Product Details

SNP ID
rs138230187
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:164908703 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGACACAAGCGTGGCTACAGTGAT[A/G]ACCATCACTGTTACAACAATGTGGA
Phenotype
MIM: 616526
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC38A11 PubMed Links

Gene Details

Gene
SLC38A11
Gene Name
solute carrier family 38 member 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199148.1 1509 Silent Mutation GTC,GTT V288V NP_001186077.1
NM_173512.2 1509 Silent Mutation GTC,GTT V266V NP_775783.1
XM_005246350.4 1509 Silent Mutation GTC,GTT V344V XP_005246407.1
XM_006712337.3 1509 Silent Mutation GTC,GTT V290V XP_006712400.1
XM_011510737.2 1509 Silent Mutation GTC,GTT V322V XP_011509039.1
XM_011510742.2 1509 Silent Mutation GTC,GTT V149V XP_011509044.1
XM_017003455.1 1509 Silent Mutation GTC,GTT V370V XP_016858944.1
XM_017003456.1 1509 Silent Mutation GTC,GTT V348V XP_016858945.1
XM_017003457.1 1509 Silent Mutation GTC,GTT V345V XP_016858946.1
XM_017003458.1 1509 Silent Mutation GTC,GTT V314V XP_016858947.1
XM_017003459.1 1509 Silent Mutation GTC,GTT V292V XP_016858948.1
XM_017003460.1 1509 Silent Mutation GTC,GTT V370V XP_016858949.1
XM_017003461.1 1509 Silent Mutation GTC,GTT V370V XP_016858950.1
XM_017003462.1 1509 Silent Mutation GTC,GTT V370V XP_016858951.1
XM_017003463.1 1509 Silent Mutation GTC,GTT V222V XP_016858952.1
XM_017003464.1 1509 Silent Mutation GTC,GTT V175V XP_016858953.1
XM_017003465.1 1509 Silent Mutation GTC,GTT V175V XP_016858954.1

View Full Product Details