Variants In Journals

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VariantValidator Portal For Variants In Journals

This web page provides a portal for using the VariantValidator validation process for variants intended for submission to Journals, either within the main manuscript or within accompanying supplementary data.

Select your chosen genome reference (default GRCh38), and select whether your transcript reference sequences are from RefSeq or Ensembl (default RefSeq), then input at least 1 genomic or transcript-based variant description for validation and click the submit button.

Select your preferred genome reference version
Select your preferred transcript reference provider