Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
C |
T |
16: 8,420,300 (GRCm39) |
|
probably benign |
Het |
Abcb10 |
G |
A |
8: 124,688,756 (GRCm39) |
R507W |
probably damaging |
Het |
Actg1 |
T |
C |
11: 120,238,586 (GRCm39) |
D80G |
possibly damaging |
Het |
Actr5 |
A |
G |
2: 158,477,264 (GRCm39) |
D405G |
possibly damaging |
Het |
Ahnak |
C |
T |
19: 8,984,512 (GRCm39) |
T1932I |
probably benign |
Het |
Ankk1 |
T |
A |
9: 49,327,371 (GRCm39) |
T603S |
possibly damaging |
Het |
Atp13a3 |
A |
T |
16: 30,155,053 (GRCm39) |
F964I |
probably damaging |
Het |
Atp6v1g3 |
A |
G |
1: 138,215,570 (GRCm39) |
T77A |
probably benign |
Het |
Bccip |
A |
G |
7: 133,319,503 (GRCm39) |
H198R |
probably damaging |
Het |
Bsx |
A |
T |
9: 40,785,519 (GRCm39) |
R16W |
probably damaging |
Het |
Ccdc88b |
C |
T |
19: 6,826,406 (GRCm39) |
R1103Q |
probably damaging |
Het |
Cd59a |
A |
C |
2: 103,941,103 (GRCm39) |
Y27S |
probably damaging |
Het |
Cdk20 |
A |
G |
13: 64,584,413 (GRCm39) |
H162R |
probably damaging |
Het |
Col6a2 |
C |
T |
10: 76,450,212 (GRCm39) |
E240K |
possibly damaging |
Het |
Ddr2 |
A |
G |
1: 169,814,634 (GRCm39) |
V603A |
possibly damaging |
Het |
Dgkz |
A |
G |
2: 91,772,980 (GRCm39) |
V359A |
probably benign |
Het |
Dis3l2 |
T |
A |
1: 86,782,153 (GRCm39) |
S223T |
probably benign |
Het |
Dpysl4 |
A |
G |
7: 138,679,734 (GRCm39) |
S535G |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,165,717 (GRCm39) |
S515T |
probably benign |
Het |
Epg5 |
A |
G |
18: 78,072,179 (GRCm39) |
E2397G |
possibly damaging |
Het |
Fam83d |
G |
A |
2: 158,627,096 (GRCm39) |
G262S |
probably damaging |
Het |
Frmd4a |
A |
T |
2: 4,595,509 (GRCm39) |
T477S |
probably damaging |
Het |
Gbp3 |
A |
G |
3: 142,274,819 (GRCm39) |
E382G |
probably benign |
Het |
Gltp |
A |
T |
5: 114,808,572 (GRCm39) |
C157S |
possibly damaging |
Het |
Grb10 |
A |
G |
11: 11,887,905 (GRCm39) |
S378P |
probably damaging |
Het |
Gulo |
G |
T |
14: 66,240,080 (GRCm39) |
T126K |
probably damaging |
Het |
H2-M10.6 |
T |
A |
17: 37,124,836 (GRCm39) |
M251K |
probably damaging |
Het |
Hecw1 |
T |
C |
13: 14,422,205 (GRCm39) |
D967G |
possibly damaging |
Het |
Htr3b |
A |
T |
9: 48,858,933 (GRCm39) |
D68E |
probably damaging |
Het |
Igkv5-39 |
G |
T |
6: 69,877,489 (GRCm39) |
S89* |
probably null |
Het |
Kctd4 |
C |
A |
14: 76,200,037 (GRCm39) |
|
probably benign |
Het |
Lmna |
T |
C |
3: 88,393,813 (GRCm39) |
Q255R |
probably damaging |
Het |
Lsmem1 |
A |
G |
12: 40,230,656 (GRCm39) |
I82T |
possibly damaging |
Het |
Lyg2 |
T |
A |
1: 37,950,194 (GRCm39) |
M45L |
probably benign |
Het |
Myo5b |
G |
A |
18: 74,750,064 (GRCm39) |
A176T |
probably damaging |
Het |
Nudt5 |
A |
T |
2: 5,869,248 (GRCm39) |
K158I |
possibly damaging |
Het |
Nufip1 |
C |
T |
14: 76,348,494 (GRCm39) |
P41L |
possibly damaging |
Het |
Or4f14b |
A |
T |
2: 111,775,739 (GRCm39) |
W21R |
probably null |
Het |
Or52z13 |
A |
T |
7: 103,247,073 (GRCm39) |
E183D |
probably damaging |
Het |
Pcp2 |
T |
C |
8: 3,674,887 (GRCm39) |
D22G |
probably damaging |
Het |
Pdk2 |
G |
C |
11: 94,930,228 (GRCm39) |
N69K |
possibly damaging |
Het |
Pdlim7 |
G |
T |
13: 55,655,905 (GRCm39) |
|
probably benign |
Het |
Ptprc |
C |
A |
1: 138,041,416 (GRCm39) |
E148* |
probably null |
Het |
Rassf5 |
A |
T |
1: 131,108,405 (GRCm39) |
V225E |
probably damaging |
Het |
Rbm6 |
A |
T |
9: 107,664,458 (GRCm39) |
M725K |
probably benign |
Het |
Scn1a |
T |
A |
2: 66,103,660 (GRCm39) |
I1867F |
probably damaging |
Het |
Sdk2 |
T |
A |
11: 113,684,581 (GRCm39) |
Q1960L |
probably damaging |
Het |
Setx |
A |
G |
2: 29,064,474 (GRCm39) |
|
probably benign |
Het |
Sgo2b |
T |
A |
8: 64,381,345 (GRCm39) |
R496* |
probably null |
Het |
Slco1a1 |
C |
T |
6: 141,878,176 (GRCm39) |
V222I |
probably damaging |
Het |
Sntg2 |
A |
C |
12: 30,308,013 (GRCm39) |
L224R |
probably damaging |
Het |
Syt16 |
C |
A |
12: 74,313,467 (GRCm39) |
C464* |
probably null |
Het |
Tapbpl |
T |
A |
6: 125,201,881 (GRCm39) |
S420C |
probably benign |
Het |
Tax1bp1 |
A |
G |
6: 52,723,694 (GRCm39) |
E528G |
probably benign |
Het |
Tmem168 |
T |
C |
6: 13,602,710 (GRCm39) |
T219A |
probably benign |
Het |
Zfp180 |
T |
C |
7: 23,804,981 (GRCm39) |
F467L |
probably damaging |
Het |
|
Other mutations in Dsp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00502:Dsp
|
APN |
13 |
38,381,822 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01337:Dsp
|
APN |
13 |
38,376,663 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01371:Dsp
|
APN |
13 |
38,377,593 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01473:Dsp
|
APN |
13 |
38,351,547 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01660:Dsp
|
APN |
13 |
38,360,471 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01723:Dsp
|
APN |
13 |
38,363,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01999:Dsp
|
APN |
13 |
38,365,162 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02313:Dsp
|
APN |
13 |
38,380,499 (GRCm39) |
nonsense |
probably null |
|
IGL02833:Dsp
|
APN |
13 |
38,376,897 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL03050:Dsp
|
APN |
13 |
38,372,421 (GRCm39) |
splice site |
probably benign |
|
IGL03353:Dsp
|
APN |
13 |
38,370,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Dsp
|
UTSW |
13 |
38,381,340 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0052:Dsp
|
UTSW |
13 |
38,381,340 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0078:Dsp
|
UTSW |
13 |
38,379,993 (GRCm39) |
missense |
probably benign |
0.22 |
R0230:Dsp
|
UTSW |
13 |
38,381,681 (GRCm39) |
missense |
probably benign |
0.03 |
R0234:Dsp
|
UTSW |
13 |
38,371,869 (GRCm39) |
missense |
probably benign |
0.13 |
R0234:Dsp
|
UTSW |
13 |
38,371,869 (GRCm39) |
missense |
probably benign |
0.13 |
R0285:Dsp
|
UTSW |
13 |
38,356,770 (GRCm39) |
missense |
probably benign |
|
R0326:Dsp
|
UTSW |
13 |
38,376,846 (GRCm39) |
nonsense |
probably null |
|
R0332:Dsp
|
UTSW |
13 |
38,366,204 (GRCm39) |
nonsense |
probably null |
|
R0471:Dsp
|
UTSW |
13 |
38,377,326 (GRCm39) |
nonsense |
probably null |
|
R0567:Dsp
|
UTSW |
13 |
38,376,414 (GRCm39) |
missense |
probably benign |
0.01 |
R0611:Dsp
|
UTSW |
13 |
38,371,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R0718:Dsp
|
UTSW |
13 |
38,380,740 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0926:Dsp
|
UTSW |
13 |
38,367,194 (GRCm39) |
missense |
probably damaging |
0.97 |
R1078:Dsp
|
UTSW |
13 |
38,367,082 (GRCm39) |
splice site |
probably benign |
|
R1183:Dsp
|
UTSW |
13 |
38,375,716 (GRCm39) |
nonsense |
probably null |
|
R1188:Dsp
|
UTSW |
13 |
38,378,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R1419:Dsp
|
UTSW |
13 |
38,370,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Dsp
|
UTSW |
13 |
38,375,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R1467:Dsp
|
UTSW |
13 |
38,376,688 (GRCm39) |
missense |
probably benign |
0.00 |
R1467:Dsp
|
UTSW |
13 |
38,376,688 (GRCm39) |
missense |
probably benign |
0.00 |
R1478:Dsp
|
UTSW |
13 |
38,365,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R1568:Dsp
|
UTSW |
13 |
38,359,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Dsp
|
UTSW |
13 |
38,379,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1676:Dsp
|
UTSW |
13 |
38,377,350 (GRCm39) |
nonsense |
probably null |
|
R1736:Dsp
|
UTSW |
13 |
38,376,966 (GRCm39) |
missense |
probably benign |
0.01 |
R1776:Dsp
|
UTSW |
13 |
38,380,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R1829:Dsp
|
UTSW |
13 |
38,377,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1878:Dsp
|
UTSW |
13 |
38,348,831 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2013:Dsp
|
UTSW |
13 |
38,375,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R2161:Dsp
|
UTSW |
13 |
38,380,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R2187:Dsp
|
UTSW |
13 |
38,360,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R2295:Dsp
|
UTSW |
13 |
38,381,022 (GRCm39) |
missense |
probably benign |
0.28 |
R2495:Dsp
|
UTSW |
13 |
38,377,453 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2566:Dsp
|
UTSW |
13 |
38,380,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R2888:Dsp
|
UTSW |
13 |
38,376,224 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3012:Dsp
|
UTSW |
13 |
38,377,318 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3614:Dsp
|
UTSW |
13 |
38,361,175 (GRCm39) |
missense |
probably damaging |
0.98 |
R3725:Dsp
|
UTSW |
13 |
38,381,594 (GRCm39) |
missense |
probably benign |
0.00 |
R3725:Dsp
|
UTSW |
13 |
38,378,665 (GRCm39) |
splice site |
probably null |
|
R3797:Dsp
|
UTSW |
13 |
38,361,260 (GRCm39) |
critical splice donor site |
probably null |
|
R3841:Dsp
|
UTSW |
13 |
38,381,681 (GRCm39) |
missense |
probably benign |
|
R4030:Dsp
|
UTSW |
13 |
38,375,404 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4124:Dsp
|
UTSW |
13 |
38,370,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4279:Dsp
|
UTSW |
13 |
38,369,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R4334:Dsp
|
UTSW |
13 |
38,380,640 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4419:Dsp
|
UTSW |
13 |
38,379,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R4615:Dsp
|
UTSW |
13 |
38,375,608 (GRCm39) |
missense |
probably damaging |
0.98 |
R4627:Dsp
|
UTSW |
13 |
38,352,617 (GRCm39) |
missense |
probably benign |
0.01 |
R4639:Dsp
|
UTSW |
13 |
38,380,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Dsp
|
UTSW |
13 |
38,375,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Dsp
|
UTSW |
13 |
38,380,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R4746:Dsp
|
UTSW |
13 |
38,379,080 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4772:Dsp
|
UTSW |
13 |
38,351,504 (GRCm39) |
nonsense |
probably null |
|
R4830:Dsp
|
UTSW |
13 |
38,376,840 (GRCm39) |
missense |
probably benign |
|
R4850:Dsp
|
UTSW |
13 |
38,376,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4959:Dsp
|
UTSW |
13 |
38,375,686 (GRCm39) |
missense |
probably benign |
0.41 |
R4963:Dsp
|
UTSW |
13 |
38,381,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R4969:Dsp
|
UTSW |
13 |
38,376,886 (GRCm39) |
missense |
probably benign |
0.00 |
R4978:Dsp
|
UTSW |
13 |
38,366,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Dsp
|
UTSW |
13 |
38,381,678 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5068:Dsp
|
UTSW |
13 |
38,381,099 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5069:Dsp
|
UTSW |
13 |
38,381,099 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5070:Dsp
|
UTSW |
13 |
38,381,099 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5133:Dsp
|
UTSW |
13 |
38,381,678 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5138:Dsp
|
UTSW |
13 |
38,379,821 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5138:Dsp
|
UTSW |
13 |
38,367,274 (GRCm39) |
missense |
probably benign |
0.37 |
R5153:Dsp
|
UTSW |
13 |
38,366,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R5199:Dsp
|
UTSW |
13 |
38,376,878 (GRCm39) |
nonsense |
probably null |
|
R5226:Dsp
|
UTSW |
13 |
38,370,746 (GRCm39) |
missense |
probably damaging |
0.99 |
R5265:Dsp
|
UTSW |
13 |
38,379,159 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5371:Dsp
|
UTSW |
13 |
38,378,865 (GRCm39) |
missense |
probably damaging |
0.97 |
R5484:Dsp
|
UTSW |
13 |
38,368,014 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5534:Dsp
|
UTSW |
13 |
38,379,818 (GRCm39) |
missense |
probably benign |
0.01 |
R5569:Dsp
|
UTSW |
13 |
38,376,628 (GRCm39) |
missense |
probably benign |
0.01 |
R5854:Dsp
|
UTSW |
13 |
38,351,477 (GRCm39) |
splice site |
probably null |
|
R5910:Dsp
|
UTSW |
13 |
38,376,445 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5929:Dsp
|
UTSW |
13 |
38,379,410 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5940:Dsp
|
UTSW |
13 |
38,380,002 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5948:Dsp
|
UTSW |
13 |
38,379,377 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5955:Dsp
|
UTSW |
13 |
38,378,934 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5970:Dsp
|
UTSW |
13 |
38,379,678 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6054:Dsp
|
UTSW |
13 |
38,351,585 (GRCm39) |
missense |
probably benign |
0.00 |
R6113:Dsp
|
UTSW |
13 |
38,376,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R6139:Dsp
|
UTSW |
13 |
38,376,382 (GRCm39) |
missense |
probably damaging |
0.97 |
R6527:Dsp
|
UTSW |
13 |
38,379,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Dsp
|
UTSW |
13 |
38,380,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R6628:Dsp
|
UTSW |
13 |
38,351,598 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6738:Dsp
|
UTSW |
13 |
38,376,186 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6898:Dsp
|
UTSW |
13 |
38,376,193 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6919:Dsp
|
UTSW |
13 |
38,351,631 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6951:Dsp
|
UTSW |
13 |
38,351,622 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7017:Dsp
|
UTSW |
13 |
38,370,683 (GRCm39) |
missense |
probably benign |
0.02 |
R7022:Dsp
|
UTSW |
13 |
38,375,716 (GRCm39) |
missense |
probably benign |
0.06 |
R7135:Dsp
|
UTSW |
13 |
38,363,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R7192:Dsp
|
UTSW |
13 |
38,379,569 (GRCm39) |
missense |
probably benign |
0.09 |
R7211:Dsp
|
UTSW |
13 |
38,372,511 (GRCm39) |
critical splice donor site |
probably null |
|
R7251:Dsp
|
UTSW |
13 |
38,377,524 (GRCm39) |
missense |
probably benign |
0.02 |
R7326:Dsp
|
UTSW |
13 |
38,376,859 (GRCm39) |
missense |
probably benign |
0.01 |
R7369:Dsp
|
UTSW |
13 |
38,381,501 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7376:Dsp
|
UTSW |
13 |
38,356,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R7406:Dsp
|
UTSW |
13 |
38,381,172 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7439:Dsp
|
UTSW |
13 |
38,379,425 (GRCm39) |
missense |
probably benign |
0.00 |
R7439:Dsp
|
UTSW |
13 |
38,360,478 (GRCm39) |
critical splice donor site |
probably null |
|
R7441:Dsp
|
UTSW |
13 |
38,379,425 (GRCm39) |
missense |
probably benign |
0.00 |
R7477:Dsp
|
UTSW |
13 |
38,356,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R7535:Dsp
|
UTSW |
13 |
38,376,765 (GRCm39) |
missense |
probably benign |
0.05 |
R7558:Dsp
|
UTSW |
13 |
38,352,742 (GRCm39) |
missense |
probably benign |
0.02 |
R7600:Dsp
|
UTSW |
13 |
38,375,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R7616:Dsp
|
UTSW |
13 |
38,375,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R7702:Dsp
|
UTSW |
13 |
38,359,183 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7738:Dsp
|
UTSW |
13 |
38,369,151 (GRCm39) |
missense |
probably damaging |
0.97 |
R7815:Dsp
|
UTSW |
13 |
38,375,446 (GRCm39) |
missense |
probably benign |
0.31 |
R7882:Dsp
|
UTSW |
13 |
38,367,994 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7917:Dsp
|
UTSW |
13 |
38,351,615 (GRCm39) |
nonsense |
probably null |
|
R7971:Dsp
|
UTSW |
13 |
38,376,499 (GRCm39) |
missense |
probably damaging |
0.97 |
R8104:Dsp
|
UTSW |
13 |
38,352,600 (GRCm39) |
missense |
probably benign |
0.03 |
R8176:Dsp
|
UTSW |
13 |
38,376,786 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8303:Dsp
|
UTSW |
13 |
38,381,319 (GRCm39) |
missense |
probably benign |
|
R8323:Dsp
|
UTSW |
13 |
38,356,806 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8326:Dsp
|
UTSW |
13 |
38,375,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R8358:Dsp
|
UTSW |
13 |
38,376,457 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8410:Dsp
|
UTSW |
13 |
38,380,791 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8552:Dsp
|
UTSW |
13 |
38,369,117 (GRCm39) |
missense |
probably damaging |
0.98 |
R8713:Dsp
|
UTSW |
13 |
38,352,701 (GRCm39) |
missense |
probably damaging |
0.99 |
R8801:Dsp
|
UTSW |
13 |
38,381,502 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8900:Dsp
|
UTSW |
13 |
38,365,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R8901:Dsp
|
UTSW |
13 |
38,365,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R8968:Dsp
|
UTSW |
13 |
38,335,596 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9014:Dsp
|
UTSW |
13 |
38,376,700 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9021:Dsp
|
UTSW |
13 |
38,380,808 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9030:Dsp
|
UTSW |
13 |
38,352,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R9124:Dsp
|
UTSW |
13 |
38,377,276 (GRCm39) |
missense |
probably benign |
0.42 |
R9129:Dsp
|
UTSW |
13 |
38,377,126 (GRCm39) |
missense |
probably benign |
0.09 |
R9143:Dsp
|
UTSW |
13 |
38,377,337 (GRCm39) |
missense |
probably benign |
0.05 |
R9450:Dsp
|
UTSW |
13 |
38,376,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R9488:Dsp
|
UTSW |
13 |
38,377,218 (GRCm39) |
missense |
probably benign |
0.04 |
R9514:Dsp
|
UTSW |
13 |
38,371,781 (GRCm39) |
missense |
probably benign |
0.02 |
R9789:Dsp
|
UTSW |
13 |
38,367,937 (GRCm39) |
missense |
probably benign |
0.03 |
R9792:Dsp
|
UTSW |
13 |
38,379,494 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0023:Dsp
|
UTSW |
13 |
38,381,660 (GRCm39) |
missense |
probably benign |
0.00 |
X0024:Dsp
|
UTSW |
13 |
38,377,231 (GRCm39) |
missense |
probably benign |
0.04 |
X0027:Dsp
|
UTSW |
13 |
38,370,622 (GRCm39) |
missense |
possibly damaging |
0.68 |
X0067:Dsp
|
UTSW |
13 |
38,366,288 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1176:Dsp
|
UTSW |
13 |
38,381,166 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1177:Dsp
|
UTSW |
13 |
38,376,830 (GRCm39) |
frame shift |
probably null |
|
Z1177:Dsp
|
UTSW |
13 |
38,335,665 (GRCm39) |
missense |
probably benign |
0.01 |
|