Product Details

SNP ID

rs141178771

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:54544667 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGAACGTGACGGCGACCGAGGGGC[A/G]GAATGTGGAGATGTCCTGCGCCTTC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

VSTM2A PubMed Links

Gene Details

Gene

VSTM2A

Gene Name

V-set and transmembrane domain containing 2A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301009.1	531	Missense Mutation	CAG,CGG	Q42R	NP_001287938.1
NM_001317843.1	531	Missense Mutation	CAG,CGG	Q42R	NP_001304772.1
NM_182546.3	531	Missense Mutation	CAG,CGG	Q42R	NP_872352.2
XM_006715665.3	531	Missense Mutation	CAG,CGG	Q42R	XP_006715728.1
XM_006715666.3	531	Missense Mutation	CAG,CGG	Q42R	XP_006715729.1
XM_017011841.1	531	Missense Mutation	CAG,CGG	Q42R	XP_016867330.1

View Full Product Details