Product Details

SNP ID
rs144769578
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:57407847 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTACGGCATTCCCGATATACCAGA[A/G]AGGGGTGGAAGAATGTCAGAAGAAT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC43A3 PubMed Links

Gene Details

Gene
SLC43A3
Gene Name
solute carrier family 43 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001278201.1 1753 Missense Mutation TCT,TTT S474F NP_001265130.1
NM_001278206.1 1753 Missense Mutation TCT,TTT S487F NP_001265135.1
NM_014096.3 1753 Missense Mutation TCT,TTT S474F NP_054815.2
NM_017611.2 1753 Missense Mutation TCT,TTT S474F NP_060081.1
NM_199329.2 1753 Missense Mutation TCT,TTT S474F NP_955361.1

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