Product Details

SNP ID
rs148962110
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:96121309 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCAACTGCCAGTTTGTAGCCCCCA[A/G]CGTGATCAGGATTCGGGGCAGGCAG
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 1987 Missense Mutation NP_001153682.1
NM_014251.2 1987 Missense Mutation NP_055066.1
XM_006715831.3 1987 Missense Mutation XP_006715894.1
XM_011515727.2 1987 Intron XP_011514029.1
XM_017011663.1 1987 Missense Mutation XP_016867152.1
XM_017011664.1 1987 Missense Mutation XP_016867153.1
XM_017011665.1 1987 Missense Mutation XP_016867154.1

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