Product Details

SNP ID
rs150082469
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:96121909 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTTCTAAAGCAGTCTATCACTCC[A/G]CTGTAAGTGGTTTGGCCAGCCCGGG
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 1757 Silent Mutation AGC,AGT S561S NP_001153682.1
NM_014251.2 1757 Silent Mutation AGC,AGT S560S NP_055066.1
XM_006715831.3 1757 Silent Mutation AGC,AGT S571S XP_006715894.1
XM_011515727.2 1757 Intron XP_011514029.1
XM_017011663.1 1757 Silent Mutation AGC,AGT S557S XP_016867152.1
XM_017011664.1 1757 Silent Mutation AGC,AGT S276S XP_016867153.1
XM_017011665.1 1757 Silent Mutation AGC,AGT S276S XP_016867154.1

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