Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26b |
C |
G |
8: 43,974,335 (GRCm39) |
M222I |
probably benign |
Het |
Ahnak |
T |
C |
19: 8,992,546 (GRCm39) |
V4610A |
possibly damaging |
Het |
Ankrd13c |
C |
T |
3: 157,653,220 (GRCm39) |
|
silent |
Het |
Cables2 |
A |
G |
2: 179,903,841 (GRCm39) |
|
probably benign |
Het |
Cabp2 |
C |
A |
19: 4,136,497 (GRCm39) |
A181D |
probably damaging |
Het |
Camsap3 |
A |
G |
8: 3,651,999 (GRCm39) |
D265G |
probably damaging |
Het |
Cbs |
G |
T |
17: 31,851,853 (GRCm39) |
T50N |
probably damaging |
Het |
Cenpa |
A |
T |
5: 30,830,381 (GRCm39) |
Q83L |
possibly damaging |
Het |
Cit |
A |
T |
5: 116,063,598 (GRCm39) |
|
probably benign |
Het |
Ckap5 |
A |
G |
2: 91,445,445 (GRCm39) |
E1694G |
possibly damaging |
Het |
Copz1 |
A |
T |
15: 103,203,197 (GRCm39) |
M104L |
probably benign |
Het |
Crot |
T |
A |
5: 9,024,192 (GRCm39) |
M335L |
probably benign |
Het |
Ctnna2 |
T |
C |
6: 77,120,904 (GRCm39) |
D373G |
probably benign |
Het |
Ctu2 |
G |
A |
8: 123,203,693 (GRCm39) |
|
probably benign |
Het |
Cyp3a59 |
T |
A |
5: 146,027,455 (GRCm39) |
Y75* |
probably null |
Het |
Dbi |
A |
G |
1: 120,048,583 (GRCm39) |
I21T |
probably benign |
Het |
Dcun1d3 |
A |
G |
7: 119,458,799 (GRCm39) |
S79P |
probably benign |
Het |
Dock10 |
T |
A |
1: 80,483,304 (GRCm39) |
|
probably benign |
Het |
Dstyk |
T |
A |
1: 132,381,875 (GRCm39) |
I543N |
probably damaging |
Het |
Epx |
G |
T |
11: 87,756,318 (GRCm39) |
A621E |
probably damaging |
Het |
Farp2 |
G |
A |
1: 93,548,367 (GRCm39) |
|
probably null |
Het |
Gm11992 |
C |
T |
11: 9,002,711 (GRCm39) |
P25S |
probably damaging |
Het |
Grik5 |
A |
T |
7: 24,758,502 (GRCm39) |
M307K |
possibly damaging |
Het |
Hnf1b |
A |
T |
11: 83,773,503 (GRCm39) |
N234I |
probably damaging |
Het |
Htr2a |
A |
G |
14: 74,882,530 (GRCm39) |
D172G |
probably damaging |
Het |
Ifit1bl2 |
T |
C |
19: 34,597,128 (GRCm39) |
T163A |
probably benign |
Het |
Igsf10 |
A |
T |
3: 59,235,578 (GRCm39) |
D1534E |
probably benign |
Het |
Il3ra |
T |
G |
14: 14,350,799 (GRCm38) |
V178G |
probably damaging |
Het |
Itgb1 |
A |
T |
8: 129,439,718 (GRCm39) |
K136* |
probably null |
Het |
Itprid1 |
A |
T |
6: 55,874,754 (GRCm39) |
R235* |
probably null |
Het |
Lama2 |
T |
A |
10: 26,891,494 (GRCm39) |
I2540F |
probably benign |
Het |
Lrp8 |
C |
A |
4: 107,714,493 (GRCm39) |
H622Q |
probably damaging |
Het |
Lrrc2 |
T |
A |
9: 110,795,629 (GRCm39) |
M138K |
probably benign |
Het |
Lrrk2 |
C |
A |
15: 91,630,034 (GRCm39) |
H1242N |
probably benign |
Het |
Lsm11 |
G |
C |
11: 45,835,445 (GRCm39) |
R99G |
probably benign |
Het |
Mif4gd |
C |
T |
11: 115,500,439 (GRCm39) |
V40M |
probably benign |
Het |
Mpp3 |
A |
T |
11: 101,916,241 (GRCm39) |
V37D |
probably damaging |
Het |
Mre11a |
T |
A |
9: 14,698,258 (GRCm39) |
D35E |
probably damaging |
Het |
Mroh4 |
C |
A |
15: 74,493,003 (GRCm39) |
V233F |
probably damaging |
Het |
Npy2r |
A |
T |
3: 82,448,068 (GRCm39) |
S123T |
possibly damaging |
Het |
Nrip2 |
A |
G |
6: 128,385,361 (GRCm39) |
Y264C |
possibly damaging |
Het |
Obscn |
A |
G |
11: 58,897,639 (GRCm39) |
S6639P |
unknown |
Het |
Or10d4 |
C |
T |
9: 39,580,386 (GRCm39) |
T11I |
probably benign |
Het |
Or51t4 |
T |
A |
7: 102,598,017 (GRCm39) |
F105Y |
probably benign |
Het |
Osbpl5 |
C |
T |
7: 143,310,695 (GRCm39) |
|
probably benign |
Het |
Panx1 |
A |
T |
9: 14,921,513 (GRCm39) |
Y121N |
probably damaging |
Het |
Pcdhb8 |
A |
G |
18: 37,489,243 (GRCm39) |
D307G |
probably damaging |
Het |
Pde1b |
A |
G |
15: 103,429,866 (GRCm39) |
K120E |
possibly damaging |
Het |
Pdzrn4 |
T |
C |
15: 92,295,255 (GRCm39) |
S154P |
probably benign |
Het |
Ppp1r13b |
T |
C |
12: 111,796,876 (GRCm39) |
K889R |
probably benign |
Het |
Ppp4r3a |
T |
A |
12: 101,017,872 (GRCm39) |
D439V |
probably damaging |
Het |
Ptk2b |
A |
G |
14: 66,411,328 (GRCm39) |
I401T |
probably damaging |
Het |
Rab24 |
T |
C |
13: 55,468,343 (GRCm39) |
T153A |
probably damaging |
Het |
Rarb |
C |
A |
14: 16,434,264 (GRCm38) |
A305S |
probably damaging |
Het |
Rc3h2 |
GCC |
GCCC |
2: 37,304,745 (GRCm39) |
|
probably null |
Het |
Scn10a |
G |
A |
9: 119,456,237 (GRCm39) |
T1194I |
probably damaging |
Het |
Scn3a |
G |
T |
2: 65,295,180 (GRCm39) |
N1514K |
probably damaging |
Het |
Serpinb3d |
T |
C |
1: 107,011,105 (GRCm39) |
T36A |
probably benign |
Het |
Shisa5 |
T |
A |
9: 108,885,751 (GRCm39) |
M229K |
possibly damaging |
Het |
Sik2 |
C |
T |
9: 50,828,431 (GRCm39) |
G204R |
probably damaging |
Het |
Sla |
C |
T |
15: 66,665,554 (GRCm39) |
G46E |
probably damaging |
Het |
Slc35g3 |
A |
T |
11: 69,652,509 (GRCm39) |
M1K |
probably null |
Het |
Slc5a7 |
A |
T |
17: 54,583,972 (GRCm39) |
Y439* |
probably null |
Het |
Slc9a1 |
T |
C |
4: 133,147,176 (GRCm39) |
|
probably benign |
Het |
Slitrk6 |
T |
G |
14: 110,987,305 (GRCm39) |
T801P |
probably benign |
Het |
Spata31d1c |
T |
C |
13: 65,184,894 (GRCm39) |
V812A |
possibly damaging |
Het |
Spata31g1 |
T |
C |
4: 42,971,465 (GRCm39) |
L230P |
probably benign |
Het |
Spef1l |
G |
A |
7: 139,556,526 (GRCm39) |
H154Y |
probably benign |
Het |
Sphkap |
A |
C |
1: 83,317,320 (GRCm39) |
L59R |
probably damaging |
Het |
Spmip8 |
A |
T |
8: 96,046,620 (GRCm39) |
T98S |
possibly damaging |
Het |
Srsf10 |
C |
A |
4: 135,583,553 (GRCm39) |
R6S |
probably damaging |
Het |
Supt5 |
T |
A |
7: 28,028,900 (GRCm39) |
R131S |
probably benign |
Het |
Syne1 |
T |
C |
10: 5,310,706 (GRCm39) |
|
probably null |
Het |
Tet2 |
T |
A |
3: 133,194,296 (GRCm39) |
H46L |
possibly damaging |
Het |
Tnfsf4 |
T |
A |
1: 161,244,819 (GRCm39) |
N169K |
probably damaging |
Het |
Tprg1 |
A |
T |
16: 25,136,011 (GRCm39) |
M1L |
possibly damaging |
Het |
Tsen2 |
A |
G |
6: 115,536,556 (GRCm39) |
Y104C |
probably damaging |
Het |
Umod |
A |
T |
7: 119,070,650 (GRCm39) |
I414N |
probably damaging |
Het |
Usp10 |
G |
T |
8: 120,673,828 (GRCm39) |
V398L |
possibly damaging |
Het |
Vmn2r23 |
A |
T |
6: 123,718,854 (GRCm39) |
I736F |
possibly damaging |
Het |
Vmn2r65 |
C |
A |
7: 84,592,869 (GRCm39) |
G446V |
probably benign |
Het |
Wbp1l |
C |
T |
19: 46,642,619 (GRCm39) |
R191* |
probably null |
Het |
Yars2 |
A |
G |
16: 16,127,335 (GRCm39) |
I467V |
probably benign |
Het |
Ykt6 |
A |
G |
11: 5,909,338 (GRCm39) |
E49G |
possibly damaging |
Het |
Zan |
T |
A |
5: 137,442,192 (GRCm39) |
M1907L |
unknown |
Het |
Zdhhc2 |
T |
C |
8: 40,917,277 (GRCm39) |
S225P |
probably damaging |
Het |
Zfc3h1 |
A |
T |
10: 115,267,262 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ttc6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03278:Ttc6
|
APN |
12 |
57,668,812 (GRCm39) |
missense |
probably damaging |
0.99 |
polonius
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
tybalt
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02802:Ttc6
|
UTSW |
12 |
57,622,654 (GRCm39) |
missense |
probably benign |
0.14 |
PIT4802001:Ttc6
|
UTSW |
12 |
57,772,462 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0698:Ttc6
|
UTSW |
12 |
57,720,002 (GRCm39) |
missense |
probably benign |
0.04 |
R0988:Ttc6
|
UTSW |
12 |
57,735,435 (GRCm39) |
splice site |
probably benign |
|
R1290:Ttc6
|
UTSW |
12 |
57,707,199 (GRCm39) |
missense |
probably benign |
0.00 |
R1338:Ttc6
|
UTSW |
12 |
57,663,155 (GRCm39) |
missense |
probably benign |
0.10 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1481:Ttc6
|
UTSW |
12 |
57,783,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Ttc6
|
UTSW |
12 |
57,696,301 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1558:Ttc6
|
UTSW |
12 |
57,733,132 (GRCm39) |
missense |
probably benign |
0.14 |
R1570:Ttc6
|
UTSW |
12 |
57,721,549 (GRCm39) |
missense |
probably damaging |
0.98 |
R1619:Ttc6
|
UTSW |
12 |
57,784,454 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1819:Ttc6
|
UTSW |
12 |
57,741,286 (GRCm39) |
critical splice donor site |
probably null |
|
R1826:Ttc6
|
UTSW |
12 |
57,707,033 (GRCm39) |
missense |
probably benign |
0.10 |
R1863:Ttc6
|
UTSW |
12 |
57,760,881 (GRCm39) |
missense |
probably benign |
0.04 |
R1872:Ttc6
|
UTSW |
12 |
57,751,338 (GRCm39) |
critical splice donor site |
probably null |
|
R1887:Ttc6
|
UTSW |
12 |
57,720,044 (GRCm39) |
missense |
probably benign |
0.04 |
R1937:Ttc6
|
UTSW |
12 |
57,663,109 (GRCm39) |
missense |
probably benign |
0.02 |
R2014:Ttc6
|
UTSW |
12 |
57,623,003 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2056:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2058:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2059:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2152:Ttc6
|
UTSW |
12 |
57,752,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R2179:Ttc6
|
UTSW |
12 |
57,719,904 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2275:Ttc6
|
UTSW |
12 |
57,749,084 (GRCm39) |
missense |
probably benign |
0.01 |
R2432:Ttc6
|
UTSW |
12 |
57,668,821 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2474:Ttc6
|
UTSW |
12 |
57,622,713 (GRCm39) |
missense |
probably benign |
0.37 |
R2853:Ttc6
|
UTSW |
12 |
57,622,967 (GRCm39) |
missense |
probably damaging |
0.96 |
R3848:Ttc6
|
UTSW |
12 |
57,723,932 (GRCm39) |
missense |
probably damaging |
0.97 |
R3853:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3950:Ttc6
|
UTSW |
12 |
57,696,292 (GRCm39) |
missense |
probably damaging |
0.97 |
R3953:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3954:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3955:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3957:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R4135:Ttc6
|
UTSW |
12 |
57,679,581 (GRCm39) |
intron |
probably benign |
|
R4387:Ttc6
|
UTSW |
12 |
57,689,836 (GRCm39) |
missense |
probably benign |
0.00 |
R4577:Ttc6
|
UTSW |
12 |
57,623,441 (GRCm39) |
missense |
probably benign |
0.22 |
R4747:Ttc6
|
UTSW |
12 |
57,721,478 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4779:Ttc6
|
UTSW |
12 |
57,776,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Ttc6
|
UTSW |
12 |
57,775,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Ttc6
|
UTSW |
12 |
57,749,142 (GRCm39) |
missense |
probably damaging |
0.96 |
R4898:Ttc6
|
UTSW |
12 |
57,707,026 (GRCm39) |
missense |
probably benign |
0.00 |
R4930:Ttc6
|
UTSW |
12 |
57,720,609 (GRCm39) |
critical splice donor site |
probably null |
|
R4946:Ttc6
|
UTSW |
12 |
57,689,926 (GRCm39) |
missense |
probably benign |
0.01 |
R5257:Ttc6
|
UTSW |
12 |
57,749,061 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5303:Ttc6
|
UTSW |
12 |
57,622,606 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5385:Ttc6
|
UTSW |
12 |
57,689,821 (GRCm39) |
splice site |
probably null |
|
R5402:Ttc6
|
UTSW |
12 |
57,783,817 (GRCm39) |
nonsense |
probably null |
|
R5428:Ttc6
|
UTSW |
12 |
57,736,620 (GRCm39) |
missense |
probably null |
0.98 |
R5436:Ttc6
|
UTSW |
12 |
57,721,380 (GRCm39) |
splice site |
probably null |
|
R5646:Ttc6
|
UTSW |
12 |
57,622,805 (GRCm39) |
missense |
probably damaging |
0.99 |
R5697:Ttc6
|
UTSW |
12 |
57,724,000 (GRCm39) |
missense |
probably benign |
0.22 |
R5792:Ttc6
|
UTSW |
12 |
57,719,990 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5808:Ttc6
|
UTSW |
12 |
57,664,397 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5842:Ttc6
|
UTSW |
12 |
57,783,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R6144:Ttc6
|
UTSW |
12 |
57,719,886 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6155:Ttc6
|
UTSW |
12 |
57,784,402 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6283:Ttc6
|
UTSW |
12 |
57,749,048 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6371:Ttc6
|
UTSW |
12 |
57,775,249 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6715:Ttc6
|
UTSW |
12 |
57,721,556 (GRCm39) |
critical splice donor site |
probably null |
|
R6738:Ttc6
|
UTSW |
12 |
57,735,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R6795:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R6959:Ttc6
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
R7053:Ttc6
|
UTSW |
12 |
57,707,318 (GRCm39) |
missense |
probably benign |
0.01 |
R7125:Ttc6
|
UTSW |
12 |
57,623,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7259:Ttc6
|
UTSW |
12 |
57,622,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7304:Ttc6
|
UTSW |
12 |
57,622,837 (GRCm39) |
missense |
probably damaging |
0.96 |
R7369:Ttc6
|
UTSW |
12 |
57,719,717 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7409:Ttc6
|
UTSW |
12 |
57,743,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R7429:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7430:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7492:Ttc6
|
UTSW |
12 |
57,719,922 (GRCm39) |
missense |
probably benign |
0.02 |
R7535:Ttc6
|
UTSW |
12 |
57,623,305 (GRCm39) |
missense |
probably benign |
0.00 |
R7866:Ttc6
|
UTSW |
12 |
57,721,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R7901:Ttc6
|
UTSW |
12 |
57,735,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R7944:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7945:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7965:Ttc6
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8062:Ttc6
|
UTSW |
12 |
57,783,764 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8119:Ttc6
|
UTSW |
12 |
57,752,429 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8142:Ttc6
|
UTSW |
12 |
57,744,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8154:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Ttc6
|
UTSW |
12 |
57,720,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R8335:Ttc6
|
UTSW |
12 |
57,707,077 (GRCm39) |
missense |
probably benign |
0.00 |
R8343:Ttc6
|
UTSW |
12 |
57,707,282 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8696:Ttc6
|
UTSW |
12 |
57,784,492 (GRCm39) |
missense |
probably benign |
0.20 |
R8875:Ttc6
|
UTSW |
12 |
57,776,194 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8875:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R8876:Ttc6
|
UTSW |
12 |
57,784,489 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8924:Ttc6
|
UTSW |
12 |
57,697,790 (GRCm39) |
nonsense |
probably null |
|
R8944:Ttc6
|
UTSW |
12 |
57,689,826 (GRCm39) |
missense |
|
|
R8956:Ttc6
|
UTSW |
12 |
57,775,196 (GRCm39) |
nonsense |
probably null |
|
R9009:Ttc6
|
UTSW |
12 |
57,744,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Ttc6
|
UTSW |
12 |
57,752,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Ttc6
|
UTSW |
12 |
57,783,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R9291:Ttc6
|
UTSW |
12 |
57,622,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R9304:Ttc6
|
UTSW |
12 |
57,776,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R9309:Ttc6
|
UTSW |
12 |
57,753,649 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9331:Ttc6
|
UTSW |
12 |
57,720,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9398:Ttc6
|
UTSW |
12 |
57,784,404 (GRCm39) |
nonsense |
probably null |
|
R9430:Ttc6
|
UTSW |
12 |
57,733,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Ttc6
|
UTSW |
12 |
57,664,299 (GRCm39) |
missense |
probably benign |
|
R9688:Ttc6
|
UTSW |
12 |
57,720,602 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9732:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
probably benign |
0.36 |
R9740:Ttc6
|
UTSW |
12 |
57,736,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Ttc6
|
UTSW |
12 |
57,701,559 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Ttc6
|
UTSW |
12 |
57,622,904 (GRCm39) |
missense |
probably damaging |
0.96 |
X0058:Ttc6
|
UTSW |
12 |
57,753,637 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Ttc6
|
UTSW |
12 |
57,744,161 (GRCm39) |
missense |
probably benign |
0.08 |
|