Product Details

SNP ID
rs3782369
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:84863448 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTATTTTGTATTTACCTTATCTTC[A/C]ATCCATGCGTTATAGCCAGGAGGAC
Phenotype
MIM: 607971
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SLC6A15 PubMed Links

Gene Details

Gene
SLC6A15
Gene Name
solute carrier family 6 member 15
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146335.2 2304 Missense Mutation ATG,ATT M496I NP_001139807.1
NM_018057.6 2304 Intron NP_060527.2
NM_182767.5 2304 Missense Mutation ATG,ATT M603I NP_877499.1
XM_011538525.2 2304 Intron XP_011536827.1

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