Product Details

SNP ID

rs16823816

Assay Type

Functionally tested

NCBI dbSNP Submissions

27

Location

Chr.1:20293136 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCCACCCAGGGTGATGACACCAGT[A/G]TTCTGTTCCAAGGAGCTAGGACACC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

VWA5B1 PubMed Links

Gene Details

Gene

VWA5B1

Gene Name

von Willebrand factor A domain containing 5B1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039500.2		Intron			NP_001034589.2
XM_006710360.3		Intron			XP_006710423.2
XM_011540683.2		Intron			XP_011538985.1
XM_011540684.2		Intron			XP_011538986.1
XM_011540685.2		Intron			XP_011538987.1
XM_011540688.2		Intron			XP_011538990.1
XM_011540690.2		Intron			XP_011538992.1
XM_011540691.2		Intron			XP_011538993.1
XM_011540692.2		Intron			XP_011538994.1
XM_011540693.1		Intron			XP_011538995.1
XM_011540695.1		Intron			XP_011538997.1
XM_011540697.2		Intron			XP_011538999.1
XM_011540698.1		Intron			XP_011539000.1
XM_017000305.1		Intron			XP_016855794.1
XM_017000306.1		Intron			XP_016855795.1

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