Variant #0001017060 (NC_000005.9:g.(?_112112293)_(112251318_?)[2], NM_000038.5:c.(?_531+859)_(*71495_?)[2] (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.(?_112112293)_(112251318_?)[2]
DNA change (hg38) g.(?_112776596)_(112915621_?)[2]
Published as GRCh37/hg19 5q22.2(chr5:112112293-112251318)x3, dup ex1-16
ISCN -
DB-ID APC_002200
Variant remarks ACMG PM2_sup
Reference PubMed: Yin 2024, Journal: Yin 2024
ClinVar ID ClinVar-1341140
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
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




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

Exon_old     

DNA change (cDNA)     

RNA change     

Protein     

Predicted     

Type/DNA     
APC NM_000038.5 ?/. - - c.(?_531+859)_(*71495_?)[2] r.? p.? - -


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