Annotation Detail

Information
Associated Genes
APC
Associated Variants
APC p.Asn1981IlefsTer63 (p.N1981Ifs*63) ( ENST00000257430.9, ENST00000504915.3, ENST00000507379.6, ENST00000508376.6, ENST00000509732.6, ENST00000512211.7, ENST00000713638.1, ENST00000713639.1 )
APC p.Asn1981IlefsTer63 (p.N1981Ifs*63) ( ENST00000257430.9, ENST00000504915.3, ENST00000507379.6, ENST00000508376.6, ENST00000509732.6, ENST00000512211.7, ENST00000713638.1, ENST00000713639.1 )
Associated Disease
familial adenomatous polyposis 1
Source Database
ClinVar
Description
NM_000038.6(APC):c.5942del (p.Asn1981fs) AND Familial adenomatous polyposis 1
ClinVar Allele ID
15859
ClinVar RefSeq Alternation Syntax
NM_001354897.2:c.5972del
ClinVar RefSeq Alternation Syntax
NM_001127510.3:c.5942del
ClinVar RefSeq Alternation Syntax
NM_001354899.2:c.5858del
ClinVar RefSeq Alternation Syntax
NM_001354900.2:c.5819del
ClinVar RefSeq Alternation Syntax
NM_001354901.2:c.5765del
ClinVar RefSeq Alternation Syntax
NM_001354896.2:c.5996del
ClinVar RefSeq Alternation Syntax
NM_001354895.2:c.5942del
ClinVar RefSeq Alternation Syntax
NM_001354904.2:c.5564del
ClinVar RefSeq Alternation Syntax
NM_001354903.2:c.5639del
ClinVar RefSeq Alternation Syntax
NM_001354902.2:c.5669del
ClinVar RefSeq Alternation Syntax
NM_001127511.3:c.5888del
ClinVar RefSeq Alternation Syntax
NM_000038.6:c.5942del
ClinVar RefSeq Alternation Syntax
NM_001354898.2:c.5867del
ClinVar RefSeq Alternation Syntax
NM_001354906.2:c.5093del
ClinVar RefSeq Alternation Syntax
NM_001354905.2:c.5462del
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
1996-12-01
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000000862
ClinVar Disease
Familial adenomatous polyposis 1
Observed Origin Sample
germline
Pubmed
8931709
Pubmed
7797123
Drugs