The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries.
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Curation History
Variant: CA121215 10880
VCEP: Mitochondrial Diseases VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000284.4(PDHA1):c.1142_1145dup (p.Trp383fs) | Pathogenic | pyruvate dehydrogenase deficiency | 2021-05-06 | 1.0 | - | PDHA1 |
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