Product Details

SNP ID

rs6534638

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:127736799 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCATAGTTAGTGCTCAAGTAATTGT[A/T]ACTAATGTGTATGTGTGTGTTCCTG

Phenotype

MIM: 610796

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

SLC25A31 PubMed Links

Additional Information

For this assay, SNP(s) [rs79716299] 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

SLC25A31

Gene Name

solute carrier family 25 member 31

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318467.1		Intron			NP_001305396.1
NM_031291.3		Intron			NP_112581.1
XM_011532298.1		Intron			XP_011530600.1

View Full Product Details