Product Details

SNP ID
rs139568359
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:42755931 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCTTCAACTTCAGGCGAGTGCTCC[A/G]AATTTTCCACCACCCACTGTAATGG
Phenotype
MIM: 606888
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CHRNA6 PubMed Links

Gene Details

Gene
CHRNA6
Gene Name
cholinergic receptor nicotinic alpha 6 subunit
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199279.1 1624 Missense Mutation TCG,TTG S408L NP_001186208.1
NM_004198.3 1624 Missense Mutation TCG,TTG S423L NP_004189.1

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