Product Details

SNP ID: rs2073078
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:18952173 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GACCTGGTTTGCCCCTCAGTCCCTC[A/G]GGCTCATACCTAGTGCCTGCGGCAG
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: SLC5A10 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042450.2	170	UTR 5			NP_001035915.1
NM_001270648.1	170	UTR 5			NP_001257577.1
NM_001270649.1	170	UTR 5			NP_001257578.1
NM_001282417.1	170	Intron			NP_001269346.1
NM_152351.4	170	UTR 5			NP_689564.3
XM_011523652.1	170	Missense Mutation	AGG,GGG	R32G	XP_011521954.1
XM_011523653.2	170	Missense Mutation	AGG,GGG	R32G	XP_011521955.1
XM_017024191.1	170	Missense Mutation	AGG,GGG	R32G	XP_016879680.1