A Ideal LSDB Homepage
| General information | Links to other servers | Information for patients or clinicians | Gene and Protein |
| Name, Web address, FTP location | Gene related sites | Disease | Species |
| Contact curator | Disease related sites | Treatment | Gene symbols and synonyms |
| Goals of Database and Guidelines | Genome databases (HUGO, GDB..) | Mutations in other Species | Genetic locus (approved nomenclature) |
| Date of Creation | Disease databases (OMIM..) | Diagnosis | Chromosome location |
| Last Update | Sequence databases | Reference sequence | |
| List of options | (DDBJ/EMBL/GenBank/NCBl..) | Protein function | |
| List of Consortium members | Protein Databases (SwissProt..) | Tissue distribution | |
| List of Contributors | Central mutation databases (HGMD..) | Structures including 3D | |
| Literature reference to the database | Bibliographic databases (MEDLINE) | Phylogenic tree | |
| Copyright notice | Expression analysis | ||
| Disclaimer | Molecular modeling |
| B Ideal LSDB Mutation or Polymorphism Data | ||
| Mutation submission form | Mutation tables | Quality control of data |
| Recommended Allele Nomenclature use | Complete Mutation table | MDI Quality Assurance checklist |
| HUGO-MDI Allele variant entry form use | Summary Tables | EMQN |
| Polymorphism Table | Approved Primer Sequences | |
| Graphical Displays | Approved Technical Protocols | |
| Statistics | ||
| Patient data | Search by mutation | Search by type of mutation |
| Unique Database Identifier | Systematic name (HUGO) | Missense |
| Sample source and ID | Trivial name | Nonsense |
| Genotype | Exon, intron, UTR, Other | Post-elongation |
| Origin-geographic | CpG site | Deletion frameshift |
| Origin-ethnic | Restriction Enzyme site | Deletion in-frame |
| Phenotype | Amino Acid change | Deletion in UTR |
| Molecular | RNA change | Deletion of exons |
| Clinical | Method of Detection | Insertion frameshift |
| Inheritance | Haplotype | Insertion in-frame |
| Environmental exposures | Population data | Complex |
| Submitter and date of report | Splice site | |
| Reference (with link to MEDLINE) | Silent substitution | |
| Multiple DNA changes in one allele | Disease-causing mutation | |
| Penetrance | Change not causing disease | |
| Comments | Don't know | |