Annotation Detail
Information
- Associated Genes
- PTCH1 LOC100507346
- Associated Variants
-
PTCH1 p.Ala578= (p.A578=)
(
ENST00000331920.11,
ENST00000429896.6,
ENST00000430669.6,
ENST00000437951.6,
ENST00000692981.1,
ENST00000711046.1 )
PTCH1 p.Ala578= (p.A578=) ( ENST00000331920.11, ENST00000429896.6, ENST00000430669.6, ENST00000437951.6, ENST00000692981.1, ENST00000711046.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_000264.5(PTCH1):c.1734G>A (p.Ala578=) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 221910
- ClinVar RefSeq Alternation Syntax
- NM_001083604.3:c.1281G>A
- ClinVar RefSeq Alternation Syntax
- NM_001083602.3:c.1536G>A
- ClinVar RefSeq Alternation Syntax
- NM_001083603.3:c.1731G>A
- ClinVar RefSeq Alternation Syntax
- NM_001083605.3:c.1281G>A
- ClinVar RefSeq Alternation Syntax
- NM_001083606.3:c.1281G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354918.2:c.1578G>A
- ClinVar RefSeq Alternation Syntax
- NR_038982.1:n.1864C>T
- ClinVar RefSeq Alternation Syntax
- NR_149061.2:n.2639G>A
- ClinVar RefSeq Alternation Syntax
- NM_001083607.3:c.1281G>A
- ClinVar RefSeq Alternation Syntax
- NM_000264.5:c.1734G>A
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2020-10-23
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002256117
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs