Product Details

SNP ID
rs145760709
Assay Type
Functionally tested
NCBI dbSNP Submissions
10
Location
Chr.1:48228851 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTGACCCAACTGTGCCTTGCAGA[C/T]TGGAGCATCTCTGATGTCCAGCAAT
Phenotype
Polymorphism
C/T, Transition 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_001011547.2 276 Missense Mutation ACT,ATT T79I NP_001011547.2
NM_001135181.1 276 Missense Mutation ACT,ATT T79I NP_001128653.1
XM_011540924.2 276 Missense Mutation ACT,ATT T79I XP_011539226.1
XM_011540925.2 276 Missense Mutation ACT,ATT T79I XP_011539227.1
XM_011540926.2 276 UTR 5 XP_011539228.1
XM_011540927.1 276 Intron XP_011539229.1
XM_011540928.1 276 UTR 5 XP_011539230.1
XM_011540929.2 276 Missense Mutation ACT,ATT T79I XP_011539231.1
XM_017000558.1 276 Missense Mutation ACT,ATT T79I XP_016856047.1

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