Product Details
- SNP ID
-
rs141782217
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:43535361 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCAGCCCAAGGCCTTGATGTTCTTC[A/C]GCCACGTGTGAATTTAGGGAGGGTT
- Phenotype
-
MIM: 600178
MIM: 610979
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
MAP1A
PubMed Links
Gene Details
- Gene
- MAP1A
- Gene Name
- microtubule associated protein 1A
There are no transcripts associated with this gene.
- Gene
- PPIP5K1
- Gene Name
- diphosphoinositol pentakisphosphate kinase 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001130858.2 |
3807 |
Silent Mutation |
GCG,GCT |
A1205A |
NP_001124330.1 |
| NM_001130859.2 |
3807 |
Silent Mutation |
GCG,GCT |
A1180A |
NP_001124331.1 |
| NM_001190214.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1178A |
NP_001177143.1 |
| NM_014659.5 |
3807 |
Silent Mutation |
GCG,GCT |
A1180A |
NP_055474.3 |
| XM_005254803.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1201A |
XP_005254860.1 |
| XM_005254804.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1180A |
XP_005254861.1 |
| XM_006720786.2 |
3807 |
Silent Mutation |
GCG,GCT |
A1138A |
XP_006720849.1 |
| XM_011522249.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1251A |
XP_011520551.1 |
| XM_011522250.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1251A |
XP_011520552.1 |
| XM_011522252.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1251A |
XP_011520554.1 |
| XM_011522254.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1251A |
XP_011520556.1 |
| XM_011522258.1 |
3807 |
Silent Mutation |
GCG,GCT |
A996A |
XP_011520560.1 |
| XM_011522259.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1193A |
XP_011520561.1 |
| XM_017022735.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1251A |
XP_016878224.1 |
| XM_017022736.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1251A |
XP_016878225.1 |
| XM_017022737.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1251A |
XP_016878226.1 |
| XM_017022738.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1243A |
XP_016878227.1 |
| XM_017022739.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1230A |
XP_016878228.1 |
| XM_017022740.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1201A |
XP_016878229.1 |
| XM_017022741.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1201A |
XP_016878230.1 |
| XM_017022742.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1201A |
XP_016878231.1 |
| XM_017022743.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1201A |
XP_016878232.1 |
| XM_017022744.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1201A |
XP_016878233.1 |
| XM_017022745.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1193A |
XP_016878234.1 |
| XM_017022746.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1193A |
XP_016878235.1 |
| XM_017022747.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1188A |
XP_016878236.1 |
| XM_017022748.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1180A |
XP_016878237.1 |
| XM_017022749.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1180A |
XP_016878238.1 |
| XM_017022750.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1180A |
XP_016878239.1 |
| XM_017022751.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1180A |
XP_016878240.1 |
| XM_017022752.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1172A |
XP_016878241.1 |
| XM_017022753.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1172A |
XP_016878242.1 |
| XM_017022754.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1138A |
XP_016878243.1 |
| XM_017022755.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1138A |
XP_016878244.1 |
| XM_017022756.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1138A |
XP_016878245.1 |
| XM_017022757.1 |
3807 |
Silent Mutation |
GCG,GCT |
A1138A |
XP_016878246.1 |
| XM_017022758.1 |
3807 |
Silent Mutation |
GCG,GCT |
A925A |
XP_016878247.1 |
| XM_017022759.1 |
3807 |
Intron |
|
|
XP_016878248.1 |
| XM_017022760.1 |
3807 |
Silent Mutation |
GCG,GCT |
A537A |
XP_016878249.1 |
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