Product Details

SNP ID
rs74440350
Assay Type
Functionally Tested
NCBI dbSNP Submissions
4
Location
Chr.1:48228891 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTCCAGCAATGTGGGCAGTGGCTT[G/T]TTCATCGGCCTGGCTGGGACAGGGG
Phenotype
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
SLC5A9 PubMed Links

Gene Details

Gene
SLC5A9
Gene Name
solute carrier family 5 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001011547.2 316 Missense Mutation TTG,TTT L92F NP_001011547.2
NM_001135181.1 316 Missense Mutation TTG,TTT L92F NP_001128653.1
XM_011540924.2 316 Missense Mutation TTG,TTT L92F XP_011539226.1
XM_011540925.2 316 Missense Mutation TTG,TTT L92F XP_011539227.1
XM_011540926.2 316 UTR 5 XP_011539228.1
XM_011540927.1 316 UTR 5 XP_011539229.1
XM_011540928.1 316 UTR 5 XP_011539230.1
XM_011540929.2 316 Missense Mutation TTG,TTT L92F XP_011539231.1
XM_017000558.1 316 Missense Mutation TTG,TTT L92F XP_016856047.1

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