Annotation Detail
Information
- Associated Genes
- APC
- Associated Variants
-
APC p.Arg805Ter (p.R805*)
(
ENST00000257430.9,
ENST00000504915.3,
ENST00000507379.6,
ENST00000508376.6,
ENST00000509732.6,
ENST00000512211.7,
ENST00000713638.1,
ENST00000713639.1 )
APC p.Arg805Ter (p.R805*) ( ENST00000257430.9, ENST00000504915.3, ENST00000507379.6, ENST00000508376.6, ENST00000509732.6, ENST00000512211.7, ENST00000713638.1, ENST00000713639.1 ) - Associated Disease
- APC-related disorder
- Source Database
- ClinVar
- Description
- NM_000038.6(APC):c.2413C>T (p.Arg805Ter) AND APC-related disorder
- ClinVar Allele ID
- 132738
- ClinVar RefSeq Alternation Syntax
- NM_001354903.2:c.2110C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354906.2:c.1564C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354900.2:c.2290C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354902.2:c.2140C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354895.2:c.2413C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354901.2:c.2236C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127510.3:c.2413C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354904.2:c.2035C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354898.2:c.2338C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354899.2:c.2329C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354905.2:c.1933C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354897.2:c.2443C>T
- ClinVar RefSeq Alternation Syntax
- NM_000038.6:c.2413C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127511.3:c.2359C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354896.2:c.2467C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2024-01-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003935094
- ClinVar Disease
- APC-related disorder
- Observed Origin Sample
- germline
Drugs