Product Details

SNP ID
rs5760076
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:23859375 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CAGGATTCTGCCCTCCAGAGCCACT[G/T]CCTCTGCTCCCCCAGCCTCCAGTGC
Phenotype
MIM: 610367
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC2A11 PubMed Links

Gene Details

Gene
SLC2A11
Gene Name
solute carrier family 2 member 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024938.3 Intron NP_001020109.1
NM_001024939.3 Intron NP_001020110.1
NM_001282864.1 Intron NP_001269793.1
NM_030807.4 Intron NP_110434.3

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