Product Details

SNP ID

rs1687228

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:184231061 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTCATCCTGGTATTTAGCAGTCG[C/T]GGGCTGGGCACCTGACCTGCGCCAG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

VWA5B2 PubMed Links

Gene Details

Gene

VWA5B2

Gene Name

von Willebrand factor A domain containing 5B2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320373.1		Intron			NP_001307302.1
NM_138345.2		Intron			NP_612354.1
XM_011513288.2		Intron			XP_011511590.1
XM_011513289.2		Intron			XP_011511591.1
XM_011513290.2		Intron			XP_011511592.1
XM_011513291.2		Intron			XP_011511593.1
XM_011513292.2		Intron			XP_011511594.1

View Full Product Details