Product Details

SNP ID
rs139861447
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32220998 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGATTCGCTCCTCTGTACTGTTCC[A/G]AAGAACCCAGCACAGGCGGTACAGC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC5A4 PubMed Links

Gene Details

Gene
SLC5A4
Gene Name
solute carrier family 5 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014227.2 1572 Missense Mutation CGG,TGG R564W NP_055042.1
XM_006724308.3 1572 Missense Mutation CGG,TGG R518W XP_006724371.1
XM_011530342.2 1572 Missense Mutation CGG,TGG R518W XP_011528644.1
XM_011530343.2 1572 Missense Mutation CGG,TGG R518W XP_011528645.1
XM_011530344.2 1572 Missense Mutation CGG,TGG R495W XP_011528646.1
XM_017028920.1 1572 Missense Mutation CGG,TGG R594W XP_016884409.1

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