Annotation Detail
Information
- Associated Genes
- APC
- Associated Variants
-
APC p.Arg499Gly (p.R499G)
(
ENST00000257430.9,
ENST00000504915.3,
ENST00000507379.6,
ENST00000508376.6,
ENST00000509732.6,
ENST00000512211.7,
ENST00000713638.1,
ENST00000713639.1 )
APC p.Arg499Gly (p.R499G) ( 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.1495C>G (p.Arg499Gly) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 49957
- ClinVar RefSeq Alternation Syntax
- NM_001354906.2:c.646C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354900.2:c.1372C>G
- ClinVar RefSeq Alternation Syntax
- NM_001127510.3:c.1495C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354905.2:c.1015C>G
- ClinVar RefSeq Alternation Syntax
- NM_000038.6:c.1495C>G
- ClinVar RefSeq Alternation Syntax
- NM_001127511.3:c.1441C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354895.2:c.1495C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354902.2:c.1222C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354901.2:c.1318C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354899.2:c.1411C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354903.2:c.1192C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354904.2:c.1117C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354897.2:c.1525C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354898.2:c.1420C>G
- ClinVar RefSeq Alternation Syntax
- NM_001354896.2:c.1549C>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-01-18
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000564391
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs