Annotation Detail
Information
- Associated Genes
- APC
- Associated Variants
-
APC p.Ala545= (p.A545=)
(
ENST00000512211.7,
ENST00000504915.3,
ENST00000257430.9,
ENST00000508376.6,
ENST00000507379.6,
ENST00000509732.6,
ENST00000713638.1,
ENST00000713639.1 )
APC p.Ala545= (p.A545=) ( ENST00000257430.9, ENST00000504915.3, ENST00000507379.6, ENST00000508376.6, ENST00000509732.6, ENST00000512211.7, ENST00000713638.1, ENST00000713639.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_000038.6(APC):c.1635G>A (p.Ala545=) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 51409
- ClinVar RefSeq Alternation Syntax
- NM_001354896.2:c.1689G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354897.2:c.1665G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354904.2:c.1257G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354900.2:c.1512G>A
- ClinVar RefSeq Alternation Syntax
- NM_001127510.3:c.1635G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354898.2:c.1560G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354905.2:c.1155G>A
- ClinVar RefSeq Alternation Syntax
- NM_000038.6:c.1635G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354903.2:c.1332G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354902.2:c.1362G>A
- ClinVar RefSeq Alternation Syntax
- NM_001127511.3:c.1581G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354899.2:c.1551G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354906.2:c.786G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354895.2:c.1635G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354901.2:c.1458G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2016-03-18
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000162371
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs