Annotation Detail
Information
- Associated Genes
- APC
- Associated Variants
-
APC p.Arg414Cys (p.R414C)
(
ENST00000504915.3,
ENST00000257430.9,
ENST00000507379.6,
ENST00000508376.6,
ENST00000509732.6,
ENST00000512211.7,
ENST00000713638.1,
ENST00000713639.1 )
APC p.Arg414Cys (p.R414C) ( ENST00000257430.9, ENST00000504915.3, ENST00000507379.6, ENST00000508376.6, ENST00000509732.6, ENST00000512211.7, ENST00000713638.1, ENST00000713639.1 ) - Associated Disease
- familial adenomatous polyposis 1
- Source Database
- ClinVar
- Description
- NM_000038.6(APC):c.1240C>T (p.Arg414Cys) AND Familial adenomatous polyposis 1
- ClinVar Allele ID
- 15836
- ClinVar RefSeq Alternation Syntax
- NM_001354900.2:c.1063C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354899.2:c.1156C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127510.3:c.1240C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354897.2:c.1270C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354896.2:c.1240C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354902.2:c.967C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354906.2:c.391C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354895.2:c.1240C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354901.2:c.1063C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354903.2:c.937C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354904.2:c.862C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354905.2:c.760C>T
- ClinVar RefSeq Alternation Syntax
- NM_000038.6:c.1240C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354898.2:c.1165C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127511.3:c.1186C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2023-02-18
- Clinical Significance Review Status
- reviewed by expert panel
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000122757
- ClinVar Disease
- Familial adenomatous polyposis 1
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs