Product Details

SNP ID

rs200329146

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:85708063 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGCACGACCCTGTCTCATCCAGC[C/G]AGACTAGGAGAAAGAGGGGATGGAC

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C16orf74 PubMed Links

Gene Details

Gene

C16orf74

Gene Name

chromosome 16 open reading frame 74

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_206967.2	352	Missense Mutation	TCG,TGG	S59W	NP_996850.1

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