Product Details

SNP ID

rs201410035

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:35059622 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGATGGCAGGATCAATGATGTCAGG[A/C]CGGTTGGTAGCGCCAATGATGAACA

Phenotype

MIM: 601023

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

VCP PubMed Links

Gene Details

Gene

VCP

Gene Name

valosin containing protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007126.3	2264	Silent Mutation	CGG,CGT	R625R	NP_009057.1

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