Annotation Detail

Information
Associated Genes
APC
Associated Variants
APC p.Glu313AsnfsTer13 (p.E313Nfs*13) ( ENST00000257430.9, ENST00000504915.3, ENST00000507379.6, ENST00000508376.6, ENST00000509732.6, ENST00000512211.7, ENST00000713638.1, ENST00000713639.1 )
APC p.Glu313AsnfsTer13 (p.E313Nfs*13) ( 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.937_938del (p.Glu313fs) AND Hereditary cancer-predisposing syndrome
ClinVar Allele ID
15870
ClinVar RefSeq Alternation Syntax
NM_001354898.2:c.862_863del
ClinVar RefSeq Alternation Syntax
NM_001354897.2:c.967_968del
ClinVar RefSeq Alternation Syntax
NM_001354896.2:c.937_938del
ClinVar RefSeq Alternation Syntax
NM_000038.6:c.937_938del
ClinVar RefSeq Alternation Syntax
NM_001354906.2:c.88_89del
ClinVar RefSeq Alternation Syntax
NM_001354900.2:c.760_761del
ClinVar RefSeq Alternation Syntax
NM_001354904.2:c.859-300_859-299del
ClinVar RefSeq Alternation Syntax
NM_001354901.2:c.760_761del
ClinVar RefSeq Alternation Syntax
NM_001354899.2:c.853_854del
ClinVar RefSeq Alternation Syntax
NM_001354902.2:c.964-300_964-299del
ClinVar RefSeq Alternation Syntax
NM_001127511.3:c.883_884del
ClinVar RefSeq Alternation Syntax
NM_001127510.3:c.937_938del
ClinVar RefSeq Alternation Syntax
NM_001354903.2:c.934-300_934-299del
ClinVar RefSeq Alternation Syntax
NM_001354895.2:c.937_938del
ClinVar RefSeq Alternation Syntax
NM_001354905.2:c.757-300_757-299del
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2020-02-24
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000772639
ClinVar Disease
Hereditary cancer-predisposing syndrome
Observed Origin Sample
germline
Drugs