Product Details

SNP ID

rs6002123

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:40774712 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAACATCTGCAGTCTAAGCTCTTCA[C/G]ATTATGTGTTTACATTATAAAAGTG

Phenotype

MIM: 606795

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC25A17 PubMed Links

Gene Details

Gene

SLC25A17

Gene Name

solute carrier family 25 member 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282726.1		Intron			NP_001269655.1
NM_001282727.1		Intron			NP_001269656.1
NM_006358.3		Intron			NP_006349.1

View Full Product Details