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SNP ID

rs74853650

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:49374055 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCACCTGTGTGCTGGAGTGGCTGG[A/G]GCGGAGGCAGGGGAAGAAGAAACAA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C16orf78 PubMed Links

Gene Details

Gene

C16orf78

Gene Name

chromosome 16 open reading frame 78

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_144602.3	248	Missense Mutation	GAG,GGG	E39G	NP_653203.1

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