Product Details

SNP ID
rs6713479
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:98099930 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGTTATTATCATGCCAATCTCTCT[G/T]ACATTTTTTATTCTGGTAACTTATG
Phenotype
MIM: 614884
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
VWA3B PubMed Links

Gene Details

Gene
VWA3B
Gene Name
von Willebrand factor A domain containing 3B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_144992.4 Intron NP_659429.4
XM_005263897.2 Intron XP_005263954.1
XM_006712357.2 Intron XP_006712420.1
XM_006712359.3 Intron XP_006712422.1
XM_006712360.3 Intron XP_006712423.1
XM_011510770.1 Intron XP_011509072.1
XM_011510771.2 Intron XP_011509073.1
XM_011510772.1 Intron XP_011509074.1
XM_011510774.1 Intron XP_011509076.1
XM_011510775.2 Intron XP_011509077.1
XM_017003560.1 Intron XP_016859049.1
XM_017003561.1 Intron XP_016859050.1
XM_017003562.1 Intron XP_016859051.1
XM_017003563.1 Intron XP_016859052.1
XM_017003564.1 Intron XP_016859053.1

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