Product Details

SNP ID

rs13278992

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:123429947 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAATAATTTAGTAGTGGTTTAACT[A/G]AAGGTATGGCTTACGAAATGTATTG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

WDYHV1 PubMed Links

Additional Information

For this assay, SNP(s) [rs74564385] 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

WDYHV1

Gene Name

WDYHV motif containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001283024.1		Intron			NP_001269953.1
NM_001283027.1		Intron			NP_001269956.1
NM_018024.2		Intron			NP_060494.1
XM_006716597.3		Intron			XP_006716660.1
XM_011517147.1		Intron			XP_011515449.1
XM_011517151.2		Intron			XP_011515453.1
XM_017013601.1		Intron			XP_016869090.1
XM_017013602.1		Intron			XP_016869091.1
XM_017013603.1		Intron			XP_016869092.1

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