Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
T |
A |
5: 77,024,203 (GRCm39) |
I991L |
probably benign |
Het |
Abtb3 |
C |
A |
10: 85,223,520 (GRCm39) |
R110S |
unknown |
Het |
Actg2 |
C |
A |
6: 83,497,745 (GRCm39) |
G96V |
probably damaging |
Het |
Adh5 |
T |
A |
3: 138,156,812 (GRCm39) |
L166* |
probably null |
Het |
Akap13 |
A |
G |
7: 75,260,010 (GRCm39) |
D75G |
probably benign |
Het |
Ank2 |
T |
C |
3: 126,739,947 (GRCm39) |
|
probably benign |
Het |
Arfgap1 |
T |
A |
2: 180,615,913 (GRCm39) |
D197E |
probably benign |
Het |
Aste1 |
T |
C |
9: 105,273,906 (GRCm39) |
|
probably null |
Het |
Atp8b2 |
T |
A |
3: 89,861,878 (GRCm39) |
N78I |
probably damaging |
Het |
Cacna2d3 |
T |
A |
14: 28,691,260 (GRCm39) |
|
probably benign |
Het |
Chrd |
T |
A |
16: 20,558,183 (GRCm39) |
W809R |
probably damaging |
Het |
Col2a1 |
C |
T |
15: 97,896,469 (GRCm39) |
G60D |
unknown |
Het |
Coro7 |
T |
A |
16: 4,497,475 (GRCm39) |
M1L |
probably damaging |
Het |
Cracdl |
A |
T |
1: 37,670,982 (GRCm39) |
F97Y |
probably damaging |
Het |
Dhx40 |
T |
C |
11: 86,688,569 (GRCm39) |
I285V |
probably benign |
Het |
Enox1 |
A |
T |
14: 77,848,764 (GRCm39) |
R358S |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,815,990 (GRCm39) |
V2724A |
probably damaging |
Het |
Fam221a |
A |
C |
6: 49,355,432 (GRCm39) |
Q178P |
probably damaging |
Het |
Fcho1 |
A |
C |
8: 72,163,141 (GRCm39) |
|
probably null |
Het |
Fndc1 |
A |
T |
17: 7,988,567 (GRCm39) |
V1165D |
unknown |
Het |
Gal3st2b |
A |
T |
1: 93,868,341 (GRCm39) |
N189Y |
possibly damaging |
Het |
Ghr |
T |
A |
15: 3,349,966 (GRCm39) |
D404V |
probably damaging |
Het |
Glis3 |
A |
T |
19: 28,508,919 (GRCm39) |
V355D |
probably damaging |
Het |
Gpr12 |
A |
C |
5: 146,520,349 (GRCm39) |
V32G |
possibly damaging |
Het |
Gspt1 |
T |
A |
16: 11,040,525 (GRCm39) |
L593F |
probably damaging |
Het |
H2-Q7 |
A |
T |
17: 35,659,007 (GRCm39) |
T153S |
probably damaging |
Het |
Hars2 |
A |
G |
18: 36,921,009 (GRCm39) |
I194V |
probably damaging |
Het |
Hdac9 |
T |
A |
12: 34,479,548 (GRCm39) |
T202S |
possibly damaging |
Het |
Hoxd13 |
T |
C |
2: 74,499,368 (GRCm39) |
Y239H |
probably damaging |
Het |
Insm2 |
C |
T |
12: 55,646,621 (GRCm39) |
Q122* |
probably null |
Het |
Insyn2b |
T |
A |
11: 34,352,677 (GRCm39) |
C240S |
possibly damaging |
Het |
Ip6k1 |
T |
A |
9: 107,922,651 (GRCm39) |
|
probably null |
Het |
Ippk |
T |
C |
13: 49,615,219 (GRCm39) |
V534A |
probably damaging |
Het |
Itch |
T |
G |
2: 155,051,914 (GRCm39) |
F611C |
probably damaging |
Het |
Itga1 |
A |
T |
13: 115,104,776 (GRCm39) |
N1083K |
probably damaging |
Het |
Itgae |
A |
C |
11: 73,006,969 (GRCm39) |
D405A |
probably damaging |
Het |
Kif18a |
T |
C |
2: 109,125,347 (GRCm39) |
S255P |
probably damaging |
Het |
Klhl24 |
C |
G |
16: 19,926,231 (GRCm39) |
T253R |
probably benign |
Het |
Krt81 |
T |
A |
15: 101,358,609 (GRCm39) |
T307S |
possibly damaging |
Het |
Lbr |
A |
T |
1: 181,656,354 (GRCm39) |
W265R |
probably damaging |
Het |
Lgals3bp |
T |
C |
11: 118,283,999 (GRCm39) |
T527A |
probably benign |
Het |
Lzts1 |
A |
C |
8: 69,593,397 (GRCm39) |
V70G |
probably damaging |
Het |
Map3k6 |
C |
T |
4: 132,979,023 (GRCm39) |
P1154S |
probably benign |
Het |
Masp1 |
T |
C |
16: 23,271,205 (GRCm39) |
D681G |
probably benign |
Het |
Mdga2 |
T |
C |
12: 66,533,526 (GRCm39) |
N948D |
probably benign |
Het |
Mettl4 |
A |
T |
17: 95,041,061 (GRCm39) |
F364L |
probably damaging |
Het |
Mosmo |
T |
C |
7: 120,277,055 (GRCm39) |
I23T |
probably benign |
Het |
Mtg1 |
G |
A |
7: 139,723,657 (GRCm39) |
V96I |
probably benign |
Het |
Myh11 |
T |
A |
16: 14,036,803 (GRCm39) |
R966S |
possibly damaging |
Het |
Ncapg2 |
A |
G |
12: 116,388,337 (GRCm39) |
|
probably null |
Het |
Nid1 |
G |
A |
13: 13,683,353 (GRCm39) |
V1144I |
probably benign |
Het |
Or4a77 |
T |
C |
2: 89,486,910 (GRCm39) |
I292V |
probably benign |
Het |
Or52a33 |
A |
T |
7: 103,289,167 (GRCm39) |
M60K |
probably damaging |
Het |
Or55b4 |
C |
A |
7: 102,133,979 (GRCm39) |
C116F |
possibly damaging |
Het |
Oscar |
T |
G |
7: 3,614,238 (GRCm39) |
Y167S |
probably damaging |
Het |
Pa2g4 |
T |
C |
10: 128,396,559 (GRCm39) |
T200A |
probably benign |
Het |
Pcdh7 |
A |
G |
5: 57,877,126 (GRCm39) |
D227G |
probably benign |
Het |
Pira1 |
C |
G |
7: 3,740,319 (GRCm39) |
A301P |
probably damaging |
Het |
Plce1 |
G |
A |
19: 38,747,384 (GRCm39) |
G1702R |
probably damaging |
Het |
Plxna2 |
C |
A |
1: 194,476,212 (GRCm39) |
T1144K |
possibly damaging |
Het |
Prl8a8 |
G |
A |
13: 27,695,450 (GRCm39) |
T99I |
probably benign |
Het |
Prr29 |
C |
A |
11: 106,267,085 (GRCm39) |
H83Q |
probably damaging |
Het |
Raly |
T |
A |
2: 154,701,664 (GRCm39) |
I108N |
possibly damaging |
Het |
Ranbp9 |
A |
T |
13: 43,573,098 (GRCm39) |
S475R |
probably benign |
Het |
Rogdi |
C |
A |
16: 4,831,362 (GRCm39) |
|
probably benign |
Het |
Rorc |
C |
T |
3: 94,280,214 (GRCm39) |
Q6* |
probably null |
Het |
Sacs |
T |
C |
14: 61,449,945 (GRCm39) |
L3997S |
probably damaging |
Het |
Scn2a |
A |
T |
2: 65,594,950 (GRCm39) |
Y1933F |
probably benign |
Het |
Sik3 |
T |
C |
9: 46,122,041 (GRCm39) |
L898P |
probably damaging |
Het |
Sipa1l1 |
A |
G |
12: 82,388,180 (GRCm39) |
I135M |
probably damaging |
Het |
Slc26a3 |
C |
A |
12: 31,500,934 (GRCm39) |
Q224K |
probably damaging |
Het |
Sobp |
G |
T |
10: 42,897,436 (GRCm39) |
N716K |
probably benign |
Het |
Spata16 |
A |
G |
3: 26,981,483 (GRCm39) |
D513G |
probably damaging |
Het |
Spata31h1 |
G |
A |
10: 82,125,777 (GRCm39) |
T2411I |
probably damaging |
Het |
Speer4a3 |
A |
T |
5: 26,154,842 (GRCm39) |
S253T |
possibly damaging |
Het |
Stac |
T |
C |
9: 111,401,394 (GRCm39) |
R351G |
possibly damaging |
Het |
Tecta |
T |
A |
9: 42,306,237 (GRCm39) |
T64S |
probably benign |
Het |
Tert |
G |
A |
13: 73,776,529 (GRCm39) |
V427M |
probably damaging |
Het |
Tex15 |
G |
A |
8: 34,060,748 (GRCm39) |
M333I |
probably benign |
Het |
Tmbim4 |
A |
T |
10: 120,056,664 (GRCm39) |
Q72L |
probably benign |
Het |
Trav9n-4 |
T |
C |
14: 53,532,256 (GRCm39) |
S37P |
probably benign |
Het |
Trpv5 |
A |
T |
6: 41,652,894 (GRCm39) |
M93K |
possibly damaging |
Het |
Ulk4 |
T |
C |
9: 121,087,876 (GRCm39) |
E272G |
probably benign |
Het |
Ulk4 |
T |
C |
9: 121,095,583 (GRCm39) |
T79A |
probably benign |
Het |
Upb1 |
A |
G |
10: 75,248,602 (GRCm39) |
N41D |
probably benign |
Het |
Wls |
A |
T |
3: 159,639,965 (GRCm39) |
Y532F |
probably damaging |
Het |
Zdhhc5 |
G |
A |
2: 84,545,355 (GRCm39) |
|
probably benign |
Het |
Zfp109 |
T |
C |
7: 23,928,785 (GRCm39) |
D216G |
probably benign |
Het |
Zfp473 |
G |
A |
7: 44,381,798 (GRCm39) |
A845V |
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 |
R5176:Dop1a
|
UTSW |
9 |
86,403,868 (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 |
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 |
|