Product Details

SNP ID

rs139629514

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:110739263 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCACTGGGTGACGACTCCCCCAGA[C/T]ATCCCCGGCAGCCGCAACCTGCACT

Phenotype

MIM: 610826

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC25A46 PubMed Links

Additional Information

For this assay, SNP(s) [rs145421520] 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

SLC25A46

Gene Name

solute carrier family 25 member 46

There are no transcripts associated with this gene.

Gene

TMEM232

Gene Name

transmembrane protein 232

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039763.3		Intron			NP_001034852.3
XM_006714670.3		Intron			XP_006714733.1
XM_011543552.2		Intron			XP_011541854.1
XM_011543553.2		Intron			XP_011541855.1
XM_011543555.2		Intron			XP_011541857.1
XM_011543556.1		Intron			XP_011541858.1
XM_011543557.2		Intron			XP_011541859.1
XM_011543559.2		Intron			XP_011541861.1
XM_011543560.2		Intron			XP_011541862.1
XM_011543561.2		Intron			XP_011541863.1
XM_011543563.2		Intron			XP_011541865.1
XM_011543564.2		Intron			XP_011541866.1
XM_011543565.2		Intron			XP_011541867.1
XM_011543566.2		Intron			XP_011541868.1
XM_011543567.2		Intron			XP_011541869.1
XM_017009704.1		Intron			XP_016865193.1
XM_017009705.1		Intron			XP_016865194.1
XM_017009706.1		Intron			XP_016865195.1
XM_017009707.1		Intron			XP_016865196.1

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