Product Details

SNP ID

rs4897614

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:132729666 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGCTTAATTTATAGGAGATGGGTC[A/T]TATGTGTGAACATAGCATAGAATGC

Phenotype

MIM: 606592

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

VNN3 PubMed Links

Gene Details

Gene

VNN3

Gene Name

vanin 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291702.1		Intron			NP_001278631.1
NM_001291703.1		Intron			NP_001278632.1

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