Annotation Detail
Information
- Associated Genes
- CFTR
- Associated Variants
-
CFTR p.Ala120Thr (p.A120T)
(
ENST00000003084.11,
ENST00000648260.1,
ENST00000649406.1,
ENST00000649781.2,
ENST00000699596.1,
ENST00000699597.1,
ENST00000699602.1,
ENST00000699605.1 )
CFTR p.Ala120Thr (p.A120T) ( ENST00000699602.1, ENST00000699605.1, ENST00000003084.11, ENST00000648260.1, ENST00000649406.1, ENST00000649781.2, ENST00000699596.1, ENST00000699597.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000492.4(CFTR):c.358G>A (p.Ala120Thr) AND not specified
- ClinVar Allele ID
- 68442
- ClinVar RefSeq Alternation Syntax
- NM_000492.4:c.358G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-10-02
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001731339
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs