Product Details

SNP ID
rs3744394
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:6687830 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CGTCTCTGGCAGATAATTCCACCTA[C/T]GGAACACTGAAGGCTGAGGTCAGAG
Phenotype
MIM: 608305
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC13A5 PubMed Links

Gene Details

Gene
SLC13A5
Gene Name
solute carrier family 13 member 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143838.2 1522 Intron NP_001137310.1
NM_001284509.1 1522 Intron NP_001271438.1
NM_001284510.1 1522 Intron NP_001271439.1
NM_177550.4 1522 Intron NP_808218.1
XM_011523795.2 1522 Missense Mutation ATA,GTA I482V XP_011522097.1

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