Annotation Detail
Information
- Associated Genes
- CYBA
- Associated Variants
-
CYBA p.Arg90Gly (p.R90G)
(
ENST00000696162.1,
ENST00000696157.1,
ENST00000696161.1,
ENST00000696156.1,
ENST00000261623.8,
ENST00000696158.1,
ENST00000569359.5,
ENST00000696163.1,
ENST00000696159.1,
ENST00000567174.5,
ENST00000696160.1 )
CYBA p.Arg90Gly (p.R90G) ( ENST00000261623.8, ENST00000567174.5, ENST00000569359.5, ENST00000696156.1, ENST00000696157.1, ENST00000696158.1, ENST00000696159.1, ENST00000696160.1, ENST00000696161.1, ENST00000696162.1, ENST00000696163.1 ) - Associated Disease
- Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
- Source Database
- ClinVar
- Description
- NM_000101.4(CYBA):c.268C>G (p.Arg90Gly) AND Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
- ClinVar Allele ID
- 1460123
- ClinVar RefSeq Alternation Syntax
- NM_000101.4:c.268C>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2023-07-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002036378
- ClinVar Disease
- Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
- Observed Origin Sample
- germline
Drugs