |
probably benign |
0.02 |
R8080:Hydin
|
UTSW |
8 |
111,261,863 (GRCm39) |
missense |
probably benign |
0.32 |
R8081:Hydin
|
UTSW |
8 |
111,092,101 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8095:Hydin
|
UTSW |
8 |
111,295,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R8157:Hydin
|
UTSW |
8 |
111,178,668 (GRCm39) |
missense |
probably benign |
0.33 |
R8186:Hydin
|
UTSW |
8 |
111,336,277 (GRCm39) |
missense |
probably benign |
0.14 |
R8205:Hydin
|
UTSW |
8 |
111,319,270 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8263:Hydin
|
UTSW |
8 |
111,178,705 (GRCm39) |
missense |
probably benign |
0.00 |
R8288:Hydin
|
UTSW |
8 |
111,233,661 (GRCm39) |
missense |
probably damaging |
0.96 |
R8298:Hydin
|
UTSW |
8 |
111,327,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8309:Hydin
|
UTSW |
8 |
111,334,534 (GRCm39) |
missense |
probably benign |
0.18 |
R8348:Hydin
|
UTSW |
8 |
111,329,878 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8356:Hydin
|
UTSW |
8 |
111,259,756 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8406:Hydin
|
UTSW |
8 |
111,336,543 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8415:Hydin
|
UTSW |
8 |
111,178,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R8417:Hydin
|
UTSW |
8 |
111,296,024 (GRCm39) |
missense |
probably benign |
0.28 |
R8432:Hydin
|
UTSW |
8 |
111,324,583 (GRCm39) |
missense |
probably benign |
0.02 |
R8437:Hydin
|
UTSW |
8 |
111,189,367 (GRCm39) |
missense |
probably damaging |
0.96 |
R8463:Hydin
|
UTSW |
8 |
111,237,553 (GRCm39) |
missense |
probably benign |
0.22 |
R8508:Hydin
|
UTSW |
8 |
111,308,650 (GRCm39) |
missense |
probably benign |
0.00 |
R8510:Hydin
|
UTSW |
8 |
111,233,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R8560:Hydin
|
UTSW |
8 |
111,265,106 (GRCm39) |
missense |
probably benign |
0.09 |
R8682:Hydin
|
UTSW |
8 |
111,035,798 (GRCm39) |
missense |
probably damaging |
0.96 |
R8697:Hydin
|
UTSW |
8 |
111,259,515 (GRCm39) |
missense |
probably benign |
|
R8857:Hydin
|
UTSW |
8 |
111,298,587 (GRCm39) |
critical splice donor site |
probably null |
|
R8866:Hydin
|
UTSW |
8 |
111,308,779 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8878:Hydin
|
UTSW |
8 |
111,035,720 (GRCm39) |
missense |
probably benign |
0.12 |
R8897:Hydin
|
UTSW |
8 |
111,316,112 (GRCm39) |
missense |
probably benign |
|
R8987:Hydin
|
UTSW |
8 |
111,239,766 (GRCm39) |
nonsense |
probably null |
|
R9072:Hydin
|
UTSW |
8 |
110,994,083 (GRCm39) |
critical splice donor site |
probably null |
|
R9073:Hydin
|
UTSW |
8 |
110,994,083 (GRCm39) |
critical splice donor site |
probably null |
|
R9102:Hydin
|
UTSW |
8 |
111,235,546 (GRCm39) |
missense |
probably benign |
0.33 |
R9224:Hydin
|
UTSW |
8 |
111,259,516 (GRCm39) |
missense |
probably benign |
|
R9255:Hydin
|
UTSW |
8 |
111,261,972 (GRCm39) |
missense |
probably benign |
0.23 |
R9257:Hydin
|
UTSW |
8 |
111,301,648 (GRCm39) |
missense |
probably damaging |
0.99 |
R9261:Hydin
|
UTSW |
8 |
110,994,047 (GRCm39) |
missense |
unknown |
|
R9273:Hydin
|
UTSW |
8 |
111,233,580 (GRCm39) |
missense |
probably damaging |
0.98 |
R9376:Hydin
|
UTSW |
8 |
111,124,695 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9380:Hydin
|
UTSW |
8 |
111,290,504 (GRCm39) |
missense |
probably benign |
0.07 |
R9386:Hydin
|
UTSW |
8 |
111,314,362 (GRCm39) |
missense |
probably benign |
|
R9406:Hydin
|
UTSW |
8 |
111,314,412 (GRCm39) |
missense |
probably null |
0.96 |
R9492:Hydin
|
UTSW |
8 |
111,326,877 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9513:Hydin
|
UTSW |
8 |
111,322,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R9562:Hydin
|
UTSW |
8 |
111,312,786 (GRCm39) |
missense |
probably benign |
0.11 |
R9664:Hydin
|
UTSW |
8 |
111,220,965 (GRCm39) |
missense |
probably benign |
0.01 |
R9733:Hydin
|
UTSW |
8 |
111,262,011 (GRCm39) |
missense |
probably benign |
|
R9753:Hydin
|
UTSW |
8 |
111,217,398 (GRCm39) |
missense |
possibly damaging |
0.85 |
X0063:Hydin
|
UTSW |
8 |
111,277,951 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Hydin
|
UTSW |
8 |
111,319,423 (GRCm39) |
frame shift |
probably null |
|
Z1088:Hydin
|
UTSW |
8 |
111,312,680 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Hydin
|
UTSW |
8 |
111,026,605 (GRCm39) |
missense |
probably benign |
0.12 |
Z1176:Hydin
|
UTSW |
8 |
111,268,232 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1177:Hydin
|
UTSW |
8 |
111,313,774 (GRCm39) |
frame shift |
probably null |
|
Z1177:Hydin
|
UTSW |
8 |
111,176,864 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Hydin
|
UTSW |
8 |
111,107,242 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Hydin
|
UTSW |
8 |
111,336,621 (GRCm39) |
missense |
probably benign |
0.10 |
Z1188:Hydin
|
UTSW |
8 |
111,142,419 (GRCm39) |
missense |
probably benign |
0.40 |
|