Product Details

SNP ID

rs9874

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:101271199 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAACATTTTCAGCTACAGAAAATA[C/T]ATTCAAGGAAGAATGTTAAAAAGTT

Phenotype

MIM: 607918

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

VIMP PubMed Links

Gene Details

Gene

VIMP

Gene Name

VCP interacting membrane selenoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018445.5	1127	Intron			NP_060915.2
NM_203472.2	1127	UTR 3			NP_982298.2

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