Product Details

SNP ID

rs111372554

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:167054441 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGAAAGTTCTCTTAGCTGCTCTG[A/G]TGGCTCCTCATAGGCTTCCCGGTTC

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	1025	Missense Mutation	CCA,TCA	P285S	NP_005805.1
XM_017000005.1	1025	Missense Mutation	CCA,TCA	P177S	XP_016855494.1

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