Product Details

SNP ID
rs140440513
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:45759079 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGGTGGAGGAGGCCACAAGCAGCC[C/T]GATGACAGCCAGTGCATAGGCCGGG
Phenotype
MIM: 605616
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC6A20 PubMed Links

Gene Details

Gene
SLC6A20
Gene Name
solute carrier family 6 member 20
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020208.3 2116 Missense Mutation AGG,GGG R560G NP_064593.1
NM_022405.3 2116 Missense Mutation AGG,GGG R523G NP_071800.1
XM_011533847.2 2116 Missense Mutation AGG,GGG R461G XP_011532149.1
XM_011533848.2 2116 Intron XP_011532150.1

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