Product Details

SNP ID

rs201186970

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:167055078 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGAGGGCTGCAACCACGCCCACC[A/G]CGATGCCCACATACAGGGCCACGTT

Phenotype

MIM: 602171

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

GPA33 PubMed Links

Gene Details

Gene

GPA33

Gene Name

glycoprotein A33

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005814.2	897	Missense Mutation	GCG,GTG	A242V	NP_005805.1
XM_017000005.1	897	Missense Mutation	GCG,GTG	A134V	XP_016855494.1

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