| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Brugada syndrome v0.44 | KCNE5 | Chirag Patel Mode of inheritance for gene: KCNE5 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to X-LINKED: hemizygous mutation in males, biallelic mutations in females | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.43 | KCNE5 | Chirag Patel Deleted their comment | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.43 | KCNE5 | Chirag Patel edited their review of gene: KCNE5: Added comment: ClinGen DISPUTED - Nov 2017; Changed mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.43 | KCNE5 | Chirag Patel Marked gene: KCNE5 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.43 | KCNE5 | Chirag Patel Gene: kcne5 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.42 | KCNE5 |
Chirag Patel gene: KCNE5 was added gene: KCNE5 was added to Brugada syndrome. Sources: ClinGen disputed tags were added to gene: KCNE5. Mode of inheritance for gene: KCNE5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: KCNE5 were set to Brugada syndrome, MONDO:0015263 Review for gene: KCNE5 was set to RED Added comment: ClinGen DISPUTED - Nov 2017 Sources: ClinGen |
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