| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Intellectual disability syndromic and non-syndromic v2.142 | AFF3_FRA2A_CGG | Zornitza Stark Marked STR: AFF3_FRA2A_CGG as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.142 | AFF3_FRA2A_CGG | Zornitza Stark Str: aff3_fra2a_cgg has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.142 | AFF3_FRA2A_CGG | Zornitza Stark Phenotypes for STR: AFF3_FRA2A_CGG were changed from Neurodevelopmental delay to Neurodevelopmental disorder, MONDO:0700092, AFF3-related | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.141 | Zornitza Stark Copied STR AFF3_FRA2A_CGG from panel Repeat Disorders | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.141 | AFF3_FRA2A_CGG |
Zornitza Stark STR: AFF3_FRA2A_CGG was added STR: AFF3_FRA2A_CGG was added to Intellectual disability syndromic and non-syndromic. Sources: Expert Review Amber,Literature paediatric-onset tags were added to STR: AFF3_FRA2A_CGG. Mode of inheritance for STR: AFF3_FRA2A_CGG was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for STR: AFF3_FRA2A_CGG were set to 24763282; 39313615; 33510257 Phenotypes for STR: AFF3_FRA2A_CGG were set to Neurodevelopmental delay |
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| Intellectual disability syndromic and non-syndromic v2.132 | AFF3 | Zornitza Stark Publications for gene: AFF3 were set to 31388108; 33961779 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.122 | AFF3 | Rylee Peters Phenotypes for gene: AFF3 were changed from KINSSHIP syndrome, MIM# 619297 to KINSSHIP syndrome, MIM# 619297; Neurodevelopmental disorder, MONDO:0700092, AFF3-related | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.121 | AFF3 | Rylee Peters Mode of inheritance for gene: AFF3 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.120 | Rylee Peters Added reviews for gene AFF3 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.0 | AFF3 | Gene migrated from ENSG00000144218 to ENSG00000144218 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v0.3761 | AFF3 | Zornitza Stark Marked gene: AFF3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v0.3761 | AFF3 | Zornitza Stark Gene: aff3 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v0.3761 | AFF3 | Zornitza Stark Phenotypes for gene: AFF3 were changed from to KINSSHIP syndrome, MIM# 619297 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v0.3760 | AFF3 | Zornitza Stark Publications for gene: AFF3 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v0.3759 | AFF3 | Zornitza Stark Mode of inheritance for gene: AFF3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v0.3758 | AFF3 | Zornitza Stark reviewed gene: AFF3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31388108, 33961779; Phenotypes: KINSSHIP syndrome, MIM# 619297; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v0.0 | AFF3 |
Zornitza Stark gene: AFF3 was added gene: AFF3 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland Mode of inheritance for gene: AFF3 was set to Unknown |
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