Product Details

SNP ID
rs9640226
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:140339107 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCACAGCTCACTGTAACTTCCCTTC[A/G]TTTCTTTTTAATGGCTCATTAGTAT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC37A3 PubMed Links

Gene Details

Gene
SLC37A3
Gene Name
solute carrier family 37 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001287498.1 Intron NP_001274427.1
NM_032295.3 Intron NP_115671.1
NM_207113.2 Intron NP_996996.1
XM_011516626.2 Intron XP_011514928.1
XM_011516627.2 Intron XP_011514929.1
XM_017012712.1 Intron XP_016868201.1
XM_017012713.1 Intron XP_016868202.1
XM_017012714.1 Intron XP_016868203.1
XM_017012715.1 Intron XP_016868204.1
XM_017012716.1 Intron XP_016868205.1
XM_017012717.1 Intron XP_016868206.1
XM_017012718.1 Intron XP_016868207.1

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