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Mitochondrial disorder with complex III deficiency v1.6 UQCR10 Arina Puzriakova Classified gene: UQCR10 as Red List (low evidence)
Mitochondrial disorder with complex III deficiency v1.6 UQCR10 Arina Puzriakova Added comment: Comment on list classification: Demoting to Red as there is no evidence for Mendelian gene-disease association at this time
Mitochondrial disorder with complex III deficiency v1.6 UQCR10 Arina Puzriakova Gene: uqcr10 has been classified as Red List (Low Evidence).
Mitochondrial disorder with complex III deficiency v0.19 UQCR10 Ellen McDonagh Marked gene: UQCR10 as ready
Mitochondrial disorder with complex III deficiency v0.19 UQCR10 Ellen McDonagh Added comment: Comment when marking as ready: This gene should remain Amber due to the overall review and evidence assessment from the GMS mitochondrial specialist test group, submitted by Carl Fratter.
Mitochondrial disorder with complex III deficiency v0.19 UQCR10 Ellen McDonagh Gene: uqcr10 has been classified as Amber List (Moderate Evidence).
Mitochondrial disorder with complex III deficiency v0.16 UQCR10 Carl Fratter reviewed gene: UQCR10: Rating: AMBER; Mode of pathogenicity: ; Publications: none found; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Mitochondrial disorder with complex III deficiency v0.14 UQCR10 Anna de Burca Classified gene: UQCR10 as Amber List (moderate evidence)
Mitochondrial disorder with complex III deficiency v0.14 UQCR10 Anna de Burca Gene: uqcr10 has been classified as Amber List (Moderate Evidence).
Mitochondrial disorder with complex III deficiency v0.3 UQCR10 Ivone Leong reviewed gene: UQCR10: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Mitochondrial disorder with complex III deficiency v0.2 UQCR10 Ivone Leong gene: UQCR10 was added
gene: UQCR10 was added to Mitochondrial disorder with complex III deficiency. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: UQCR10 was set to Unknown
Phenotypes for gene: UQCR10 were set to No OMIM phenotype