Incidentalome_PREGEN_DRAFT
Gene: TFG
TFG (TRK-fused gene)
EnsemblGeneIds (GRCh38): ENSG00000114354
EnsemblGeneIds (GRCh37): ENSG00000114354
OMIM: 602498, Gene2Phenotype
TFG is in 7 panels
EnsemblGeneIds (GRCh38): ENSG00000114354
EnsemblGeneIds (GRCh37): ENSG00000114354
OMIM: 602498, Gene2Phenotype
TFG is in 7 panels
1 review
Tony Roscioli (New South Wales Health Pathology)
Comment when marking as ready: may present in childhoodCreated: 20 Jan 2021, 5:19 a.m. | Last Modified: 20 Jan 2021, 5:19 a.m.
Panel Version: 0.27
may present in childhoodCreated: 20 Jan 2021, 5:18 a.m. | Last Modified: 20 Jan 2021, 5:18 a.m.
Panel Version: 0.26
may present in childhoodCreated: 20 Jan 2021, 5:09 a.m. | Last Modified: 20 Jan 2021, 5:09 a.m.
Panel Version: 0.19
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- NSW Health Pathology
- OMIM
- 602498
- Clinvar variants
- Variants in TFG
- Penetrance
- None
- Panels with this gene
History Filter Activity
20 Jan 2021, Gel status: 1
Entity classified by Genomics England curator
Tony Roscioli (New South Wales Health Pathology)Gene: tfg has been classified as Red List (Low Evidence).
20 Jan 2021, Gel status: 1
Entity classified by Genomics England curator
Tony Roscioli (New South Wales Health Pathology)Gene: tfg has been classified as Red List (Low Evidence).
9 Nov 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: TFG was added gene: TFG was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: TFG was set to Unknown