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Brugada syndrome v0.44 SCN2B Chirag Patel Marked gene: SCN2B as ready
Brugada syndrome v0.44 SCN2B Chirag Patel Gene: scn2b has been classified as Red List (Low Evidence).
Brugada syndrome v0.44 TRPM4 Chirag Patel Marked gene: TRPM4 as ready
Brugada syndrome v0.44 TRPM4 Chirag Patel Gene: trpm4 has been classified as Red List (Low Evidence).
Brugada syndrome v0.44 SLMAP Chirag Patel Marked gene: SLMAP as ready
Brugada syndrome v0.44 SLMAP Chirag Patel Gene: slmap has been classified as Red List (Low Evidence).
Brugada syndrome v0.44 PKP2 Chirag Patel Marked gene: PKP2 as ready
Brugada syndrome v0.44 PKP2 Chirag Patel Gene: pkp2 has been classified as Red List (Low Evidence).
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 v0.43 HCN4 Chirag Patel Marked gene: HCN4 as ready
Brugada syndrome v0.43 HCN4 Chirag Patel Gene: hcn4 has been classified as Red List (Low Evidence).
Brugada syndrome v0.43 ANK2 Chirag Patel Marked gene: ANK2 as ready
Brugada syndrome v0.43 ANK2 Chirag Patel Gene: ank2 has been classified as Red List (Low Evidence).
Brugada syndrome v0.43 PKP2 Chirag Patel gene: PKP2 was added
gene: PKP2 was added to Brugada syndrome. Sources: ClinGen
disputed tags were added to gene: PKP2.
Mode of inheritance for gene: PKP2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: PKP2 were set to Brugada syndrome, MONDO:0015263
Review for gene: PKP2 was set to RED
Added comment: ClinGen DISPUTED - Nov 2017
Sources: ClinGen
Brugada syndrome v0.43 SLMAP Chirag Patel gene: SLMAP was added
gene: SLMAP was added to Brugada syndrome. Sources: ClinGen
disputed tags were added to gene: SLMAP.
Mode of inheritance for gene: SLMAP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: SLMAP were set to Brugada syndrome, MONDO:0015263
Review for gene: SLMAP was set to RED
Added comment: ClinGen DISPUTED - Nov 2017
Sources: ClinGen
Brugada syndrome v0.43 SCN2B Chirag Patel gene: SCN2B was added
gene: SCN2B was added to Brugada syndrome. Sources: ClinGen
disputed tags were added to gene: SCN2B.
Mode of inheritance for gene: SCN2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: SCN2B were set to Brugada syndrome, MONDO:0015263
Review for gene: SCN2B was set to RED
Added comment: ClinGen DISPUTED - Nov 2017
Sources: ClinGen
Brugada syndrome v0.43 TRPM4 Chirag Patel gene: TRPM4 was added
gene: TRPM4 was added to Brugada syndrome. Sources: ClinGen
disputed tags were added to gene: TRPM4.
Mode of inheritance for gene: TRPM4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: TRPM4 were set to Brugada syndrome, MONDO:0015263
Review for gene: TRPM4 was set to RED
Added comment: ClinGen DISPUTED - Nov 2017
Sources: ClinGen
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
Brugada syndrome v0.42 HCN4 Chirag Patel gene: HCN4 was added
gene: HCN4 was added to Brugada syndrome. Sources: ClinGen
disputed tags were added to gene: HCN4.
Mode of inheritance for gene: HCN4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: HCN4 were set to Brugada syndrome, MONDO:0015263
Review for gene: HCN4 was set to RED
Added comment: ClinGen DISPUTED - Nov 2017
Sources: ClinGen
Brugada syndrome v0.42 ANK2 Chirag Patel gene: ANK2 was added
gene: ANK2 was added to Brugada syndrome. Sources: ClinGen
disputed tags were added to gene: ANK2.
Mode of inheritance for gene: ANK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: ANK2 were set to Brugada syndrome, MONDO:0015263
Review for gene: ANK2 was set to RED
Added comment: ClinGen DISPUTED - Nov 2017
Sources: ClinGen
Brugada syndrome v0.41 KCNE3 Chirag Patel Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263
Brugada syndrome v0.41 KCNE3 Chirag Patel Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263
Brugada syndrome v0.41 KCNE3 Chirag Patel Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263
Brugada syndrome v0.41 KCNE3 Chirag Patel Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263
Brugada syndrome v0.41 KCNE3 Chirag Patel Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263
Brugada syndrome v0.41 KCNE3 Chirag Patel Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263
Brugada syndrome v0.40 KCNE3 Chirag Patel Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263
Brugada syndrome v0.40 KCNE3 Chirag Patel Phenotypes for gene: KCNE3 were changed from Brugada syndrome, MONDO:0015263 to Brugada syndrome, MONDO:0015263
Brugada syndrome v0.40 KCNE3 Chirag Patel Phenotypes for gene: KCNE3 were changed from to Brugada syndrome, MONDO:0015263
Brugada syndrome v0.39 CACNA2D1 Chirag Patel Phenotypes for gene: CACNA2D1 were changed from to Brugada syndrome 1, MONDO:0011001
Brugada syndrome v0.38 KCNJ8 Chirag Patel Phenotypes for gene: KCNJ8 were changed from Brugada syndrome 1, MONDO:0011001 to Brugada syndrome 1, MONDO:0011001
Brugada syndrome v0.38 KCNJ8 Chirag Patel Phenotypes for gene: KCNJ8 were changed from Brugada syndrome to Brugada syndrome 1, MONDO:0011001
Brugada syndrome v0.37 SCN1B Chirag Patel Phenotypes for gene: SCN1B were changed from Brugada syndrome 1, MONDO:0011001 to Brugada syndrome 1, MONDO:0011001
Brugada syndrome v0.37 SCN1B Chirag Patel Phenotypes for gene: SCN1B were changed from to Brugada syndrome 1, MONDO:0011001
Brugada syndrome v0.36 KCNH2 Chirag Patel Marked gene: KCNH2 as ready
Brugada syndrome v0.36 KCNH2 Chirag Patel Gene: kcnh2 has been classified as Red List (Low Evidence).
Brugada syndrome v0.36 ABCC9 Chirag Patel Marked gene: ABCC9 as ready
Brugada syndrome v0.36 ABCC9 Chirag Patel Gene: abcc9 has been classified as Red List (Low Evidence).
Brugada syndrome v0.36 ABCC9 Chirag Patel gene: ABCC9 was added
gene: ABCC9 was added to Brugada syndrome. Sources: ClinGen
disputed tags were added to gene: ABCC9.
Mode of inheritance for gene: ABCC9 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: ABCC9 were set to Brugada syndrome, MONDO:0015263
Review for gene: ABCC9 was set to RED
Added comment: ClinGen DISPUTED - Oct 2025
Sources: ClinGen
Brugada syndrome v0.36 KCNH2 Chirag Patel gene: KCNH2 was added
gene: KCNH2 was added to Brugada syndrome. Sources: ClinGen
disputed tags were added to gene: KCNH2.
Mode of inheritance for gene: KCNH2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: KCNH2 were set to Brugada syndrome, MONDO:0015263
Review for gene: KCNH2 was set to RED
Added comment: ClinGen DISPUTED - Jun 2025
Sources: ClinGen
Brugada syndrome v0.35 RANGRF Chirag Patel Marked gene: RANGRF as ready
Brugada syndrome v0.35 RANGRF Chirag Patel Gene: rangrf has been classified as Red List (Low Evidence).
Brugada syndrome v0.35 RANGRF Chirag Patel gene: RANGRF was added
gene: RANGRF was added to Brugada syndrome. Sources: ClinGen
refuted tags were added to gene: RANGRF.
Mode of inheritance for gene: RANGRF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: RANGRF were set to Brugada syndrome, MONDO:0015263
Review for gene: RANGRF was set to RED
Added comment: ClinGen REFUTED - Oct 2025
Sources: ClinGen
Brugada syndrome v0.34 KCND3 Zornitza Stark Phenotypes for gene: KCND3 were changed from to Brugada syndrome
Brugada syndrome v0.33 KCND3 Zornitza Stark Tag disputed tag was added to gene: KCND3.
Brugada syndrome v0.33 CACNB2 Zornitza Stark Tag disputed tag was added to gene: CACNB2.
Brugada syndrome v0.33 CACNA2D1 Zornitza Stark Tag disputed tag was added to gene: CACNA2D1.
Brugada syndrome v0.33 CACNA1C Zornitza Stark Tag disputed tag was added to gene: CACNA1C.
Brugada syndrome v0.33 GPD1L Zornitza Stark Publications for gene: GPD1L were set to 17967977; 19666841
Brugada syndrome v0.32 GPD1L Zornitza Stark Classified gene: GPD1L as Red List (low evidence)
Brugada syndrome v0.32 GPD1L Zornitza Stark Gene: gpd1l has been classified as Red List (Low Evidence).
Brugada syndrome v0.31 SCN1B Zornitza Stark Marked gene: SCN1B as ready
Brugada syndrome v0.31 SCN1B Zornitza Stark Gene: scn1b has been classified as Red List (Low Evidence).
Brugada syndrome v0.31 SCN1B Zornitza Stark Publications for gene: SCN1B were set to
Brugada syndrome v0.30 SCN1B Zornitza Stark Classified gene: SCN1B as Red List (low evidence)
Brugada syndrome v0.30 SCN1B Zornitza Stark Gene: scn1b has been classified as Red List (Low Evidence).
Brugada syndrome v0.29 SCN1B Zornitza Stark Tag disputed tag was added to gene: SCN1B.
Brugada syndrome v0.29 SCN10A Zornitza Stark Marked gene: SCN10A as ready
Brugada syndrome v0.29 SCN10A Zornitza Stark Gene: scn10a has been classified as Red List (Low Evidence).
Brugada syndrome v0.29 SCN10A Zornitza Stark Phenotypes for gene: SCN10A were changed from to Brugada syndrome
Brugada syndrome v0.28 SCN10A Zornitza Stark Publications for gene: SCN10A were set to
Brugada syndrome v0.27 SCN10A Zornitza Stark Classified gene: SCN10A as Red List (low evidence)
Brugada syndrome v0.27 SCN10A Zornitza Stark Gene: scn10a has been classified as Red List (Low Evidence).
Brugada syndrome v0.26 SCN10A Zornitza Stark Tag disputed tag was added to gene: SCN10A.
Brugada syndrome v0.26 KCNJ8 Zornitza Stark Phenotypes for gene: KCNJ8 were changed from to Brugada syndrome
Brugada syndrome v0.25 KCNJ8 Zornitza Stark Marked gene: KCNJ8 as ready
Brugada syndrome v0.25 KCNJ8 Zornitza Stark Gene: kcnj8 has been classified as Red List (Low Evidence).
Brugada syndrome v0.25 KCNJ8 Zornitza Stark Tag disputed tag was added to gene: KCNJ8.
Brugada syndrome v0.25 KCNJ8 Zornitza Stark Publications for gene: KCNJ8 were set to
Brugada syndrome v0.24 KCNJ8 Zornitza Stark Classified gene: KCNJ8 as Red List (low evidence)
Brugada syndrome v0.24 KCNJ8 Zornitza Stark Gene: kcnj8 has been classified as Red List (Low Evidence).
Brugada syndrome v0.23 KCNE3 Zornitza Stark Marked gene: KCNE3 as ready
Brugada syndrome v0.23 KCNE3 Zornitza Stark Gene: kcne3 has been classified as Red List (Low Evidence).
Brugada syndrome v0.23 KCNE3 Zornitza Stark Tag disputed tag was added to gene: KCNE3.
Brugada syndrome v0.23 KCNE3 Zornitza Stark Publications for gene: KCNE3 were set to
Brugada syndrome v0.22 KCNE3 Zornitza Stark Classified gene: KCNE3 as Red List (low evidence)
Brugada syndrome v0.22 KCNE3 Zornitza Stark Gene: kcne3 has been classified as Red List (Low Evidence).
Brugada syndrome v0.21 KCND3 Zornitza Stark Marked gene: KCND3 as ready
Brugada syndrome v0.21 KCND3 Zornitza Stark Gene: kcnd3 has been classified as Red List (Low Evidence).
Brugada syndrome v0.21 KCND3 Zornitza Stark Publications for gene: KCND3 were set to
Brugada syndrome v0.20 KCND3 Zornitza Stark Classified gene: KCND3 as Red List (low evidence)
Brugada syndrome v0.20 KCND3 Zornitza Stark Gene: kcnd3 has been classified as Red List (Low Evidence).
Brugada syndrome v0.19 CACNB2 Zornitza Stark Marked gene: CACNB2 as ready
Brugada syndrome v0.19 CACNB2 Zornitza Stark Gene: cacnb2 has been classified as Red List (Low Evidence).
Brugada syndrome v0.19 CACNB2 Zornitza Stark Publications for gene: CACNB2 were set to
Brugada syndrome v0.18 CACNB2 Zornitza Stark Classified gene: CACNB2 as Red List (low evidence)
Brugada syndrome v0.18 CACNB2 Zornitza Stark Gene: cacnb2 has been classified as Red List (Low Evidence).
Brugada syndrome v0.17 CACNA2D1 Zornitza Stark Marked gene: CACNA2D1 as ready
Brugada syndrome v0.17 CACNA2D1 Zornitza Stark Gene: cacna2d1 has been classified as Red List (Low Evidence).
Brugada syndrome v0.17 CACNA2D1 Zornitza Stark Publications for gene: CACNA2D1 were set to
Brugada syndrome v0.16 CACNA2D1 Zornitza Stark Classified gene: CACNA2D1 as Red List (low evidence)
Brugada syndrome v0.16 CACNA2D1 Zornitza Stark Gene: cacna2d1 has been classified as Red List (Low Evidence).
Brugada syndrome v0.15 CACNA1C Zornitza Stark Marked gene: CACNA1C as ready
Brugada syndrome v0.15 CACNA1C Zornitza Stark Gene: cacna1c has been classified as Red List (Low Evidence).
Brugada syndrome v0.15 CACNA1C Zornitza Stark Publications for gene: CACNA1C were set to
Brugada syndrome v0.14 CACNA1C Zornitza Stark Classified gene: CACNA1C as Red List (low evidence)
Brugada syndrome v0.14 CACNA1C Zornitza Stark Gene: cacna1c has been classified as Red List (Low Evidence).
Brugada syndrome v0.13 SCN3B Ivan Macciocca reviewed gene: SCN3B: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: Brugada syndrome; Mode of inheritance: None
Brugada syndrome v0.13 GPD1L Ivan Macciocca reviewed gene: GPD1L: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.13 SCN5A Ivan Macciocca reviewed gene: SCN5A: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: Brugada syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Brugada syndrome v0.13 SCN1B Ivan Macciocca reviewed gene: SCN1B: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.13 SCN10A Ivan Macciocca reviewed gene: SCN10A: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.13 KCNJ8 Ivan Macciocca reviewed gene: KCNJ8: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.13 KCNE3 Ivan Macciocca reviewed gene: KCNE3: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.13 CACNB2 Ivan Macciocca changed review comment from: disputed by ClinGen (21/11/2017) and recent publication: Circulation. 2018;138:1195–1205 (PMID: 29959160); to: disputed by ClinGen (21/11/2017) and as reported in Circulation. 2018;138:1195–1205 (PMID: 29959160)
Brugada syndrome v0.13 CACNA2D1 Ivan Macciocca changed review comment from: disputed by ClinGen (21/11/2017) and recent publication: Circulation. 2018;138:1195–1205; to: disputed by ClinGen (21/11/2017) and as reported in Circulation. 2018;138:1195–1205 (PMID: 29959160)
Brugada syndrome v0.13 CACNA1C Ivan Macciocca changed review comment from: disputed by ClinGen (21/11/2017) and recent publication: Circulation. 2018;138:1195–1205; to: disputed by ClinGen (21/11/2017) and as reported in Circulation. 2018;138:1195–1205 (PMID: 29959160)
Brugada syndrome v0.13 KCND3 Ivan Macciocca reviewed gene: KCND3: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.13 CACNB2 Ivan Macciocca reviewed gene: CACNB2: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.13 CACNA2D1 Ivan Macciocca reviewed gene: CACNA2D1: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.13 CACNA1C Ivan Macciocca reviewed gene: CACNA1C: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.13 SCN3B Zornitza Stark Phenotypes for gene: SCN3B were changed from Brugada syndrome 7 MIM#613120 to Brugada syndrome 7 MIM#613120
Brugada syndrome v0.13 SCN3B Zornitza Stark Marked gene: SCN3B as ready
Brugada syndrome v0.13 SCN3B Zornitza Stark Gene: scn3b has been classified as Red List (Low Evidence).
Brugada syndrome v0.13 SCN3B Zornitza Stark Phenotypes for gene: SCN3B were changed from to Brugada syndrome 7 MIM#613120
Brugada syndrome v0.12 SCN3B Zornitza Stark Mode of inheritance for gene: SCN3B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Brugada syndrome v0.11 SCN3B Zornitza Stark Classified gene: SCN3B as Red List (low evidence)
Brugada syndrome v0.11 SCN3B Zornitza Stark Gene: scn3b has been classified as Red List (Low Evidence).
Brugada syndrome v0.10 SCN3B Zornitza Stark Tag disputed tag was added to gene: SCN3B.
Brugada syndrome v0.10 GPD1L Zornitza Stark Marked gene: GPD1L as ready
Brugada syndrome v0.10 GPD1L Zornitza Stark Added comment: Comment when marking as ready: Rated as DISPUTED by ClinGen.
Brugada syndrome v0.10 GPD1L Zornitza Stark Gene: gpd1l has been classified as Amber List (Moderate Evidence).
Brugada syndrome v0.10 GPD1L Zornitza Stark Phenotypes for gene: GPD1L were changed from to Brugada syndrome 2, MIM# 611777
Brugada syndrome v0.9 GPD1L Zornitza Stark Publications for gene: GPD1L were set to
Brugada syndrome v0.8 GPD1L Zornitza Stark Mode of inheritance for gene: GPD1L was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Brugada syndrome v0.7 GPD1L Zornitza Stark Tag disputed tag was added to gene: GPD1L.
Brugada syndrome v0.7 GPD1L Zornitza Stark Classified gene: GPD1L as Amber List (moderate evidence)
Brugada syndrome v0.7 GPD1L Zornitza Stark Gene: gpd1l has been classified as Amber List (Moderate Evidence).
Brugada syndrome v0.6 GPD1L Elena Savva reviewed gene: GPD1L: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 17967977, 19666841; Phenotypes: Brugada syndrome 2 611777; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Brugada syndrome v0.6 SCN3B Bryony Thompson reviewed gene: SCN3B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Brugada syndrome 7 MIM#613120; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Brugada syndrome v0.6 SCN5A Zornitza Stark Marked gene: SCN5A as ready
Brugada syndrome v0.6 SCN5A Zornitza Stark Gene: scn5a has been classified as Green List (High Evidence).
Brugada syndrome v0.6 SCN5A Zornitza Stark Phenotypes for gene: SCN5A were changed from to Atrial fibrillation, familial, 10; Brugada syndrome 1; Cardiomyopathy, dilated, 1E; Heart block, nonprogressive; Heart block, progressive, type IA; Long QT syndrome 3; Sick sinus syndrome 1; Ventricular fibrillation, familial, 1; {Sudden infant death syndrome, susceptibility to}
Brugada syndrome v0.6 SCN5A Zornitza Stark Publications for gene: SCN5A were set to
Brugada syndrome v0.5 SCN5A Zornitza Stark Mode of pathogenicity for gene: SCN5A was changed from to Other
Brugada syndrome v0.5 SCN5A Zornitza Stark Mode of inheritance for gene: SCN5A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Brugada syndrome v0.4 SCN5A Elena Savva reviewed gene: SCN5A: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 29806494, 18929244; Phenotypes: Atrial fibrillation, familial, 10, Brugada syndrome 1, Cardiomyopathy, dilated, 1E, Heart block, nonprogressive, Heart block, progressive, type IA, Long QT syndrome 3, Sick sinus syndrome 1, Ventricular fibrillation, familial, 1, {Sudden infant death syndrome, susceptibility to}; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Brugada syndrome v0.4 Zornitza Stark Panel types changed to Victorian Clinical Genetics Services; Rare Disease
Brugada syndrome v0.2 Zornitza Stark Panel name changed from Brugada syndrome_VCGS to Brugada syndrome
Brugada syndrome v0.1 Zornitza Stark Panel types changed to Victorian Clinical Genetics Services
Brugada syndrome v0.0 SCN5A Zornitza Stark gene: SCN5A was added
gene: SCN5A was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: SCN5A was set to Unknown
Brugada syndrome v0.0 SCN3B Zornitza Stark gene: SCN3B was added
gene: SCN3B was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: SCN3B was set to Unknown
Brugada syndrome v0.0 SCN1B Zornitza Stark gene: SCN1B was added
gene: SCN1B was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: SCN1B was set to Unknown
Brugada syndrome v0.0 SCN10A Zornitza Stark gene: SCN10A was added
gene: SCN10A was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: SCN10A was set to Unknown
Brugada syndrome v0.0 KCNJ8 Zornitza Stark gene: KCNJ8 was added
gene: KCNJ8 was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: KCNJ8 was set to Unknown
Brugada syndrome v0.0 KCNE3 Zornitza Stark gene: KCNE3 was added
gene: KCNE3 was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: KCNE3 was set to Unknown
Brugada syndrome v0.0 KCND3 Zornitza Stark gene: KCND3 was added
gene: KCND3 was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: KCND3 was set to Unknown
Brugada syndrome v0.0 GPD1L Zornitza Stark gene: GPD1L was added
gene: GPD1L was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: GPD1L was set to Unknown
Brugada syndrome v0.0 CACNB2 Zornitza Stark gene: CACNB2 was added
gene: CACNB2 was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CACNB2 was set to Unknown
Brugada syndrome v0.0 CACNA2D1 Zornitza Stark gene: CACNA2D1 was added
gene: CACNA2D1 was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CACNA2D1 was set to Unknown
Brugada syndrome v0.0 CACNA1C Zornitza Stark gene: CACNA1C was added
gene: CACNA1C was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CACNA1C was set to Unknown
Brugada syndrome v0.0 Zornitza Stark Added panel Brugada syndrome_VCGS