Product Details

SNP ID
rs218691
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:6686687 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCATTGCTCACCCCAGTGCCTTAAC[C/T]ATCCTACAAGGACGTGCCAGCTTCC
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 Intron NP_001137310.1
NM_001284509.1 Intron NP_001271438.1
NM_001284510.1 Intron NP_001271439.1
NM_177550.4 Intron NP_808218.1
XM_011523795.2 Intron XP_011522097.1

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