Product Details

SNP ID
rs80074725
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35224982 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGCCCCGCAGGGCCTTCCTTGCC[C/T]CCCGCCACTGGGCATCGTTCTCTCT
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FAM187B PubMed Links

Gene Details

Gene
FAM187B
Gene Name
family with sequence similarity 187 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152481.1 998 Missense Mutation GAG,GGG E318G NP_689694.1

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