Annotation Detail
Information
- Associated Genes
- CFTR CFTR-AS1 LOC111674472
- Associated Variants
-
CFTR p.Phe508del (p.F508del)
(
ENST00000003084.11,
ENST00000648260.1,
ENST00000649406.1,
ENST00000649781.2,
ENST00000699596.1,
ENST00000699597.1,
ENST00000699602.1,
ENST00000699605.1 )
CFTR p.Phe508del (p.F508del) ( ENST00000003084.11, ENST00000648260.1, ENST00000649406.1, ENST00000649781.2, ENST00000699596.1, ENST00000699597.1, ENST00000699602.1, ENST00000699605.1 )
CFTR p.Ile1027Thr (p.I1027T) ( ENST00000003084.11, ENST00000648260.1, ENST00000649406.1, ENST00000649781.2, ENST00000699602.1, ENST00000699605.1 )
CFTR p.Ile1027Thr (p.I1027T) ( ENST00000003084.11, ENST00000648260.1, ENST00000649406.1, ENST00000649781.2, ENST00000699602.1, ENST00000699605.1 ) - Associated Disease
- cystic fibrosis
- Source Database
- ClinVar
- Description
- NM_000492.3(CFTR):c.[1521_1523delCTT;3080T>C] AND Cystic fibrosis
- ClinVar Allele ID
- 44524
- ClinVar Allele ID
- 22144
- ClinVar RefSeq Alternation Syntax
- NM_000492.4:c.3080T>C
- ClinVar RefSeq Alternation Syntax
- NM_000492.4:c.1521_1523del
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-03-11
- Clinical Significance Review Status
- reviewed by expert panel
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000785641
- ClinVar Disease
- Cystic fibrosis
- Observed Origin Sample
- germline
Drugs