Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930004D18Rik |
A |
G |
2: 18,031,848 (GRCm39) |
I90T |
probably damaging |
Het |
Acox3 |
A |
G |
5: 35,761,987 (GRCm39) |
N444D |
probably damaging |
Het |
Adamts16 |
A |
G |
13: 70,927,743 (GRCm39) |
Y499H |
probably damaging |
Het |
Ajm1 |
T |
A |
2: 25,469,661 (GRCm39) |
R83S |
possibly damaging |
Het |
Ank2 |
A |
T |
3: 126,752,612 (GRCm39) |
V368D |
probably damaging |
Het |
Atad5 |
T |
C |
11: 79,986,017 (GRCm39) |
V368A |
probably damaging |
Het |
Atp13a5 |
T |
C |
16: 29,067,090 (GRCm39) |
|
probably null |
Het |
Bdh1 |
A |
T |
16: 31,254,954 (GRCm39) |
|
probably benign |
Het |
Bmp6 |
A |
T |
13: 38,653,701 (GRCm39) |
Y256F |
probably damaging |
Het |
Bub1b |
C |
A |
2: 118,453,657 (GRCm39) |
S496* |
probably null |
Het |
Capn15 |
C |
T |
17: 26,178,811 (GRCm39) |
R1128H |
probably damaging |
Het |
Ccnf |
T |
A |
17: 24,450,303 (GRCm39) |
R461* |
probably null |
Het |
Col6a1 |
C |
T |
10: 76,547,191 (GRCm39) |
V725I |
unknown |
Het |
Cp |
T |
C |
3: 20,011,599 (GRCm39) |
|
probably null |
Het |
Cul2 |
T |
C |
18: 3,430,957 (GRCm39) |
V577A |
probably benign |
Het |
Cux2 |
A |
T |
5: 121,998,716 (GRCm39) |
I1408K |
probably benign |
Het |
Cyp2c69 |
T |
A |
19: 39,869,630 (GRCm39) |
T130S |
possibly damaging |
Het |
Cyp3a57 |
A |
G |
5: 145,311,074 (GRCm39) |
T278A |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,608,554 (GRCm39) |
S1802G |
probably damaging |
Het |
Dner |
T |
C |
1: 84,361,537 (GRCm39) |
S691G |
probably damaging |
Het |
Dzip1l |
A |
T |
9: 99,529,267 (GRCm39) |
Q332L |
probably damaging |
Het |
Eprs1 |
A |
G |
1: 185,133,804 (GRCm39) |
Y827C |
probably damaging |
Het |
Ermp1 |
A |
T |
19: 29,594,051 (GRCm39) |
N706K |
probably damaging |
Het |
F830045P16Rik |
A |
G |
2: 129,305,423 (GRCm39) |
L317S |
probably damaging |
Het |
Fam120c |
G |
T |
X: 150,219,179 (GRCm39) |
G696W |
probably damaging |
Het |
Fance |
T |
A |
17: 28,536,125 (GRCm39) |
|
probably null |
Het |
Fancl |
G |
T |
11: 26,418,423 (GRCm39) |
|
probably null |
Het |
Fbxo30 |
T |
A |
10: 11,165,293 (GRCm39) |
V5E |
probably benign |
Het |
Foxn4 |
A |
T |
5: 114,394,886 (GRCm39) |
I347N |
possibly damaging |
Het |
Galr2 |
A |
T |
11: 116,172,325 (GRCm39) |
D5V |
probably benign |
Het |
Gm4845 |
T |
G |
1: 141,184,865 (GRCm39) |
|
noncoding transcript |
Het |
Gnao1 |
A |
T |
8: 94,693,532 (GRCm39) |
Q73L |
probably damaging |
Het |
Gnpat |
T |
A |
8: 125,605,241 (GRCm39) |
|
probably null |
Het |
H2-T5 |
C |
T |
17: 36,472,649 (GRCm39) |
|
probably benign |
Het |
Hectd1 |
A |
G |
12: 51,791,356 (GRCm39) |
M2594T |
probably damaging |
Het |
Hint3 |
T |
C |
10: 30,486,428 (GRCm39) |
H117R |
probably damaging |
Het |
Hsd3b6 |
A |
G |
3: 98,713,541 (GRCm39) |
F253L |
probably damaging |
Het |
Itgal |
A |
G |
7: 126,904,466 (GRCm39) |
D313G |
possibly damaging |
Het |
Kbtbd2 |
A |
T |
6: 56,755,893 (GRCm39) |
D614E |
probably damaging |
Het |
Ksr2 |
A |
T |
5: 117,894,335 (GRCm39) |
I825F |
probably damaging |
Het |
L3mbtl4 |
A |
T |
17: 69,071,635 (GRCm39) |
S521C |
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,123,015 (GRCm39) |
N725S |
probably damaging |
Het |
Med1 |
T |
G |
11: 98,049,248 (GRCm39) |
E516A |
possibly damaging |
Het |
Mical3 |
A |
T |
6: 120,935,660 (GRCm39) |
V1622E |
probably benign |
Het |
Miip |
G |
A |
4: 147,945,518 (GRCm39) |
P373S |
probably damaging |
Het |
Myo7a |
C |
A |
7: 97,722,400 (GRCm39) |
S1175I |
probably damaging |
Het |
Ndst3 |
A |
T |
3: 123,340,474 (GRCm39) |
D781E |
probably benign |
Het |
Nf1 |
T |
A |
11: 79,359,583 (GRCm39) |
V1407E |
probably damaging |
Het |
Opalin |
A |
G |
19: 41,056,196 (GRCm39) |
L33P |
probably damaging |
Het |
Or2f2 |
A |
T |
6: 42,767,458 (GRCm39) |
I162F |
probably benign |
Het |
Or2n1b |
G |
C |
17: 38,460,296 (GRCm39) |
K272N |
probably damaging |
Het |
Or4c111 |
T |
C |
2: 88,843,488 (GRCm39) |
I307V |
probably benign |
Het |
Or8b12i |
G |
T |
9: 20,082,410 (GRCm39) |
S152R |
probably damaging |
Het |
Or8k28 |
T |
C |
2: 86,285,859 (GRCm39) |
Y252C |
probably damaging |
Het |
Or8s10 |
A |
T |
15: 98,335,560 (GRCm39) |
D70V |
probably damaging |
Het |
Pcdhb2 |
T |
A |
18: 37,429,168 (GRCm39) |
N23K |
probably damaging |
Het |
Pdap1 |
A |
G |
5: 145,073,691 (GRCm39) |
|
probably benign |
Het |
Pds5b |
A |
G |
5: 150,670,197 (GRCm39) |
E395G |
probably damaging |
Het |
Pex1 |
C |
A |
5: 3,668,880 (GRCm39) |
R624S |
probably benign |
Het |
Pitrm1 |
G |
A |
13: 6,608,261 (GRCm39) |
V329I |
probably benign |
Het |
Pop1 |
G |
A |
15: 34,515,970 (GRCm39) |
|
probably benign |
Het |
Prkaa1 |
A |
G |
15: 5,190,082 (GRCm39) |
|
probably null |
Het |
Slc38a6 |
G |
T |
12: 73,335,298 (GRCm39) |
|
probably null |
Het |
Slc5a9 |
T |
A |
4: 111,750,384 (GRCm39) |
Y158F |
probably damaging |
Het |
Spata3 |
T |
A |
1: 85,954,175 (GRCm39) |
V114E |
probably damaging |
Het |
Tbcb |
T |
A |
7: 29,931,019 (GRCm39) |
I34F |
possibly damaging |
Het |
Tek |
T |
A |
4: 94,751,903 (GRCm39) |
Y1014* |
probably null |
Het |
Togaram1 |
G |
T |
12: 65,014,681 (GRCm39) |
C644F |
probably damaging |
Het |
Trim56 |
A |
C |
5: 137,142,918 (GRCm39) |
D199E |
possibly damaging |
Het |
Tssk3 |
A |
T |
4: 129,383,110 (GRCm39) |
D187E |
probably benign |
Het |
Ttn |
G |
A |
2: 76,727,147 (GRCm39) |
|
probably benign |
Het |
Twf2 |
G |
A |
9: 106,090,025 (GRCm39) |
R126Q |
probably benign |
Het |
Ugt1a10 |
T |
C |
1: 87,983,838 (GRCm39) |
M212T |
probably benign |
Het |
Vmn1r177 |
A |
T |
7: 23,565,772 (GRCm39) |
F35I |
possibly damaging |
Het |
Vmn1r44 |
T |
A |
6: 89,870,915 (GRCm39) |
H77Q |
possibly damaging |
Het |
Zfp1004 |
T |
A |
2: 150,034,143 (GRCm39) |
Y186N |
probably damaging |
Het |
Zfp524 |
G |
A |
7: 5,021,347 (GRCm39) |
V292I |
probably benign |
Het |
Zfp788 |
T |
G |
7: 41,297,018 (GRCm39) |
I56S |
probably benign |
Het |
|
Other mutations in Dchs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00235:Dchs1
|
APN |
7 |
105,407,950 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00422:Dchs1
|
APN |
7 |
105,407,236 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00427:Dchs1
|
APN |
7 |
105,407,631 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00469:Dchs1
|
APN |
7 |
105,404,468 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00470:Dchs1
|
APN |
7 |
105,407,414 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00534:Dchs1
|
APN |
7 |
105,407,150 (GRCm39) |
missense |
probably benign |
|
IGL01292:Dchs1
|
APN |
7 |
105,410,098 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01380:Dchs1
|
APN |
7 |
105,411,418 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01396:Dchs1
|
APN |
7 |
105,421,490 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01448:Dchs1
|
APN |
7 |
105,421,134 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01759:Dchs1
|
APN |
7 |
105,404,509 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01829:Dchs1
|
APN |
7 |
105,404,604 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01946:Dchs1
|
APN |
7 |
105,408,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01955:Dchs1
|
APN |
7 |
105,406,798 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02012:Dchs1
|
APN |
7 |
105,413,504 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02222:Dchs1
|
APN |
7 |
105,414,094 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02261:Dchs1
|
APN |
7 |
105,421,776 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02365:Dchs1
|
APN |
7 |
105,404,395 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02430:Dchs1
|
APN |
7 |
105,421,178 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02500:Dchs1
|
APN |
7 |
105,405,013 (GRCm39) |
missense |
probably benign |
|
IGL02741:Dchs1
|
APN |
7 |
105,406,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02890:Dchs1
|
APN |
7 |
105,405,698 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03213:Dchs1
|
APN |
7 |
105,404,279 (GRCm39) |
missense |
probably damaging |
1.00 |
G1patch:Dchs1
|
UTSW |
7 |
105,408,000 (GRCm39) |
missense |
probably damaging |
0.99 |
P0026:Dchs1
|
UTSW |
7 |
105,407,612 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4377001:Dchs1
|
UTSW |
7 |
105,406,795 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4791001:Dchs1
|
UTSW |
7 |
105,408,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Dchs1
|
UTSW |
7 |
105,405,043 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0090:Dchs1
|
UTSW |
7 |
105,405,139 (GRCm39) |
missense |
probably benign |
0.18 |
R0091:Dchs1
|
UTSW |
7 |
105,415,301 (GRCm39) |
splice site |
probably benign |
|
R0193:Dchs1
|
UTSW |
7 |
105,414,190 (GRCm39) |
missense |
probably benign |
0.40 |
R0395:Dchs1
|
UTSW |
7 |
105,407,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R0448:Dchs1
|
UTSW |
7 |
105,415,134 (GRCm39) |
missense |
probably benign |
0.00 |
R0480:Dchs1
|
UTSW |
7 |
105,420,696 (GRCm39) |
missense |
probably benign |
0.14 |
R0485:Dchs1
|
UTSW |
7 |
105,421,934 (GRCm39) |
missense |
probably benign |
0.00 |
R0566:Dchs1
|
UTSW |
7 |
105,408,402 (GRCm39) |
missense |
probably benign |
0.00 |
R0571:Dchs1
|
UTSW |
7 |
105,421,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Dchs1
|
UTSW |
7 |
105,407,985 (GRCm39) |
missense |
probably damaging |
0.98 |
R0577:Dchs1
|
UTSW |
7 |
105,413,462 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0622:Dchs1
|
UTSW |
7 |
105,412,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R0654:Dchs1
|
UTSW |
7 |
105,421,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R0677:Dchs1
|
UTSW |
7 |
105,414,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1171:Dchs1
|
UTSW |
7 |
105,406,921 (GRCm39) |
missense |
probably benign |
|
R1241:Dchs1
|
UTSW |
7 |
105,407,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R1389:Dchs1
|
UTSW |
7 |
105,404,778 (GRCm39) |
missense |
probably benign |
0.40 |
R1427:Dchs1
|
UTSW |
7 |
105,415,398 (GRCm39) |
missense |
probably benign |
0.06 |
R1458:Dchs1
|
UTSW |
7 |
105,404,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Dchs1
|
UTSW |
7 |
105,421,278 (GRCm39) |
nonsense |
probably null |
|
R1524:Dchs1
|
UTSW |
7 |
105,413,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R1525:Dchs1
|
UTSW |
7 |
105,408,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Dchs1
|
UTSW |
7 |
105,421,247 (GRCm39) |
missense |
probably damaging |
0.98 |
R1567:Dchs1
|
UTSW |
7 |
105,421,068 (GRCm39) |
missense |
probably benign |
0.01 |
R1577:Dchs1
|
UTSW |
7 |
105,415,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R1603:Dchs1
|
UTSW |
7 |
105,411,977 (GRCm39) |
missense |
probably benign |
0.24 |
R1676:Dchs1
|
UTSW |
7 |
105,404,128 (GRCm39) |
missense |
probably benign |
0.40 |
R1794:Dchs1
|
UTSW |
7 |
105,420,927 (GRCm39) |
missense |
probably benign |
0.02 |
R1826:Dchs1
|
UTSW |
7 |
105,406,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R1892:Dchs1
|
UTSW |
7 |
105,413,363 (GRCm39) |
missense |
probably benign |
0.00 |
R1924:Dchs1
|
UTSW |
7 |
105,421,487 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1932:Dchs1
|
UTSW |
7 |
105,415,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Dchs1
|
UTSW |
7 |
105,413,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1985:Dchs1
|
UTSW |
7 |
105,421,605 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1993:Dchs1
|
UTSW |
7 |
105,411,755 (GRCm39) |
missense |
probably benign |
0.00 |
R2007:Dchs1
|
UTSW |
7 |
105,404,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R2316:Dchs1
|
UTSW |
7 |
105,413,411 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2351:Dchs1
|
UTSW |
7 |
105,403,301 (GRCm39) |
missense |
probably benign |
|
R2474:Dchs1
|
UTSW |
7 |
105,422,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R2474:Dchs1
|
UTSW |
7 |
105,404,281 (GRCm39) |
missense |
probably benign |
0.37 |
R3429:Dchs1
|
UTSW |
7 |
105,405,711 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3430:Dchs1
|
UTSW |
7 |
105,405,711 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3737:Dchs1
|
UTSW |
7 |
105,411,523 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3767:Dchs1
|
UTSW |
7 |
105,406,292 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3874:Dchs1
|
UTSW |
7 |
105,410,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R3883:Dchs1
|
UTSW |
7 |
105,411,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R4105:Dchs1
|
UTSW |
7 |
105,414,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R4209:Dchs1
|
UTSW |
7 |
105,415,397 (GRCm39) |
missense |
probably damaging |
0.99 |
R4329:Dchs1
|
UTSW |
7 |
105,402,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R4516:Dchs1
|
UTSW |
7 |
105,404,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Dchs1
|
UTSW |
7 |
105,403,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R4588:Dchs1
|
UTSW |
7 |
105,405,248 (GRCm39) |
missense |
probably benign |
|
R4613:Dchs1
|
UTSW |
7 |
105,421,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R4632:Dchs1
|
UTSW |
7 |
105,403,562 (GRCm39) |
missense |
probably benign |
0.02 |
R4696:Dchs1
|
UTSW |
7 |
105,413,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Dchs1
|
UTSW |
7 |
105,414,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Dchs1
|
UTSW |
7 |
105,404,460 (GRCm39) |
missense |
probably damaging |
0.98 |
R4738:Dchs1
|
UTSW |
7 |
105,407,880 (GRCm39) |
missense |
probably damaging |
0.96 |
R4768:Dchs1
|
UTSW |
7 |
105,420,827 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4784:Dchs1
|
UTSW |
7 |
105,415,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Dchs1
|
UTSW |
7 |
105,404,460 (GRCm39) |
missense |
probably damaging |
0.98 |
R4880:Dchs1
|
UTSW |
7 |
105,404,937 (GRCm39) |
missense |
probably benign |
0.00 |
R4909:Dchs1
|
UTSW |
7 |
105,415,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R5102:Dchs1
|
UTSW |
7 |
105,421,384 (GRCm39) |
missense |
probably benign |
0.09 |
R5109:Dchs1
|
UTSW |
7 |
105,414,221 (GRCm39) |
missense |
probably benign |
|
R5126:Dchs1
|
UTSW |
7 |
105,402,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R5149:Dchs1
|
UTSW |
7 |
105,404,865 (GRCm39) |
missense |
probably damaging |
0.98 |
R5330:Dchs1
|
UTSW |
7 |
105,403,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Dchs1
|
UTSW |
7 |
105,421,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Dchs1
|
UTSW |
7 |
105,407,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Dchs1
|
UTSW |
7 |
105,407,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5622:Dchs1
|
UTSW |
7 |
105,404,500 (GRCm39) |
missense |
probably benign |
0.11 |
R5623:Dchs1
|
UTSW |
7 |
105,421,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R5708:Dchs1
|
UTSW |
7 |
105,422,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R5718:Dchs1
|
UTSW |
7 |
105,404,955 (GRCm39) |
missense |
probably benign |
0.01 |
R5743:Dchs1
|
UTSW |
7 |
105,420,803 (GRCm39) |
missense |
probably benign |
|
R5759:Dchs1
|
UTSW |
7 |
105,413,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R5772:Dchs1
|
UTSW |
7 |
105,422,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R5860:Dchs1
|
UTSW |
7 |
105,421,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Dchs1
|
UTSW |
7 |
105,408,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R5965:Dchs1
|
UTSW |
7 |
105,405,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R5997:Dchs1
|
UTSW |
7 |
105,403,302 (GRCm39) |
missense |
probably benign |
0.08 |
R6065:Dchs1
|
UTSW |
7 |
105,404,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R6136:Dchs1
|
UTSW |
7 |
105,410,132 (GRCm39) |
missense |
probably benign |
|
R6137:Dchs1
|
UTSW |
7 |
105,414,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R6324:Dchs1
|
UTSW |
7 |
105,414,145 (GRCm39) |
missense |
probably benign |
0.05 |
R6363:Dchs1
|
UTSW |
7 |
105,407,679 (GRCm39) |
missense |
probably benign |
0.12 |
R6466:Dchs1
|
UTSW |
7 |
105,413,748 (GRCm39) |
missense |
probably benign |
0.09 |
R6544:Dchs1
|
UTSW |
7 |
105,407,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R6572:Dchs1
|
UTSW |
7 |
105,408,013 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6579:Dchs1
|
UTSW |
7 |
105,412,120 (GRCm39) |
missense |
probably benign |
0.17 |
R6632:Dchs1
|
UTSW |
7 |
105,411,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R6725:Dchs1
|
UTSW |
7 |
105,408,000 (GRCm39) |
missense |
probably damaging |
0.99 |
R6789:Dchs1
|
UTSW |
7 |
105,406,210 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6868:Dchs1
|
UTSW |
7 |
105,412,710 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7058:Dchs1
|
UTSW |
7 |
105,406,228 (GRCm39) |
missense |
probably benign |
|
R7064:Dchs1
|
UTSW |
7 |
105,412,392 (GRCm39) |
missense |
probably damaging |
0.99 |
R7076:Dchs1
|
UTSW |
7 |
105,411,078 (GRCm39) |
missense |
probably benign |
0.04 |
R7191:Dchs1
|
UTSW |
7 |
105,414,646 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7298:Dchs1
|
UTSW |
7 |
105,404,338 (GRCm39) |
nonsense |
probably null |
|
R7380:Dchs1
|
UTSW |
7 |
105,407,835 (GRCm39) |
missense |
probably benign |
0.35 |
R7438:Dchs1
|
UTSW |
7 |
105,404,155 (GRCm39) |
missense |
probably benign |
0.30 |
R7496:Dchs1
|
UTSW |
7 |
105,411,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R7534:Dchs1
|
UTSW |
7 |
105,421,580 (GRCm39) |
missense |
probably benign |
0.00 |
R7604:Dchs1
|
UTSW |
7 |
105,415,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7631:Dchs1
|
UTSW |
7 |
105,408,445 (GRCm39) |
missense |
probably benign |
|
R7821:Dchs1
|
UTSW |
7 |
105,414,352 (GRCm39) |
missense |
probably benign |
0.00 |
R7834:Dchs1
|
UTSW |
7 |
105,414,774 (GRCm39) |
missense |
probably benign |
0.39 |
R7841:Dchs1
|
UTSW |
7 |
105,412,180 (GRCm39) |
missense |
probably benign |
|
R7913:Dchs1
|
UTSW |
7 |
105,408,435 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8041:Dchs1
|
UTSW |
7 |
105,404,395 (GRCm39) |
missense |
probably benign |
0.45 |
R8076:Dchs1
|
UTSW |
7 |
105,411,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R8076:Dchs1
|
UTSW |
7 |
105,405,128 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8087:Dchs1
|
UTSW |
7 |
105,402,706 (GRCm39) |
missense |
probably benign |
0.41 |
R8125:Dchs1
|
UTSW |
7 |
105,414,089 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8223:Dchs1
|
UTSW |
7 |
105,411,824 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8239:Dchs1
|
UTSW |
7 |
105,414,718 (GRCm39) |
missense |
probably benign |
0.22 |
R8476:Dchs1
|
UTSW |
7 |
105,408,015 (GRCm39) |
missense |
probably benign |
0.05 |
R8497:Dchs1
|
UTSW |
7 |
105,408,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Dchs1
|
UTSW |
7 |
105,420,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R8856:Dchs1
|
UTSW |
7 |
105,410,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R8866:Dchs1
|
UTSW |
7 |
105,404,597 (GRCm39) |
missense |
probably benign |
0.00 |
R8948:Dchs1
|
UTSW |
7 |
105,408,212 (GRCm39) |
missense |
probably benign |
0.30 |
R8950:Dchs1
|
UTSW |
7 |
105,408,212 (GRCm39) |
missense |
probably benign |
0.30 |
R9029:Dchs1
|
UTSW |
7 |
105,402,919 (GRCm39) |
missense |
probably benign |
0.13 |
R9039:Dchs1
|
UTSW |
7 |
105,405,215 (GRCm39) |
missense |
probably benign |
0.11 |
R9081:Dchs1
|
UTSW |
7 |
105,403,636 (GRCm39) |
missense |
probably benign |
0.00 |
R9134:Dchs1
|
UTSW |
7 |
105,404,910 (GRCm39) |
missense |
probably damaging |
0.96 |
R9159:Dchs1
|
UTSW |
7 |
105,415,126 (GRCm39) |
missense |
probably benign |
|
R9162:Dchs1
|
UTSW |
7 |
105,414,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R9169:Dchs1
|
UTSW |
7 |
105,422,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R9262:Dchs1
|
UTSW |
7 |
105,404,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9292:Dchs1
|
UTSW |
7 |
105,403,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R9325:Dchs1
|
UTSW |
7 |
105,415,402 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9376:Dchs1
|
UTSW |
7 |
105,414,981 (GRCm39) |
critical splice donor site |
probably null |
|
R9392:Dchs1
|
UTSW |
7 |
105,421,869 (GRCm39) |
missense |
probably benign |
0.09 |
R9619:Dchs1
|
UTSW |
7 |
105,413,662 (GRCm39) |
missense |
probably benign |
0.07 |
R9680:Dchs1
|
UTSW |
7 |
105,411,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R9687:Dchs1
|
UTSW |
7 |
105,407,191 (GRCm39) |
missense |
probably damaging |
0.99 |
R9747:Dchs1
|
UTSW |
7 |
105,412,682 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dchs1
|
UTSW |
7 |
105,406,900 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dchs1
|
UTSW |
7 |
105,407,758 (GRCm39) |
missense |
probably benign |
0.00 |
|