Product Details

SNP ID

rs140017632

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:74714196 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGGAGGGGGTGGGAGTTGTCACTG[C/G]GTCTTCAGGTGGGGTTTCTCTGGAG

Phenotype

MIM: 611026

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FA2H PubMed Links

Gene Details

Gene

FA2H

Gene Name

fatty acid 2-hydroxylase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024306.4	888	Silent Mutation	ACC,ACG	T371T	NP_077282.3
XM_011523317.2	888	Intron			XP_011521619.1
XM_011523319.2	888	Silent Mutation	ACC,ACG	T291T	XP_011521621.1

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