Annotation Detail
Information
- Associated Genes
- APC
- Associated Variants
-
APC p.Gln1406Ter (p.Q1406*)
(
ENST00000512211.7,
ENST00000508376.6,
ENST00000257430.9,
ENST00000504915.3,
ENST00000507379.6,
ENST00000509732.6,
ENST00000713638.1,
ENST00000713639.1 )
APC p.Gln1406Ter (p.Q1406*) ( 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.4216C>T (p.Gln1406Ter) AND Familial adenomatous polyposis 1
- ClinVar Allele ID
- 152233
- ClinVar RefSeq Alternation Syntax
- NM_001354906.2:c.3367C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354902.2:c.3943C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354904.2:c.3838C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354895.2:c.4216C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354901.2:c.4039C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354903.2:c.3913C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354900.2:c.4093C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354897.2:c.4246C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354905.2:c.3736C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354899.2:c.4132C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354896.2:c.4270C>T
- ClinVar RefSeq Alternation Syntax
- NM_000038.6:c.4216C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127511.3:c.4162C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127510.3:c.4216C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354898.2:c.4141C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-05-10
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003337237
- ClinVar Disease
- Familial adenomatous polyposis 1
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs