Product Details

SNP ID
rs28610064
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:75087913 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTGGAAGGTGGGTCCCCGCCCAC[A/G]CCGCCCTGGGCCCGCCCTGCCTGGC
Phenotype
MIM: 603879
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC16A5 PubMed Links

Gene Details

Gene
SLC16A5
Gene Name
solute carrier family 16 member 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001271765.1 Intron NP_001258694.1
NM_004695.3 Intron NP_004686.1
XM_005257790.1 Intron XP_005257847.1
XM_011525462.1 Intron XP_011523764.1
XM_017025293.1 Intron XP_016880782.1

View Full Product Details