Annotation Detail
Information
- Associated Genes
- CDKN2A
- Associated Variants
-
CDKN2A p.Ala148Thr (p.A148T)
(
ENST00000498628.6,
ENST00000578845.2,
ENST00000494262.5,
ENST00000530628.2,
ENST00000498124.1,
ENST00000497750.1,
ENST00000579122.1,
ENST00000304494.10,
ENST00000479692.2,
ENST00000579755.2 )
CDKN2A p.Ala148Thr (p.A148T) ( ENST00000579122.1, ENST00000579755.2, ENST00000304494.10, ENST00000479692.2, ENST00000494262.5, ENST00000497750.1, ENST00000498124.1, ENST00000498628.6, ENST00000530628.2, ENST00000578845.2 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_000077.5(CDKN2A):c.442G>A (p.Ala148Thr) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 50019
- ClinVar RefSeq Alternation Syntax
- NM_058195.4:c.*86G>A
- ClinVar RefSeq Alternation Syntax
- NM_001363763.2:c.289G>A
- ClinVar RefSeq Alternation Syntax
- NM_000077.5:c.442G>A
- ClinVar RefSeq Alternation Syntax
- NM_001195132.2:c.442G>A
- ClinVar RefSeq Alternation Syntax
- NM_058197.5:c.*365G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2020-05-10
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000157755
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs