Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp6 |
T |
C |
3: 97,075,891 (GRCm39) |
|
probably null |
Het |
Adam33 |
C |
A |
2: 130,896,399 (GRCm39) |
G437C |
probably damaging |
Het |
Aldh1a1 |
T |
A |
19: 20,579,377 (GRCm39) |
M1K |
probably null |
Het |
Amotl2 |
C |
A |
9: 102,597,718 (GRCm39) |
P126Q |
probably damaging |
Het |
Ap1g1 |
T |
A |
8: 110,580,275 (GRCm39) |
M576K |
possibly damaging |
Het |
Apob |
C |
A |
12: 8,040,406 (GRCm39) |
A581E |
probably damaging |
Het |
Asb7 |
A |
T |
7: 66,328,907 (GRCm39) |
D44E |
probably damaging |
Het |
Bcl2 |
G |
A |
1: 106,640,292 (GRCm39) |
R107C |
probably damaging |
Het |
C9orf72 |
G |
A |
4: 35,193,257 (GRCm39) |
T232I |
probably benign |
Het |
Ccdc65 |
A |
T |
15: 98,615,348 (GRCm39) |
H118L |
probably benign |
Het |
Cdc25b |
A |
G |
2: 131,039,204 (GRCm39) |
E523G |
probably damaging |
Het |
Cdk11b |
A |
G |
4: 155,731,999 (GRCm39) |
|
probably benign |
Het |
Cilk1 |
G |
T |
9: 78,062,799 (GRCm39) |
|
probably null |
Het |
Clec1b |
A |
G |
6: 129,378,570 (GRCm39) |
|
probably benign |
Het |
Cntrl |
A |
G |
2: 35,017,392 (GRCm39) |
T400A |
probably benign |
Het |
Cpne4 |
T |
G |
9: 104,899,481 (GRCm39) |
|
probably null |
Het |
Cyp2j6 |
T |
A |
4: 96,419,985 (GRCm39) |
R249* |
probably null |
Het |
Dock2 |
T |
C |
11: 34,579,380 (GRCm39) |
I678V |
probably benign |
Het |
Dqx1 |
C |
T |
6: 83,036,407 (GRCm39) |
|
probably benign |
Het |
Eif2b2 |
T |
C |
12: 85,266,957 (GRCm39) |
F121S |
probably benign |
Het |
Ephx4 |
T |
C |
5: 107,561,379 (GRCm39) |
V69A |
possibly damaging |
Het |
Epn2 |
T |
C |
11: 61,426,134 (GRCm39) |
Q281R |
probably damaging |
Het |
Fgf3 |
A |
C |
7: 144,396,547 (GRCm39) |
D187A |
probably damaging |
Het |
Galnt18 |
C |
A |
7: 111,378,506 (GRCm39) |
|
probably benign |
Het |
Gm4871 |
C |
T |
5: 144,968,402 (GRCm39) |
|
probably benign |
Het |
Inpp4b |
T |
C |
8: 82,768,528 (GRCm39) |
I679T |
possibly damaging |
Het |
Itpkb |
A |
G |
1: 180,245,820 (GRCm39) |
E779G |
probably damaging |
Het |
Itsn1 |
G |
A |
16: 91,696,477 (GRCm39) |
V27M |
probably damaging |
Het |
Lrp2 |
C |
A |
2: 69,355,578 (GRCm39) |
R422L |
probably damaging |
Het |
Mmp25 |
G |
A |
17: 23,858,858 (GRCm39) |
A231V |
possibly damaging |
Het |
Mprip |
T |
C |
11: 59,650,561 (GRCm39) |
S1422P |
probably damaging |
Het |
Mro |
A |
T |
18: 74,009,860 (GRCm39) |
Q176L |
probably benign |
Het |
Mrpl12 |
A |
G |
11: 120,379,229 (GRCm39) |
E192G |
probably damaging |
Het |
Myo5b |
A |
T |
18: 74,862,025 (GRCm39) |
|
probably benign |
Het |
Ncam2 |
G |
T |
16: 80,997,772 (GRCm39) |
|
probably benign |
Het |
Nip7 |
T |
C |
8: 107,783,949 (GRCm39) |
L63P |
probably damaging |
Het |
Nsd3 |
T |
C |
8: 26,138,450 (GRCm39) |
|
probably benign |
Het |
Nup98 |
A |
T |
7: 101,788,004 (GRCm39) |
V1022D |
probably benign |
Het |
Or2y1e |
T |
A |
11: 49,218,744 (GRCm39) |
C169S |
probably damaging |
Het |
Or5d43 |
A |
G |
2: 88,104,559 (GRCm39) |
V278A |
possibly damaging |
Het |
Or5h22 |
A |
G |
16: 58,894,633 (GRCm39) |
I270T |
probably benign |
Het |
Or7g28 |
A |
T |
9: 19,272,177 (GRCm39) |
L158* |
probably null |
Het |
P4ha2 |
T |
C |
11: 54,008,434 (GRCm39) |
Y214H |
possibly damaging |
Het |
Pacrg |
A |
T |
17: 10,795,407 (GRCm39) |
F184L |
possibly damaging |
Het |
Parpbp |
T |
A |
10: 87,929,569 (GRCm39) |
R426S |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,454,359 (GRCm39) |
Y246* |
probably null |
Het |
Pik3cg |
T |
A |
12: 32,244,770 (GRCm39) |
T895S |
probably damaging |
Het |
Prkch |
T |
C |
12: 73,738,426 (GRCm39) |
Y178H |
probably benign |
Het |
Rusc2 |
G |
T |
4: 43,425,486 (GRCm39) |
R1197L |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,054,700 (GRCm39) |
E3296G |
possibly damaging |
Het |
Svs3a |
A |
G |
2: 164,131,801 (GRCm39) |
K123R |
probably benign |
Het |
Sycp2l |
A |
G |
13: 41,304,006 (GRCm39) |
|
probably null |
Het |
Syne3 |
T |
C |
12: 104,909,685 (GRCm39) |
H717R |
probably benign |
Het |
Tiprl |
A |
G |
1: 165,050,092 (GRCm39) |
|
probably null |
Het |
Trim24 |
T |
G |
6: 37,892,130 (GRCm39) |
V151G |
possibly damaging |
Het |
Trim33 |
T |
C |
3: 103,234,217 (GRCm39) |
V56A |
possibly damaging |
Het |
Trim67 |
C |
A |
8: 125,521,397 (GRCm39) |
T253K |
probably benign |
Het |
Trip12 |
T |
C |
1: 84,703,928 (GRCm39) |
E698G |
probably damaging |
Het |
Tspan14 |
T |
C |
14: 40,637,353 (GRCm39) |
D145G |
probably damaging |
Het |
Ushbp1 |
G |
A |
8: 71,847,021 (GRCm39) |
Q204* |
probably null |
Het |
Vmn1r71 |
G |
C |
7: 10,482,019 (GRCm39) |
S223C |
possibly damaging |
Het |
Vmn2r75 |
G |
T |
7: 85,814,721 (GRCm39) |
N257K |
probably benign |
Het |
Washc4 |
T |
C |
10: 83,394,598 (GRCm39) |
|
probably benign |
Het |
Zc3h7b |
G |
A |
15: 81,666,169 (GRCm39) |
D560N |
probably damaging |
Het |
Zscan21 |
T |
C |
5: 138,123,402 (GRCm39) |
V27A |
probably benign |
Het |
Zzef1 |
A |
C |
11: 72,813,937 (GRCm39) |
E2842A |
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 |
|
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 |
R6328:Dsp
|
UTSW |
13 |
38,380,982 (GRCm39) |
nonsense |
probably null |
|
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 |
|