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- SNP ID:
- rs16969968
- Gene
-
CHRNA3CHRNA5 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.15: 78590583 - 78590583 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
TAGAAACACATTGGAAGCTGCGCTC[A/G]ATTCTATTCGCTACATTACAAGACA
Genomic Map
Back To TopAssay Details
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 118503
MIM: 118505
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Literature Links: |
CHRNA3 PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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| CHRNA3 - cholinergic receptor nicotinic alpha 3 subunit | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| CHRNA5 - cholinergic receptor nicotinic alpha 5 subunit | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000745.3 | 1392 | Missense Mutation | AAT,GAT | N,D 398 | NP_000736.2 | |
| NM_001307945.1 | 1392 | Intron | NP_001294874.1 | |||
| XM_005254142.3 | 1392 | Intron | XP_005254199.1 | |||
| XM_017021881.1 | 1392 | Intron | XP_016877370.1 | |||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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