Variant #0000859652 (NC_000005.9:g.112043492C>A, NM_000038.5:c.-30149C>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.112043492C>A
DNA change (hg38) -
Published as APC(NM_001127511.2):c.78C>A (p.(Ser26Arg)), APC(NM_001354897.2):c.78C>A (p.S26R)
ISCN -
DB-ID APC_001971 See all 2 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) 0.00191 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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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.-30149C>A r.(?) p.(=) - -


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