Variant ID: -

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Source: NCBI ClinVar ( ID 985863 )

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 : -

Variation Set

Variation set ID	Names	Clinical significance	Review status	Last evaluated	Releated variation

Releated Interpretations

Interpretation ID	Variation set ID	Clinical significance	Condition	Phenotype	Review status	Last evaluated	Submitter	Comment

Releated Evidences

Origin	Ethnicity	Affetcted	Literature	Method	Description	Interpretation id

Call ID	Assembly	Chr	Start	End	Validation	Copy number	Zygosity	Origin	Phenotype	HGVS/Genome Variation	Coverage	Description

Call ID	Population name	Population class	Group	Allele: frequency (count)	Genotype: frequency (count)

Project

Project ID	Title	Data type	Accession in other database	Release date	Description

Sample

Sample ID	Sample name	Sample title	Organism	Sample type	Related accession	Accession in other database	Release date	Description

Experiment

Experiment ID	Title	Platform	Strategy	Source	Selection	Related accession	Accession in other database	Release date