Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars2 |
T |
A |
17: 45,819,887 (GRCm39) |
Y221* |
probably null |
Het |
AC166344.1 |
T |
A |
14: 43,158,245 (GRCm39) |
F97I |
|
Het |
Ankmy2 |
T |
C |
12: 36,246,311 (GRCm39) |
S412P |
probably benign |
Het |
Ap1s3 |
T |
C |
1: 79,586,919 (GRCm39) |
T144A |
probably benign |
Het |
Armh2 |
T |
C |
13: 24,925,489 (GRCm39) |
S78P |
probably benign |
Het |
Asb3 |
T |
A |
11: 30,948,501 (GRCm39) |
L59* |
probably null |
Het |
Asxl3 |
G |
T |
18: 22,650,758 (GRCm39) |
G916* |
probably null |
Het |
Asxl3 |
G |
C |
18: 22,650,759 (GRCm39) |
G916A |
probably damaging |
Het |
Birc2 |
A |
C |
9: 7,818,762 (GRCm39) |
F610V |
probably damaging |
Het |
Camk4 |
G |
A |
18: 33,240,996 (GRCm39) |
|
probably null |
Het |
Ccdc162 |
A |
G |
10: 41,549,855 (GRCm39) |
S343P |
probably benign |
Het |
Ccnk |
T |
A |
12: 108,152,734 (GRCm39) |
L17Q |
probably damaging |
Het |
Cd59b |
G |
A |
2: 103,914,792 (GRCm39) |
W63* |
probably null |
Het |
Chrm3 |
C |
T |
13: 9,927,837 (GRCm39) |
V400I |
probably benign |
Het |
Crb1 |
C |
A |
1: 139,171,105 (GRCm39) |
V762F |
probably damaging |
Het |
Cspp1 |
C |
T |
1: 10,159,161 (GRCm39) |
T529I |
possibly damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,448,446 (GRCm39) |
I71T |
possibly damaging |
Het |
Cyb561 |
C |
A |
11: 105,826,393 (GRCm39) |
G90V |
probably damaging |
Het |
Cyld |
T |
A |
8: 89,471,520 (GRCm39) |
D804E |
possibly damaging |
Het |
Ddx31 |
G |
A |
2: 28,738,318 (GRCm39) |
V160I |
probably benign |
Het |
Dgkg |
T |
C |
16: 22,319,132 (GRCm39) |
D643G |
probably damaging |
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
Dnah12 |
T |
G |
14: 26,523,370 (GRCm39) |
I1953S |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,178,870 (GRCm39) |
W848R |
probably damaging |
Het |
Dnah7c |
C |
T |
1: 46,572,368 (GRCm39) |
T947M |
probably damaging |
Het |
Dnmt3c |
C |
A |
2: 153,556,872 (GRCm39) |
|
probably null |
Het |
Espl1 |
T |
A |
15: 102,227,959 (GRCm39) |
C1603* |
probably null |
Het |
Faiml |
G |
T |
9: 99,116,496 (GRCm39) |
R65S |
probably benign |
Het |
Gfpt2 |
T |
C |
11: 49,695,782 (GRCm39) |
I4T |
probably damaging |
Het |
Gm10376 |
T |
A |
14: 42,867,950 (GRCm39) |
M179L |
probably benign |
Het |
Gm4302 |
T |
A |
10: 100,177,589 (GRCm39) |
M291K |
unknown |
Het |
Gnb1l |
T |
A |
16: 18,363,918 (GRCm39) |
D154E |
probably benign |
Het |
Igkv10-94 |
T |
C |
6: 68,681,727 (GRCm39) |
R38G |
possibly damaging |
Het |
Inmt |
A |
T |
6: 55,148,013 (GRCm39) |
Y205* |
probably null |
Het |
Krba1 |
A |
G |
6: 48,393,233 (GRCm39) |
Q1049R |
probably benign |
Het |
Lpxn |
T |
A |
19: 12,810,683 (GRCm39) |
C376S |
probably damaging |
Het |
Lrrc52 |
T |
A |
1: 167,294,019 (GRCm39) |
I89F |
probably damaging |
Het |
Map9 |
A |
T |
3: 82,270,765 (GRCm39) |
T110S |
probably benign |
Het |
Mccc1 |
T |
C |
3: 36,049,967 (GRCm39) |
Y75C |
probably damaging |
Het |
Mff |
T |
A |
1: 82,724,812 (GRCm39) |
L203* |
probably null |
Het |
Micall1 |
C |
A |
15: 78,993,624 (GRCm39) |
D47E |
unknown |
Het |
Mink1 |
T |
C |
11: 70,494,329 (GRCm39) |
F243S |
probably damaging |
Het |
Mlycd |
C |
T |
8: 120,129,216 (GRCm39) |
R228W |
probably damaging |
Het |
Msr1 |
A |
T |
8: 40,042,465 (GRCm39) |
V370E |
possibly damaging |
Het |
Naip6 |
T |
C |
13: 100,436,927 (GRCm39) |
E532G |
probably damaging |
Het |
Nepn |
G |
A |
10: 52,267,815 (GRCm39) |
C27Y |
probably damaging |
Het |
Ninl |
T |
C |
2: 150,797,524 (GRCm39) |
H592R |
probably benign |
Het |
Nr4a2 |
A |
G |
2: 57,002,261 (GRCm39) |
M64T |
possibly damaging |
Het |
Oprm1 |
A |
T |
10: 6,780,203 (GRCm39) |
I171F |
possibly damaging |
Het |
Or4g16 |
T |
A |
2: 111,137,365 (GRCm39) |
F272I |
probably benign |
Het |
Or5p60 |
T |
C |
7: 107,723,781 (GRCm39) |
K230E |
probably damaging |
Het |
Pcbp1 |
A |
T |
6: 86,502,488 (GRCm39) |
M137K |
possibly damaging |
Het |
Pcf11 |
A |
T |
7: 92,306,524 (GRCm39) |
S1215T |
probably benign |
Het |
Pdlim5 |
A |
T |
3: 142,017,683 (GRCm39) |
|
probably null |
Het |
Pecam1 |
T |
C |
11: 106,579,857 (GRCm39) |
I402V |
probably damaging |
Het |
Pex12 |
T |
C |
11: 83,188,468 (GRCm39) |
T176A |
probably benign |
Het |
Phf3 |
T |
C |
1: 30,870,190 (GRCm39) |
K286R |
possibly damaging |
Het |
Pik3ap1 |
T |
A |
19: 41,320,760 (GRCm39) |
D153V |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,448,374 (GRCm39) |
|
probably null |
Het |
Plekhn1 |
A |
G |
4: 156,307,792 (GRCm39) |
V378A |
probably benign |
Het |
Pramel26 |
A |
T |
4: 143,537,233 (GRCm39) |
L366Q |
probably damaging |
Het |
Ptprm |
A |
T |
17: 67,251,283 (GRCm39) |
D531E |
possibly damaging |
Het |
Pum2 |
A |
T |
12: 8,778,952 (GRCm39) |
Q508L |
possibly damaging |
Het |
Rad54l |
A |
G |
4: 115,963,027 (GRCm39) |
S324P |
probably damaging |
Het |
Recql5 |
C |
T |
11: 115,821,498 (GRCm39) |
|
probably null |
Het |
Reln |
A |
T |
5: 22,181,594 (GRCm39) |
V1763D |
possibly damaging |
Het |
Rp1 |
T |
C |
1: 4,418,391 (GRCm39) |
N907S |
possibly damaging |
Het |
Scaf11 |
T |
A |
15: 96,318,209 (GRCm39) |
N452Y |
possibly damaging |
Het |
Scgb2b3 |
T |
A |
7: 31,059,639 (GRCm39) |
H45L |
possibly damaging |
Het |
Sim1 |
A |
G |
10: 50,772,023 (GRCm39) |
T11A |
probably damaging |
Het |
Slc5a12 |
T |
A |
2: 110,447,059 (GRCm39) |
M189K |
possibly damaging |
Het |
Slco2b1 |
C |
T |
7: 99,344,270 (GRCm39) |
G10S |
probably null |
Het |
Speer1j |
C |
T |
5: 11,555,198 (GRCm39) |
P83S |
probably damaging |
Het |
Stxbp3 |
A |
G |
3: 108,708,071 (GRCm39) |
L410P |
probably damaging |
Het |
Sugct |
T |
C |
13: 17,476,594 (GRCm39) |
N297D |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,183,409 (GRCm39) |
I4132T |
probably benign |
Het |
Teddm1b |
A |
T |
1: 153,750,912 (GRCm39) |
L240F |
probably damaging |
Het |
Tlr5 |
C |
A |
1: 182,803,088 (GRCm39) |
D797E |
possibly damaging |
Het |
Tmprss13 |
G |
T |
9: 45,249,643 (GRCm39) |
G327C |
probably damaging |
Het |
Tnrc18 |
G |
T |
5: 142,773,572 (GRCm39) |
A419D |
|
Het |
Ttc28 |
T |
C |
5: 111,427,873 (GRCm39) |
Y1790H |
probably damaging |
Het |
Vmn1r125 |
T |
G |
7: 21,006,327 (GRCm39) |
M75R |
probably damaging |
Het |
Vwa3a |
T |
A |
7: 120,372,253 (GRCm39) |
D276E |
possibly damaging |
Het |
Wdfy3 |
C |
T |
5: 102,063,303 (GRCm39) |
V1322M |
probably damaging |
Het |
Wdr11 |
T |
C |
7: 129,229,830 (GRCm39) |
S872P |
possibly damaging |
Het |
Zc3h13 |
T |
C |
14: 75,559,161 (GRCm39) |
S357P |
unknown |
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 |
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 |
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 |
|