Product Details

SNP ID

hCV90256770

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:51993815 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTTAGCTGTTAGACTTGAATATGG[A/T]GATAATGGTACGTTTTGTGGGGAAT

Phenotype

MIM: 610858

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

C14orf166 PubMed Links

Gene Details

Gene

C14orf166

Gene Name

chromosome 14 open reading frame 166

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016039.2		Intron			NP_057123.1

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