Product Details

SNP ID
rs79886797
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:96121918 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCAGTCTATCACTCCGCTGTAAGT[A/G]GTTTGGCCAGCCCGGGCAGCCACCT
Phenotype
MIM: 603859
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC25A13 PubMed Links

Gene Details

Gene
SLC25A13
Gene Name
solute carrier family 25 member 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001160210.1 1748 Silent Mutation ACC,ACT T558T NP_001153682.1
NM_014251.2 1748 Silent Mutation ACC,ACT T557T NP_055066.1
XM_006715831.3 1748 Silent Mutation ACC,ACT T568T XP_006715894.1
XM_011515727.2 1748 Intron XP_011514029.1
XM_017011663.1 1748 Silent Mutation ACC,ACT T554T XP_016867152.1
XM_017011664.1 1748 Silent Mutation ACC,ACT T273T XP_016867153.1
XM_017011665.1 1748 Silent Mutation ACC,ACT T273T XP_016867154.1

View Full Product Details