Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
A |
T |
11: 110,110,144 (GRCm39) |
S600T |
probably benign |
Het |
Acly |
T |
A |
11: 100,386,717 (GRCm39) |
Q615L |
probably benign |
Het |
Adgrf1 |
C |
A |
17: 43,620,924 (GRCm39) |
T387K |
probably benign |
Het |
Afg3l1 |
G |
T |
8: 124,228,670 (GRCm39) |
K745N |
probably damaging |
Het |
Armc8 |
T |
C |
9: 99,418,312 (GRCm39) |
T39A |
possibly damaging |
Het |
Atm |
C |
A |
9: 53,403,533 (GRCm39) |
|
probably benign |
Het |
Babam2 |
A |
G |
5: 32,214,890 (GRCm39) |
T324A |
probably damaging |
Het |
Btd |
C |
A |
14: 31,384,246 (GRCm39) |
D77E |
possibly damaging |
Het |
Cadm1 |
T |
A |
9: 47,740,668 (GRCm39) |
|
probably benign |
Het |
Card11 |
A |
T |
5: 140,871,315 (GRCm39) |
D729E |
probably benign |
Het |
Ccni |
G |
T |
5: 93,335,967 (GRCm39) |
T144K |
possibly damaging |
Het |
Ceacam23 |
C |
T |
7: 17,607,255 (GRCm39) |
|
noncoding transcript |
Het |
Cecr2 |
A |
G |
6: 120,708,228 (GRCm39) |
T77A |
probably damaging |
Het |
Cgas |
A |
G |
9: 78,341,593 (GRCm39) |
|
probably null |
Het |
Cpsf7 |
T |
C |
19: 10,512,803 (GRCm39) |
F296L |
possibly damaging |
Het |
Cyfip1 |
C |
A |
7: 55,523,196 (GRCm39) |
N70K |
possibly damaging |
Het |
Cyp4a12b |
A |
G |
4: 115,271,259 (GRCm39) |
|
probably benign |
Het |
Ddx20 |
A |
T |
3: 105,585,896 (GRCm39) |
Y816* |
probably null |
Het |
Ddx59 |
A |
G |
1: 136,360,245 (GRCm39) |
I420V |
probably damaging |
Het |
Dgat1 |
T |
A |
15: 76,386,703 (GRCm39) |
M445L |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,246,546 (GRCm39) |
L628* |
probably null |
Het |
Dnah7a |
A |
C |
1: 53,598,307 (GRCm39) |
D1409E |
probably benign |
Het |
Dnmt1 |
T |
C |
9: 20,838,422 (GRCm39) |
T215A |
probably benign |
Het |
Dsg4 |
C |
T |
18: 20,604,302 (GRCm39) |
T923M |
probably damaging |
Het |
Enox1 |
A |
G |
14: 77,852,915 (GRCm39) |
I394V |
possibly damaging |
Het |
Esrp2 |
A |
T |
8: 106,861,250 (GRCm39) |
M183K |
probably damaging |
Het |
Fam171a1 |
C |
T |
2: 3,179,410 (GRCm39) |
P79S |
probably benign |
Het |
Fga |
A |
G |
3: 82,939,082 (GRCm39) |
T486A |
probably benign |
Het |
Fkbp10 |
G |
T |
11: 100,306,715 (GRCm39) |
A36S |
probably benign |
Het |
Fnip1 |
A |
G |
11: 54,393,279 (GRCm39) |
T572A |
probably benign |
Het |
Fxn |
A |
C |
19: 24,257,765 (GRCm39) |
|
probably null |
Het |
Gaa |
C |
T |
11: 119,175,324 (GRCm39) |
Q901* |
probably null |
Het |
Gabrg1 |
A |
G |
5: 70,911,594 (GRCm39) |
M344T |
probably benign |
Het |
Galnt7 |
C |
T |
8: 57,991,212 (GRCm39) |
V433M |
probably damaging |
Het |
Gin1 |
A |
G |
1: 97,712,951 (GRCm39) |
|
probably null |
Het |
Igsf6 |
T |
C |
7: 120,670,031 (GRCm39) |
Y37C |
probably damaging |
Het |
Il18rap |
A |
G |
1: 40,570,687 (GRCm39) |
I210V |
probably benign |
Het |
Kif3a |
T |
C |
11: 53,489,561 (GRCm39) |
Y138H |
probably damaging |
Het |
Klra17 |
A |
G |
6: 129,845,681 (GRCm39) |
|
probably null |
Het |
Lcorl |
A |
T |
5: 45,952,688 (GRCm39) |
I55N |
probably damaging |
Het |
Lrrc49 |
A |
G |
9: 60,510,059 (GRCm39) |
S398P |
possibly damaging |
Het |
Ltv1 |
A |
G |
10: 13,055,018 (GRCm39) |
L384S |
probably damaging |
Het |
Mageb3 |
A |
T |
2: 121,784,918 (GRCm39) |
Y261* |
probably null |
Het |
Mical3 |
T |
G |
6: 121,019,196 (GRCm39) |
T9P |
probably benign |
Het |
Myrip |
C |
T |
9: 120,217,228 (GRCm39) |
S49L |
probably damaging |
Het |
Nrap |
T |
C |
19: 56,372,487 (GRCm39) |
|
probably benign |
Het |
Or2m12 |
T |
C |
16: 19,104,627 (GRCm39) |
N289D |
probably damaging |
Het |
Or4k5 |
A |
G |
14: 50,385,728 (GRCm39) |
V201A |
probably benign |
Het |
Otoa |
A |
T |
7: 120,759,753 (GRCm39) |
|
probably benign |
Het |
Pals2 |
T |
G |
6: 50,140,411 (GRCm39) |
F144V |
probably benign |
Het |
Parp11 |
T |
A |
6: 127,467,008 (GRCm39) |
I133N |
probably damaging |
Het |
Pcnx1 |
A |
G |
12: 81,965,416 (GRCm39) |
T528A |
probably benign |
Het |
Pde4c |
A |
G |
8: 71,179,638 (GRCm39) |
H63R |
probably benign |
Het |
Pdpk1 |
T |
C |
17: 24,329,878 (GRCm39) |
K53E |
probably damaging |
Het |
Pdzd7 |
A |
T |
19: 45,024,615 (GRCm39) |
M468K |
probably damaging |
Het |
Perm1 |
C |
A |
4: 156,303,061 (GRCm39) |
P535Q |
possibly damaging |
Het |
Pgap1 |
C |
A |
1: 54,575,128 (GRCm39) |
A265S |
probably benign |
Het |
Pik3c2a |
A |
T |
7: 115,975,747 (GRCm39) |
|
probably null |
Het |
Plxnd1 |
T |
C |
6: 115,957,562 (GRCm39) |
T491A |
possibly damaging |
Het |
Pms1 |
A |
T |
1: 53,246,128 (GRCm39) |
D470E |
probably benign |
Het |
Prf1 |
C |
A |
10: 61,138,762 (GRCm39) |
T240N |
probably damaging |
Het |
Prune2 |
A |
G |
19: 17,099,445 (GRCm39) |
T1650A |
probably benign |
Het |
Ptprf |
A |
G |
4: 118,080,462 (GRCm39) |
L1264P |
probably benign |
Het |
Ptprs |
A |
G |
17: 56,726,527 (GRCm39) |
S948P |
probably damaging |
Het |
Rapgef1 |
T |
C |
2: 29,576,268 (GRCm39) |
V117A |
probably damaging |
Het |
Rnf123 |
A |
G |
9: 107,940,125 (GRCm39) |
V756A |
probably benign |
Het |
Sez6l2 |
A |
G |
7: 126,566,291 (GRCm39) |
E741G |
probably damaging |
Het |
Shc3 |
A |
T |
13: 51,626,888 (GRCm39) |
I125K |
possibly damaging |
Het |
Smr3a |
A |
T |
5: 88,155,917 (GRCm39) |
|
probably benign |
Het |
Spef2 |
C |
T |
15: 9,584,194 (GRCm39) |
E1624K |
probably damaging |
Het |
St6gal1 |
A |
T |
16: 23,140,083 (GRCm39) |
K85* |
probably null |
Het |
Taf1b |
T |
G |
12: 24,597,121 (GRCm39) |
D353E |
possibly damaging |
Het |
Tcp10b |
C |
T |
17: 13,286,590 (GRCm39) |
P180S |
possibly damaging |
Het |
Tlr9 |
A |
T |
9: 106,102,142 (GRCm39) |
M478L |
probably benign |
Het |
Tpr |
A |
T |
1: 150,295,654 (GRCm39) |
E892D |
probably damaging |
Het |
Trio |
C |
T |
15: 27,742,581 (GRCm39) |
W22* |
probably null |
Het |
Usp14 |
A |
G |
18: 10,024,673 (GRCm39) |
V8A |
probably damaging |
Het |
Vmn2r19 |
A |
T |
6: 123,307,011 (GRCm39) |
K506N |
possibly damaging |
Het |
Vmn2r45 |
T |
A |
7: 8,475,372 (GRCm39) |
N552I |
probably damaging |
Het |
Vmn2r56 |
A |
T |
7: 12,449,542 (GRCm39) |
M232K |
probably benign |
Het |
Vps13b |
T |
A |
15: 35,910,788 (GRCm39) |
F3517L |
possibly damaging |
Het |
Yif1a |
C |
T |
19: 5,142,333 (GRCm39) |
R247* |
probably null |
Het |
Zbtb5 |
A |
G |
4: 44,993,767 (GRCm39) |
V539A |
probably benign |
Het |
Zfp180 |
G |
A |
7: 23,804,652 (GRCm39) |
R357Q |
probably damaging |
Het |
Zfp536 |
A |
G |
7: 37,268,042 (GRCm39) |
L458P |
probably damaging |
Het |
Zfp646 |
G |
A |
7: 127,482,292 (GRCm39) |
G1490S |
probably benign |
Het |
Zfp970 |
C |
T |
2: 177,167,976 (GRCm39) |
H517Y |
probably damaging |
Het |
Zranb3 |
A |
T |
1: 127,945,293 (GRCm39) |
|
probably null |
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 |
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 |
|
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 |
|