Product Details

SNP ID

rs349358

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:72539240 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CACATGTGTATGCGCATTTAATTGC[C/T]GTTTGAGGTGGTGTTTTTAATTTAA

Phenotype

MIM: 607738

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

KCNB2 PubMed Links

Gene Details

Gene

KCNB2

Gene Name

potassium voltage-gated channel subfamily B member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004770.2		Intron			NP_004761.2
XM_017013981.1		Intron			XP_016869470.1
XM_017013982.1		Intron			XP_016869471.1

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