Product Details

SNP ID
rs140968602
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:96120939 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCCCCAAATCATGTTAGTGTTGAC[C/T]AAATCCCATCAATTTTCAGATGCAA
Phenotype
MIM: 603859
Polymorphism
C/T, 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 2357 UTR 3 NP_001153682.1
NM_014251.2 2357 UTR 3 NP_055066.1
XM_006715831.3 2357 UTR 3 XP_006715894.1
XM_011515727.2 2357 Intron XP_011514029.1
XM_017011663.1 2357 UTR 3 XP_016867152.1
XM_017011664.1 2357 UTR 3 XP_016867153.1
XM_017011665.1 2357 UTR 3 XP_016867154.1

View Full Product Details