Annotation Detail
Information
- Associated Genes
- APC
- Associated Variants
-
APC p.Glu991Ter (p.E991*)
(
ENST00000512211.7,
ENST00000257430.9,
ENST00000508376.6,
ENST00000504915.3,
ENST00000507379.6,
ENST00000509732.6,
ENST00000713638.1,
ENST00000713639.1 )
APC p.Glu991Ter (p.E991*) ( 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.2971G>T (p.Glu991Ter) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 182372
- ClinVar RefSeq Alternation Syntax
- NM_001354899.2:c.2887G>T
- ClinVar RefSeq Alternation Syntax
- NM_001127511.3:c.2917G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354900.2:c.2848G>T
- ClinVar RefSeq Alternation Syntax
- NM_000038.6:c.2971G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354897.2:c.3001G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354904.2:c.2593G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354895.2:c.2971G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354901.2:c.2794G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354905.2:c.2491G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354898.2:c.2896G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354903.2:c.2668G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354906.2:c.2122G>T
- ClinVar RefSeq Alternation Syntax
- NM_001127510.3:c.2971G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354902.2:c.2698G>T
- ClinVar RefSeq Alternation Syntax
- NM_001354896.2:c.3025G>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-09-30
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000166096
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs