Other mutations in this stock |
Total: 14 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acin1 |
G |
A |
14: 54,884,257 (GRCm39) |
T67I |
probably damaging |
Het |
Agmo |
T |
C |
12: 37,407,716 (GRCm39) |
I200T |
probably damaging |
Het |
Cep95 |
A |
G |
11: 106,697,220 (GRCm39) |
T248A |
probably benign |
Het |
Cmya5 |
C |
T |
13: 93,234,441 (GRCm39) |
V216M |
possibly damaging |
Het |
Gas6 |
T |
G |
8: 13,526,171 (GRCm39) |
T256P |
probably damaging |
Het |
Gbf1 |
T |
C |
19: 46,272,559 (GRCm39) |
|
probably null |
Het |
Klhl10 |
G |
A |
11: 100,347,110 (GRCm39) |
V435I |
possibly damaging |
Het |
Lama2 |
T |
A |
10: 27,245,011 (GRCm39) |
K257* |
probably null |
Het |
Lrriq1 |
A |
T |
10: 102,997,757 (GRCm39) |
V1286E |
probably damaging |
Het |
Mtbp |
T |
A |
15: 55,421,894 (GRCm39) |
|
probably benign |
Het |
Nedd1 |
A |
G |
10: 92,525,548 (GRCm39) |
V587A |
possibly damaging |
Het |
Srbd1 |
T |
C |
17: 86,437,698 (GRCm39) |
E215G |
probably damaging |
Het |
Stxbp4 |
A |
G |
11: 90,426,338 (GRCm39) |
V490A |
probably benign |
Het |
Vmn2r124 |
A |
G |
17: 18,282,932 (GRCm39) |
M209V |
probably benign |
Het |
|
Other mutations in 1700010I14Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01569:1700010I14Rik
|
APN |
17 |
9,215,827 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03024:1700010I14Rik
|
APN |
17 |
9,212,464 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03410:1700010I14Rik
|
APN |
17 |
9,220,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R0017:1700010I14Rik
|
UTSW |
17 |
9,226,938 (GRCm39) |
utr 3 prime |
probably benign |
|
R0017:1700010I14Rik
|
UTSW |
17 |
9,226,938 (GRCm39) |
utr 3 prime |
probably benign |
|
R0324:1700010I14Rik
|
UTSW |
17 |
9,219,989 (GRCm39) |
missense |
probably benign |
0.33 |
R0361:1700010I14Rik
|
UTSW |
17 |
9,211,378 (GRCm39) |
missense |
probably benign |
0.39 |
R0482:1700010I14Rik
|
UTSW |
17 |
9,207,255 (GRCm39) |
critical splice donor site |
probably null |
|
R0529:1700010I14Rik
|
UTSW |
17 |
9,211,228 (GRCm39) |
missense |
probably benign |
0.32 |
R1102:1700010I14Rik
|
UTSW |
17 |
9,211,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R1964:1700010I14Rik
|
UTSW |
17 |
9,211,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R3620:1700010I14Rik
|
UTSW |
17 |
9,226,864 (GRCm39) |
missense |
probably benign |
0.15 |
R4259:1700010I14Rik
|
UTSW |
17 |
9,214,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R4261:1700010I14Rik
|
UTSW |
17 |
9,214,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:1700010I14Rik
|
UTSW |
17 |
9,210,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:1700010I14Rik
|
UTSW |
17 |
9,224,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:1700010I14Rik
|
UTSW |
17 |
9,226,845 (GRCm39) |
missense |
probably benign |
0.41 |
R4979:1700010I14Rik
|
UTSW |
17 |
9,220,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R5225:1700010I14Rik
|
UTSW |
17 |
9,226,839 (GRCm39) |
nonsense |
probably null |
|
R5383:1700010I14Rik
|
UTSW |
17 |
9,211,532 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6031:1700010I14Rik
|
UTSW |
17 |
9,214,084 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6031:1700010I14Rik
|
UTSW |
17 |
9,214,084 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6505:1700010I14Rik
|
UTSW |
17 |
9,220,772 (GRCm39) |
missense |
probably benign |
0.08 |
R6736:1700010I14Rik
|
UTSW |
17 |
9,211,100 (GRCm39) |
missense |
probably benign |
0.01 |
R7089:1700010I14Rik
|
UTSW |
17 |
9,226,927 (GRCm39) |
missense |
probably benign |
0.00 |
R7097:1700010I14Rik
|
UTSW |
17 |
9,224,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:1700010I14Rik
|
UTSW |
17 |
9,215,861 (GRCm39) |
nonsense |
probably null |
|
R7405:1700010I14Rik
|
UTSW |
17 |
9,220,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R7567:1700010I14Rik
|
UTSW |
17 |
9,226,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:1700010I14Rik
|
UTSW |
17 |
9,220,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:1700010I14Rik
|
UTSW |
17 |
9,226,939 (GRCm39) |
missense |
unknown |
|
R8805:1700010I14Rik
|
UTSW |
17 |
9,226,737 (GRCm39) |
nonsense |
probably null |
|
R9007:1700010I14Rik
|
UTSW |
17 |
9,226,935 (GRCm39) |
missense |
probably benign |
0.01 |
R9308:1700010I14Rik
|
UTSW |
17 |
9,220,667 (GRCm39) |
nonsense |
probably null |
|
R9400:1700010I14Rik
|
UTSW |
17 |
9,211,118 (GRCm39) |
missense |
probably benign |
0.01 |
|