Product Details

SNP ID

rs5257

Assay Type

Functionally tested

NCBI dbSNP Submissions

86

Location

Chr.1:16046629 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGTGGCCCTCGTCTCTTTCTCTTC[A/G]GGCTTCTCTCAGAGCATCACACCCT

Phenotype

MIM: 602023

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CLCNKB PubMed Links

Gene Details

Gene

CLCNKB

Gene Name

chloride voltage-gated channel Kb

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000085.4	476	Silent Mutation	TCA,TCG	S108S	NP_000076.2
NM_001165945.2	476	Intron			NP_001159417.2

View Full Product Details