Product Details

SNP ID
rs10192920
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:164902959 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATTCATAGCACCTGAATACAAATTA[A/G]TATCTACAAAGGTACACAAAAAATA
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 2900 Intron NP_001186077.1
NM_173512.2 2900 Intron NP_775783.1
XM_005246350.4 2900 Intron XP_005246407.1
XM_006712337.3 2900 Intron XP_006712400.1
XM_011510737.2 2900 Intron XP_011509039.1
XM_011510742.2 2900 Intron XP_011509044.1
XM_017003455.1 2900 Intron XP_016858944.1
XM_017003456.1 2900 Intron XP_016858945.1
XM_017003457.1 2900 Intron XP_016858946.1
XM_017003458.1 2900 Intron XP_016858947.1
XM_017003459.1 2900 Intron XP_016858948.1
XM_017003460.1 2900 Intron XP_016858949.1
XM_017003461.1 2900 UTR 3 XP_016858950.1
XM_017003462.1 2900 Intron XP_016858951.1
XM_017003463.1 2900 Intron XP_016858952.1
XM_017003464.1 2900 Intron XP_016858953.1
XM_017003465.1 2900 Intron XP_016858954.1

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