Product Details

SNP ID

rs9836566

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:184231277 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTTAGGCTGCACACCTCAATCCG[C/G]CCCCGCGTGGGCCAGTGAATCAAGT

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

VWA5B2 PubMed Links

Additional Information

For this assay, SNP(s) [rs115111989] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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

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