Variant #0000262626 (NC_000005.9:g.112162854T>C, NM_000038.5:c.1458T>C (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.112162854T>C
DNA change (hg38) g.112827157T>C
Published as APC(NM_000038.4):c.1458T>C (p.Y486=), APC(NM_000038.6):c.1458T>C (p.Y486=), APC(NM_001127510.3):c.1458T>C (p.Y486=)
ISCN -
DB-ID APC_001726 See all 22 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) 0.58541 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.1458T>C r.(?) p.(Tyr486=) - -


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