Variant #0001017071 (NC_000005.9:g.(?_112102013)_(112179833_?)dup, NM_000038.5:c.(?_136-10)_(*10_?)dup (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.(?_112102013)_(112179833_?)dup
DNA change (hg38) g.(?_112766316)_(112844136_?)dup
Published as dup ex3-16
ISCN -
DB-ID APC_002248
Variant remarks ACMG PM2_sup
Reference PubMed: Yin 2024, Journal: Yin 2024
ClinVar ID ClinVar-831727
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.(?_136-10)_(*10_?)dup r.? p.? - -


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