Product Details

SNP ID
rs2121467
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:93146351 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TAATTTTCAACTCATTTTATATCAA[A/G]CTATAAAGTTTTTTAAACATCTAAT
Phenotype
MIM: 613760
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC36A4 PubMed Links

Gene Details

Gene
SLC36A4
Gene Name
solute carrier family 36 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286139.1 3844 UTR 3 NP_001273068.1
NM_152313.3 3844 UTR 3 NP_689526.2
XM_017017174.1 3844 Intron XP_016872663.1
XM_017017175.1 3844 Intron XP_016872664.1
XM_017017176.1 3844 Intron XP_016872665.1
XM_017017177.1 3844 Intron XP_016872666.1

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