Product Details

SNP ID

rs145354319

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:49775441 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGCCGGGACGTGGTAGGGGATGCC[C/T]AGCTCCACTGCGATGGCAGTTGGCG

Phenotype

MIM: 611108

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

VWC2 PubMed Links

Gene Details

Gene

VWC2

Gene Name

von Willebrand factor C domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198570.4	562	Silent Mutation	CCC,CCT	P2P	NP_940972.2

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