Variant #0000350359 (NC_000005.9:g.112176756T>A, NM_000038.5:c.5465T>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.112176756T>A
DNA change (hg38) g.112841059T>A
Published as APC(NM_000038.4):c.5465T>A (p.V1822D), APC(NM_000038.6):c.5465T>A (p.V1822D), APC(NM_001127510.3):c.5465T>A (p.V1822D)
ISCN -
DB-ID APC_001694 See all 29 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) 0.79376 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.5465T>A r.(?) p.(Val1822Asp) - -


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