Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568A12Rik |
A |
G |
1: 34,524,661 (GRCm39) |
|
noncoding transcript |
Het |
A2ml1 |
T |
C |
6: 128,518,024 (GRCm39) |
T1421A |
probably benign |
Het |
Actr8 |
T |
A |
14: 29,708,242 (GRCm39) |
Y150* |
probably null |
Het |
Adamts1 |
A |
G |
16: 85,595,432 (GRCm39) |
C249R |
probably damaging |
Het |
Adgre1 |
T |
A |
17: 57,752,034 (GRCm39) |
I594N |
probably damaging |
Het |
Atf6 |
A |
T |
1: 170,669,344 (GRCm39) |
L119H |
probably damaging |
Het |
Atf6 |
G |
A |
1: 170,669,345 (GRCm39) |
L119F |
possibly damaging |
Het |
B3gat2 |
G |
A |
1: 23,854,400 (GRCm39) |
W33* |
probably null |
Het |
Bach2 |
A |
G |
4: 32,580,268 (GRCm39) |
D831G |
probably damaging |
Het |
Ccnk |
A |
T |
12: 108,153,466 (GRCm39) |
I76F |
probably damaging |
Het |
Cdyl |
A |
C |
13: 36,042,066 (GRCm39) |
K368T |
possibly damaging |
Het |
Chi3l1 |
A |
G |
1: 134,112,909 (GRCm39) |
T114A |
probably benign |
Het |
Cnppd1 |
A |
G |
1: 75,113,131 (GRCm39) |
V379A |
probably benign |
Het |
Col11a2 |
C |
A |
17: 34,283,159 (GRCm39) |
|
probably benign |
Het |
Creb3l1 |
T |
C |
2: 91,854,399 (GRCm39) |
S18G |
probably benign |
Het |
Crybg3 |
A |
C |
16: 59,385,632 (GRCm39) |
D197E |
probably damaging |
Het |
Cryga |
T |
C |
1: 65,142,527 (GRCm39) |
|
probably benign |
Het |
Cthrc1 |
T |
C |
15: 38,950,080 (GRCm39) |
C146R |
probably damaging |
Het |
Cyp2c39 |
A |
T |
19: 39,525,270 (GRCm39) |
D191V |
probably damaging |
Het |
Dhx30 |
G |
A |
9: 109,913,645 (GRCm39) |
T1126I |
probably damaging |
Het |
Dock2 |
C |
T |
11: 34,206,562 (GRCm39) |
G1345R |
probably damaging |
Het |
Dsc1 |
T |
C |
18: 20,228,081 (GRCm39) |
E425G |
probably damaging |
Het |
Dynlt2b |
A |
G |
16: 32,247,614 (GRCm39) |
Y143C |
probably damaging |
Het |
Exosc8 |
C |
T |
3: 54,642,463 (GRCm39) |
|
probably benign |
Het |
Fat1 |
C |
T |
8: 45,504,166 (GRCm39) |
A4553V |
probably benign |
Het |
Flnb |
T |
A |
14: 7,931,135 (GRCm38) |
L2119Q |
probably damaging |
Het |
Fnbp4 |
T |
A |
2: 90,587,826 (GRCm39) |
D401E |
probably benign |
Het |
Glyctk |
T |
C |
9: 106,032,906 (GRCm39) |
E369G |
possibly damaging |
Het |
Gm14149 |
C |
A |
2: 151,066,225 (GRCm39) |
|
noncoding transcript |
Het |
Golga4 |
T |
C |
9: 118,387,174 (GRCm39) |
L1432P |
probably damaging |
Het |
Gtpbp4 |
A |
T |
13: 9,023,196 (GRCm39) |
S623T |
probably benign |
Het |
Insc |
A |
C |
7: 114,390,383 (GRCm39) |
S85R |
probably damaging |
Het |
Lgr4 |
G |
A |
2: 109,821,496 (GRCm39) |
R126H |
probably damaging |
Het |
M1ap |
T |
A |
6: 82,980,795 (GRCm39) |
L227Q |
probably damaging |
Het |
Marchf7 |
T |
C |
2: 60,067,187 (GRCm39) |
I569T |
probably damaging |
Het |
Mbd1 |
C |
A |
18: 74,409,768 (GRCm39) |
C339* |
probably null |
Het |
Moxd2 |
T |
A |
6: 40,857,341 (GRCm39) |
Y473F |
probably damaging |
Het |
Mrgpra6 |
T |
C |
7: 46,839,099 (GRCm39) |
H2R |
probably benign |
Het |
Mtus1 |
T |
G |
8: 41,529,303 (GRCm39) |
L742F |
probably damaging |
Het |
Nek11 |
A |
G |
9: 105,270,160 (GRCm39) |
Y21H |
probably benign |
Het |
Notch4 |
G |
T |
17: 34,801,392 (GRCm39) |
C1080F |
probably damaging |
Het |
Nsd3 |
C |
A |
8: 26,156,107 (GRCm39) |
P558Q |
probably damaging |
Het |
Oas1e |
A |
T |
5: 120,930,015 (GRCm39) |
S168T |
probably benign |
Het |
Ogfr |
T |
C |
2: 180,234,285 (GRCm39) |
S119P |
probably damaging |
Het |
Or2y15 |
A |
G |
11: 49,350,563 (GRCm39) |
D19G |
probably damaging |
Het |
Or8g20 |
T |
A |
9: 39,395,767 (GRCm39) |
M261L |
probably benign |
Het |
Pde4dip |
A |
G |
3: 97,631,504 (GRCm39) |
I1135T |
possibly damaging |
Het |
Prex1 |
G |
A |
2: 166,486,604 (GRCm39) |
|
probably benign |
Het |
Ptprf |
T |
C |
4: 118,068,486 (GRCm39) |
|
probably benign |
Het |
Rapsn |
T |
C |
2: 90,875,859 (GRCm39) |
V359A |
probably damaging |
Het |
Ric1 |
A |
G |
19: 29,577,245 (GRCm39) |
S1050G |
possibly damaging |
Het |
Rnft2 |
A |
G |
5: 118,366,868 (GRCm39) |
I290T |
possibly damaging |
Het |
Senp7 |
C |
A |
16: 55,975,722 (GRCm39) |
A476E |
possibly damaging |
Het |
Serpinh1 |
G |
A |
7: 98,995,571 (GRCm39) |
S337L |
probably damaging |
Het |
Slc5a12 |
C |
A |
2: 110,427,969 (GRCm39) |
A8D |
probably benign |
Het |
Smg5 |
T |
A |
3: 88,250,214 (GRCm39) |
C109S |
probably damaging |
Het |
Speer4b |
T |
C |
5: 27,705,226 (GRCm39) |
H49R |
possibly damaging |
Het |
Tas2r109 |
T |
C |
6: 132,957,664 (GRCm39) |
I89V |
probably benign |
Het |
Tet1 |
A |
G |
10: 62,648,399 (GRCm39) |
|
probably null |
Het |
Tmed6 |
G |
T |
8: 107,790,786 (GRCm39) |
T87K |
probably damaging |
Het |
Tpgs1 |
G |
A |
10: 79,505,545 (GRCm39) |
G101D |
probably damaging |
Het |
Trim13 |
T |
G |
14: 61,842,188 (GRCm39) |
S68R |
probably damaging |
Het |
Vwf |
A |
G |
6: 125,620,053 (GRCm39) |
N1577S |
|
Het |
Vwf |
G |
T |
6: 125,656,228 (GRCm39) |
|
probably benign |
Het |
Xpr1 |
T |
C |
1: 155,207,868 (GRCm39) |
|
probably benign |
Het |
Ylpm1 |
C |
T |
12: 85,087,660 (GRCm39) |
P1148L |
probably damaging |
Het |
Zftraf1 |
A |
T |
15: 76,532,391 (GRCm39) |
I239N |
probably damaging |
Het |
Zftraf1 |
T |
C |
15: 76,540,615 (GRCm39) |
Y101C |
probably damaging |
Het |
Zscan29 |
G |
T |
2: 120,994,518 (GRCm39) |
T489N |
probably damaging |
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 |
105,404,281 (GRCm39) |
missense |
probably benign |
0.37 |
R2474:Dchs1
|
UTSW |
7 |
105,422,045 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|