Annotation Detail
Information
- Associated Genes
- APC
- Associated Variants
-
APC p.Asn1979ThrfsTer64 (p.N1979Tfs*64)
(
ENST00000257430.9,
ENST00000504915.3,
ENST00000507379.6,
ENST00000508376.6,
ENST00000509732.6,
ENST00000512211.7,
ENST00000713638.1,
ENST00000713639.1 )
APC p.Asn1979ThrfsTer64 (p.N1979Tfs*64) ( 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.5936_5939del (p.Asn1979fs) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 150577
- ClinVar RefSeq Alternation Syntax
- NM_001354899.2:c.5852_5855del
- ClinVar RefSeq Alternation Syntax
- NM_001354903.2:c.5633_5636del
- ClinVar RefSeq Alternation Syntax
- NM_001354904.2:c.5558_5561del
- ClinVar RefSeq Alternation Syntax
- NM_001127511.3:c.5882_5885del
- ClinVar RefSeq Alternation Syntax
- NM_001127510.3:c.5936_5939del
- ClinVar RefSeq Alternation Syntax
- NM_001354897.2:c.5966_5969del
- ClinVar RefSeq Alternation Syntax
- NM_001354901.2:c.5759_5762del
- ClinVar RefSeq Alternation Syntax
- NM_001354898.2:c.5861_5864del
- ClinVar RefSeq Alternation Syntax
- NM_001354906.2:c.5087_5090del
- ClinVar RefSeq Alternation Syntax
- NM_001354900.2:c.5813_5816del
- ClinVar RefSeq Alternation Syntax
- NM_001354905.2:c.5456_5459del
- ClinVar RefSeq Alternation Syntax
- NM_000038.6:c.5936_5939del
- ClinVar RefSeq Alternation Syntax
- NM_001354902.2:c.5663_5666del
- ClinVar RefSeq Alternation Syntax
- NM_001354896.2:c.5990_5993del
- ClinVar RefSeq Alternation Syntax
- NM_001354895.2:c.5936_5939del
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2012-12-19
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000129077
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs