Variant #0001047697 (NC_000022.10:g.41513352C>T, NM_001429.3:c.256C>T (EP300))

Chromosome 22
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.41513352C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID EP300_000265
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1601598122
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-09-05 15:50:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EP300 NM_001429.3 +/. - c.256C>T r.(?) p.(Arg86Ter)


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