Product Details

SNP ID
rs2108976
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:28489005 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCTTGTAATGTCTGGGCTCCCCA[C/G]GGTCAAAGACAAGGTGATATTGAGT
Phenotype
MIM: 604148
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SLC13A2 PubMed Links

Gene Details

Gene
SLC13A2
Gene Name
solute carrier family 13 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145975.1 Intron NP_001139447.1
NM_003984.3 Intron NP_003975.1
XM_006722165.2 Intron XP_006722228.1
XM_011525450.2 Intron XP_011523752.1
XM_011525451.1 Intron XP_011523753.1
XM_011525452.1 Intron XP_011523754.1
XM_011525453.2 Intron XP_011523755.1
XM_011525454.2 Intron XP_011523756.1

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