Variant #0001017083 (NC_000005.9:g.(?_112090569)_(112181936_?)del, NM_000038.5:c.(?_-18-1)_(*2113_?)del (APC))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_112090569)_(112181936_?)del
DNA change (hg38) g.(?_112754872)_(112846239_?)del
Published as whole gene deletion
ISCN -
DB-ID APC_002228
Variant remarks ACMG PVS1, PS4_very strong, PM2_sup
Reference PubMed: Yin 2024, Journal: Yin 2024
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Stefan Aretz
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-14 12:22:32 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

Exon_old     

DNA change (cDNA)     

RNA change     

Protein     

Predicted     

Type/DNA     
APC NM_000038.5 +/. - - c.(?_-18-1)_(*2113_?)del r.? p.0 - -


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