Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
T |
A |
5: 88,120,649 (GRCm39) |
Y469N |
probably benign |
Het |
Actl11 |
T |
C |
9: 107,805,964 (GRCm39) |
S96P |
possibly damaging |
Het |
Ankrd13b |
T |
A |
11: 77,363,198 (GRCm39) |
|
probably null |
Het |
Apobec4 |
T |
A |
1: 152,632,017 (GRCm39) |
I15K |
probably damaging |
Het |
Arhgef28 |
G |
T |
13: 98,090,401 (GRCm39) |
D1039E |
probably damaging |
Het |
Atp1a1 |
C |
T |
3: 101,498,769 (GRCm39) |
G175R |
probably damaging |
Het |
AU040320 |
T |
A |
4: 126,763,171 (GRCm39) |
|
probably benign |
Het |
Bcl9l |
G |
A |
9: 44,418,121 (GRCm39) |
R653H |
probably damaging |
Het |
Ccdc141 |
T |
A |
2: 76,958,669 (GRCm39) |
I144L |
possibly damaging |
Het |
Cdh20 |
C |
T |
1: 104,875,154 (GRCm39) |
T312I |
possibly damaging |
Het |
Cdh23 |
C |
T |
10: 60,220,848 (GRCm39) |
V1297I |
possibly damaging |
Het |
Cfap57 |
T |
C |
4: 118,467,792 (GRCm39) |
Y315C |
probably damaging |
Het |
Chd8 |
A |
G |
14: 52,442,044 (GRCm39) |
|
probably benign |
Het |
Cog5 |
A |
G |
12: 31,944,095 (GRCm39) |
D660G |
probably benign |
Het |
Cps1 |
T |
C |
1: 67,196,945 (GRCm39) |
I332T |
probably damaging |
Het |
Csgalnact2 |
T |
C |
6: 118,103,288 (GRCm39) |
T225A |
probably damaging |
Het |
Dgki |
T |
C |
6: 36,977,025 (GRCm39) |
N695S |
probably damaging |
Het |
Gas7 |
T |
A |
11: 67,543,740 (GRCm39) |
|
probably null |
Het |
Gm21286 |
T |
C |
4: 60,794,323 (GRCm39) |
|
noncoding transcript |
Het |
Gm4799 |
C |
T |
10: 82,790,518 (GRCm39) |
|
noncoding transcript |
Het |
Hdac4 |
T |
C |
1: 91,887,196 (GRCm39) |
|
probably benign |
Het |
Hif1a |
T |
A |
12: 73,987,307 (GRCm39) |
S467T |
probably benign |
Het |
Ier5 |
A |
G |
1: 154,974,296 (GRCm39) |
V294A |
probably damaging |
Het |
Ifna11 |
T |
C |
4: 88,738,314 (GRCm39) |
V40A |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,436,191 (GRCm39) |
|
probably benign |
Het |
Lbx1 |
G |
T |
19: 45,222,670 (GRCm39) |
Q118K |
probably benign |
Het |
Lta |
A |
T |
17: 35,423,061 (GRCm39) |
|
probably null |
Het |
Matr3 |
A |
G |
18: 35,721,442 (GRCm39) |
Y471C |
probably damaging |
Het |
Nrg2 |
A |
T |
18: 36,178,905 (GRCm39) |
|
probably benign |
Het |
Or4c103 |
C |
T |
2: 88,513,575 (GRCm39) |
C167Y |
probably damaging |
Het |
Or4k51 |
T |
C |
2: 111,584,848 (GRCm39) |
F85L |
probably benign |
Het |
Or4k51 |
T |
A |
2: 111,584,948 (GRCm39) |
M118K |
probably damaging |
Het |
Or5l13 |
G |
T |
2: 87,780,207 (GRCm39) |
F123L |
probably damaging |
Het |
Patl1 |
A |
G |
19: 11,901,247 (GRCm39) |
K299R |
probably damaging |
Het |
Pdgfrb |
A |
G |
18: 61,205,736 (GRCm39) |
E574G |
probably damaging |
Het |
Phf3 |
G |
A |
1: 30,843,386 (GRCm39) |
Q1858* |
probably null |
Het |
Prkca |
T |
C |
11: 107,905,148 (GRCm39) |
K197E |
possibly damaging |
Het |
Psmc6 |
C |
A |
14: 45,581,124 (GRCm39) |
Q307K |
probably benign |
Het |
Rasa1 |
T |
C |
13: 85,406,561 (GRCm39) |
I181V |
probably benign |
Het |
Scel |
A |
G |
14: 103,845,530 (GRCm39) |
|
probably benign |
Het |
Scn5a |
A |
T |
9: 119,363,770 (GRCm39) |
S457T |
probably damaging |
Het |
Sesn3 |
A |
G |
9: 14,232,374 (GRCm39) |
T216A |
probably benign |
Het |
Slc25a21 |
A |
G |
12: 57,205,974 (GRCm39) |
V19A |
probably benign |
Het |
Slc34a1 |
A |
G |
13: 55,550,546 (GRCm39) |
T81A |
probably damaging |
Het |
Slc35a5 |
A |
G |
16: 44,971,866 (GRCm39) |
Y117H |
probably damaging |
Het |
Sptbn4 |
A |
G |
7: 27,114,196 (GRCm39) |
V569A |
probably benign |
Het |
Sqle |
A |
G |
15: 59,195,723 (GRCm39) |
Y333C |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,068,552 (GRCm39) |
E3078G |
possibly damaging |
Het |
Tacc2 |
T |
A |
7: 130,360,919 (GRCm39) |
I2737N |
probably damaging |
Het |
Tet3 |
A |
T |
6: 83,346,620 (GRCm39) |
Y1272* |
probably null |
Het |
Tnr |
G |
T |
1: 159,724,594 (GRCm39) |
R1095L |
possibly damaging |
Het |
Vmn1r184 |
T |
C |
7: 25,966,862 (GRCm39) |
S203P |
probably damaging |
Het |
Vmn2r94 |
A |
G |
17: 18,477,301 (GRCm39) |
L370P |
probably damaging |
Het |
Xrcc5 |
A |
G |
1: 72,393,404 (GRCm39) |
H559R |
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 |
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 |
105,408,180 (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 |
|