Annotation Detail
Information
- Associated Genes
- CYBA
- Associated Variants
-
CYBA p.Pro156Gln (p.P156Q)
(
ENST00000696163.1,
ENST00000696159.1,
ENST00000696160.1,
ENST00000696157.1,
ENST00000696162.1,
ENST00000696161.1,
ENST00000261623.8,
ENST00000696156.1,
ENST00000696158.1 )
CYBA p.Pro156Gln (p.P156Q) ( ENST00000261623.8, 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.467C>A (p.Pro156Gln) AND Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
- ClinVar Allele ID
- 17299
- ClinVar RefSeq Alternation Syntax
- NM_000101.4:c.467C>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1991-12-15
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000002348
- ClinVar Disease
- Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
- Observed Origin Sample
- germline
- Pubmed
- 1763037
Drugs