Update the Coordinate Search result page to provide a hyperlink directly to ClinVar, based on ClinVar AlleleID (CLNALLELEID).
Be careful about the Variation ID and Allele ID in ClinVar, as they are different. The ID in PubMind is Allele ID, but the ID in ClinVar URL and webpage is Variation ID. The ClinVar version used in PubMind-DB is 20240917.
The website has been updated to support more search functions and improved user interface.
(1) All fields support multiple-term search now — separate each term by a new line.
(2) The Identifier Search allows users to search a variant based on the cDNA or protein change, e.g. BRCA1:c.A122T, BRCA1:p.Arg133Cys
(3) The result page lets users customize which columns to display.
(4) Added genomic variant search under Coordinate Search (VCF-style, e.g. chr17_43100863_C_T).
The latest version is presented at the American Society of Human Genetics (ASHG) 2025 Annual Meeting. The website interface and search functions are still in development, but the content (database itself) is fixed and notification will be sent if database is changed.
Updated: October 16, 2025