Product Details

SNP ID
rs201931382
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:96121350 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGCAGGCAGGTTGATCCTGGATTT[A/G]GGAACTGGCTCTGATCCCATGGGTT
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 1946 Silent Mutation CCC,CCT P624P NP_001153682.1
NM_014251.2 1946 Silent Mutation CCC,CCT P623P NP_055066.1
XM_006715831.3 1946 Silent Mutation CCC,CCT P634P XP_006715894.1
XM_011515727.2 1946 Intron XP_011514029.1
XM_017011663.1 1946 Silent Mutation CCC,CCT P620P XP_016867152.1
XM_017011664.1 1946 Silent Mutation CCC,CCT P339P XP_016867153.1
XM_017011665.1 1946 Silent Mutation CCC,CCT P339P XP_016867154.1

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