Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Brd10 |
T |
C |
19: 29,731,212 (GRCm39) |
H600R |
possibly damaging |
Het |
Cacnb3 |
A |
T |
15: 98,537,469 (GRCm39) |
Q49L |
probably benign |
Het |
Dapk1 |
A |
G |
13: 60,878,845 (GRCm39) |
|
probably benign |
Het |
Dop1b |
T |
A |
16: 93,566,846 (GRCm39) |
L1091* |
probably null |
Het |
Epb42 |
A |
G |
2: 120,858,169 (GRCm39) |
V263A |
probably damaging |
Het |
Fig4 |
T |
G |
10: 41,132,490 (GRCm39) |
S439R |
probably benign |
Het |
Gatc |
A |
T |
5: 115,479,048 (GRCm39) |
V54E |
possibly damaging |
Het |
Hook2 |
T |
C |
8: 85,729,618 (GRCm39) |
L686P |
probably benign |
Het |
Med12l |
A |
T |
3: 59,169,680 (GRCm39) |
T1615S |
probably damaging |
Het |
Msr1 |
C |
T |
8: 40,064,714 (GRCm39) |
G320D |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,256,414 (GRCm39) |
F220I |
probably damaging |
Het |
Or14j2 |
T |
A |
17: 37,885,679 (GRCm39) |
I212F |
possibly damaging |
Het |
Or2l5 |
G |
A |
16: 19,334,228 (GRCm39) |
H53Y |
probably benign |
Het |
Pcdh10 |
A |
T |
3: 45,334,078 (GRCm39) |
I131F |
probably damaging |
Het |
Phlpp2 |
A |
G |
8: 110,660,697 (GRCm39) |
E784G |
possibly damaging |
Het |
Prr36 |
A |
T |
8: 4,264,043 (GRCm39) |
|
probably benign |
Het |
Ptprq |
G |
A |
10: 107,535,457 (GRCm39) |
S436L |
probably benign |
Het |
Rock1 |
T |
A |
18: 10,132,119 (GRCm39) |
|
probably benign |
Het |
Sash1 |
T |
G |
10: 8,617,341 (GRCm39) |
T522P |
probably damaging |
Het |
Serpinb2 |
T |
C |
1: 107,447,503 (GRCm39) |
|
probably null |
Het |
Supt16 |
T |
C |
14: 52,414,647 (GRCm39) |
K422E |
probably damaging |
Het |
Syt14 |
T |
G |
1: 192,669,073 (GRCm39) |
D60A |
probably damaging |
Het |
Tbc1d2b |
A |
C |
9: 90,097,526 (GRCm39) |
|
probably benign |
Het |
Thsd7b |
T |
C |
1: 129,605,954 (GRCm39) |
I565T |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,564,536 (GRCm39) |
Y28534H |
probably damaging |
Het |
Vmn1r177 |
T |
A |
7: 23,565,765 (GRCm39) |
H37L |
probably damaging |
Het |
Vps13b |
A |
T |
15: 35,455,103 (GRCm39) |
N671Y |
possibly damaging |
Het |
|
Other mutations in Adamts19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00156:Adamts19
|
APN |
18 |
59,157,537 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00331:Adamts19
|
APN |
18 |
59,140,397 (GRCm39) |
splice site |
probably benign |
|
IGL00970:Adamts19
|
APN |
18 |
59,144,149 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01328:Adamts19
|
APN |
18 |
59,181,954 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01385:Adamts19
|
APN |
18 |
59,105,851 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01529:Adamts19
|
APN |
18 |
59,096,535 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01557:Adamts19
|
APN |
18 |
59,101,792 (GRCm39) |
splice site |
probably null |
|
IGL01705:Adamts19
|
APN |
18 |
59,166,038 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01803:Adamts19
|
APN |
18 |
59,085,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02116:Adamts19
|
APN |
18 |
58,970,571 (GRCm39) |
missense |
probably benign |
|
IGL02131:Adamts19
|
APN |
18 |
59,185,732 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02312:Adamts19
|
APN |
18 |
59,060,369 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02755:Adamts19
|
APN |
18 |
59,103,005 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02866:Adamts19
|
APN |
18 |
59,181,914 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02964:Adamts19
|
APN |
18 |
59,122,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Adamts19
|
APN |
18 |
59,157,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03040:Adamts19
|
APN |
18 |
59,036,080 (GRCm39) |
missense |
probably benign |
0.05 |
R0081:Adamts19
|
UTSW |
18 |
59,036,137 (GRCm39) |
critical splice donor site |
probably null |
|
R0194:Adamts19
|
UTSW |
18 |
59,144,220 (GRCm39) |
missense |
probably null |
1.00 |
R0195:Adamts19
|
UTSW |
18 |
59,102,942 (GRCm39) |
splice site |
probably benign |
|
R0541:Adamts19
|
UTSW |
18 |
59,060,372 (GRCm39) |
critical splice donor site |
probably null |
|
R0659:Adamts19
|
UTSW |
18 |
59,140,565 (GRCm39) |
splice site |
probably benign |
|
R0967:Adamts19
|
UTSW |
18 |
59,105,812 (GRCm39) |
nonsense |
probably null |
|
R1512:Adamts19
|
UTSW |
18 |
59,181,917 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1536:Adamts19
|
UTSW |
18 |
59,185,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1582:Adamts19
|
UTSW |
18 |
59,103,013 (GRCm39) |
missense |
probably damaging |
0.98 |
R1629:Adamts19
|
UTSW |
18 |
59,087,691 (GRCm39) |
missense |
probably damaging |
0.97 |
R1653:Adamts19
|
UTSW |
18 |
59,023,365 (GRCm39) |
missense |
probably benign |
0.00 |
R1718:Adamts19
|
UTSW |
18 |
59,105,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R1733:Adamts19
|
UTSW |
18 |
59,165,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Adamts19
|
UTSW |
18 |
59,140,444 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1776:Adamts19
|
UTSW |
18 |
59,087,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R1905:Adamts19
|
UTSW |
18 |
59,166,017 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1958:Adamts19
|
UTSW |
18 |
59,103,078 (GRCm39) |
missense |
probably benign |
0.09 |
R1994:Adamts19
|
UTSW |
18 |
59,105,903 (GRCm39) |
critical splice donor site |
probably null |
|
R2177:Adamts19
|
UTSW |
18 |
59,087,626 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3730:Adamts19
|
UTSW |
18 |
59,033,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R4342:Adamts19
|
UTSW |
18 |
59,075,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R4772:Adamts19
|
UTSW |
18 |
58,970,848 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4822:Adamts19
|
UTSW |
18 |
59,023,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R4891:Adamts19
|
UTSW |
18 |
59,166,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Adamts19
|
UTSW |
18 |
59,164,876 (GRCm39) |
nonsense |
probably null |
|
R5116:Adamts19
|
UTSW |
18 |
59,036,066 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5205:Adamts19
|
UTSW |
18 |
59,101,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R5765:Adamts19
|
UTSW |
18 |
59,185,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5781:Adamts19
|
UTSW |
18 |
58,971,040 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5792:Adamts19
|
UTSW |
18 |
58,970,584 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6082:Adamts19
|
UTSW |
18 |
59,101,846 (GRCm39) |
missense |
probably benign |
0.18 |
R6088:Adamts19
|
UTSW |
18 |
59,035,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7060:Adamts19
|
UTSW |
18 |
58,970,712 (GRCm39) |
nonsense |
probably null |
|
R7251:Adamts19
|
UTSW |
18 |
58,970,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R7295:Adamts19
|
UTSW |
18 |
58,970,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Adamts19
|
UTSW |
18 |
59,144,094 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7991:Adamts19
|
UTSW |
18 |
59,185,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Adamts19
|
UTSW |
18 |
59,140,559 (GRCm39) |
critical splice donor site |
probably null |
|
R8297:Adamts19
|
UTSW |
18 |
58,970,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R8336:Adamts19
|
UTSW |
18 |
59,140,444 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8358:Adamts19
|
UTSW |
18 |
59,181,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Adamts19
|
UTSW |
18 |
59,023,497 (GRCm39) |
nonsense |
probably null |
|
R9051:Adamts19
|
UTSW |
18 |
59,034,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R9253:Adamts19
|
UTSW |
18 |
59,103,013 (GRCm39) |
missense |
probably damaging |
0.98 |
R9423:Adamts19
|
UTSW |
18 |
59,023,427 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9610:Adamts19
|
UTSW |
18 |
59,023,399 (GRCm39) |
missense |
probably benign |
0.26 |
R9611:Adamts19
|
UTSW |
18 |
59,023,399 (GRCm39) |
missense |
probably benign |
0.26 |
R9686:Adamts19
|
UTSW |
18 |
58,971,093 (GRCm39) |
missense |
probably benign |
0.00 |
R9697:Adamts19
|
UTSW |
18 |
59,101,834 (GRCm39) |
missense |
probably damaging |
0.99 |
R9747:Adamts19
|
UTSW |
18 |
59,023,487 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1177:Adamts19
|
UTSW |
18 |
59,023,446 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Adamts19
|
UTSW |
18 |
58,971,147 (GRCm39) |
missense |
probably damaging |
1.00 |
|