Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
C |
A |
10: 79,834,123 (GRCm39) |
H116Q |
probably benign |
Het |
Akap12 |
G |
T |
10: 4,303,947 (GRCm39) |
E252D |
probably benign |
Het |
Apobr |
A |
G |
7: 126,184,188 (GRCm39) |
D2G |
probably damaging |
Het |
Arhgef12 |
A |
T |
9: 42,931,982 (GRCm39) |
H168Q |
probably damaging |
Het |
Asb3 |
T |
A |
11: 31,031,357 (GRCm39) |
|
probably null |
Het |
Brip1 |
T |
C |
11: 85,968,710 (GRCm39) |
Y825C |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,525,143 (GRCm39) |
Y1679N |
probably damaging |
Het |
Ccdc69 |
C |
T |
11: 54,951,296 (GRCm39) |
A42T |
probably benign |
Het |
Cds1 |
G |
T |
5: 101,929,286 (GRCm39) |
D55Y |
possibly damaging |
Het |
Cep135 |
C |
A |
5: 76,784,873 (GRCm39) |
D989E |
probably benign |
Het |
Cpsf6 |
C |
A |
10: 117,197,189 (GRCm39) |
|
probably benign |
Het |
Ctif |
C |
T |
18: 75,770,290 (GRCm39) |
V32M |
probably damaging |
Het |
Cylc2 |
T |
C |
4: 51,228,587 (GRCm39) |
|
probably benign |
Het |
Dao |
T |
C |
5: 114,158,070 (GRCm39) |
|
probably null |
Het |
Dop1b |
A |
G |
16: 93,536,931 (GRCm39) |
Y14C |
probably damaging |
Het |
Fam187a |
C |
T |
11: 102,777,290 (GRCm39) |
R365C |
probably damaging |
Het |
Fastkd2 |
A |
G |
1: 63,770,598 (GRCm39) |
|
probably benign |
Het |
Fhip2a |
A |
G |
19: 57,359,613 (GRCm39) |
N51S |
probably damaging |
Het |
Fkbp15 |
G |
T |
4: 62,230,560 (GRCm39) |
L718I |
possibly damaging |
Het |
Gabbr2 |
C |
A |
4: 46,681,208 (GRCm39) |
V118F |
probably damaging |
Het |
Gm13991 |
T |
A |
2: 116,358,508 (GRCm39) |
|
noncoding transcript |
Het |
H2-M9 |
T |
C |
17: 36,952,523 (GRCm39) |
I174M |
probably damaging |
Het |
Ift70a2 |
T |
C |
2: 75,807,421 (GRCm39) |
M364V |
probably benign |
Het |
Insr |
T |
A |
8: 3,208,742 (GRCm39) |
M1240L |
probably benign |
Het |
Ints15 |
G |
T |
5: 143,300,830 (GRCm39) |
S7* |
probably null |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Mad2l1bp |
T |
A |
17: 46,463,738 (GRCm39) |
E95D |
probably benign |
Het |
Marchf9 |
T |
C |
10: 126,895,319 (GRCm39) |
D102G |
probably benign |
Het |
Muc19 |
A |
G |
15: 91,776,374 (GRCm39) |
|
noncoding transcript |
Het |
Nr1h4 |
T |
A |
10: 89,334,117 (GRCm39) |
Y91F |
probably benign |
Het |
Nr5a2 |
A |
T |
1: 136,876,540 (GRCm39) |
M1K |
probably null |
Het |
Oprd1 |
T |
C |
4: 131,841,104 (GRCm39) |
T285A |
probably benign |
Het |
Optc |
T |
C |
1: 133,829,822 (GRCm39) |
N196S |
probably benign |
Het |
Or51f5 |
T |
A |
7: 102,424,513 (GRCm39) |
S261T |
probably damaging |
Het |
Or5g29 |
A |
C |
2: 85,421,779 (GRCm39) |
K298N |
possibly damaging |
Het |
Or7g21 |
A |
T |
9: 19,032,656 (GRCm39) |
Y132F |
probably damaging |
Het |
Panx2 |
G |
T |
15: 88,944,431 (GRCm39) |
R52L |
probably damaging |
Het |
Pdzd8 |
A |
G |
19: 59,333,389 (GRCm39) |
F211L |
probably damaging |
Het |
Pot1b |
T |
A |
17: 56,006,995 (GRCm39) |
T41S |
probably benign |
Het |
Prss56 |
T |
C |
1: 87,111,880 (GRCm39) |
L37S |
probably damaging |
Het |
Ptk2b |
T |
C |
14: 66,393,864 (GRCm39) |
T870A |
probably damaging |
Het |
Rabep2 |
C |
A |
7: 126,033,465 (GRCm39) |
|
probably benign |
Het |
Rbm48 |
A |
C |
5: 3,645,444 (GRCm39) |
V80G |
probably damaging |
Het |
Rhou |
G |
T |
8: 124,380,848 (GRCm39) |
C55F |
possibly damaging |
Het |
Rnaseh2c |
A |
G |
19: 5,652,070 (GRCm39) |
D45G |
probably benign |
Het |
Rusc1 |
A |
G |
3: 88,996,389 (GRCm39) |
S109P |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,588,012 (GRCm39) |
D2643G |
possibly damaging |
Het |
Septin4 |
T |
A |
11: 87,458,358 (GRCm39) |
M244K |
probably benign |
Het |
Sik2 |
T |
C |
9: 50,810,703 (GRCm39) |
E471G |
probably benign |
Het |
Sipa1 |
A |
G |
19: 5,709,406 (GRCm39) |
S310P |
probably damaging |
Het |
Sp140l1 |
C |
T |
1: 85,066,521 (GRCm39) |
|
probably benign |
Het |
Spen |
T |
C |
4: 141,203,587 (GRCm39) |
E1680G |
unknown |
Het |
Steap3 |
C |
T |
1: 120,171,497 (GRCm39) |
|
probably null |
Het |
Tmeff2 |
T |
A |
1: 51,110,700 (GRCm39) |
C171* |
probably null |
Het |
Tmem138 |
A |
T |
19: 10,552,634 (GRCm39) |
M33K |
probably benign |
Het |
Trappc11 |
C |
A |
8: 47,963,998 (GRCm39) |
V601L |
possibly damaging |
Het |
Ttll4 |
C |
A |
1: 74,718,445 (GRCm39) |
H99N |
probably damaging |
Het |
Uchl4 |
A |
T |
9: 64,143,022 (GRCm39) |
K168* |
probably null |
Het |
Wdr17 |
C |
T |
8: 55,106,913 (GRCm39) |
|
probably null |
Het |
Xpo1 |
A |
G |
11: 23,245,977 (GRCm39) |
D1029G |
probably damaging |
Het |
Zfp719 |
G |
T |
7: 43,240,549 (GRCm39) |
K712N |
probably damaging |
Het |
|
Other mutations in Dop1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Dop1a
|
APN |
9 |
86,433,732 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL00427:Dop1a
|
APN |
9 |
86,403,552 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00427:Dop1a
|
APN |
9 |
86,403,551 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00427:Dop1a
|
APN |
9 |
86,403,553 (GRCm39) |
missense |
probably benign |
0.09 |
IGL00577:Dop1a
|
APN |
9 |
86,402,999 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00741:Dop1a
|
APN |
9 |
86,404,859 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL00959:Dop1a
|
APN |
9 |
86,369,484 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01339:Dop1a
|
APN |
9 |
86,433,730 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01608:Dop1a
|
APN |
9 |
86,389,614 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01760:Dop1a
|
APN |
9 |
86,401,976 (GRCm39) |
missense |
probably benign |
|
IGL01788:Dop1a
|
APN |
9 |
86,413,772 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01844:Dop1a
|
APN |
9 |
86,396,138 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01923:Dop1a
|
APN |
9 |
86,404,920 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02036:Dop1a
|
APN |
9 |
86,413,818 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02308:Dop1a
|
APN |
9 |
86,402,141 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02494:Dop1a
|
APN |
9 |
86,408,871 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02698:Dop1a
|
APN |
9 |
86,406,412 (GRCm39) |
splice site |
probably benign |
|
IGL02731:Dop1a
|
APN |
9 |
86,369,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02821:Dop1a
|
APN |
9 |
86,402,209 (GRCm39) |
missense |
probably benign |
|
IGL02952:Dop1a
|
APN |
9 |
86,414,975 (GRCm39) |
splice site |
probably benign |
|
IGL03071:Dop1a
|
APN |
9 |
86,371,668 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03271:Dop1a
|
APN |
9 |
86,386,275 (GRCm39) |
nonsense |
probably null |
|
IGL03344:Dop1a
|
APN |
9 |
86,418,197 (GRCm39) |
missense |
probably damaging |
1.00 |
Beg
|
UTSW |
9 |
86,430,225 (GRCm39) |
nonsense |
probably null |
|
covet
|
UTSW |
9 |
86,397,396 (GRCm39) |
missense |
probably damaging |
1.00 |
crave
|
UTSW |
9 |
86,399,092 (GRCm39) |
missense |
probably benign |
|
desire
|
UTSW |
9 |
86,402,109 (GRCm39) |
missense |
possibly damaging |
0.47 |
groak
|
UTSW |
9 |
86,403,710 (GRCm39) |
missense |
probably damaging |
1.00 |
Querer
|
UTSW |
9 |
86,386,265 (GRCm39) |
missense |
probably damaging |
1.00 |
yearn
|
UTSW |
9 |
86,386,220 (GRCm39) |
splice site |
probably null |
|
R0055:Dop1a
|
UTSW |
9 |
86,394,705 (GRCm39) |
missense |
probably benign |
0.08 |
R0285:Dop1a
|
UTSW |
9 |
86,394,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0415:Dop1a
|
UTSW |
9 |
86,388,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R0427:Dop1a
|
UTSW |
9 |
86,389,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Dop1a
|
UTSW |
9 |
86,402,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Dop1a
|
UTSW |
9 |
86,367,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R1118:Dop1a
|
UTSW |
9 |
86,397,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1158:Dop1a
|
UTSW |
9 |
86,367,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R1272:Dop1a
|
UTSW |
9 |
86,403,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Dop1a
|
UTSW |
9 |
86,424,785 (GRCm39) |
splice site |
probably null |
|
R1584:Dop1a
|
UTSW |
9 |
86,430,225 (GRCm39) |
nonsense |
probably null |
|
R1601:Dop1a
|
UTSW |
9 |
86,418,303 (GRCm39) |
missense |
probably damaging |
0.99 |
R1674:Dop1a
|
UTSW |
9 |
86,418,213 (GRCm39) |
missense |
probably damaging |
0.98 |
R1706:Dop1a
|
UTSW |
9 |
86,436,133 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1856:Dop1a
|
UTSW |
9 |
86,374,057 (GRCm39) |
missense |
probably damaging |
0.99 |
R1926:Dop1a
|
UTSW |
9 |
86,405,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Dop1a
|
UTSW |
9 |
86,376,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Dop1a
|
UTSW |
9 |
86,403,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Dop1a
|
UTSW |
9 |
86,403,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Dop1a
|
UTSW |
9 |
86,403,652 (GRCm39) |
missense |
probably benign |
0.00 |
R2271:Dop1a
|
UTSW |
9 |
86,376,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R2312:Dop1a
|
UTSW |
9 |
86,403,495 (GRCm39) |
nonsense |
probably null |
|
R2379:Dop1a
|
UTSW |
9 |
86,403,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R2507:Dop1a
|
UTSW |
9 |
86,395,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R3737:Dop1a
|
UTSW |
9 |
86,376,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R3804:Dop1a
|
UTSW |
9 |
86,403,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R3916:Dop1a
|
UTSW |
9 |
86,403,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R3921:Dop1a
|
UTSW |
9 |
86,402,324 (GRCm39) |
missense |
probably benign |
0.06 |
R4035:Dop1a
|
UTSW |
9 |
86,376,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4392:Dop1a
|
UTSW |
9 |
86,385,196 (GRCm39) |
intron |
probably benign |
|
R4404:Dop1a
|
UTSW |
9 |
86,404,866 (GRCm39) |
nonsense |
probably null |
|
R4513:Dop1a
|
UTSW |
9 |
86,402,612 (GRCm39) |
missense |
probably benign |
0.39 |
R4624:Dop1a
|
UTSW |
9 |
86,403,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R4659:Dop1a
|
UTSW |
9 |
86,384,085 (GRCm39) |
intron |
probably benign |
|
R4910:Dop1a
|
UTSW |
9 |
86,374,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R4919:Dop1a
|
UTSW |
9 |
86,402,109 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5061:Dop1a
|
UTSW |
9 |
86,385,161 (GRCm39) |
splice site |
probably benign |
|
R5079:Dop1a
|
UTSW |
9 |
86,369,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R5118:Dop1a
|
UTSW |
9 |
86,388,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R5169:Dop1a
|
UTSW |
9 |
86,415,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R5190:Dop1a
|
UTSW |
9 |
86,369,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Dop1a
|
UTSW |
9 |
86,397,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R5346:Dop1a
|
UTSW |
9 |
86,402,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R5484:Dop1a
|
UTSW |
9 |
86,427,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R5501:Dop1a
|
UTSW |
9 |
86,389,783 (GRCm39) |
missense |
probably benign |
0.04 |
R5554:Dop1a
|
UTSW |
9 |
86,403,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R5707:Dop1a
|
UTSW |
9 |
86,385,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5826:Dop1a
|
UTSW |
9 |
86,389,623 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5921:Dop1a
|
UTSW |
9 |
86,383,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R5934:Dop1a
|
UTSW |
9 |
86,424,495 (GRCm39) |
nonsense |
probably null |
|
R5936:Dop1a
|
UTSW |
9 |
86,418,565 (GRCm39) |
nonsense |
probably null |
|
R6046:Dop1a
|
UTSW |
9 |
86,397,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R6053:Dop1a
|
UTSW |
9 |
86,397,347 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6072:Dop1a
|
UTSW |
9 |
86,389,750 (GRCm39) |
missense |
probably benign |
0.00 |
R6104:Dop1a
|
UTSW |
9 |
86,402,860 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6125:Dop1a
|
UTSW |
9 |
86,403,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Dop1a
|
UTSW |
9 |
86,386,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R6930:Dop1a
|
UTSW |
9 |
86,413,825 (GRCm39) |
critical splice donor site |
probably null |
|
R6949:Dop1a
|
UTSW |
9 |
86,382,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R6979:Dop1a
|
UTSW |
9 |
86,403,695 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7035:Dop1a
|
UTSW |
9 |
86,406,355 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7069:Dop1a
|
UTSW |
9 |
86,432,222 (GRCm39) |
critical splice donor site |
probably null |
|
R7101:Dop1a
|
UTSW |
9 |
86,389,722 (GRCm39) |
missense |
probably benign |
|
R7202:Dop1a
|
UTSW |
9 |
86,386,220 (GRCm39) |
splice site |
probably null |
|
R7222:Dop1a
|
UTSW |
9 |
86,404,929 (GRCm39) |
critical splice donor site |
probably null |
|
R7233:Dop1a
|
UTSW |
9 |
86,403,749 (GRCm39) |
missense |
probably benign |
0.00 |
R7236:Dop1a
|
UTSW |
9 |
86,397,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R7252:Dop1a
|
UTSW |
9 |
86,382,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R7268:Dop1a
|
UTSW |
9 |
86,394,830 (GRCm39) |
nonsense |
probably null |
|
R7353:Dop1a
|
UTSW |
9 |
86,394,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R7481:Dop1a
|
UTSW |
9 |
86,417,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Dop1a
|
UTSW |
9 |
86,376,464 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7507:Dop1a
|
UTSW |
9 |
86,418,002 (GRCm39) |
missense |
probably benign |
0.01 |
R7525:Dop1a
|
UTSW |
9 |
86,388,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Dop1a
|
UTSW |
9 |
86,403,626 (GRCm39) |
missense |
probably benign |
0.03 |
R7751:Dop1a
|
UTSW |
9 |
86,389,783 (GRCm39) |
missense |
probably benign |
0.00 |
R7753:Dop1a
|
UTSW |
9 |
86,371,755 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7839:Dop1a
|
UTSW |
9 |
86,424,818 (GRCm39) |
nonsense |
probably null |
|
R7868:Dop1a
|
UTSW |
9 |
86,384,037 (GRCm39) |
critical splice donor site |
probably null |
|
R8061:Dop1a
|
UTSW |
9 |
86,403,246 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8067:Dop1a
|
UTSW |
9 |
86,400,392 (GRCm39) |
missense |
probably benign |
0.00 |
R8156:Dop1a
|
UTSW |
9 |
86,376,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R8196:Dop1a
|
UTSW |
9 |
86,405,151 (GRCm39) |
missense |
probably benign |
0.12 |
R8223:Dop1a
|
UTSW |
9 |
86,400,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R8267:Dop1a
|
UTSW |
9 |
86,396,054 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8276:Dop1a
|
UTSW |
9 |
86,399,092 (GRCm39) |
missense |
probably benign |
|
R8306:Dop1a
|
UTSW |
9 |
86,402,259 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8353:Dop1a
|
UTSW |
9 |
86,403,639 (GRCm39) |
missense |
probably damaging |
0.97 |
R8362:Dop1a
|
UTSW |
9 |
86,395,941 (GRCm39) |
missense |
probably benign |
0.02 |
R8403:Dop1a
|
UTSW |
9 |
86,382,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R8817:Dop1a
|
UTSW |
9 |
86,396,003 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8862:Dop1a
|
UTSW |
9 |
86,406,404 (GRCm39) |
critical splice donor site |
probably null |
|
R8888:Dop1a
|
UTSW |
9 |
86,403,587 (GRCm39) |
missense |
probably benign |
|
R8972:Dop1a
|
UTSW |
9 |
86,403,300 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9001:Dop1a
|
UTSW |
9 |
86,436,374 (GRCm39) |
makesense |
probably null |
|
R9011:Dop1a
|
UTSW |
9 |
86,397,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R9021:Dop1a
|
UTSW |
9 |
86,402,490 (GRCm39) |
missense |
probably benign |
0.35 |
R9039:Dop1a
|
UTSW |
9 |
86,382,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R9128:Dop1a
|
UTSW |
9 |
86,395,208 (GRCm39) |
missense |
probably benign |
|
R9178:Dop1a
|
UTSW |
9 |
86,371,796 (GRCm39) |
nonsense |
probably null |
|
R9238:Dop1a
|
UTSW |
9 |
86,415,027 (GRCm39) |
missense |
probably benign |
|
R9313:Dop1a
|
UTSW |
9 |
86,406,641 (GRCm39) |
makesense |
probably null |
|
R9334:Dop1a
|
UTSW |
9 |
86,403,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9422:Dop1a
|
UTSW |
9 |
86,425,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R9562:Dop1a
|
UTSW |
9 |
86,424,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R9584:Dop1a
|
UTSW |
9 |
86,385,151 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9677:Dop1a
|
UTSW |
9 |
86,425,098 (GRCm39) |
missense |
|
|
RF004:Dop1a
|
UTSW |
9 |
86,436,244 (GRCm39) |
missense |
probably benign |
|
X0019:Dop1a
|
UTSW |
9 |
86,413,803 (GRCm39) |
missense |
probably damaging |
0.98 |
X0019:Dop1a
|
UTSW |
9 |
86,388,280 (GRCm39) |
missense |
probably damaging |
1.00 |
ZE80:Dop1a
|
UTSW |
9 |
86,382,895 (GRCm39) |
missense |
probably damaging |
1.00 |
|