Product Details

SNP ID
rs200236841
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:96121883 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCTTTTGGTCCTTCTTCACGCAGT[A/G]TCTTTCTAAAGCAGTCTATCACTCC
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 1783 Missense Mutation ACA,ATA T570I NP_001153682.1
NM_014251.2 1783 Missense Mutation ACA,ATA T569I NP_055066.1
XM_006715831.3 1783 Missense Mutation ACA,ATA T580I XP_006715894.1
XM_011515727.2 1783 Intron XP_011514029.1
XM_017011663.1 1783 Missense Mutation ACA,ATA T566I XP_016867152.1
XM_017011664.1 1783 Missense Mutation ACA,ATA T285I XP_016867153.1
XM_017011665.1 1783 Missense Mutation ACA,ATA T285I XP_016867154.1

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