Phommarinh, M.

mutation database genome population information findbase browser phenotype disorder variant ucsc genome browser query frequency table region source project group locus genome browser track locus variants track encode sequence entry nemdb institute result figure university issue disease phencode patrino search page curator blood mutat example research variation world map mutation frequencies encode project consortium data source color ¢ gure number acids research fibrosis deletion hbvar genetic software format script home page data sources details page data entry pennsylvania state university function 2002. genet patient apoa 5 gene 10.1002/ content reference study swiss-prot detail thalassemia mutations hemoglobin variants consortium grant frequency range query results query returns search genomic