Product Details

SNP ID
rs201283753
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:96121931 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCGCTGTAAGTGGTTTGGCCAGCC[C/T]GGGCAGCCACCTGTAATCTCGTCTT
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 1735 Missense Mutation NP_001153682.1
NM_014251.2 1735 Missense Mutation NP_055066.1
XM_006715831.3 1735 Missense Mutation XP_006715894.1
XM_011515727.2 1735 Intron XP_011514029.1
XM_017011663.1 1735 Missense Mutation XP_016867152.1
XM_017011664.1 1735 Missense Mutation XP_016867153.1
XM_017011665.1 1735 Missense Mutation XP_016867154.1

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