Product Details

SNP ID
rs6725198
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:98102611 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACCTAATTCAGTCAAGGAAGTTAGC[A/G]AAAATACCAATTTCTTACATTTTGT
Phenotype
MIM: 614884
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
VWA3B PubMed Links
Additional Information
For this assay, SNP(s) [rs76101908,rs76206971] 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
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

View Full Product Details