Variant ID: -

-

Names: -

Organism: -

Variant type: -

Location: -

Frequence: -

Sequence ID: -

Reference bases: -

Alternate bases: -

Ancestral allele: -

Allele origin: -

Svlen: -

HGVS/Genome Variation: -

Molecular consequence : -

Molecular type: -

Clinical significance : -

Gene(s): -

Condition(s): -

Phenotype(s): -

Literature ID: -

Project : -

Identifier(s): -

Variation Set
Variation set IDNamesClinical significanceReview statusLast evaluatedReleated variation
Releated Interpretations
Interpretation IDVariation set IDClinical significanceConditionPhenotypeReview statusLast evaluatedSubmitterComment
Releated Evidences
OriginEthnicityAffetctedLiteratureMethodDescriptionInterpretation id
Call IDAssemblyChrStartEndValidationCopy numberZygosityOriginPhenotypeHGVS/Genome VariationCoverageDescription
Call IDPopulation namePopulation classGroupAllele: frequency (count)Genotype: frequency (count)
Project
Project IDTitleData typeAccession in other databaseRelease dateDescription
Sample
Sample IDSample nameSample titleOrganismSample typeRelated accessionAccession in other databaseRelease dateDescription
Experiment
Experiment IDTitlePlatformStrategySourceSelectionRelated accessionAccession in other databaseRelease date