Product Details

SNP ID

rs10739707

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:128084830 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCAGCCTCTATTGTCTAGATTCTTA[A/G]AACAGTGGTTATTTCTGCAGGTATT

Phenotype

MIM: 608745

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC25A25 PubMed Links

Additional Information

For this assay, SNP(s) [rs79598605] 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

SLC25A25

Gene Name

solute carrier family 25 member 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001006641.3		Intron			NP_001006642.1
NM_001006642.3		Intron			NP_001006643.1
NM_001265614.2		Intron			NP_001252543.1
NM_052901.4		Intron			NP_443133.2
XM_005251688.1		Intron			XP_005251745.1
XM_005251689.4		Intron			XP_005251746.1
XM_006716948.2		Intron			XP_006717011.1
XM_006716949.3		Intron			XP_006717012.1

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