Product Details

SNP ID
rs199992589
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:10816386 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCGGCGCCCGCGCGCCACCCGCGC[A/G]TCAAGCGCGACAAGGCGGTCCACGA
Phenotype
MIM: 607952
Polymorphism
A/G, 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_001317406.1 187 Missense Mutation ATC,GTC I41V NP_001304335.1
NM_014229.2 187 Missense Mutation ATC,GTC I41V NP_055044.1
XM_011534033.2 187 Missense Mutation ATC,GTC I41V XP_011532335.1
XM_017007073.1 187 Intron XP_016862562.1

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