Variant #0001016967 (NC_000005.9:g.(?_112073556)_(112090723_112102022)del, NC_000005.9(NM_000038.5):c.(?_-85)_(135+1_136-1)del (APC))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_112073556)_(112090723_112102022)del
DNA change (hg38) g.(?_112737859)_(112755026_112766325)del
Published as del ex1-2
ISCN -
DB-ID APC_000526 See all 4 reported entries
Variant remarks ACMG PS4_sup, 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.(?_-85)_(135+1_136-1)del r.0 p.0 - -


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