Variant #0001052044 (NC_000005.9:g.112174096C>A, NM_000038.5:c.2805C>A (APC))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.112174096C>A
DNA change (hg38) -
Published as APC(NM_000038.5):c.2805C>A (p.(Tyr935Ter)), APC(NM_000038.6):c.2805C>A (p.Y935*)
ISCN -
DB-ID APC_000054 See all 54 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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.2805C>A r.(?) p.(Tyr935Ter) - -


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