Other mutations in this stock |
Total: 132 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
A |
G |
5: 125,583,224 (GRCm39) |
D260G |
possibly damaging |
Het |
Aadacl4 |
T |
A |
4: 144,340,362 (GRCm39) |
L29H |
probably damaging |
Het |
Abca7 |
T |
C |
10: 79,848,022 (GRCm39) |
|
probably null |
Het |
Adgre1 |
G |
A |
17: 57,754,832 (GRCm39) |
M643I |
possibly damaging |
Het |
Adgrl2 |
A |
T |
3: 148,596,099 (GRCm39) |
M79K |
probably damaging |
Het |
Ankrd55 |
T |
A |
13: 112,459,573 (GRCm39) |
|
probably null |
Het |
Aopep |
A |
T |
13: 63,318,753 (GRCm39) |
|
probably null |
Het |
Arhgap21 |
A |
G |
2: 20,863,800 (GRCm39) |
I1257T |
probably damaging |
Het |
Arhgap26 |
T |
A |
18: 39,126,690 (GRCm39) |
|
probably benign |
Het |
Arhgap39 |
A |
G |
15: 76,622,005 (GRCm39) |
S199P |
probably damaging |
Het |
Arhgef5 |
A |
G |
6: 43,249,762 (GRCm39) |
D171G |
probably benign |
Het |
Atp7a |
T |
C |
X: 105,163,980 (GRCm39) |
V1305A |
probably damaging |
Het |
B3gnt3 |
T |
A |
8: 72,145,578 (GRCm39) |
R263S |
probably benign |
Het |
B9d1 |
A |
C |
11: 61,398,497 (GRCm39) |
D59A |
probably benign |
Het |
Bag2 |
A |
T |
1: 33,787,357 (GRCm39) |
I55N |
probably benign |
Het |
Bank1 |
T |
C |
3: 135,990,004 (GRCm39) |
I29V |
probably benign |
Het |
Bbs2 |
A |
T |
8: 94,815,743 (GRCm39) |
D174E |
probably damaging |
Het |
Bmp8b |
T |
C |
4: 123,009,030 (GRCm39) |
W203R |
probably damaging |
Het |
Cacnb2 |
A |
T |
2: 14,986,151 (GRCm39) |
E359D |
possibly damaging |
Het |
Camp |
T |
A |
9: 109,676,651 (GRCm39) |
|
probably null |
Het |
Casp4 |
C |
T |
9: 5,328,580 (GRCm39) |
|
probably benign |
Het |
Ccdc110 |
A |
T |
8: 46,395,944 (GRCm39) |
T612S |
probably benign |
Het |
Cd209b |
T |
A |
8: 3,976,640 (GRCm39) |
|
probably null |
Het |
Cemip |
T |
C |
7: 83,632,461 (GRCm39) |
D367G |
probably damaging |
Het |
Cers5 |
T |
A |
15: 99,644,960 (GRCm39) |
N131I |
probably damaging |
Het |
Cfhr4 |
T |
G |
1: 139,702,301 (GRCm39) |
D61A |
probably damaging |
Het |
Chd5 |
T |
G |
4: 152,445,129 (GRCm39) |
V370G |
probably damaging |
Het |
Cipc |
C |
A |
12: 86,999,531 (GRCm39) |
Q20K |
probably benign |
Het |
Cnr2 |
T |
A |
4: 135,644,512 (GRCm39) |
F197I |
possibly damaging |
Het |
Col7a1 |
G |
A |
9: 108,804,287 (GRCm39) |
G2233S |
unknown |
Het |
Dcdc2b |
T |
A |
4: 129,505,060 (GRCm39) |
I125F |
possibly damaging |
Het |
Ddi2 |
A |
G |
4: 141,411,713 (GRCm39) |
S400P |
probably benign |
Het |
Ddx31 |
C |
A |
2: 28,794,696 (GRCm39) |
T664K |
probably benign |
Het |
Dhx30 |
C |
A |
9: 109,929,992 (GRCm39) |
G35C |
probably damaging |
Het |
Dmxl2 |
G |
A |
9: 54,318,937 (GRCm39) |
T1576I |
probably damaging |
Het |
Dnah1 |
T |
C |
14: 31,017,280 (GRCm39) |
Y1510C |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,389,930 (GRCm39) |
|
probably null |
Het |
Dock10 |
C |
A |
1: 80,583,953 (GRCm39) |
G163C |
probably damaging |
Het |
Edar |
T |
C |
10: 58,457,146 (GRCm39) |
N144S |
probably benign |
Het |
Elavl2 |
T |
A |
4: 91,196,915 (GRCm39) |
E54D |
possibly damaging |
Het |
Enam |
T |
G |
5: 88,650,173 (GRCm39) |
S561A |
probably benign |
Het |
Ercc5 |
C |
A |
1: 44,206,031 (GRCm39) |
H315N |
possibly damaging |
Het |
Esp31 |
A |
G |
17: 38,955,552 (GRCm39) |
E65G |
possibly damaging |
Het |
Faap100 |
T |
C |
11: 120,262,939 (GRCm39) |
I806M |
probably benign |
Het |
Fbxw21 |
T |
C |
9: 108,974,731 (GRCm39) |
Y263C |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,811,837 (GRCm39) |
S2719T |
possibly damaging |
Het |
Fv1 |
T |
C |
4: 147,953,875 (GRCm39) |
V147A |
probably benign |
Het |
Gal |
T |
C |
19: 3,461,590 (GRCm39) |
E65G |
probably benign |
Het |
Galnt2l |
A |
G |
8: 123,807,343 (GRCm39) |
|
probably benign |
Het |
Galnt6 |
T |
C |
15: 100,614,059 (GRCm39) |
T81A |
probably benign |
Het |
Gcc2 |
A |
G |
10: 58,106,261 (GRCm39) |
E399G |
probably damaging |
Het |
Gfi1b |
A |
T |
2: 28,500,114 (GRCm39) |
C306S |
probably damaging |
Het |
Gm10654 |
T |
A |
8: 71,384,496 (GRCm39) |
|
noncoding transcript |
Het |
Gm4953 |
T |
A |
1: 158,995,929 (GRCm39) |
|
noncoding transcript |
Het |
Gorasp2 |
T |
C |
2: 70,518,683 (GRCm39) |
|
probably benign |
Het |
Gse1 |
T |
C |
8: 121,295,205 (GRCm39) |
|
probably benign |
Het |
H2-D1 |
A |
G |
17: 35,484,973 (GRCm39) |
E278G |
probably damaging |
Het |
Herc2 |
T |
C |
7: 55,877,640 (GRCm39) |
L4569P |
probably damaging |
Het |
Hgs |
T |
A |
11: 120,368,028 (GRCm39) |
S246T |
probably damaging |
Het |
Hs2st1 |
T |
C |
3: 144,170,843 (GRCm39) |
T110A |
probably benign |
Het |
Ighv1-23 |
C |
A |
12: 114,728,372 (GRCm39) |
V17F |
possibly damaging |
Het |
Ighv8-14 |
A |
T |
12: 115,772,185 (GRCm39) |
|
noncoding transcript |
Het |
Igsf21 |
C |
T |
4: 139,761,934 (GRCm39) |
R248H |
probably benign |
Het |
Il22b |
T |
C |
10: 118,130,894 (GRCm39) |
M1V |
probably null |
Het |
Il23r |
T |
C |
6: 67,400,545 (GRCm39) |
N595S |
probably benign |
Het |
Il5ra |
G |
T |
6: 106,692,629 (GRCm39) |
P372Q |
probably damaging |
Het |
Inppl1 |
A |
G |
7: 101,481,516 (GRCm39) |
V222A |
possibly damaging |
Het |
Ints10 |
T |
C |
8: 69,279,964 (GRCm39) |
V697A |
probably damaging |
Het |
Isg15 |
T |
A |
4: 156,284,217 (GRCm39) |
T104S |
probably benign |
Het |
Kif11 |
A |
G |
19: 37,406,385 (GRCm39) |
T983A |
probably benign |
Het |
Kif3b |
A |
T |
2: 153,159,212 (GRCm39) |
K338* |
probably null |
Het |
Kpna2 |
T |
A |
11: 106,881,545 (GRCm39) |
I362F |
probably damaging |
Het |
Lama2 |
G |
A |
10: 27,014,923 (GRCm39) |
T1595M |
probably damaging |
Het |
Lrrc36 |
A |
G |
8: 106,153,567 (GRCm39) |
T126A |
probably benign |
Het |
Lrrk1 |
T |
A |
7: 65,945,202 (GRCm39) |
D604V |
probably damaging |
Het |
Map7d1 |
T |
C |
4: 126,130,484 (GRCm39) |
K409E |
probably damaging |
Het |
Mast2 |
T |
C |
4: 116,210,254 (GRCm39) |
T110A |
probably benign |
Het |
Micall2 |
G |
A |
5: 139,702,580 (GRCm39) |
T221M |
probably damaging |
Het |
Morc2b |
T |
A |
17: 33,356,351 (GRCm39) |
N474Y |
probably damaging |
Het |
Myo1e |
T |
A |
9: 70,250,378 (GRCm39) |
M528K |
probably benign |
Het |
Nlrp1c-ps |
G |
T |
11: 71,151,195 (GRCm39) |
|
noncoding transcript |
Het |
Nostrin |
T |
C |
2: 68,991,486 (GRCm39) |
S160P |
possibly damaging |
Het |
Nup133 |
T |
C |
8: 124,653,870 (GRCm39) |
R530G |
possibly damaging |
Het |
Or2f2 |
T |
A |
6: 42,767,138 (GRCm39) |
L55H |
probably damaging |
Het |
Or5p64 |
T |
C |
7: 107,855,244 (GRCm39) |
I34V |
possibly damaging |
Het |
Or8c16 |
A |
G |
9: 38,130,392 (GRCm39) |
E91G |
probably damaging |
Het |
Pabpc4l |
A |
T |
3: 46,400,597 (GRCm39) |
M349K |
possibly damaging |
Het |
Pah |
G |
A |
10: 87,406,129 (GRCm39) |
G256S |
probably benign |
Het |
Pigk |
T |
C |
3: 152,445,841 (GRCm39) |
S151P |
probably damaging |
Het |
Plcd4 |
A |
C |
1: 74,603,572 (GRCm39) |
T658P |
possibly damaging |
Het |
Pld4 |
A |
T |
12: 112,730,951 (GRCm39) |
S178C |
probably benign |
Het |
Polr1a |
G |
A |
6: 71,886,213 (GRCm39) |
E23K |
possibly damaging |
Het |
Pomt1 |
T |
C |
2: 32,131,691 (GRCm39) |
S127P |
probably damaging |
Het |
Pon2 |
A |
G |
6: 5,269,029 (GRCm39) |
V215A |
possibly damaging |
Het |
Ppp3cb |
A |
T |
14: 20,559,508 (GRCm39) |
M416K |
probably damaging |
Het |
Prdm1 |
A |
T |
10: 44,318,048 (GRCm39) |
N273K |
possibly damaging |
Het |
Prg4 |
T |
A |
1: 150,331,574 (GRCm39) |
|
probably benign |
Het |
Prkn |
G |
T |
17: 11,059,359 (GRCm39) |
|
probably benign |
Het |
Ptch1 |
G |
A |
13: 63,670,866 (GRCm39) |
T888M |
probably damaging |
Het |
Pusl1 |
T |
G |
4: 155,975,899 (GRCm39) |
|
probably benign |
Het |
Rapgef6 |
A |
T |
11: 54,513,143 (GRCm39) |
E122D |
probably damaging |
Het |
Rif1 |
C |
T |
2: 52,000,530 (GRCm39) |
T1328I |
probably damaging |
Het |
Rngtt |
T |
G |
4: 33,500,292 (GRCm39) |
|
probably null |
Het |
Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
Samd1 |
A |
G |
8: 84,725,618 (GRCm39) |
|
probably benign |
Het |
Scamp5 |
A |
T |
9: 57,358,735 (GRCm39) |
F14I |
probably damaging |
Het |
Shank3 |
C |
T |
15: 89,388,547 (GRCm39) |
R380C |
probably damaging |
Het |
Shisal2a |
T |
C |
4: 108,234,658 (GRCm39) |
T70A |
probably benign |
Het |
Slc1a4 |
C |
A |
11: 20,282,166 (GRCm39) |
A103S |
probably damaging |
Het |
Slc39a14 |
A |
G |
14: 70,547,371 (GRCm39) |
V325A |
probably benign |
Het |
Slc5a9 |
C |
A |
4: 111,748,941 (GRCm39) |
|
probably null |
Het |
Spata6l |
G |
A |
19: 28,874,903 (GRCm39) |
|
probably benign |
Het |
Spta1 |
T |
A |
1: 174,013,213 (GRCm39) |
S375T |
probably damaging |
Het |
Sval1 |
A |
G |
6: 41,932,378 (GRCm39) |
N76S |
probably benign |
Het |
Synpo |
C |
T |
18: 60,762,936 (GRCm39) |
|
probably benign |
Het |
Sytl5 |
C |
T |
X: 9,781,841 (GRCm39) |
P181L |
possibly damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,622 (GRCm39) |
M111T |
possibly damaging |
Het |
Tec |
T |
C |
5: 72,913,694 (GRCm39) |
D613G |
probably benign |
Het |
Tecpr2 |
C |
T |
12: 110,897,921 (GRCm39) |
T391I |
possibly damaging |
Het |
Thop1 |
G |
A |
10: 80,909,125 (GRCm39) |
G52D |
probably damaging |
Het |
Tmco5 |
T |
A |
2: 116,722,689 (GRCm39) |
V270D |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,556,973 (GRCm39) |
E28265K |
possibly damaging |
Het |
Tuft1 |
T |
C |
3: 94,542,750 (GRCm39) |
D72G |
probably damaging |
Het |
Tyrp1 |
C |
T |
4: 80,769,144 (GRCm39) |
|
probably benign |
Het |
Usp9y |
T |
C |
Y: 1,308,041 (GRCm39) |
D2265G |
probably damaging |
Het |
Vmn2r104 |
G |
A |
17: 20,250,288 (GRCm39) |
A661V |
probably benign |
Het |
Vwa5a |
A |
T |
9: 38,649,268 (GRCm39) |
N672I |
probably benign |
Het |
Wdr95 |
A |
T |
5: 149,535,157 (GRCm39) |
K772* |
probably null |
Het |
Ybx1 |
T |
C |
4: 119,140,010 (GRCm39) |
T106A |
probably benign |
Het |
Ypel3 |
T |
C |
7: 126,376,961 (GRCm39) |
S14P |
probably benign |
Het |
Zfp518a |
T |
A |
19: 40,903,972 (GRCm39) |
S1300R |
probably benign |
Het |
Zscan5b |
A |
T |
7: 6,242,189 (GRCm39) |
*469Y |
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 |
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 |
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 |
|