Product Details

SNP ID

rs199999862

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:154569519 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGGAGCATCTCCTGGATCCTTCCC[A/G]CTACAACAAGCTTATCCGCCCAGCC

Phenotype

MIM: 118507

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CHRNB2 PubMed Links

Gene Details

Gene

CHRNB2

Gene Name

cholinergic receptor nicotinic beta 2 subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000748.2	368	Missense Mutation	CAC,CGC	H41R	NP_000739.1
XM_017000180.1	368	UTR 5			XP_016855669.1

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