Product Details

SNP ID
rs61746357
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:10819816 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGAGCAACTGCTTCACTACTGAG[C/T]TACCCTGGGCTACCTGTGGGCATGA
Phenotype
MIM: 607952
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC6A11 PubMed Links

Gene Details

Gene
SLC6A11
Gene Name
solute carrier family 6 member 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001317406.1 562 Silent Mutation CTA,TTA L166L NP_001304335.1
NM_014229.2 562 Silent Mutation CTA,TTA L166L NP_055044.1
XM_011534033.2 562 Silent Mutation CTA,TTA L166L XP_011532335.1
XM_017007073.1 562 UTR 5 XP_016862562.1

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