Product Details

SNP ID

rs12663367

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:132746043 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCACAAAGTGTCTTCACATGCATTA[C/T]CATATTTGATCCTCACCAAATCAGT

Phenotype

MIM: 603571

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

VNN2 PubMed Links

Gene Details

Gene

VNN2

Gene Name

vanin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242350.2		Intron			NP_001229279.1
NM_004665.4		Intron			NP_004656.2
NM_078488.2		Intron			NP_511043.1
XM_006715593.3		Intron			XP_006715656.1
XM_011536231.1		Intron			XP_011534533.1
XM_017011407.1		Intron			XP_016866896.1
XM_017011408.1		Intron			XP_016866897.1
XM_017011409.1		Intron			XP_016866898.1

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