Genes in panel
Regions in panel
Prev Next

Mendeliome

Gene: CYP2A6

Red List (low evidence)

CYP2A6 (cytochrome P450 family 2 subfamily A member 6)
EnsemblGeneIds (GRCh38): ENSG00000255974
EnsemblGeneIds (GRCh37): ENSG00000255974
OMIM: 122720, Gene2Phenotype
CYP2A6 is in 1 panel

1 review

Ain Roesley (Victorian Clinical Genetics Services)

Red List (low evidence)

Only risk alleles mentioned in OMIM.

No other disease associations found via punned
Created: 5 May 2022, 10:27 a.m. | Last Modified: 5 May 2022, 10:27 a.m.
Panel Version: 0.13851

Phenotypes
Coumarin resistance MIM#122700

Variants in this GENE are reported as part of current diagnostic practice

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Coumarin resistance MIM#122700
OMIM
122720
Clinvar variants
Variants in CYP2A6
Penetrance
None
Panels with this gene

History Filter Activity

5 May 2022, Gel status: 1

Entity classified by Genomics England curator

Ain Roesley (Victorian Clinical Genetics Services)

Gene: cyp2a6 has been classified as Red List (Low Evidence).

5 May 2022, Gel status: 1

Set Phenotypes

Ain Roesley (Victorian Clinical Genetics Services)

Phenotypes for gene: CYP2A6 were changed from to Coumarin resistance MIM#122700

5 May 2022, Gel status: 1

Entity classified by Genomics England curator

Ain Roesley (Victorian Clinical Genetics Services)

Gene: cyp2a6 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: CYP2A6 was added gene: CYP2A6 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CYP2A6 was set to Unknown