Product Details

SNP ID

rs3815531

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:12331880 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTTTAGCACCTTTTTCTTCCTTT[A/G]CTTATTTTCCCTTTCTCTGTGTTTC

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

VWDE PubMed Links

Additional Information

For this assay, SNP(s) [rs78617014] 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

VWDE

Gene Name

von Willebrand factor D and EGF domains

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135924.1		Intron			NP_001129396.1
XM_005249641.1		Intron			XP_005249698.1
XM_011515174.1		Intron			XP_011513476.1
XM_011515175.1		Intron			XP_011513477.1
XM_017011828.1		Intron			XP_016867317.1
XM_017011829.1		Intron			XP_016867318.1
XM_017011830.1		Intron			XP_016867319.1

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