Annotation Detail
Information
- Associated Genes
- APC
- Associated Variants
-
APC p.Cys1578Gly (p.C1578G)
(
ENST00000257430.9,
ENST00000504915.3,
ENST00000507379.6,
ENST00000508376.6,
ENST00000509732.6,
ENST00000512211.7,
ENST00000713638.1,
ENST00000713639.1 )
APC p.Cys1578Gly (p.C1578G) ( 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.4732T>G (p.Cys1578Gly) AND Familial adenomatous polyposis 1
- ClinVar Allele ID
- 150553
- ClinVar RefSeq Alternation Syntax
- NM_001354903.2:c.4429T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354906.2:c.3883T>G
- ClinVar RefSeq Alternation Syntax
- NM_000038.6:c.4732T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354898.2:c.4657T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354902.2:c.4459T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354905.2:c.4252T>G
- ClinVar RefSeq Alternation Syntax
- NM_001127511.3:c.4678T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354897.2:c.4762T>G
- ClinVar RefSeq Alternation Syntax
- NM_001127510.3:c.4732T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354896.2:c.4786T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354899.2:c.4648T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354895.2:c.4732T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354901.2:c.4555T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354904.2:c.4354T>G
- ClinVar RefSeq Alternation Syntax
- NM_001354900.2:c.4609T>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-02-26
- Clinical Significance Review Status
- reviewed by expert panel
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002514708
- ClinVar Disease
- Familial adenomatous polyposis 1
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs