Product Details

SNP ID
rs1805064
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:55656899 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAAGAAGATCGACTTCCTGCTGTCC[A/G]TAGTCGGCTTCGCAGTGGACCTGGC
Phenotype
MIM: 163970
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC6A2 PubMed Links

Gene Details

Gene
SLC6A2
Gene Name
solute carrier family 6 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001043.3 796 Missense Mutation ATA,GTA I69V NP_001034.1
NM_001172501.1 796 Missense Mutation ATA,GTA I69V NP_001165972.1
NM_001172502.1 796 Intron NP_001165973.1
NM_001172504.1 796 Missense Mutation ATA,GTA I69V NP_001165975.1
XM_006721263.2 796 Missense Mutation ATA,GTA I69V XP_006721326.1
XM_011523295.1 796 Missense Mutation ATA,GTA I69V XP_011521597.1
XM_011523296.1 796 Missense Mutation ATA,GTA I69V XP_011521598.1
XM_011523297.2 796 Missense Mutation ATA,GTA I69V XP_011521599.1
XM_011523298.1 796 Missense Mutation ATA,GTA I69V XP_011521600.1
XM_011523299.2 796 Intron XP_011521601.1
XM_011523300.2 796 Intron XP_011521602.1

View Full Product Details