Product Details

SNP ID
rs11594979
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:114245218 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AATGAGCAGAAACTTGGGCGCCTCT[A/G]GAAAAACATGCAGCTGGGCAAGCAG
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 Intron NP_001258975.1
NM_001320804.1 Intron NP_001307733.1
XM_011539754.2 Intron XP_011538056.1
XM_011539757.2 Intron XP_011538059.1
XM_017016177.1 Intron XP_016871666.1
XM_017016178.1 Intron XP_016871667.1
XM_017016179.1 Intron XP_016871668.1
XM_017016180.1 Intron XP_016871669.1
XM_017016181.1 Intron XP_016871670.1

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