Product Details

SNP ID

rs6569837

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:132730507 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTTTCTGTAACACAAAACTGAAA[C/G]GTTGTCATTTGAATAAGTAGGTGTA

Phenotype

MIM: 606592

Polymorphism

C/G, 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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