Product Details

SNP ID

rs141979531

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:114248740 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCCCCTTTCCTGTTGCTGGAAGC[C/T]GTCTGTGTTTTCCTGTTTTCCAGAG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

VWA2 PubMed Links

Additional Information

For this assay, SNP(s) [rs9664945] are located under a probe 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

VWA2

Gene Name

von Willebrand factor A domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001272046.1	295	Silent Mutation	GCC,GCT	A9A	NP_001258975.1
NM_001320804.1	295	Silent Mutation	GCC,GCT	A9A	NP_001307733.1
XM_011539754.2	295	UTR 5			XP_011538056.1
XM_011539757.2	295	Silent Mutation	GCC,GCT	A9A	XP_011538059.1
XM_017016177.1	295	Silent Mutation	GCC,GCT	A19A	XP_016871666.1
XM_017016178.1	295	Silent Mutation	GCC,GCT	A19A	XP_016871667.1
XM_017016179.1	295	Silent Mutation	GCC,GCT	A15A	XP_016871668.1
XM_017016180.1	295	Intron			XP_016871669.1
XM_017016181.1	295	Silent Mutation	GCC,GCT	A19A	XP_016871670.1

View Full Product Details