Product Details

SNP ID
rs143706021
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:96121951 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCCCGGGCAGCCACCTGTAATCT[C/T]GTCTTGATAACATCAGCAGGGGTCA
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 1715 Silent Mutation ACA,ACG T547T NP_001153682.1
NM_014251.2 1715 Silent Mutation ACA,ACG T546T NP_055066.1
XM_006715831.3 1715 Silent Mutation ACA,ACG T557T XP_006715894.1
XM_011515727.2 1715 Intron XP_011514029.1
XM_017011663.1 1715 Silent Mutation ACA,ACG T543T XP_016867152.1
XM_017011664.1 1715 Silent Mutation ACA,ACG T262T XP_016867153.1
XM_017011665.1 1715 Silent Mutation ACA,ACG T262T XP_016867154.1

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