Variant #0000330477 (NC_000005.9:g.112176556G>A, NM_000038.5:c.5265G>A (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.112176556G>A
DNA change (hg38) g.112840859G>A
Published as APC(NM_000038.4):c.5265G>A (p.A1755=), APC(NM_000038.5):c.5265G>A (p.(Ala1755=)), APC(NM_000038.6):c.5265G>A (p.A1755=), APC(NM_001127510.1):c.5265...
ISCN -
DB-ID APC_001690 See all 7 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) 0.00453 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.5265G>A r.(?) p.(Ala1755=) - -


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