Product Details

SNP ID

rs9664945

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:114248738 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CATGCCCCCTTTCCTGTTGCTGGAA[A/G]CCGTCTGTGTTTTCCTGTTTTCCAG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

VWA2 PubMed Links

Gene Details

Gene

VWA2

Gene Name

von Willebrand factor A domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001272046.1	293	Missense Mutation	ACC,GCC	T9A	NP_001258975.1
NM_001320804.1	293	Missense Mutation	ACC,GCC	T9A	NP_001307733.1
XM_011539754.2	293	UTR 5			XP_011538056.1
XM_011539757.2	293	Missense Mutation	ACC,GCC	T9A	XP_011538059.1
XM_017016177.1	293	Missense Mutation	ACC,GCC	T19A	XP_016871666.1
XM_017016178.1	293	Missense Mutation	ACC,GCC	T19A	XP_016871667.1
XM_017016179.1	293	Missense Mutation	ACC,GCC	T15A	XP_016871668.1
XM_017016180.1	293	Intron			XP_016871669.1
XM_017016181.1	293	Missense Mutation	ACC,GCC	T19A	XP_016871670.1

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