Product Details

SNP ID
rs62175628
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:164906408 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGAAATAGATCCTGAACTGTAGTC[C/T]CAAGGTGCAATCACCCATGCAATAA
Phenotype
MIM: 616526
Polymorphism
C/T, 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 Intron NP_001186077.1
NM_173512.2 Intron NP_775783.1
XM_005246350.4 Intron XP_005246407.1
XM_006712337.3 Intron XP_006712400.1
XM_011510737.2 Intron XP_011509039.1
XM_011510742.2 Intron XP_011509044.1
XM_017003455.1 Intron XP_016858944.1
XM_017003456.1 Intron XP_016858945.1
XM_017003457.1 Intron XP_016858946.1
XM_017003458.1 Intron XP_016858947.1
XM_017003459.1 Intron XP_016858948.1
XM_017003460.1 Intron XP_016858949.1
XM_017003461.1 Intron XP_016858950.1
XM_017003462.1 Intron XP_016858951.1
XM_017003463.1 Intron XP_016858952.1
XM_017003464.1 Intron XP_016858953.1
XM_017003465.1 Intron XP_016858954.1

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