Product Details

SNP ID

rs115072733

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:39383902 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACCCTTTTCCGCGCCCCAGGGTGC[G/T]CTCAGGATTTAGGATGCGGCGGGAG

Phenotype

MIM: 610819

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

SLC25A38 PubMed Links

Additional Information

For this assay, SNP(s) [rs116056544] 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

SLC25A38

Gene Name

solute carrier family 25 member 38

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017875.2		Intron			NP_060345.2
XM_006713214.1		Intron			XP_006713277.1
XM_011533869.2		Intron			XP_011532171.1
XM_017006710.1		Intron			XP_016862199.1

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