Product Details

SNP ID
rs7610064
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:170997547 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AATGATATTCAAATATATAAATATT[A/T]GTTGCATCCTCAGGTTTCTAGTTAT
Phenotype
MIM: 138160
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC2A2 PubMed Links

Gene Details

Gene
SLC2A2
Gene Name
solute carrier family 2 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000340.1 2240 UTR 3 NP_000331.1
NM_001278658.1 2240 UTR 3 NP_001265587.1
NM_001278659.1 2240 UTR 3 NP_001265588.1
XM_011513087.2 2240 UTR 3 XP_011511389.1
XM_011513089.2 2240 UTR 3 XP_011511391.1

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