Other mutations in this stock |
Total: 128 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700069L16Rik |
T |
C |
5: 113,830,813 (GRCm39) |
K59R |
unknown |
Het |
Abcb4 |
T |
C |
5: 8,977,931 (GRCm39) |
V503A |
probably benign |
Het |
Actn4 |
A |
G |
7: 28,596,398 (GRCm39) |
V699A |
probably benign |
Het |
Adam26a |
T |
A |
8: 44,022,358 (GRCm39) |
K377N |
probably benign |
Het |
Adam6b |
C |
T |
12: 113,454,748 (GRCm39) |
R522C |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 20,839,683 (GRCm39) |
Y198C |
probably damaging |
Het |
Ankrd44 |
G |
A |
1: 54,700,349 (GRCm39) |
Q720* |
probably null |
Het |
Arhgap26 |
A |
T |
18: 39,490,652 (GRCm39) |
M297L |
|
Het |
Arhgef11 |
C |
T |
3: 87,637,788 (GRCm39) |
T1093I |
probably damaging |
Het |
Arhgef25 |
C |
A |
10: 127,018,735 (GRCm39) |
R609S |
probably damaging |
Het |
Arhgef28 |
G |
T |
13: 98,190,472 (GRCm39) |
H162Q |
possibly damaging |
Het |
Atg4b |
A |
G |
1: 93,706,081 (GRCm39) |
E178G |
possibly damaging |
Het |
Atxn1l |
T |
C |
8: 110,459,117 (GRCm39) |
T382A |
probably benign |
Het |
Bdp1 |
A |
G |
13: 100,204,021 (GRCm39) |
V667A |
probably benign |
Het |
C6 |
T |
C |
15: 4,844,344 (GRCm39) |
I922T |
|
Het |
Ccdc191 |
A |
G |
16: 43,751,710 (GRCm39) |
T347A |
probably benign |
Het |
Cd22 |
G |
T |
7: 30,577,172 (GRCm39) |
P45H |
probably damaging |
Het |
Cdc45 |
A |
G |
16: 18,630,300 (GRCm39) |
F6L |
probably benign |
Het |
Cenpj |
T |
C |
14: 56,764,383 (GRCm39) |
E1343G |
possibly damaging |
Het |
Chtf8 |
T |
A |
8: 107,612,735 (GRCm39) |
N68I |
probably benign |
Het |
Cldn8 |
C |
T |
16: 88,359,733 (GRCm39) |
C64Y |
probably damaging |
Het |
Cntnap2 |
G |
T |
6: 46,460,983 (GRCm39) |
S673I |
probably benign |
Het |
Cyp3a13 |
C |
T |
5: 137,909,849 (GRCm39) |
R158K |
probably benign |
Het |
Cyp3a57 |
A |
T |
5: 145,311,039 (GRCm39) |
|
probably null |
Het |
Cyp3a57 |
G |
T |
5: 145,311,040 (GRCm39) |
|
probably null |
Het |
D630045J12Rik |
A |
G |
6: 38,173,898 (GRCm39) |
I90T |
probably benign |
Het |
Dapk2 |
A |
G |
9: 66,157,602 (GRCm39) |
|
probably benign |
Het |
Dmxl1 |
A |
G |
18: 50,026,919 (GRCm39) |
D2009G |
|
Het |
Dnah1 |
C |
T |
14: 31,033,704 (GRCm39) |
V290I |
possibly damaging |
Het |
Doc2g |
A |
T |
19: 4,054,511 (GRCm39) |
|
probably null |
Het |
Dpysl2 |
C |
T |
14: 67,045,402 (GRCm39) |
G457D |
probably damaging |
Het |
Drc1 |
A |
T |
5: 30,521,439 (GRCm39) |
Y700F |
probably damaging |
Het |
Ehbp1 |
A |
G |
11: 22,003,531 (GRCm39) |
Y1073H |
probably damaging |
Het |
Epm2aip1 |
T |
A |
9: 111,101,036 (GRCm39) |
M3K |
probably benign |
Het |
Erich3 |
G |
A |
3: 154,415,340 (GRCm39) |
R152Q |
|
Het |
Exoc5 |
C |
T |
14: 49,252,986 (GRCm39) |
R609H |
probably damaging |
Het |
Fam135b |
T |
A |
15: 71,334,189 (GRCm39) |
T1002S |
probably benign |
Het |
Fanca |
C |
T |
8: 124,024,538 (GRCm39) |
E528K |
probably damaging |
Het |
Fsd2 |
C |
A |
7: 81,209,766 (GRCm39) |
M25I |
probably benign |
Het |
Fyco1 |
T |
C |
9: 123,658,139 (GRCm39) |
E679G |
possibly damaging |
Het |
Gas6 |
T |
A |
8: 13,520,294 (GRCm39) |
M465L |
probably damaging |
Het |
Gfra3 |
A |
G |
18: 34,823,879 (GRCm39) |
V365A |
probably benign |
Het |
Gm10269 |
T |
G |
18: 20,815,981 (GRCm39) |
K14Q |
possibly damaging |
Het |
Gm21798 |
G |
A |
15: 64,689,756 (GRCm39) |
|
probably null |
Het |
Gm5916 |
T |
A |
9: 36,032,286 (GRCm39) |
R49S |
probably benign |
Het |
Gpam |
G |
T |
19: 55,072,227 (GRCm39) |
T266N |
possibly damaging |
Het |
Gtse1 |
A |
G |
15: 85,753,109 (GRCm39) |
E408G |
probably benign |
Het |
Hmgcll1 |
A |
T |
9: 76,037,592 (GRCm39) |
|
probably null |
Het |
Hspa12a |
T |
A |
19: 58,787,903 (GRCm39) |
R640* |
probably null |
Het |
Hspa9 |
T |
C |
18: 35,080,982 (GRCm39) |
D233G |
probably damaging |
Het |
Htt |
T |
G |
5: 34,977,368 (GRCm39) |
I751M |
probably benign |
Het |
Ift43 |
A |
C |
12: 86,208,275 (GRCm39) |
M138L |
probably benign |
Het |
Il11 |
C |
T |
7: 4,779,029 (GRCm39) |
V93M |
probably damaging |
Het |
Iws1 |
T |
A |
18: 32,226,645 (GRCm39) |
F741L |
possibly damaging |
Het |
Jmy |
A |
T |
13: 93,589,397 (GRCm39) |
I620N |
probably damaging |
Het |
Kap |
T |
A |
6: 133,830,689 (GRCm39) |
|
probably benign |
Het |
Kcnk15 |
A |
G |
2: 163,700,217 (GRCm39) |
N152S |
probably damaging |
Het |
Kif16b |
C |
T |
2: 142,691,783 (GRCm39) |
|
probably null |
Het |
Kif16b |
T |
C |
2: 142,743,278 (GRCm39) |
K5R |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,992,400 (GRCm39) |
R555H |
probably damaging |
Het |
Krt36 |
A |
G |
11: 99,994,372 (GRCm39) |
V235A |
possibly damaging |
Het |
Lca5 |
A |
G |
9: 83,283,796 (GRCm39) |
S246P |
probably damaging |
Het |
Maml1 |
T |
C |
11: 50,157,575 (GRCm39) |
D200G |
probably damaging |
Het |
Maml3 |
T |
C |
3: 51,597,868 (GRCm39) |
R939G |
probably damaging |
Het |
Mgam |
A |
T |
6: 40,706,570 (GRCm39) |
T74S |
probably damaging |
Het |
Mib2 |
G |
T |
4: 155,745,351 (GRCm39) |
D125E |
probably benign |
Het |
Muc16 |
A |
T |
9: 18,462,981 (GRCm39) |
L7407* |
probably null |
Het |
Mycbp2 |
A |
T |
14: 103,446,232 (GRCm39) |
N1865K |
probably damaging |
Het |
Naip1 |
A |
G |
13: 100,563,434 (GRCm39) |
L577S |
probably damaging |
Het |
Nell1 |
A |
T |
7: 50,498,399 (GRCm39) |
D652V |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nxph1 |
G |
A |
6: 8,950,312 (GRCm39) |
|
probably benign |
Het |
Oas1h |
T |
A |
5: 121,005,152 (GRCm39) |
I200N |
probably damaging |
Het |
Or2h2b-ps1 |
A |
G |
17: 37,480,867 (GRCm39) |
L122P |
probably damaging |
Het |
Or2h2b-ps1 |
A |
T |
17: 37,480,990 (GRCm39) |
I81N |
probably damaging |
Het |
Or8g53 |
A |
T |
9: 39,683,688 (GRCm39) |
M136K |
probably benign |
Het |
Otog |
A |
T |
7: 45,936,878 (GRCm39) |
Q1529L |
probably benign |
Het |
Otop1 |
A |
T |
5: 38,457,071 (GRCm39) |
I277F |
probably damaging |
Het |
Pax5 |
G |
A |
4: 44,645,661 (GRCm39) |
Q223* |
probably null |
Het |
Pcdha9 |
T |
A |
18: 37,132,998 (GRCm39) |
I689N |
probably benign |
Het |
Pcsk6 |
A |
T |
7: 65,576,975 (GRCm39) |
R138* |
probably null |
Het |
Pitpnm3 |
A |
T |
11: 72,003,132 (GRCm39) |
N59K |
probably damaging |
Het |
Pla2g4d |
G |
A |
2: 120,100,442 (GRCm39) |
T630I |
probably damaging |
Het |
Plekhg5 |
T |
A |
4: 152,188,372 (GRCm39) |
|
probably benign |
Het |
Plxnb1 |
T |
A |
9: 108,937,178 (GRCm39) |
|
probably benign |
Het |
Prss28 |
T |
A |
17: 25,528,395 (GRCm39) |
L6H |
probably damaging |
Het |
Pyroxd1 |
T |
A |
6: 142,302,251 (GRCm39) |
V228E |
|
Het |
Ripk2 |
G |
A |
4: 16,123,699 (GRCm39) |
T492M |
possibly damaging |
Het |
Satb1 |
A |
T |
17: 52,112,381 (GRCm39) |
C78S |
probably damaging |
Het |
Scaf11 |
A |
T |
15: 96,316,557 (GRCm39) |
C1002* |
probably null |
Het |
Scarf2 |
A |
C |
16: 17,622,768 (GRCm39) |
Q499P |
probably damaging |
Het |
Selenbp1 |
T |
A |
3: 94,847,425 (GRCm39) |
M244K |
probably benign |
Het |
Sik2 |
T |
C |
9: 50,806,647 (GRCm39) |
N921S |
probably benign |
Het |
Slc25a1 |
A |
T |
16: 17,743,744 (GRCm39) |
V290E |
probably damaging |
Het |
Slc28a3 |
C |
T |
13: 58,719,254 (GRCm39) |
|
probably benign |
Het |
Slc35b4 |
A |
T |
6: 34,137,442 (GRCm39) |
D213E |
probably benign |
Het |
Slc40a1 |
A |
C |
1: 45,950,495 (GRCm39) |
M319R |
probably damaging |
Het |
Slc8a1 |
A |
T |
17: 81,955,282 (GRCm39) |
F585L |
possibly damaging |
Het |
Slco3a1 |
T |
A |
7: 73,970,324 (GRCm39) |
N428Y |
possibly damaging |
Het |
Slfn2 |
G |
A |
11: 82,960,363 (GRCm39) |
C114Y |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,267,714 (GRCm39) |
|
probably null |
Het |
Spata13 |
T |
A |
14: 60,993,896 (GRCm39) |
L1116Q |
possibly damaging |
Het |
Spmap1 |
C |
T |
11: 97,666,510 (GRCm39) |
V59M |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,177,579 (GRCm39) |
V4965A |
possibly damaging |
Het |
Tacc3 |
G |
T |
5: 33,826,169 (GRCm39) |
V472F |
possibly damaging |
Het |
Tacr3 |
T |
A |
3: 134,560,573 (GRCm39) |
Y171N |
probably damaging |
Het |
Tacr3 |
T |
G |
3: 134,560,718 (GRCm39) |
L219R |
probably damaging |
Het |
Tbx3 |
C |
A |
5: 119,818,886 (GRCm39) |
A507E |
possibly damaging |
Het |
Telo2 |
A |
T |
17: 25,324,402 (GRCm39) |
D494E |
probably damaging |
Het |
Tfip11 |
T |
C |
5: 112,484,921 (GRCm39) |
F744S |
possibly damaging |
Het |
Tgm3 |
A |
C |
2: 129,880,403 (GRCm39) |
N403T |
probably benign |
Het |
Thoc3 |
A |
T |
13: 54,615,708 (GRCm39) |
S119T |
possibly damaging |
Het |
Tmem176b |
A |
T |
6: 48,812,530 (GRCm39) |
I145N |
probably damaging |
Het |
Trio |
T |
A |
15: 27,732,773 (GRCm39) |
Q3036L |
probably benign |
Het |
Trpc4 |
T |
C |
3: 54,102,132 (GRCm39) |
V10A |
probably benign |
Het |
Trpm3 |
A |
G |
19: 22,896,124 (GRCm39) |
Y987C |
probably damaging |
Het |
Tspoap1 |
A |
G |
11: 87,654,394 (GRCm39) |
K225E |
probably damaging |
Het |
Txnrd3 |
A |
T |
6: 89,638,477 (GRCm39) |
Q222L |
possibly damaging |
Het |
Usp34 |
A |
T |
11: 23,414,267 (GRCm39) |
M2756L |
|
Het |
Vmn2r81 |
C |
T |
10: 79,129,704 (GRCm39) |
T865I |
probably damaging |
Het |
Vnn1 |
A |
G |
10: 23,776,714 (GRCm39) |
Y355C |
probably damaging |
Het |
Wipf2 |
A |
T |
11: 98,783,092 (GRCm39) |
S173C |
probably damaging |
Het |
Wnt1 |
A |
T |
15: 98,689,624 (GRCm39) |
H137L |
probably damaging |
Het |
Xylt2 |
A |
T |
11: 94,561,278 (GRCm39) |
C162S |
probably damaging |
Het |
Zfp426 |
T |
C |
9: 20,387,744 (GRCm39) |
E33G |
probably damaging |
Het |
Zfp811 |
A |
C |
17: 33,017,801 (GRCm39) |
C80G |
possibly damaging |
Het |
Zfp931 |
T |
C |
2: 177,709,591 (GRCm39) |
H265R |
probably damaging |
Het |
Zfp931 |
G |
A |
2: 177,709,592 (GRCm39) |
H265Y |
probably damaging |
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 |
R4965:Hydin
|
UTSW |
8 |
111,124,727 (GRCm39) |
missense |
probably benign |
|
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 |
|
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 |
|