Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg1 |
T |
C |
8: 95,739,559 (GRCm39) |
S670P |
probably damaging |
Het |
Ap5m1 |
T |
A |
14: 49,317,797 (GRCm39) |
F351L |
probably damaging |
Het |
Cacnb2 |
A |
G |
2: 14,619,079 (GRCm39) |
Y38C |
probably damaging |
Het |
Ccdc28a |
C |
T |
10: 18,095,262 (GRCm39) |
A151T |
possibly damaging |
Het |
Cgnl1 |
T |
C |
9: 71,557,604 (GRCm39) |
E976G |
probably damaging |
Het |
Cyp2c39 |
A |
G |
19: 39,525,264 (GRCm39) |
Y189C |
probably damaging |
Het |
Dbt |
T |
C |
3: 116,326,954 (GRCm39) |
V101A |
probably damaging |
Het |
Evc |
A |
G |
5: 37,477,578 (GRCm39) |
|
probably null |
Het |
Fastkd5 |
A |
G |
2: 130,457,532 (GRCm39) |
Y353H |
probably benign |
Het |
Lhx8 |
A |
G |
3: 154,027,992 (GRCm39) |
S156P |
probably damaging |
Het |
Mki67 |
T |
C |
7: 135,300,686 (GRCm39) |
I1449M |
probably damaging |
Het |
Mtrr |
A |
T |
13: 68,728,719 (GRCm39) |
V27E |
possibly damaging |
Het |
Myh14 |
A |
G |
7: 44,307,363 (GRCm39) |
V226A |
probably benign |
Het |
Nek1 |
T |
C |
8: 61,577,246 (GRCm39) |
S1076P |
possibly damaging |
Het |
Or52z14 |
C |
T |
7: 103,253,548 (GRCm39) |
A229V |
probably benign |
Het |
Or6ae1 |
G |
T |
7: 139,742,841 (GRCm39) |
N7K |
probably benign |
Het |
Pcdhb7 |
A |
G |
18: 37,475,548 (GRCm39) |
D228G |
possibly damaging |
Het |
Pias3 |
T |
C |
3: 96,611,073 (GRCm39) |
S414P |
probably benign |
Het |
Plcd4 |
G |
A |
1: 74,591,192 (GRCm39) |
V196I |
probably benign |
Het |
Proca1 |
A |
G |
11: 78,095,737 (GRCm39) |
D123G |
probably damaging |
Het |
Ptpn3 |
A |
G |
4: 57,254,915 (GRCm39) |
|
probably null |
Het |
Ptprq |
C |
A |
10: 107,535,469 (GRCm39) |
R432L |
probably damaging |
Het |
Rasgrp4 |
A |
G |
7: 28,838,475 (GRCm39) |
K108E |
possibly damaging |
Het |
Siglecg |
A |
G |
7: 43,060,888 (GRCm39) |
|
probably null |
Het |
Srpra |
A |
G |
9: 35,126,201 (GRCm39) |
T465A |
possibly damaging |
Het |
Tmpo |
G |
A |
10: 90,999,104 (GRCm39) |
R228C |
probably benign |
Het |
Zeb1 |
G |
A |
18: 5,767,867 (GRCm39) |
V793M |
possibly damaging |
Het |
|
Other mutations in Gm6408 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01695:Gm6408
|
APN |
5 |
146,418,939 (GRCm39) |
splice site |
probably benign |
|
R0211:Gm6408
|
UTSW |
5 |
146,419,870 (GRCm39) |
missense |
probably benign |
0.04 |
R1763:Gm6408
|
UTSW |
5 |
146,419,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R3745:Gm6408
|
UTSW |
5 |
146,421,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R4393:Gm6408
|
UTSW |
5 |
146,419,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Gm6408
|
UTSW |
5 |
146,421,267 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5734:Gm6408
|
UTSW |
5 |
146,419,192 (GRCm39) |
missense |
probably benign |
0.07 |
R5999:Gm6408
|
UTSW |
5 |
146,421,067 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6181:Gm6408
|
UTSW |
5 |
146,420,582 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7007:Gm6408
|
UTSW |
5 |
146,420,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7063:Gm6408
|
UTSW |
5 |
146,420,594 (GRCm39) |
missense |
probably benign |
0.01 |
R7224:Gm6408
|
UTSW |
5 |
146,421,180 (GRCm39) |
missense |
probably benign |
0.10 |
R7734:Gm6408
|
UTSW |
5 |
146,421,160 (GRCm39) |
nonsense |
probably null |
|
R8676:Gm6408
|
UTSW |
5 |
146,419,237 (GRCm39) |
missense |
probably benign |
0.02 |
R8847:Gm6408
|
UTSW |
5 |
146,420,602 (GRCm39) |
missense |
probably benign |
0.20 |
R9758:Gm6408
|
UTSW |
5 |
146,420,628 (GRCm39) |
missense |
probably benign |
0.28 |
|