Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700037C18Rik |
A |
G |
16: 3,725,511 (GRCm39) |
V5A |
probably damaging |
Het |
Abi3bp |
A |
G |
16: 56,424,375 (GRCm39) |
|
probably null |
Het |
Acot11 |
G |
A |
4: 106,619,224 (GRCm39) |
R184C |
probably damaging |
Het |
Adgre5 |
A |
T |
8: 84,458,627 (GRCm39) |
I133N |
probably damaging |
Het |
Afap1 |
A |
T |
5: 36,108,347 (GRCm39) |
Q231L |
probably damaging |
Het |
Alg12 |
T |
C |
15: 88,695,630 (GRCm39) |
T289A |
probably benign |
Het |
Ank3 |
T |
A |
10: 69,718,374 (GRCm39) |
S542T |
possibly damaging |
Het |
Ankmy2 |
G |
A |
12: 36,232,389 (GRCm39) |
R138Q |
possibly damaging |
Het |
Ascc2 |
C |
T |
11: 4,622,302 (GRCm39) |
A456V |
probably benign |
Het |
Atg4c |
G |
A |
4: 99,112,719 (GRCm39) |
V289I |
probably benign |
Het |
Bbs7 |
A |
T |
3: 36,657,022 (GRCm39) |
Y269N |
probably damaging |
Het |
Bcas3 |
T |
A |
11: 85,386,676 (GRCm39) |
D370E |
probably damaging |
Het |
Bicc1 |
T |
G |
10: 70,761,145 (GRCm39) |
E955A |
probably damaging |
Het |
Bok |
T |
C |
1: 93,616,999 (GRCm39) |
F115S |
probably damaging |
Het |
Caap1 |
A |
T |
4: 94,438,758 (GRCm39) |
|
probably null |
Het |
Cacna2d3 |
T |
A |
14: 29,256,476 (GRCm39) |
M95L |
possibly damaging |
Het |
Calcrl |
T |
A |
2: 84,200,435 (GRCm39) |
D115V |
probably benign |
Het |
Car7 |
A |
T |
8: 105,270,170 (GRCm39) |
M57L |
probably benign |
Het |
Casq1 |
G |
T |
1: 172,037,957 (GRCm39) |
|
probably benign |
Het |
Cep290 |
A |
T |
10: 100,385,206 (GRCm39) |
D1894V |
possibly damaging |
Het |
Clec4a2 |
T |
A |
6: 123,100,588 (GRCm39) |
N14K |
probably damaging |
Het |
Col16a1 |
G |
T |
4: 129,984,290 (GRCm39) |
|
probably benign |
Het |
Col5a1 |
T |
C |
2: 27,880,109 (GRCm39) |
|
probably benign |
Het |
Col5a2 |
A |
T |
1: 45,417,642 (GRCm39) |
I1311N |
probably damaging |
Het |
Col5a3 |
T |
C |
9: 20,694,004 (GRCm39) |
T1050A |
probably damaging |
Het |
Colgalt2 |
A |
T |
1: 152,360,622 (GRCm39) |
I220F |
probably damaging |
Het |
Cpb1 |
A |
T |
3: 20,329,792 (GRCm39) |
V8E |
unknown |
Het |
Dhx37 |
A |
G |
5: 125,499,295 (GRCm39) |
Y638H |
probably benign |
Het |
Dhx40 |
T |
G |
11: 86,662,088 (GRCm39) |
|
probably benign |
Het |
Ehd2 |
T |
A |
7: 15,686,001 (GRCm39) |
Q357L |
probably benign |
Het |
Ewsr1 |
T |
C |
11: 5,020,737 (GRCm39) |
|
probably benign |
Het |
Fcho1 |
C |
T |
8: 72,165,204 (GRCm39) |
A418T |
probably benign |
Het |
Gid8 |
T |
A |
2: 180,355,004 (GRCm39) |
Y3* |
probably null |
Het |
Gm10212 |
A |
C |
19: 11,548,174 (GRCm39) |
|
noncoding transcript |
Het |
Grin3b |
T |
A |
10: 79,809,890 (GRCm39) |
N465K |
possibly damaging |
Het |
H1f3 |
A |
T |
13: 23,739,924 (GRCm39) |
K221* |
probably null |
Het |
Htr4 |
A |
T |
18: 62,561,225 (GRCm39) |
N162I |
probably damaging |
Het |
Irag2 |
T |
C |
6: 145,110,938 (GRCm39) |
C248R |
probably damaging |
Het |
Itga3 |
T |
C |
11: 94,952,796 (GRCm39) |
D325G |
probably benign |
Het |
Itpr3 |
T |
G |
17: 27,330,903 (GRCm39) |
V1737G |
probably damaging |
Het |
Kcnab2 |
C |
T |
4: 152,479,439 (GRCm39) |
V251I |
probably benign |
Het |
Kcnn2 |
A |
T |
18: 45,693,215 (GRCm39) |
I264L |
probably benign |
Het |
Klhl41 |
T |
C |
2: 69,501,600 (GRCm39) |
Y354H |
probably damaging |
Het |
Klra6 |
T |
C |
6: 130,000,601 (GRCm39) |
I68V |
probably benign |
Het |
Letm2 |
G |
T |
8: 26,082,574 (GRCm39) |
P178Q |
probably damaging |
Het |
Lypd11 |
C |
A |
7: 24,422,170 (GRCm39) |
C193F |
possibly damaging |
Het |
Mbtps1 |
A |
T |
8: 120,249,340 (GRCm39) |
|
probably benign |
Het |
Mecom |
C |
T |
3: 30,035,121 (GRCm39) |
|
probably benign |
Het |
Mrps5 |
T |
A |
2: 127,433,745 (GRCm39) |
S45T |
possibly damaging |
Het |
Msra |
T |
A |
14: 64,678,210 (GRCm39) |
I29F |
possibly damaging |
Het |
Mup5 |
T |
C |
4: 61,751,229 (GRCm39) |
|
probably null |
Het |
Myo1a |
T |
C |
10: 127,555,111 (GRCm39) |
|
probably benign |
Het |
Myrip |
C |
A |
9: 120,270,443 (GRCm39) |
N564K |
probably benign |
Het |
Naa20 |
T |
A |
2: 145,757,592 (GRCm39) |
D148E |
probably damaging |
Het |
Naga |
T |
G |
15: 82,220,956 (GRCm39) |
|
probably benign |
Het |
Npc1 |
A |
G |
18: 12,346,503 (GRCm39) |
V231A |
probably benign |
Het |
Nphs1 |
T |
C |
7: 30,166,940 (GRCm39) |
F716L |
probably benign |
Het |
Or8s5 |
T |
C |
15: 98,238,810 (GRCm39) |
H20R |
probably benign |
Het |
Parn |
G |
C |
16: 13,472,299 (GRCm39) |
|
probably benign |
Het |
Polk |
A |
T |
13: 96,620,272 (GRCm39) |
C664S |
probably benign |
Het |
Prkar2b |
A |
G |
12: 32,026,034 (GRCm39) |
|
probably benign |
Het |
Prkdc |
A |
G |
16: 15,651,604 (GRCm39) |
E3747G |
probably damaging |
Het |
Prmt5 |
A |
T |
14: 54,748,712 (GRCm39) |
M362K |
probably damaging |
Het |
Prob1 |
T |
C |
18: 35,786,878 (GRCm39) |
T459A |
possibly damaging |
Het |
Rttn |
C |
T |
18: 89,108,543 (GRCm39) |
|
probably benign |
Het |
Scn1a |
T |
C |
2: 66,104,269 (GRCm39) |
M1664V |
probably damaging |
Het |
Sez6 |
T |
A |
11: 77,844,639 (GRCm39) |
L154H |
probably damaging |
Het |
Sh3tc1 |
A |
G |
5: 35,859,356 (GRCm39) |
|
probably benign |
Het |
Shkbp1 |
C |
T |
7: 27,048,006 (GRCm39) |
G334D |
probably damaging |
Het |
Slc8a1 |
A |
T |
17: 81,955,422 (GRCm39) |
F539I |
probably damaging |
Het |
Spata31e5 |
G |
T |
1: 28,817,223 (GRCm39) |
Q270K |
probably damaging |
Het |
Sptan1 |
T |
C |
2: 29,903,860 (GRCm39) |
|
probably benign |
Het |
Ssc5d |
C |
T |
7: 4,940,470 (GRCm39) |
T861M |
probably damaging |
Het |
Tbx5 |
A |
T |
5: 120,021,523 (GRCm39) |
M510L |
probably benign |
Het |
Tdp1 |
A |
G |
12: 99,876,101 (GRCm39) |
T351A |
probably benign |
Het |
Tmc8 |
T |
A |
11: 117,682,904 (GRCm39) |
|
probably benign |
Het |
Tmco5 |
T |
A |
2: 116,720,588 (GRCm39) |
D205E |
probably benign |
Het |
Tmprss2 |
T |
C |
16: 97,373,194 (GRCm39) |
|
probably benign |
Het |
Top6bl |
A |
T |
19: 4,708,442 (GRCm39) |
I350N |
probably damaging |
Het |
Tph1 |
T |
A |
7: 46,299,448 (GRCm39) |
K364N |
probably benign |
Het |
Trim24 |
T |
C |
6: 37,934,001 (GRCm39) |
L648P |
probably damaging |
Het |
Trmt6 |
C |
A |
2: 132,650,950 (GRCm39) |
|
probably benign |
Het |
Ube2i |
A |
T |
17: 25,488,259 (GRCm39) |
|
probably benign |
Het |
Vcan |
A |
C |
13: 89,852,779 (GRCm39) |
L727R |
possibly damaging |
Het |
Vmn2r28 |
T |
C |
7: 5,491,689 (GRCm39) |
Y186C |
probably damaging |
Het |
Wars1 |
C |
A |
12: 108,841,083 (GRCm39) |
D232Y |
probably damaging |
Het |
Xrcc5 |
T |
C |
1: 72,378,104 (GRCm39) |
|
probably benign |
Het |
Zbtb24 |
T |
A |
10: 41,340,532 (GRCm39) |
S543T |
probably damaging |
Het |
Zfp91 |
A |
G |
19: 12,753,353 (GRCm39) |
|
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 |
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 |
105,408,180 (GRCm39) |
missense |
probably benign |
|
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 |
|