Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
A |
G |
7: 130,959,389 (GRCm39) |
S150P |
probably damaging |
Het |
5530400C23Rik |
T |
G |
6: 133,270,174 (GRCm39) |
|
probably benign |
Het |
Ahctf1 |
A |
C |
1: 179,591,033 (GRCm39) |
|
probably null |
Het |
Ang5 |
T |
C |
14: 44,200,206 (GRCm39) |
V90A |
probably benign |
Het |
Ano9 |
C |
T |
7: 140,684,623 (GRCm39) |
G442R |
probably damaging |
Het |
Apaf1 |
G |
A |
10: 90,895,914 (GRCm39) |
T386I |
probably damaging |
Het |
Apob |
C |
A |
12: 8,056,440 (GRCm39) |
H1608N |
probably damaging |
Het |
Arhgap12 |
C |
A |
18: 6,064,433 (GRCm39) |
|
probably benign |
Het |
Asxl1 |
T |
A |
2: 153,241,824 (GRCm39) |
D791E |
probably benign |
Het |
Avl9 |
T |
C |
6: 56,713,891 (GRCm39) |
V383A |
probably benign |
Het |
Btbd1 |
A |
C |
7: 81,465,754 (GRCm39) |
D197E |
probably damaging |
Het |
Camta2 |
T |
C |
11: 70,564,785 (GRCm39) |
I938V |
possibly damaging |
Het |
Ccn5 |
G |
A |
2: 163,667,233 (GRCm39) |
C78Y |
probably damaging |
Het |
Cdca7 |
C |
A |
2: 72,313,811 (GRCm39) |
A200D |
possibly damaging |
Het |
Cep104 |
A |
T |
4: 154,091,249 (GRCm39) |
Y923F |
possibly damaging |
Het |
Cep135 |
G |
C |
5: 76,769,152 (GRCm39) |
V601L |
probably benign |
Het |
Ces2b |
G |
A |
8: 105,562,542 (GRCm39) |
G291S |
probably benign |
Het |
Col6a6 |
C |
T |
9: 105,638,639 (GRCm39) |
G1400D |
probably damaging |
Het |
Cyth2 |
T |
C |
7: 45,462,541 (GRCm39) |
E1G |
probably damaging |
Het |
Dand5 |
A |
T |
8: 85,542,921 (GRCm39) |
L185Q |
probably damaging |
Het |
Dck |
T |
C |
5: 88,929,080 (GRCm39) |
V253A |
probably benign |
Het |
Ddx20 |
A |
G |
3: 105,586,396 (GRCm39) |
S650P |
probably damaging |
Het |
Dicer1 |
G |
A |
12: 104,673,123 (GRCm39) |
P799S |
probably damaging |
Het |
Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
Eya2 |
G |
A |
2: 165,611,157 (GRCm39) |
C477Y |
probably damaging |
Het |
Fip1l1 |
T |
A |
5: 74,756,503 (GRCm39) |
N498K |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,527,166 (GRCm39) |
|
probably benign |
Het |
Galntl6 |
T |
C |
8: 58,290,217 (GRCm39) |
|
probably null |
Het |
Gda |
A |
T |
19: 21,411,667 (GRCm39) |
F44I |
possibly damaging |
Het |
Gli2 |
G |
A |
1: 118,768,119 (GRCm39) |
R703C |
probably damaging |
Het |
Golgb1 |
T |
A |
16: 36,736,633 (GRCm39) |
L1960Q |
probably damaging |
Het |
Gramd1b |
T |
C |
9: 40,219,651 (GRCm39) |
D341G |
probably damaging |
Het |
Grid2 |
G |
T |
6: 63,480,419 (GRCm39) |
A78S |
probably benign |
Het |
Hao2 |
A |
T |
3: 98,790,876 (GRCm39) |
|
probably benign |
Het |
Hook3 |
A |
G |
8: 26,609,014 (GRCm39) |
V10A |
probably benign |
Het |
Kif20a |
A |
G |
18: 34,762,262 (GRCm39) |
E425G |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,403,252 (GRCm39) |
D2107G |
probably benign |
Het |
Lrriq3 |
T |
C |
3: 154,893,373 (GRCm39) |
I358T |
possibly damaging |
Het |
Mad2l2 |
A |
G |
4: 148,225,381 (GRCm39) |
D17G |
possibly damaging |
Het |
Mastl |
G |
T |
2: 23,023,358 (GRCm39) |
T455K |
probably benign |
Het |
Mkln1 |
G |
T |
6: 31,409,862 (GRCm39) |
|
probably benign |
Het |
Mmp1b |
A |
T |
9: 7,387,947 (GRCm39) |
Y16N |
possibly damaging |
Het |
Mmp24 |
C |
T |
2: 155,634,517 (GRCm39) |
A79V |
probably benign |
Het |
Mrps35 |
T |
A |
6: 146,972,232 (GRCm39) |
C292S |
possibly damaging |
Het |
Myom1 |
T |
C |
17: 71,427,643 (GRCm39) |
F1435L |
possibly damaging |
Het |
Nars2 |
C |
T |
7: 96,689,130 (GRCm39) |
H351Y |
probably damaging |
Het |
Nat2 |
A |
T |
8: 67,953,919 (GRCm39) |
I10F |
probably damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Olfm5 |
A |
T |
7: 103,803,076 (GRCm39) |
Y462* |
probably null |
Het |
Or13p5 |
C |
T |
4: 118,591,986 (GRCm39) |
H87Y |
probably damaging |
Het |
Or1j12 |
C |
A |
2: 36,342,660 (GRCm39) |
A21E |
probably benign |
Het |
Or2w3 |
C |
A |
11: 58,556,986 (GRCm39) |
F200L |
probably damaging |
Het |
Or4c122 |
C |
A |
2: 89,079,742 (GRCm39) |
E87* |
probably null |
Het |
Or4e1 |
T |
C |
14: 52,700,966 (GRCm39) |
I167V |
probably benign |
Het |
Or5p70 |
T |
A |
7: 107,994,438 (GRCm39) |
I37N |
probably damaging |
Het |
Or7g35 |
T |
C |
9: 19,496,600 (GRCm39) |
S256P |
possibly damaging |
Het |
Or8d2b |
T |
A |
9: 38,789,111 (GRCm39) |
I213N |
probably damaging |
Het |
Or8g20 |
A |
T |
9: 39,396,284 (GRCm39) |
F85L |
probably benign |
Het |
Otog |
A |
T |
7: 45,900,819 (GRCm39) |
|
probably benign |
Het |
Pdcd2l |
A |
T |
7: 33,892,232 (GRCm39) |
D212E |
possibly damaging |
Het |
Pex5 |
T |
C |
6: 124,381,596 (GRCm39) |
N213S |
probably benign |
Het |
Pkn3 |
C |
T |
2: 29,971,146 (GRCm39) |
P238S |
probably benign |
Het |
Pramel32 |
A |
T |
4: 88,547,536 (GRCm39) |
I45K |
probably damaging |
Het |
Prl2b1 |
A |
T |
13: 27,574,723 (GRCm39) |
|
probably null |
Het |
Ptprb |
A |
T |
10: 116,204,712 (GRCm39) |
I1849L |
possibly damaging |
Het |
Rasal3 |
G |
T |
17: 32,612,500 (GRCm39) |
S787Y |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,532,177 (GRCm39) |
D596E |
possibly damaging |
Het |
Sdhd |
A |
T |
9: 50,515,064 (GRCm39) |
V9D |
possibly damaging |
Het |
Serinc5 |
T |
C |
13: 92,844,565 (GRCm39) |
S436P |
probably damaging |
Het |
Slc27a1 |
C |
T |
8: 72,036,808 (GRCm39) |
P348L |
probably damaging |
Het |
Slc28a2b |
A |
T |
2: 122,344,879 (GRCm39) |
I162F |
probably damaging |
Het |
Smg1 |
G |
A |
7: 117,759,606 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
A |
T |
9: 41,955,196 (GRCm39) |
|
probably benign |
Het |
Sprtn |
T |
A |
8: 125,626,957 (GRCm39) |
H112Q |
probably damaging |
Het |
Tet2 |
A |
G |
3: 133,173,363 (GRCm39) |
M1633T |
probably benign |
Het |
Tet2 |
T |
A |
3: 133,173,486 (GRCm39) |
D1592V |
probably benign |
Het |
Tmem68 |
A |
T |
4: 3,569,667 (GRCm39) |
C8S |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 122,771,039 (GRCm39) |
I943N |
probably benign |
Het |
Trib2 |
A |
T |
12: 15,844,069 (GRCm39) |
V191D |
probably damaging |
Het |
Tsc22d4 |
T |
C |
5: 137,760,917 (GRCm39) |
S113P |
probably damaging |
Het |
Ttc21b |
T |
C |
2: 66,069,914 (GRCm39) |
R250G |
probably damaging |
Het |
Ubr2 |
T |
C |
17: 47,278,174 (GRCm39) |
Y721C |
probably damaging |
Het |
Ubtfl1 |
A |
T |
9: 18,320,660 (GRCm39) |
I63F |
probably damaging |
Het |
Ush1c |
G |
A |
7: 45,874,332 (GRCm39) |
P171S |
probably benign |
Het |
Utp20 |
A |
T |
10: 88,603,323 (GRCm39) |
N1843K |
probably damaging |
Het |
Vangl1 |
A |
G |
3: 102,074,253 (GRCm39) |
Y285H |
probably damaging |
Het |
Virma |
A |
G |
4: 11,498,769 (GRCm39) |
D70G |
probably damaging |
Het |
Vmn2r102 |
T |
C |
17: 19,898,277 (GRCm39) |
F431L |
probably benign |
Het |
Wdr17 |
A |
G |
8: 55,114,530 (GRCm39) |
I662T |
probably damaging |
Het |
Wdr87-ps |
T |
A |
7: 29,232,690 (GRCm39) |
|
noncoding transcript |
Het |
Zfp160 |
G |
A |
17: 21,247,268 (GRCm39) |
R606H |
probably benign |
Het |
Zfp369 |
C |
T |
13: 65,444,248 (GRCm39) |
R464C |
probably 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 |
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 |
R8263:Tasor2
|
UTSW |
13 |
3,625,286 (GRCm39) |
missense |
possibly damaging |
0.70 |
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 |
|