Product Details

SNP ID
rs201074878
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:7041761 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAGCGGGAAGCAGCTCCCCCGTC[G/T]CTGGGGGAGGCGTGGCTGGAGGGGA
Phenotype
MIM: 615765
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC16A11 PubMed Links

Gene Details

Gene
SLC16A11
Gene Name
solute carrier family 16 member 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_153357.1 1905 Missense Mutation GAG,GCG E445A NP_699188.1
XM_005256488.3 1905 Missense Mutation GAG,GCG E540A XP_005256545.2
XM_017024281.1 1905 Intron XP_016879770.1
XM_017024282.1 1905 Missense Mutation GAG,GCG E284A XP_016879771.1
Gene
SLC16A13
Gene Name
solute carrier family 16 member 13
There are no transcripts associated with this gene.

View Full Product Details