Product Details

SNP ID
rs9904626
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:75095226 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGTGAGCTCTGAATCTGCCACATGG[C/T]CTCTGGCCTGCAGGGTTGGGGCAGG
Phenotype
MIM: 603879
Polymorphism
C/T, 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

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