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SNP ID

rs4347635

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:23296612 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTGGGAAATATTGGAGACAGAAA[A/G]AGGGATAACAAAAAGGACATGGATC

Phenotype

MIM: 600760

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SCNN1B PubMed Links

Gene Details

Gene

SCNN1B

Gene Name

sodium channel epithelial 1 beta subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000336.2		Intron			NP_000327.2

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