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Load variants

Choose from an example: NA12878 , ClinVar pathogenic

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Dataset:

Select variant

to compare its ΔΔG with known background variants in the same gene, and click

to rerun Maestro, or reload variants:

Missense SNV scatterplot:

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Missense SNVs in selected gene

(Note that this may be across multiple samples in the VCF/dataset)

Rerun Maestro on combined SNVs

Not found