Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630095N17Rik |
T |
A |
1: 75,208,683 (GRCm39) |
R12S |
unknown |
Het |
Ankrd10 |
C |
T |
8: 11,665,707 (GRCm39) |
V298I |
probably benign |
Het |
Atg4d |
T |
A |
9: 21,178,335 (GRCm39) |
M151K |
probably damaging |
Het |
Calhm5 |
C |
A |
10: 33,972,192 (GRCm39) |
C81F |
probably damaging |
Het |
Casp8ap2 |
T |
A |
4: 32,644,072 (GRCm39) |
H1048Q |
probably damaging |
Het |
Cd300ld2 |
A |
G |
11: 114,903,192 (GRCm39) |
S218P |
unknown |
Het |
Clec3a |
T |
C |
8: 115,152,369 (GRCm39) |
V125A |
probably benign |
Het |
Cnot6 |
A |
T |
11: 49,573,002 (GRCm39) |
Y241N |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 31,015,134 (GRCm39) |
F1686Y |
probably damaging |
Het |
Dnah12 |
A |
G |
14: 26,613,421 (GRCm39) |
K1285E |
noncoding transcript |
Het |
Dop1b |
T |
C |
16: 93,559,083 (GRCm39) |
S610P |
possibly damaging |
Het |
Ehhadh |
A |
T |
16: 21,592,295 (GRCm39) |
L136H |
probably damaging |
Het |
Epha7 |
A |
G |
4: 28,821,149 (GRCm39) |
T105A |
probably damaging |
Het |
Etl4 |
A |
T |
2: 20,748,965 (GRCm39) |
E434D |
probably benign |
Het |
Fastkd2 |
T |
C |
1: 63,770,968 (GRCm39) |
V108A |
probably benign |
Het |
Fat2 |
G |
A |
11: 55,174,962 (GRCm39) |
T1917I |
probably benign |
Het |
Fbxo45 |
A |
G |
16: 32,065,533 (GRCm39) |
S33P |
unknown |
Het |
Fig4 |
A |
T |
10: 41,143,711 (GRCm39) |
Y249* |
probably null |
Het |
Fryl |
T |
C |
5: 73,238,348 (GRCm39) |
Y1466C |
probably damaging |
Het |
G530012D18Rik |
C |
G |
1: 85,504,935 (GRCm39) |
D113E |
unknown |
Het |
Glod4 |
T |
C |
11: 76,125,318 (GRCm39) |
D147G |
possibly damaging |
Het |
Gm12695 |
T |
G |
4: 96,651,046 (GRCm39) |
M136L |
probably benign |
Het |
Gm5422 |
A |
G |
10: 31,125,099 (GRCm39) |
T313A |
noncoding transcript |
Het |
Hydin |
C |
A |
8: 111,178,705 (GRCm39) |
A1100D |
probably benign |
Het |
Ift172 |
G |
A |
5: 31,422,681 (GRCm39) |
A923V |
possibly damaging |
Het |
Irgc |
G |
A |
7: 24,132,107 (GRCm39) |
H237Y |
probably damaging |
Het |
Itga11 |
T |
C |
9: 62,604,262 (GRCm39) |
I50T |
possibly damaging |
Het |
Itpr3 |
C |
T |
17: 27,334,887 (GRCm39) |
Q2134* |
probably null |
Het |
Kat8 |
A |
T |
7: 127,523,653 (GRCm39) |
D292V |
possibly damaging |
Het |
Kdm2a |
A |
G |
19: 4,374,392 (GRCm39) |
M913T |
possibly damaging |
Het |
Larp4 |
T |
C |
15: 99,883,961 (GRCm39) |
V66A |
probably benign |
Het |
Loxhd1 |
A |
G |
18: 77,462,858 (GRCm39) |
D899G |
probably damaging |
Het |
Lrrc47 |
G |
T |
4: 154,100,486 (GRCm39) |
R354L |
probably damaging |
Het |
Lss |
C |
T |
10: 76,367,739 (GRCm39) |
R24C |
probably damaging |
Het |
Mmp14 |
C |
T |
14: 54,673,244 (GRCm39) |
R51C |
probably damaging |
Het |
Mon1a |
C |
T |
9: 107,775,993 (GRCm39) |
T37I |
probably benign |
Het |
Mtcl2 |
A |
G |
2: 156,869,510 (GRCm39) |
W1042R |
possibly damaging |
Het |
Nacc2 |
A |
C |
2: 25,952,240 (GRCm39) |
V372G |
probably damaging |
Het |
Ncapg |
T |
C |
5: 45,849,134 (GRCm39) |
V690A |
probably benign |
Het |
Nhej1 |
A |
G |
1: 75,006,896 (GRCm39) |
L152P |
probably damaging |
Het |
Nol4l |
A |
T |
2: 153,259,337 (GRCm39) |
S522R |
probably damaging |
Het |
Nr0b2 |
A |
G |
4: 133,281,241 (GRCm39) |
Y169C |
probably damaging |
Het |
Numa1 |
A |
G |
7: 101,648,491 (GRCm39) |
M741V |
probably benign |
Het |
Or10d1b |
A |
G |
9: 39,613,453 (GRCm39) |
M204T |
possibly damaging |
Het |
Or8g28 |
A |
G |
9: 39,169,899 (GRCm39) |
L26P |
probably damaging |
Het |
Pebp1 |
C |
A |
5: 117,425,473 (GRCm39) |
|
probably null |
Het |
Pik3ip1 |
A |
T |
11: 3,291,581 (GRCm39) |
I217F |
probably damaging |
Het |
Plekhg1 |
T |
A |
10: 3,907,651 (GRCm39) |
I911N |
|
Het |
Pnpla8 |
T |
C |
12: 44,342,846 (GRCm39) |
I534T |
probably damaging |
Het |
Ppp2r2a |
A |
T |
14: 67,261,205 (GRCm39) |
F172I |
probably damaging |
Het |
Rab7 |
C |
T |
6: 87,989,292 (GRCm39) |
M59I |
probably benign |
Het |
Rbm34 |
T |
C |
8: 127,692,139 (GRCm39) |
N201S |
probably benign |
Het |
Rfx1 |
G |
T |
8: 84,821,483 (GRCm39) |
R764L |
probably damaging |
Het |
Rnase12 |
T |
A |
14: 51,294,580 (GRCm39) |
D33V |
probably damaging |
Het |
Rnf121 |
A |
G |
7: 101,684,532 (GRCm39) |
L127P |
probably damaging |
Het |
Rtl1 |
C |
A |
12: 109,560,180 (GRCm39) |
R553L |
probably damaging |
Het |
Scn8a |
T |
C |
15: 100,881,736 (GRCm39) |
L601P |
probably damaging |
Het |
Scyl2 |
G |
T |
10: 89,476,525 (GRCm39) |
Q867K |
possibly damaging |
Het |
Sgtb |
T |
C |
13: 104,268,692 (GRCm39) |
F213L |
probably benign |
Het |
Slc35f4 |
A |
G |
14: 49,551,084 (GRCm39) |
V260A |
probably damaging |
Het |
Slfn14 |
A |
G |
11: 83,174,299 (GRCm39) |
Y231H |
possibly damaging |
Het |
Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
Stard13 |
G |
A |
5: 151,157,106 (GRCm39) |
A25V |
possibly damaging |
Het |
Stk38 |
C |
T |
17: 29,203,161 (GRCm39) |
R135H |
probably damaging |
Het |
Svil |
A |
G |
18: 5,108,679 (GRCm39) |
D1939G |
probably damaging |
Het |
Tbc1d7 |
A |
G |
13: 43,323,340 (GRCm39) |
V17A |
possibly damaging |
Het |
Trpc4 |
T |
C |
3: 54,129,756 (GRCm39) |
V174A |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,619,028 (GRCm39) |
T16117K |
probably damaging |
Het |
Tubb3 |
T |
A |
8: 124,147,868 (GRCm39) |
M267K |
possibly damaging |
Het |
Upk1b |
T |
C |
16: 38,604,585 (GRCm39) |
T147A |
probably damaging |
Het |
Vmn2r107 |
G |
T |
17: 20,580,614 (GRCm39) |
C517F |
probably damaging |
Het |
Vmn2r112 |
A |
G |
17: 22,824,140 (GRCm39) |
D465G |
probably damaging |
Het |
Vmn2r73 |
A |
T |
7: 85,507,619 (GRCm39) |
H564Q |
probably benign |
Het |
Vmn2r79 |
A |
G |
7: 86,686,726 (GRCm39) |
I702M |
possibly damaging |
Het |
Vmn2r84 |
A |
G |
10: 130,227,037 (GRCm39) |
V267A |
probably damaging |
Het |
Zfp445 |
T |
C |
9: 122,681,878 (GRCm39) |
I688V |
probably benign |
Het |
Zfp955a |
C |
T |
17: 33,463,087 (GRCm39) |
V15M |
probably damaging |
Het |
Zfp960 |
T |
A |
17: 17,308,202 (GRCm39) |
C305* |
probably null |
Het |
Zfp964 |
A |
G |
8: 70,116,345 (GRCm39) |
D315G |
possibly damaging |
Het |
Zmynd10 |
T |
A |
9: 107,426,516 (GRCm39) |
I183K |
possibly damaging |
Het |
|
Other mutations in Tasor2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Tasor2
|
APN |
13 |
3,624,832 (GRCm39) |
missense |
probably benign |
|
IGL00670:Tasor2
|
APN |
13 |
3,635,241 (GRCm39) |
missense |
probably benign |
0.14 |
IGL00957:Tasor2
|
APN |
13 |
3,627,101 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01311:Tasor2
|
APN |
13 |
3,625,885 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01318:Tasor2
|
APN |
13 |
3,625,067 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01767:Tasor2
|
APN |
13 |
3,626,633 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02073:Tasor2
|
APN |
13 |
3,624,721 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02152:Tasor2
|
APN |
13 |
3,635,371 (GRCm39) |
missense |
probably benign |
|
IGL02431:Tasor2
|
APN |
13 |
3,624,736 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02478:Tasor2
|
APN |
13 |
3,624,661 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02732:Tasor2
|
APN |
13 |
3,623,626 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02745:Tasor2
|
APN |
13 |
3,635,140 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02800:Tasor2
|
APN |
13 |
3,635,154 (GRCm39) |
missense |
probably benign |
|
IGL02989:Tasor2
|
APN |
13 |
3,634,820 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03124:Tasor2
|
APN |
13 |
3,624,704 (GRCm39) |
missense |
probably benign |
0.41 |
IGL03154:Tasor2
|
APN |
13 |
3,625,255 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL03216:Tasor2
|
APN |
13 |
3,624,553 (GRCm39) |
missense |
probably damaging |
0.98 |
BB001:Tasor2
|
UTSW |
13 |
3,644,331 (GRCm39) |
missense |
possibly damaging |
0.92 |
BB011:Tasor2
|
UTSW |
13 |
3,644,331 (GRCm39) |
missense |
possibly damaging |
0.92 |
H8562:Tasor2
|
UTSW |
13 |
3,627,000 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4585001:Tasor2
|
UTSW |
13 |
3,624,979 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0016:Tasor2
|
UTSW |
13 |
3,635,170 (GRCm39) |
splice site |
probably null |
|
R0016:Tasor2
|
UTSW |
13 |
3,635,170 (GRCm39) |
splice site |
probably null |
|
R0157:Tasor2
|
UTSW |
13 |
3,625,550 (GRCm39) |
missense |
probably benign |
0.06 |
R0375:Tasor2
|
UTSW |
13 |
3,646,842 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0403:Tasor2
|
UTSW |
13 |
3,632,052 (GRCm39) |
nonsense |
probably null |
|
R0472:Tasor2
|
UTSW |
13 |
3,638,364 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0517:Tasor2
|
UTSW |
13 |
3,616,964 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0586:Tasor2
|
UTSW |
13 |
3,640,321 (GRCm39) |
missense |
probably damaging |
0.99 |
R0600:Tasor2
|
UTSW |
13 |
3,626,054 (GRCm39) |
missense |
probably benign |
|
R0659:Tasor2
|
UTSW |
13 |
3,624,448 (GRCm39) |
missense |
probably damaging |
0.99 |
R1257:Tasor2
|
UTSW |
13 |
3,625,049 (GRCm39) |
missense |
probably benign |
0.25 |
R1375:Tasor2
|
UTSW |
13 |
3,626,029 (GRCm39) |
missense |
probably benign |
0.06 |
R1443:Tasor2
|
UTSW |
13 |
3,625,543 (GRCm39) |
missense |
probably benign |
0.00 |
R1497:Tasor2
|
UTSW |
13 |
3,620,409 (GRCm39) |
missense |
probably damaging |
0.96 |
R1544:Tasor2
|
UTSW |
13 |
3,640,413 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1554:Tasor2
|
UTSW |
13 |
3,626,374 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1629:Tasor2
|
UTSW |
13 |
3,624,121 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1633:Tasor2
|
UTSW |
13 |
3,631,771 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1661:Tasor2
|
UTSW |
13 |
3,623,860 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1673:Tasor2
|
UTSW |
13 |
3,634,498 (GRCm39) |
critical splice donor site |
probably null |
|
R1675:Tasor2
|
UTSW |
13 |
3,619,507 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1781:Tasor2
|
UTSW |
13 |
3,634,759 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1792:Tasor2
|
UTSW |
13 |
3,640,559 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1826:Tasor2
|
UTSW |
13 |
3,631,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R1920:Tasor2
|
UTSW |
13 |
3,626,612 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1983:Tasor2
|
UTSW |
13 |
3,624,853 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2016:Tasor2
|
UTSW |
13 |
3,626,770 (GRCm39) |
missense |
probably benign |
0.41 |
R2017:Tasor2
|
UTSW |
13 |
3,626,770 (GRCm39) |
missense |
probably benign |
0.41 |
R2220:Tasor2
|
UTSW |
13 |
3,631,872 (GRCm39) |
missense |
probably benign |
0.00 |
R2513:Tasor2
|
UTSW |
13 |
3,632,150 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2898:Tasor2
|
UTSW |
13 |
3,635,122 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2904:Tasor2
|
UTSW |
13 |
3,632,185 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3149:Tasor2
|
UTSW |
13 |
3,624,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R3623:Tasor2
|
UTSW |
13 |
3,645,556 (GRCm39) |
missense |
probably benign |
|
R3624:Tasor2
|
UTSW |
13 |
3,645,556 (GRCm39) |
missense |
probably benign |
|
R3725:Tasor2
|
UTSW |
13 |
3,640,538 (GRCm39) |
missense |
probably benign |
0.33 |
R3835:Tasor2
|
UTSW |
13 |
3,625,292 (GRCm39) |
missense |
probably benign |
0.01 |
R3890:Tasor2
|
UTSW |
13 |
3,646,785 (GRCm39) |
missense |
probably damaging |
0.96 |
R4023:Tasor2
|
UTSW |
13 |
3,634,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R4024:Tasor2
|
UTSW |
13 |
3,634,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R4025:Tasor2
|
UTSW |
13 |
3,634,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R4050:Tasor2
|
UTSW |
13 |
3,623,507 (GRCm39) |
missense |
probably benign |
0.09 |
R4308:Tasor2
|
UTSW |
13 |
3,619,498 (GRCm39) |
missense |
probably damaging |
0.97 |
R4484:Tasor2
|
UTSW |
13 |
3,631,831 (GRCm39) |
missense |
probably benign |
0.12 |
R4674:Tasor2
|
UTSW |
13 |
3,623,686 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4718:Tasor2
|
UTSW |
13 |
3,624,495 (GRCm39) |
missense |
probably benign |
0.00 |
R4745:Tasor2
|
UTSW |
13 |
3,640,069 (GRCm39) |
missense |
probably benign |
0.26 |
R4776:Tasor2
|
UTSW |
13 |
3,620,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:Tasor2
|
UTSW |
13 |
3,634,807 (GRCm39) |
missense |
probably damaging |
0.96 |
R4855:Tasor2
|
UTSW |
13 |
3,616,680 (GRCm39) |
splice site |
probably null |
|
R5049:Tasor2
|
UTSW |
13 |
3,624,000 (GRCm39) |
missense |
probably benign |
0.00 |
R5076:Tasor2
|
UTSW |
13 |
3,626,357 (GRCm39) |
missense |
probably benign |
0.41 |
R5287:Tasor2
|
UTSW |
13 |
3,625,744 (GRCm39) |
missense |
probably benign |
0.41 |
R5298:Tasor2
|
UTSW |
13 |
3,645,613 (GRCm39) |
splice site |
probably null |
|
R5379:Tasor2
|
UTSW |
13 |
3,638,496 (GRCm39) |
missense |
probably benign |
0.41 |
R5512:Tasor2
|
UTSW |
13 |
3,645,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R5624:Tasor2
|
UTSW |
13 |
3,634,996 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5750:Tasor2
|
UTSW |
13 |
3,623,642 (GRCm39) |
nonsense |
probably null |
|
R6114:Tasor2
|
UTSW |
13 |
3,640,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6118:Tasor2
|
UTSW |
13 |
3,631,891 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6119:Tasor2
|
UTSW |
13 |
3,631,891 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6269:Tasor2
|
UTSW |
13 |
3,631,891 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6270:Tasor2
|
UTSW |
13 |
3,631,891 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6271:Tasor2
|
UTSW |
13 |
3,631,891 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6272:Tasor2
|
UTSW |
13 |
3,631,891 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6525:Tasor2
|
UTSW |
13 |
3,626,540 (GRCm39) |
nonsense |
probably null |
|
R6550:Tasor2
|
UTSW |
13 |
3,640,519 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6714:Tasor2
|
UTSW |
13 |
3,644,189 (GRCm39) |
missense |
probably benign |
0.00 |
R6797:Tasor2
|
UTSW |
13 |
3,626,769 (GRCm39) |
missense |
probably benign |
0.26 |
R6967:Tasor2
|
UTSW |
13 |
3,624,819 (GRCm39) |
missense |
probably benign |
0.22 |
R7016:Tasor2
|
UTSW |
13 |
3,626,857 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7219:Tasor2
|
UTSW |
13 |
3,640,521 (GRCm39) |
missense |
probably damaging |
0.99 |
R7454:Tasor2
|
UTSW |
13 |
3,635,332 (GRCm39) |
missense |
probably benign |
0.21 |
R7570:Tasor2
|
UTSW |
13 |
3,623,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R7571:Tasor2
|
UTSW |
13 |
3,625,292 (GRCm39) |
missense |
probably benign |
0.01 |
R7580:Tasor2
|
UTSW |
13 |
3,624,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R7587:Tasor2
|
UTSW |
13 |
3,618,849 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7657:Tasor2
|
UTSW |
13 |
3,623,777 (GRCm39) |
missense |
probably damaging |
0.98 |
R7810:Tasor2
|
UTSW |
13 |
3,625,714 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7909:Tasor2
|
UTSW |
13 |
3,623,765 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7924:Tasor2
|
UTSW |
13 |
3,644,331 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7945:Tasor2
|
UTSW |
13 |
3,626,085 (GRCm39) |
missense |
probably benign |
|
R8005:Tasor2
|
UTSW |
13 |
3,625,681 (GRCm39) |
missense |
probably benign |
|
R8067:Tasor2
|
UTSW |
13 |
3,619,602 (GRCm39) |
missense |
probably benign |
|
R8112:Tasor2
|
UTSW |
13 |
3,619,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R8162:Tasor2
|
UTSW |
13 |
3,649,691 (GRCm39) |
missense |
probably damaging |
0.96 |
R8170:Tasor2
|
UTSW |
13 |
3,624,881 (GRCm39) |
nonsense |
probably null |
|
R8240:Tasor2
|
UTSW |
13 |
3,624,388 (GRCm39) |
missense |
probably benign |
|
R8263:Tasor2
|
UTSW |
13 |
3,640,016 (GRCm39) |
missense |
probably benign |
0.03 |
R8477:Tasor2
|
UTSW |
13 |
3,625,079 (GRCm39) |
missense |
probably benign |
0.18 |
R9022:Tasor2
|
UTSW |
13 |
3,626,659 (GRCm39) |
missense |
probably benign |
|
R9140:Tasor2
|
UTSW |
13 |
3,638,441 (GRCm39) |
missense |
probably benign |
0.04 |
R9167:Tasor2
|
UTSW |
13 |
3,624,724 (GRCm39) |
missense |
probably benign |
|
R9527:Tasor2
|
UTSW |
13 |
3,635,191 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9535:Tasor2
|
UTSW |
13 |
3,623,559 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9711:Tasor2
|
UTSW |
13 |
3,649,667 (GRCm39) |
missense |
probably benign |
|
X0024:Tasor2
|
UTSW |
13 |
3,649,837 (GRCm39) |
missense |
probably null |
0.99 |
X0025:Tasor2
|
UTSW |
13 |
3,626,827 (GRCm39) |
missense |
probably benign |
0.15 |
X0066:Tasor2
|
UTSW |
13 |
3,638,441 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:Tasor2
|
UTSW |
13 |
3,638,429 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Tasor2
|
UTSW |
13 |
3,626,636 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Tasor2
|
UTSW |
13 |
3,624,234 (GRCm39) |
missense |
probably damaging |
0.96 |
|