Product Details

SNP ID

rs4579962

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:117821619 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGTGATCAGCTGCCACCCGGCACT[A/G]CCCTCCGGGAGCTGCCACGGGCAAC

Phenotype

MIM: 601814

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FXYD2 PubMed Links

Additional Information

For this assay, SNP(s) [rs373825817] 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

FXYD2

Gene Name

FXYD domain containing ion transport regulator 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001680.4		Intron			NP_001671.2
NM_021603.3		Intron			NP_067614.1

Gene

FXYD6-FXYD2

Gene Name

FXYD6-FXYD2 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204268.1		Intron			NP_001191197.1
NM_001243598.2		Intron			NP_001230527.1

View Full Product Details