Product Details

SNP ID

rs12447354

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:2896054 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCCTTCGTCCGTGCTCAGCATGTG[A/G]GAGGCCCATTGGTAGTGGCTGAGTT

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FLYWCH2 PubMed Links

Additional Information

For this assay, SNP(s) [rs115755910] 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

FLYWCH2

Gene Name

FLYWCH family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142499.1		Intron			NP_001135971.1
NM_001142500.1		Intron			NP_001135972.1
NM_138439.2		Intron			NP_612448.1
XM_005255078.4		Intron			XP_005255135.1

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