Product Details

SNP ID
rs199760707
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:48224742 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTCCAGTCGTCCATCCGTGCAAGT[C/T]GAGGGACCATTGGCGGCTATTTCCT
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_001011547.2 221 Nonsense Mutation CGA,TGA R61* NP_001011547.2
NM_001135181.1 221 Nonsense Mutation CGA,TGA R61* NP_001128653.1
XM_011540924.2 221 Nonsense Mutation CGA,TGA R61* XP_011539226.1
XM_011540925.2 221 Nonsense Mutation CGA,TGA R61* XP_011539227.1
XM_011540926.2 221 UTR 5 XP_011539228.1
XM_011540927.1 221 Intron XP_011539229.1
XM_011540928.1 221 UTR 5 XP_011539230.1
XM_011540929.2 221 Nonsense Mutation CGA,TGA R61* XP_011539231.1
XM_017000558.1 221 Nonsense Mutation CGA,TGA R61* XP_016856047.1

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