Product Details

SNP ID

rs141275388

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:35059601 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATCAAGACGGCCAGGTCTGAGGAT[G/T]GCAGGATCAATGATGTCAGGCCGGT

Phenotype

MIM: 601023

Polymorphism

G/T, 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	2285	Silent Mutation	GCA,GCC	A632A	NP_009057.1

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