Product Details

SNP ID
rs2280456
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:1575871 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAAGGGGAGAAGGTCACGGGGTGGA[A/G]GGGGGAACGAAACAGGAAGGCCCAC
Phenotype
MIM: 610791
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC43A2 PubMed Links

Gene Details

Gene
SLC43A2
Gene Name
solute carrier family 43 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001284498.1 Intron NP_001271427.1
NM_001284499.1 Intron NP_001271428.1
NM_001321364.1 Intron NP_001308293.1
NM_001321365.1 Intron NP_001308294.1
NM_152346.2 Intron NP_689559.1
XM_017024177.1 Intron XP_016879666.1
XM_017024178.1 Intron XP_016879667.1
XM_017024179.1 Intron XP_016879668.1

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