Annotation Detail
Information
- Associated Genes
- CFTR
- Associated Variants
-
CFTR p.Gln1352His (p.Q1352H)
(
ENST00000003084.11,
ENST00000649781.2,
ENST00000699602.1,
ENST00000699605.1 )
CFTR p.Gln1352His (p.Q1352H) ( ENST00000003084.11, ENST00000649781.2, ENST00000699602.1, ENST00000699605.1 ) - Associated Disease
- CFTR-related disorder
- Source Database
- ClinVar
- Description
- NM_000492.4(CFTR):c.4056G>C (p.Gln1352His) AND CFTR-related disorder
- ClinVar Allele ID
- 22276
- ClinVar RefSeq Alternation Syntax
- NM_000492.4:c.4056G>C
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2024-01-18
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001009487
- ClinVar Disease
- CFTR-related disorder
- Observed Origin Sample
- germline
Drugs