Product Details

SNP ID: rs72551392
Assay Type: DME
NCBI dbSNP Submissions: NA
Location: Chr.4:68670110 on Build GRCh38
Set Membership: DME Validated Inventoried
Context Sequence [VIC/FAM]: GCCAACAGAGAATCGAAGACTGTAC[A/G]GAAAGGGTATGTTAAATAGTTCAGC
Phenotype: MIM: 600069
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: UGT2B15 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001076.3	667	Missense Mutation	CCG,CTG	P170L	NP_001067.2