Product Details

SNP ID

rs111903589

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:35057142 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTAGCCATACAGGTCATCATCATTG[C/T]CTTCTGTGTATACACTGCCACCTGT

Phenotype

MIM: 601023

Polymorphism

C/T, Transition 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	2785	Missense Mutation	GAC,GGC	D799G	NP_009057.1

View Full Product Details