Product Details

SNP ID

rs6770808

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:184347276 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTGACGGAGAAATAGGATGGGGGA[A/G]TAATTCTTAGTCCCATGTTAGAAAG

Phenotype

MIM: 600570

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CLCN2 PubMed Links

Gene Details

Gene

CLCN2

Gene Name

chloride voltage-gated channel 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001171087.2		Intron			NP_001164558.1
NM_001171088.2		Intron			NP_001164559.1
NM_001171089.2		Intron			NP_001164560.1
NM_004366.5		Intron			NP_004357.3
XM_006713489.1		Intron			XP_006713552.1
XM_006713490.2		Intron			XP_006713553.1
XM_011512401.1		Intron			XP_011510703.1

Gene

FAM131A

Gene Name

family with sequence similarity 131 member A

There are no transcripts associated with this gene.

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