BRCA1 ProteinGenes, BRCA1BRCA2 ProteinGenes, BRCA2Genetic VariationMutationGenetic Predisposition to DiseasePolymorphism, Single NucleotideGerm-Line MutationDNA Mutational AnalysisBreast NeoplasmsSequence Analysis, DNAGenetic TestingGenotypeHeterozygoteMolecular Sequence DataOvarian NeoplasmsBase SequenceExonsPedigreeAllelesMutation, MissenseHaplotypesGene FrequencyPolymorphism, GeneticPolymerase Chain ReactionCase-Control StudiesPolymorphism, Single-Stranded ConformationalAnophthalmosPhenotypeJewsFounder EffectGenomic Structural VariationExomeAmino Acid SequenceNeoplastic Syndromes, HereditaryToll-Like Receptor 10Rad51 RecombinaseGenome-Wide Association StudyNeoplasm ProteinsAlternative SplicingMicrophthalmosGenetic Association StudiesIntronsViroidsGenome, HumanBreast Neoplasms, MaleHeteroduplex AnalysisFrameshift MutationTranscription FactorsHomozygotePoint MutationDNA PrimersFamily HealthLinkage DisequilibriumGenetic LinkageIcelandDNA RepairToll-Like Receptor 6Sequence DeletionChromosome MappingGenetic CounselingAmino Acid SubstitutionDNA DamageDNA, NeoplasmDNADNA-Binding ProteinsGenetic MarkersRisk FactorsPromoter Regions, GeneticEye ProteinsGlaucoma, Open-AngleCodon, NonsenseCohort StudiesTransition TemperaturePenetranceExfoliation SyndromeSequence AlignmentVitelliform Macular DystrophyEuropean Continental Ancestry GroupCell Line, TumorNuclear ProteinsModels, GeneticPhylogenyProstatic NeoplasmsGenetic HeterogeneityRNA, MessengerINDEL MutationCell LineHigh-Throughput Nucleotide SequencingGenetic LociUntranslated RegionsTumor Suppressor ProteinsRecombination, GeneticSalpingectomyProtein Structure, TertiaryChromosomes, Human, Pair 17Homologous RecombinationAge of OnsetProtein Isoforms