Product Details

SNP ID

rs150910497

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:49775438 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCCCGCCGGGACGTGGTAGGGGAT[A/G]CCCAGCTCCACTGCGATGGCAGTTG

Phenotype

MIM: 611108

Polymorphism

A/G, 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	559	Missense Mutation	ATA,ATG	I1M	NP_940972.2

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