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Mendeliome v1.4124 SCN10A Chirag Patel changed review comment from: Comment on mode of pathogenicity: AD - GOF
AR - LOF; to: Episodic pain syndrome, familial, 2 MIM#615551 - AD - GOF (green)
Neurodevelopmental disorder (MONDO#0700092), SCN10A-related - AR - LOF (amber)
Mendeliome v1.4124 SCN10A Chirag Patel Deleted their comment
Mendeliome v1.4124 SCN10A Chirag Patel Phenotypes for gene: SCN10A were changed from s) Episodic pain syndrome, familial, 2 MIM#615551; Neurodevelopmental disorder (MONDO#0700092), SCN10A-related to Episodic pain syndrome, familial, 2 MIM#615551; Neurodevelopmental disorder (MONDO#0700092), SCN10A-related
Mendeliome v1.4123 SCN10A Chirag Patel Phenotypes for gene: SCN10A were changed from Episodic pain syndrome, familial, 2, MIM# 615551 to s) Episodic pain syndrome, familial, 2 MIM#615551; Neurodevelopmental disorder (MONDO#0700092), SCN10A-related
Mendeliome v1.4122 SCN10A Chirag Patel Publications for gene: SCN10A were set to 23115331; 33775738; 30731422; 30554136
Mendeliome v1.4121 SCN10A Chirag Patel Mode of inheritance for gene: SCN10A was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v1.4120 SCN10A Chirag Patel Added comment: Comment on mode of pathogenicity: AD - GOF
AR - LOF
Mendeliome v1.4120 SCN10A Chirag Patel Mode of pathogenicity for gene: SCN10A was changed from to Other
Mendeliome v1.4119 Chirag Patel Added reviews for gene SCN10A from panel Genetic Epilepsy
Mendeliome v1.4110 SCN10A Chirag Patel reviewed gene: SCN10A: Rating: GREEN; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.7655 SCN10A Zornitza Stark Marked gene: SCN10A as ready
Mendeliome v0.7655 SCN10A Zornitza Stark Gene: scn10a has been classified as Green List (High Evidence).
Mendeliome v0.7655 SCN10A Zornitza Stark Phenotypes for gene: SCN10A were changed from to Episodic pain syndrome, familial, 2, MIM# 615551
Mendeliome v0.7654 SCN10A Zornitza Stark Publications for gene: SCN10A were set to
Mendeliome v0.7653 SCN10A Zornitza Stark Mode of inheritance for gene: SCN10A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.7652 SCN10A Zornitza Stark reviewed gene: SCN10A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23115331, 33775738, 30731422, 30554136; Phenotypes: Episodic pain syndrome, familial, 2, MIM# 615551; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.0 SCN10A Zornitza Stark gene: SCN10A was added
gene: SCN10A was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: SCN10A was set to Unknown