Variant #0000859658 (NC_000005.9:g.112111322del, NC_000005.9(NM_000038.5):c.423-4del (APC))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.112111322del
DNA change (hg38) -
Published as APC(NM_000038.4):c.423-4delA, APC(NM_000038.5):c.423-4del (p.?), APC(NM_000038.6):c.423-4delA, APC(NM_001127510.3):c.423-4delA
ISCN -
DB-ID APC_000744 See all 13 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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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.423-4del r.spl? p.? - -


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