Annotation Detail

Information
Associated Genes
APC
Associated Variants
APC p.Ser1068GlyfsTer57 (p.S1068Gfs*57) ( ENST00000257430.9, ENST00000504915.3, ENST00000507379.6, ENST00000508376.6, ENST00000509732.6, ENST00000512211.7, ENST00000713638.1, ENST00000713639.1 )
APC p.Ser1068GlyfsTer57 (p.S1068Gfs*57) ( 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.3202_3205del (p.Ser1068fs) AND Familial adenomatous polyposis 1
ClinVar Allele ID
94473
ClinVar RefSeq Alternation Syntax
NM_001354897.2:c.3232_3235del
ClinVar RefSeq Alternation Syntax
NM_001127511.3:c.3148_3151del
ClinVar RefSeq Alternation Syntax
NM_001354898.2:c.3127_3130del
ClinVar RefSeq Alternation Syntax
NM_001354901.2:c.3025_3028del
ClinVar RefSeq Alternation Syntax
NM_001354905.2:c.2722_2725del
ClinVar RefSeq Alternation Syntax
NM_001354899.2:c.3118_3121del
ClinVar RefSeq Alternation Syntax
NM_001354900.2:c.3079_3082del
ClinVar RefSeq Alternation Syntax
NM_001354902.2:c.2929_2932del
ClinVar RefSeq Alternation Syntax
NM_000038.6:c.3202_3205del
ClinVar RefSeq Alternation Syntax
NM_001354906.2:c.2353_2356del
ClinVar RefSeq Alternation Syntax
NM_001354904.2:c.2824_2827del
ClinVar RefSeq Alternation Syntax
NM_001127510.3:c.3202_3205del
ClinVar RefSeq Alternation Syntax
NM_001354903.2:c.2899_2902del
ClinVar RefSeq Alternation Syntax
NM_001354895.2:c.3202_3205del
ClinVar RefSeq Alternation Syntax
NM_001354896.2:c.3256_3259del
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2023-12-18
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000206027
ClinVar Disease
Familial adenomatous polyposis 1
Observed Origin Sample
germline
Observed Origin Sample
unknown
Drugs