Product Details

SNP ID

rs45439105

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:132724881 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGCAGGGTAGGTGGGCTCACGGC[A/G]GGGCCGAGACTTCAGTTCTGATAGC

Phenotype

MIM: 606592

Polymorphism

A/G, Transition 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	1046	Missense Mutation			NP_001278631.1
NM_001291703.1	1046	Missense Mutation			NP_001278632.1

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