Product Details

SNP ID

rs6948526

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:143319902 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGATGGGGACTGAGGAATAAAGAAA[A/T]CTGGAGTAGAAACAGGTACAGGGAT

Phenotype

MIM: 118425

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

CLCN1 PubMed Links

Gene Details

Gene

CLCN1

Gene Name

chloride voltage-gated channel 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000083.2		Intron			NP_000074.2
XM_011515782.2		Intron			XP_011514084.1
XM_017011739.1		Intron			XP_016867228.1
XM_017011740.1		Intron			XP_016867229.1

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