Product Details

SNP ID

rs11640350

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:22108555 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATTGGAGGCAAAATCACTTGCTGG[C/G]AGAGTACAGAAAGGGAGTGCTGGAG

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

VWA3A PubMed Links

Additional Information

For this assay, SNP(s) [rs76514362] 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

VWA3A

Gene Name

von Willebrand factor A domain containing 3A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173615.4	778	Intron			NP_775886.3
XM_011545742.2	778	Missense Mutation	GCA,GGA	A171G	XP_011544044.1
XM_011545744.2	778	Intron			XP_011544046.1
XM_011545745.1	778	Intron			XP_011544047.1
XM_011545746.2	778	Intron			XP_011544048.1
XM_017022947.1	778	Missense Mutation	GCA,GGA	A171G	XP_016878436.1
XM_017022948.1	778	Intron			XP_016878437.1
XM_017022949.1	778	Intron			XP_016878438.1

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