Product Details

SNP ID
rs16891583
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:42755859 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACACACATTTACCTCCTTGGTTTCA[C/T]TGTGGCTCTTCATGTTTTCTGCTAT
Phenotype
MIM: 606888
Polymorphism
C/T, 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 1696 Missense Mutation AAT,AGT N432S NP_001186208.1
NM_004198.3 1696 Missense Mutation AAT,AGT N447S NP_004189.1

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