Product Details

SNP ID

rs148351388

Assay Type

Functionally tested

NCBI dbSNP Submissions

22

Location

Chr.1:167054353 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCTGTCACTGGTCGAGGTGGTCC[A/G]GGGATTCACGCCCAGTGCTCCTCTG

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	1113	Missense Mutation			NP_005805.1
XM_017000005.1	1113	Missense Mutation			XP_016855494.1

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