Product Details

SNP ID

rs148037017

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:167055007 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCATCCTCCTTGTCTTCAGTGTTGT[C/T]GTCCTTCCCTCGGCAGCAGCAGCAG

Phenotype

MIM: 602171

Polymorphism

C/T, 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	968	Missense Mutation	AAC,GAC	N266D	NP_005805.1
XM_017000005.1	968	Missense Mutation	AAC,GAC	N158D	XP_016855494.1

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