Product Details

SNP ID
rs11890866
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:164907638 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTGAGAATGCACAGGTCCTTTCTTA[C/T]TGCATTCATCCTTATATTCTATTGT
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 2100 Intron NP_001186077.1
NM_173512.2 2100 Intron NP_775783.1
XM_005246350.4 2100 Intron XP_005246407.1
XM_006712337.3 2100 Intron XP_006712400.1
XM_011510737.2 2100 Intron XP_011509039.1
XM_011510742.2 2100 Intron XP_011509044.1
XM_017003455.1 2100 Intron XP_016858944.1
XM_017003456.1 2100 Intron XP_016858945.1
XM_017003457.1 2100 Intron XP_016858946.1
XM_017003458.1 2100 Intron XP_016858947.1
XM_017003459.1 2100 Intron XP_016858948.1
XM_017003460.1 2100 Intron XP_016858949.1
XM_017003461.1 2100 Intron XP_016858950.1
XM_017003462.1 2100 UTR 3 XP_016858951.1
XM_017003463.1 2100 Intron XP_016858952.1
XM_017003464.1 2100 Intron XP_016858953.1
XM_017003465.1 2100 Intron XP_016858954.1

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