Variant #0000032862 (NC_000005.9:g.112103031del, APC(NM_000038.5):c.366del)

Individual ID 00013269
Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.112103031del
DNA change (hg38) g.112767334del
Published as 366delG
ISCN -
DB-ID APC_000160 See all 3 reported entries
Variant remarks -
Reference PubMed: Friedl and Aretz 2005
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Stefan Aretz
Database submission license No license selected
Created by Stefan Aretz
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

Exon_old     

DNA change (cDNA)     

RNA change     

Protein     

Predicted     

Predict/PolyPhenScore     

Type/DNA     
APC NM_000038.5 +/+ 6 3 c.366del r.(?) p.(Phe123Leufs*2) frameshift - deletion, small



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000013185 DNA SEQ leukocytes screen APC gene (index patient) APC 1 Stefan Aretz