Product Details

SNP ID
rs202181933
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:30198523 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGTGTTTCTGGGGTAATACTTTTA[A/G]TAATACGCTATTGGGAAGAAAATAC
Phenotype
MIM: 182138
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC6A4 PubMed Links

Gene Details

Gene
SLC6A4
Gene Name
solute carrier family 6 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001045.5 2402 Missense Mutation ACT,ATT T609I NP_001036.1

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