Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acer1 |
T |
C |
17: 57,265,423 (GRCm39) |
I135M |
probably benign |
Het |
Ano7 |
A |
G |
1: 93,308,158 (GRCm39) |
E63G |
possibly damaging |
Het |
Asah1 |
A |
G |
8: 41,796,765 (GRCm39) |
|
probably null |
Het |
B3gat2 |
C |
T |
1: 23,801,873 (GRCm39) |
P53L |
probably benign |
Het |
Bmp8b |
A |
T |
4: 123,016,815 (GRCm39) |
M339L |
possibly damaging |
Het |
Bpifb9b |
C |
A |
2: 154,155,574 (GRCm39) |
Q358K |
probably benign |
Het |
Cbs |
T |
C |
17: 31,843,238 (GRCm39) |
D231G |
probably damaging |
Het |
Chd6 |
A |
G |
2: 160,825,673 (GRCm39) |
Y1144H |
probably damaging |
Het |
Clca3a2 |
T |
A |
3: 144,519,685 (GRCm39) |
I230L |
probably benign |
Het |
Clec2d |
A |
T |
6: 129,161,831 (GRCm39) |
T155S |
possibly damaging |
Het |
Cpxm1 |
G |
T |
2: 130,235,117 (GRCm39) |
F567L |
probably damaging |
Het |
Cyp4f16 |
G |
T |
17: 32,756,078 (GRCm39) |
A36S |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 117,993,235 (GRCm39) |
|
probably benign |
Het |
Eml5 |
T |
C |
12: 98,791,676 (GRCm39) |
D1280G |
probably damaging |
Het |
Ergic1 |
C |
A |
17: 26,860,566 (GRCm39) |
A218D |
possibly damaging |
Het |
Eva1a |
A |
G |
6: 82,068,894 (GRCm39) |
R74G |
probably benign |
Het |
Fhip1a |
A |
G |
3: 85,637,628 (GRCm39) |
S224P |
probably damaging |
Het |
Fus |
T |
A |
7: 127,576,400 (GRCm39) |
N273K |
probably damaging |
Het |
Ipo13 |
A |
C |
4: 117,762,100 (GRCm39) |
|
probably null |
Het |
Itgb3 |
T |
A |
11: 104,531,812 (GRCm39) |
|
probably null |
Het |
Lrif1 |
T |
A |
3: 106,641,874 (GRCm39) |
S63R |
probably damaging |
Het |
Lrig3 |
A |
G |
10: 125,832,478 (GRCm39) |
|
probably null |
Het |
Lrp1b |
A |
T |
2: 41,174,177 (GRCm39) |
N1547K |
probably benign |
Het |
Mme |
A |
T |
3: 63,287,713 (GRCm39) |
N738I |
possibly damaging |
Het |
Morc2a |
A |
G |
11: 3,633,919 (GRCm39) |
N677S |
probably benign |
Het |
Mrpl35 |
A |
C |
6: 71,794,723 (GRCm39) |
L82V |
probably benign |
Het |
Mybpc1 |
A |
T |
10: 88,391,557 (GRCm39) |
N313K |
probably damaging |
Het |
Podn |
T |
C |
4: 107,879,787 (GRCm39) |
D66G |
probably damaging |
Het |
Ptpru |
A |
T |
4: 131,548,124 (GRCm39) |
N52K |
probably damaging |
Het |
Pyroxd1 |
G |
T |
6: 142,304,808 (GRCm39) |
R345L |
probably benign |
Het |
Qser1 |
A |
G |
2: 104,619,358 (GRCm39) |
S485P |
probably damaging |
Het |
Rbm46 |
A |
T |
3: 82,771,351 (GRCm39) |
D421E |
probably benign |
Het |
Rgs10 |
T |
C |
7: 127,990,761 (GRCm39) |
E109G |
probably damaging |
Het |
Samd8 |
C |
T |
14: 21,825,388 (GRCm39) |
P178S |
probably benign |
Het |
Scaf11 |
T |
C |
15: 96,318,404 (GRCm39) |
K387E |
probably damaging |
Het |
Sec22a |
A |
T |
16: 35,134,527 (GRCm39) |
V285E |
probably damaging |
Het |
Slc19a3 |
A |
G |
1: 83,000,664 (GRCm39) |
S118P |
probably damaging |
Het |
Sun1 |
C |
A |
5: 139,216,974 (GRCm39) |
R338S |
probably benign |
Het |
Taf1c |
A |
G |
8: 120,325,417 (GRCm39) |
F815S |
probably benign |
Het |
Zcchc14 |
A |
T |
8: 122,332,167 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Sccpdh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02026:Sccpdh
|
APN |
1 |
179,505,634 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02225:Sccpdh
|
APN |
1 |
179,507,264 (GRCm39) |
missense |
probably benign |
|
IGL02428:Sccpdh
|
APN |
1 |
179,508,070 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02516:Sccpdh
|
APN |
1 |
179,509,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02622:Sccpdh
|
APN |
1 |
179,504,025 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Sccpdh
|
APN |
1 |
179,508,074 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03209:Sccpdh
|
APN |
1 |
179,514,238 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0508:Sccpdh
|
UTSW |
1 |
179,508,080 (GRCm39) |
splice site |
probably null |
|
R1160:Sccpdh
|
UTSW |
1 |
179,511,775 (GRCm39) |
missense |
probably benign |
0.01 |
R1462:Sccpdh
|
UTSW |
1 |
179,509,125 (GRCm39) |
splice site |
probably benign |
|
R1965:Sccpdh
|
UTSW |
1 |
179,511,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R2104:Sccpdh
|
UTSW |
1 |
179,498,162 (GRCm39) |
missense |
probably benign |
|
R4693:Sccpdh
|
UTSW |
1 |
179,495,975 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5954:Sccpdh
|
UTSW |
1 |
179,508,153 (GRCm39) |
missense |
probably benign |
0.08 |
R6248:Sccpdh
|
UTSW |
1 |
179,495,957 (GRCm39) |
missense |
probably benign |
0.00 |
R6355:Sccpdh
|
UTSW |
1 |
179,498,165 (GRCm39) |
missense |
probably benign |
0.01 |
R6447:Sccpdh
|
UTSW |
1 |
179,506,453 (GRCm39) |
makesense |
probably null |
|
R6692:Sccpdh
|
UTSW |
1 |
179,511,792 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8117:Sccpdh
|
UTSW |
1 |
179,504,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R8551:Sccpdh
|
UTSW |
1 |
179,509,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|