Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
G |
10: 100,446,579 (GRCm39) |
|
probably null |
Het |
Ace |
A |
G |
11: 105,863,353 (GRCm39) |
D376G |
probably damaging |
Het |
Adgrb1 |
C |
T |
15: 74,458,654 (GRCm39) |
T1252I |
probably damaging |
Het |
Ckap5 |
T |
C |
2: 91,425,186 (GRCm39) |
|
probably benign |
Het |
Clcn4 |
T |
C |
7: 7,299,065 (GRCm39) |
T37A |
probably benign |
Het |
Cnmd |
C |
T |
14: 79,899,400 (GRCm39) |
V18I |
probably benign |
Het |
Cryl1 |
C |
T |
14: 57,513,478 (GRCm39) |
V248M |
probably benign |
Het |
D830039M14Rik |
C |
T |
10: 61,311,262 (GRCm39) |
|
probably benign |
Het |
Dido1 |
T |
C |
2: 180,331,128 (GRCm39) |
T107A |
possibly damaging |
Het |
Efna5 |
C |
A |
17: 62,958,023 (GRCm39) |
V78F |
probably damaging |
Het |
Eml1 |
A |
G |
12: 108,503,625 (GRCm39) |
I741V |
probably benign |
Het |
Gfap |
A |
G |
11: 102,787,780 (GRCm39) |
L55P |
probably damaging |
Het |
Itga6 |
A |
G |
2: 71,669,027 (GRCm39) |
I606V |
probably benign |
Het |
Kif2c |
G |
T |
4: 117,019,802 (GRCm39) |
D579E |
probably damaging |
Het |
Lef1 |
T |
C |
3: 130,988,442 (GRCm39) |
|
probably null |
Het |
Lrrc1 |
T |
A |
9: 77,342,404 (GRCm39) |
I357L |
probably benign |
Het |
Lrrc37 |
A |
G |
11: 103,504,109 (GRCm39) |
S2620P |
probably benign |
Het |
Map3k20 |
T |
A |
2: 72,202,239 (GRCm39) |
F157I |
probably damaging |
Het |
Naga |
A |
T |
15: 82,214,337 (GRCm39) |
N391K |
probably damaging |
Het |
Ncaph |
T |
C |
2: 126,968,025 (GRCm39) |
|
probably benign |
Het |
Or11g2 |
C |
A |
14: 50,856,185 (GRCm39) |
Q169K |
probably benign |
Het |
Or12d13 |
T |
A |
17: 37,647,887 (GRCm39) |
M79L |
probably benign |
Het |
Or5ae1 |
T |
G |
7: 84,565,567 (GRCm39) |
Y193* |
probably null |
Het |
Or6b9 |
T |
A |
7: 106,555,598 (GRCm39) |
I182F |
possibly damaging |
Het |
Or6c2b |
T |
G |
10: 128,947,904 (GRCm39) |
Y130S |
probably damaging |
Het |
Or8g55 |
T |
A |
9: 39,784,906 (GRCm39) |
C112S |
possibly damaging |
Het |
Pappa |
C |
A |
4: 65,074,863 (GRCm39) |
D472E |
possibly damaging |
Het |
Pdxk |
G |
A |
10: 78,287,319 (GRCm39) |
L81F |
probably damaging |
Het |
Pkhd1 |
G |
T |
1: 20,380,934 (GRCm39) |
T2635K |
probably damaging |
Het |
Psmb6 |
A |
T |
11: 70,417,248 (GRCm39) |
H99L |
possibly damaging |
Het |
Ptpn6 |
C |
T |
6: 124,705,623 (GRCm39) |
G135E |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 22,972,844 (GRCm39) |
D251E |
probably benign |
Het |
Ralgapa1 |
A |
G |
12: 55,689,234 (GRCm39) |
V1955A |
possibly damaging |
Het |
Rsph4a |
T |
C |
10: 33,781,148 (GRCm39) |
|
probably benign |
Het |
Sh2d4b |
T |
C |
14: 40,542,700 (GRCm39) |
T359A |
probably benign |
Het |
Sh3bp5l |
A |
G |
11: 58,237,087 (GRCm39) |
D348G |
probably damaging |
Het |
Skint5 |
A |
T |
4: 113,797,932 (GRCm39) |
M217K |
probably damaging |
Het |
Slc30a6 |
T |
C |
17: 74,711,054 (GRCm39) |
L49P |
probably damaging |
Het |
Slc8a1 |
C |
T |
17: 81,956,173 (GRCm39) |
M288I |
probably benign |
Het |
Tmem127 |
C |
A |
2: 127,097,922 (GRCm39) |
|
probably null |
Het |
Tnfrsf17 |
T |
C |
16: 11,131,811 (GRCm39) |
|
probably benign |
Het |
Trak1 |
A |
T |
9: 121,277,967 (GRCm39) |
N341I |
probably damaging |
Het |
Ubr5 |
A |
G |
15: 38,002,692 (GRCm39) |
I1453T |
probably benign |
Het |
Wdr62 |
T |
C |
7: 29,944,709 (GRCm39) |
|
probably null |
Het |
Xrn2 |
T |
C |
2: 146,880,216 (GRCm39) |
|
probably benign |
Het |
Zscan10 |
C |
T |
17: 23,827,119 (GRCm39) |
A144V |
possibly damaging |
Het |
|
Other mutations in Bhmt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01730:Bhmt
|
APN |
13 |
93,761,917 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02365:Bhmt
|
APN |
13 |
93,754,146 (GRCm39) |
missense |
probably benign |
|
R0279:Bhmt
|
UTSW |
13 |
93,761,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Bhmt
|
UTSW |
13 |
93,761,843 (GRCm39) |
missense |
probably damaging |
0.98 |
R2012:Bhmt
|
UTSW |
13 |
93,761,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R2065:Bhmt
|
UTSW |
13 |
93,754,120 (GRCm39) |
missense |
probably benign |
0.01 |
R2283:Bhmt
|
UTSW |
13 |
93,756,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R3429:Bhmt
|
UTSW |
13 |
93,763,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Bhmt
|
UTSW |
13 |
93,763,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Bhmt
|
UTSW |
13 |
93,762,007 (GRCm39) |
splice site |
probably benign |
|
R4729:Bhmt
|
UTSW |
13 |
93,763,871 (GRCm39) |
missense |
probably damaging |
0.97 |
R5135:Bhmt
|
UTSW |
13 |
93,763,831 (GRCm39) |
missense |
probably damaging |
0.99 |
R5277:Bhmt
|
UTSW |
13 |
93,761,393 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7233:Bhmt
|
UTSW |
13 |
93,758,025 (GRCm39) |
nonsense |
probably null |
|
R7553:Bhmt
|
UTSW |
13 |
93,756,589 (GRCm39) |
critical splice donor site |
probably null |
|
R7828:Bhmt
|
UTSW |
13 |
93,754,156 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8499:Bhmt
|
UTSW |
13 |
93,756,600 (GRCm39) |
missense |
probably benign |
0.18 |
R9621:Bhmt
|
UTSW |
13 |
93,758,079 (GRCm39) |
missense |
possibly damaging |
0.82 |
|