Product Details

SNP ID

rs5733

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:23186416 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTCGCCGCATCGTGGTGTCCCGC[G/T]GCCGTCTGCGCCGCCTCCTCTGGAT

Phenotype

MIM: 600761

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SCNN1G PubMed Links

Gene Details

Gene

SCNN1G

Gene Name

sodium channel epithelial 1 gamma subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039.3	284	Missense Mutation	GGC,TGC	G49C	NP_001030.2

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