Product Details

SNP ID
rs201619296
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:22097602 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGAAACACTGGCAGAGATTCAAA[G/A]AAGCCACTAAAGCAGAAGAATATGA
Phenotype
Polymorphism
G/A, Transition substitution
Allele Nomenclature
Literature Links
VWA3A PubMed Links

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_173615.4 398 Silent Mutation AAA,AAG K44K NP_775886.3
XM_011545742.2 398 Silent Mutation AAA,AAG K44K XP_011544044.1
XM_011545744.2 398 Intron XP_011544046.1
XM_011545745.1 398 Intron XP_011544047.1
XM_011545746.2 398 Intron XP_011544048.1
XM_017022947.1 398 Silent Mutation AAA,AAG K44K XP_016878436.1
XM_017022948.1 398 Intron XP_016878437.1
XM_017022949.1 398 Intron XP_016878438.1

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