Product Details

SNP ID
rs61736602
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:20601391 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAACTCAGTAGCCCGCGGGCGCAGG[A/C]GGCCTCTGCAGCTCTGCGGGACTTG
Phenotype
MIM: 604159
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SLC6A5 PubMed Links

Gene Details

Gene
SLC6A5
Gene Name
solute carrier family 6 member 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318369.1 539 UTR 5 NP_001305298.1
NM_004211.4 539 Missense Mutation GAG,GCG E89A NP_004202.3
XM_017018544.1 539 Intron XP_016874033.1
XM_017018545.1 539 Intron XP_016874034.1

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