Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
G |
A |
3: 121,856,353 (GRCm39) |
|
probably null |
Het |
C530025M09Rik |
C |
A |
2: 149,672,646 (GRCm39) |
|
probably benign |
Het |
Cep192 |
T |
G |
18: 67,953,407 (GRCm39) |
W475G |
probably damaging |
Het |
Col28a1 |
T |
C |
6: 8,014,795 (GRCm39) |
Y870C |
probably damaging |
Het |
Cyp2a22 |
A |
T |
7: 26,637,163 (GRCm39) |
M207K |
probably benign |
Het |
Dpm1 |
A |
G |
2: 168,052,495 (GRCm39) |
V247A |
probably benign |
Het |
Glt1d1 |
T |
C |
5: 127,709,349 (GRCm39) |
M1T |
probably null |
Het |
Gm9507 |
A |
T |
10: 77,647,114 (GRCm39) |
C188* |
probably null |
Het |
Hectd4 |
T |
C |
5: 121,501,933 (GRCm39) |
V4222A |
possibly damaging |
Het |
Igkv3-3 |
T |
A |
6: 70,664,397 (GRCm39) |
S80T |
possibly damaging |
Het |
Lrrc49 |
T |
C |
9: 60,508,603 (GRCm39) |
K520E |
probably damaging |
Het |
Ltbp1 |
A |
T |
17: 75,692,155 (GRCm39) |
Y1273F |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,823,463 (GRCm39) |
H1478Q |
probably benign |
Het |
Mre11a |
A |
G |
9: 14,736,504 (GRCm39) |
D518G |
probably benign |
Het |
Or1e22 |
T |
A |
11: 73,377,398 (GRCm39) |
N84I |
probably benign |
Het |
Or4a71 |
C |
T |
2: 89,358,551 (GRCm39) |
D68N |
probably damaging |
Het |
Or7e168 |
T |
C |
9: 19,719,692 (GRCm39) |
I26T |
probably benign |
Het |
Pkd1l1 |
T |
A |
11: 8,900,515 (GRCm39) |
S9C |
probably damaging |
Het |
Prrc2b |
A |
G |
2: 32,098,731 (GRCm39) |
H681R |
probably damaging |
Het |
Rapgef1 |
A |
G |
2: 29,612,281 (GRCm39) |
S644G |
probably benign |
Het |
Sgce |
T |
A |
6: 4,689,750 (GRCm39) |
H361L |
probably damaging |
Het |
Specc1 |
G |
T |
11: 62,008,835 (GRCm39) |
W117L |
probably benign |
Het |
Srrm4 |
A |
G |
5: 116,584,616 (GRCm39) |
S485P |
possibly damaging |
Het |
Traf2 |
G |
T |
2: 25,410,463 (GRCm39) |
Y395* |
probably null |
Het |
Trf |
A |
G |
9: 103,098,156 (GRCm39) |
I34T |
probably benign |
Het |
Vdac2 |
T |
C |
14: 21,888,592 (GRCm39) |
Y165H |
possibly damaging |
Het |
Wwp1 |
T |
C |
4: 19,650,360 (GRCm39) |
T269A |
probably benign |
Het |
|
Other mutations in Adamts19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
IGL01535:Adamts19
|
APN |
18 |
59,101,891 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|