Product Details

SNP ID
rs202153952
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:27200458 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACATCACAGGGAGGTCTCCTGGAGG[A/G]TGCAGGTGGAGCTGCTCCCCTGATA
Phenotype
MIM: 604024
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC5A6 PubMed Links

Gene Details

Gene
SLC5A6
Gene Name
solute carrier family 5 member 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_021095.2 2176 Missense Mutation ACC,ATC T629I NP_066918.2
XM_006712128.1 2176 Missense Mutation ACC,ATC T629I XP_006712191.1
XM_006712129.1 2176 Missense Mutation ACC,ATC T629I XP_006712192.1
XM_006712130.1 2176 Missense Mutation ACC,ATC T629I XP_006712193.1
XM_011533146.2 2176 Missense Mutation ACC,ATC T406I XP_011531448.1
XM_017005216.1 2176 Missense Mutation ACC,ATC T420I XP_016860705.1

View Full Product Details