Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
G |
C |
8: 120,872,209 (GRCm39) |
E46Q |
probably damaging |
Het |
9130401M01Rik |
A |
G |
15: 57,885,823 (GRCm39) |
I353T |
possibly damaging |
Het |
A830031A19Rik |
G |
A |
11: 23,999,438 (GRCm39) |
R53C |
unknown |
Het |
Adam10 |
A |
G |
9: 70,668,922 (GRCm39) |
N413D |
probably benign |
Het |
Csmd2 |
T |
C |
4: 128,415,807 (GRCm39) |
V2712A |
probably benign |
Het |
Dnhd1 |
T |
C |
7: 105,358,378 (GRCm39) |
F3289S |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,795,440 (GRCm39) |
S2330P |
probably damaging |
Het |
Ift74 |
C |
T |
4: 94,524,072 (GRCm39) |
A196V |
probably benign |
Het |
Kifc1 |
G |
A |
17: 34,103,685 (GRCm39) |
R195C |
probably benign |
Het |
Lipo2 |
A |
T |
19: 33,708,257 (GRCm39) |
C252* |
probably null |
Het |
Mrgpra1 |
C |
G |
7: 46,984,833 (GRCm39) |
C282S |
probably benign |
Het |
Nfatc2 |
A |
T |
2: 168,346,799 (GRCm39) |
L765Q |
probably damaging |
Het |
Or13a26 |
C |
T |
7: 140,284,407 (GRCm39) |
P81L |
probably damaging |
Het |
Or1l8 |
A |
G |
2: 36,817,764 (GRCm39) |
F121L |
probably benign |
Het |
Otof |
C |
A |
5: 30,528,087 (GRCm39) |
V1924L |
probably damaging |
Het |
Pdhb |
T |
C |
14: 8,171,442 (GRCm38) |
Q62R |
probably benign |
Het |
Plbd1 |
A |
G |
6: 136,628,903 (GRCm39) |
V55A |
probably benign |
Het |
Poteg |
T |
A |
8: 27,937,852 (GRCm39) |
F3I |
possibly damaging |
Het |
Rptor |
A |
G |
11: 119,734,569 (GRCm39) |
D46G |
probably damaging |
Het |
Slc18a1 |
C |
T |
8: 69,527,685 (GRCm39) |
|
probably null |
Het |
Slc37a1 |
A |
G |
17: 31,534,568 (GRCm39) |
N80S |
probably benign |
Het |
Slc6a18 |
T |
A |
13: 73,825,998 (GRCm39) |
R17S |
probably damaging |
Het |
Spata31d1a |
A |
G |
13: 59,850,182 (GRCm39) |
S649P |
probably benign |
Het |
Syngr3 |
G |
T |
17: 24,906,534 (GRCm39) |
Q94K |
possibly damaging |
Het |
Tgm2 |
C |
A |
2: 157,966,074 (GRCm39) |
E527* |
probably null |
Het |
Tnc |
T |
A |
4: 63,880,319 (GRCm39) |
T1952S |
probably damaging |
Het |
Ubqln3 |
C |
T |
7: 103,790,593 (GRCm39) |
R499Q |
probably benign |
Het |
Uck1 |
A |
G |
2: 32,146,205 (GRCm39) |
V230A |
possibly damaging |
Het |
Unc13d |
G |
A |
11: 115,958,900 (GRCm39) |
R754C |
probably benign |
Het |
Zfp708 |
C |
T |
13: 67,222,162 (GRCm39) |
A73T |
probably benign |
Het |
|
Other mutations in Abcc6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01589:Abcc6
|
APN |
7 |
45,652,096 (GRCm39) |
splice site |
probably benign |
|
IGL01731:Abcc6
|
APN |
7 |
45,652,034 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01743:Abcc6
|
APN |
7 |
45,646,238 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01757:Abcc6
|
APN |
7 |
45,639,705 (GRCm39) |
splice site |
probably benign |
|
IGL01895:Abcc6
|
APN |
7 |
45,678,482 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01942:Abcc6
|
APN |
7 |
45,635,997 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02251:Abcc6
|
APN |
7 |
45,626,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02277:Abcc6
|
APN |
7 |
45,650,485 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02548:Abcc6
|
APN |
7 |
45,654,686 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03063:Abcc6
|
APN |
7 |
45,665,856 (GRCm39) |
missense |
probably benign |
|
IGL03092:Abcc6
|
APN |
7 |
45,635,894 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03251:Abcc6
|
APN |
7 |
45,631,661 (GRCm39) |
unclassified |
probably benign |
|
R0057:Abcc6
|
UTSW |
7 |
45,669,567 (GRCm39) |
missense |
probably benign |
0.03 |
R0944:Abcc6
|
UTSW |
7 |
45,664,929 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1183:Abcc6
|
UTSW |
7 |
45,634,677 (GRCm39) |
missense |
probably damaging |
0.99 |
R1543:Abcc6
|
UTSW |
7 |
45,665,928 (GRCm39) |
missense |
probably benign |
0.01 |
R1550:Abcc6
|
UTSW |
7 |
45,654,668 (GRCm39) |
missense |
probably benign |
0.25 |
R1725:Abcc6
|
UTSW |
7 |
45,641,781 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1907:Abcc6
|
UTSW |
7 |
45,663,593 (GRCm39) |
missense |
probably benign |
0.04 |
R1908:Abcc6
|
UTSW |
7 |
45,669,558 (GRCm39) |
splice site |
probably null |
|
R1909:Abcc6
|
UTSW |
7 |
45,669,558 (GRCm39) |
splice site |
probably null |
|
R2138:Abcc6
|
UTSW |
7 |
45,630,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R2145:Abcc6
|
UTSW |
7 |
45,648,165 (GRCm39) |
missense |
probably benign |
0.01 |
R2402:Abcc6
|
UTSW |
7 |
45,664,999 (GRCm39) |
missense |
probably benign |
0.04 |
R3983:Abcc6
|
UTSW |
7 |
45,644,713 (GRCm39) |
missense |
probably benign |
|
R4013:Abcc6
|
UTSW |
7 |
45,668,104 (GRCm39) |
missense |
probably benign |
0.01 |
R4051:Abcc6
|
UTSW |
7 |
45,635,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R4052:Abcc6
|
UTSW |
7 |
45,635,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R4208:Abcc6
|
UTSW |
7 |
45,635,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R4362:Abcc6
|
UTSW |
7 |
45,648,256 (GRCm39) |
splice site |
probably benign |
|
R4385:Abcc6
|
UTSW |
7 |
45,644,752 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4399:Abcc6
|
UTSW |
7 |
45,652,031 (GRCm39) |
missense |
probably benign |
|
R4479:Abcc6
|
UTSW |
7 |
45,654,663 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4480:Abcc6
|
UTSW |
7 |
45,654,663 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4780:Abcc6
|
UTSW |
7 |
45,646,115 (GRCm39) |
missense |
probably benign |
|
R4791:Abcc6
|
UTSW |
7 |
45,631,584 (GRCm39) |
missense |
probably benign |
0.00 |
R4895:Abcc6
|
UTSW |
7 |
45,630,414 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4898:Abcc6
|
UTSW |
7 |
45,639,111 (GRCm39) |
missense |
probably damaging |
0.96 |
R4905:Abcc6
|
UTSW |
7 |
45,644,649 (GRCm39) |
missense |
probably benign |
|
R4941:Abcc6
|
UTSW |
7 |
45,661,947 (GRCm39) |
missense |
probably benign |
0.00 |
R5040:Abcc6
|
UTSW |
7 |
45,669,578 (GRCm39) |
missense |
probably benign |
0.04 |
R5128:Abcc6
|
UTSW |
7 |
45,639,070 (GRCm39) |
missense |
probably benign |
0.00 |
R5284:Abcc6
|
UTSW |
7 |
45,630,483 (GRCm39) |
missense |
probably benign |
0.05 |
R5328:Abcc6
|
UTSW |
7 |
45,641,735 (GRCm39) |
missense |
probably benign |
0.01 |
R5459:Abcc6
|
UTSW |
7 |
45,631,607 (GRCm39) |
missense |
probably benign |
0.00 |
R5543:Abcc6
|
UTSW |
7 |
45,638,960 (GRCm39) |
critical splice donor site |
probably null |
|
R6178:Abcc6
|
UTSW |
7 |
45,678,468 (GRCm39) |
missense |
probably benign |
|
R6228:Abcc6
|
UTSW |
7 |
45,679,680 (GRCm39) |
missense |
probably benign |
0.02 |
R6532:Abcc6
|
UTSW |
7 |
45,626,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R6605:Abcc6
|
UTSW |
7 |
45,630,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7000:Abcc6
|
UTSW |
7 |
45,654,946 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7067:Abcc6
|
UTSW |
7 |
45,668,114 (GRCm39) |
missense |
probably benign |
|
R7553:Abcc6
|
UTSW |
7 |
45,648,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Abcc6
|
UTSW |
7 |
45,644,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R7718:Abcc6
|
UTSW |
7 |
45,626,816 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7781:Abcc6
|
UTSW |
7 |
45,655,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R7798:Abcc6
|
UTSW |
7 |
45,626,277 (GRCm39) |
nonsense |
probably null |
|
R7896:Abcc6
|
UTSW |
7 |
45,626,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R8098:Abcc6
|
UTSW |
7 |
45,646,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R8443:Abcc6
|
UTSW |
7 |
45,629,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R8773:Abcc6
|
UTSW |
7 |
45,634,569 (GRCm39) |
missense |
probably benign |
|
R8784:Abcc6
|
UTSW |
7 |
45,652,025 (GRCm39) |
missense |
probably benign |
|
R8802:Abcc6
|
UTSW |
7 |
45,658,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R8807:Abcc6
|
UTSW |
7 |
45,648,431 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9006:Abcc6
|
UTSW |
7 |
45,665,820 (GRCm39) |
missense |
probably benign |
0.00 |
R9127:Abcc6
|
UTSW |
7 |
45,629,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9475:Abcc6
|
UTSW |
7 |
45,665,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R9480:Abcc6
|
UTSW |
7 |
45,629,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R9535:Abcc6
|
UTSW |
7 |
45,626,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R9642:Abcc6
|
UTSW |
7 |
45,639,765 (GRCm39) |
missense |
probably benign |
0.07 |
R9715:Abcc6
|
UTSW |
7 |
45,629,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R9731:Abcc6
|
UTSW |
7 |
45,669,660 (GRCm39) |
nonsense |
probably null |
|
X0065:Abcc6
|
UTSW |
7 |
45,669,621 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Abcc6
|
UTSW |
7 |
45,641,730 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Abcc6
|
UTSW |
7 |
45,629,158 (GRCm39) |
missense |
probably damaging |
1.00 |
|