Variant #0001017062 (NC_000005.9:g.(?_111420575)_(112116548_?)[2], NM_000038.5:c.(?_-653066)_(593_?)[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.(?_111420575)_(112116548_?)[2]
DNA change (hg38) g.(?_112084878)_(112780851_?)[2]
Published as GRCh37/hg19 5q22.1-22.2(chr5:111420575-112116548)x3, dup ex1-16
ISCN -
DB-ID APC_002202
Variant remarks ACMG PM2_sup
Reference PubMed: Yin 2024, Journal: Yin 2024
ClinVar ID ClinVar-980178
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.(?_-653066)_(593_?)[2] r.? p.? - -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.