Variant #0001047998 (NC_000002.11:g.25470905C>T, NC_000002.11(NM_022552.4):c.855+1G>A (DNMT3A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25470905C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID DNMT3A_000134
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs772041639
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 2025-09-15 14:07:01 +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     
DNMT3A NM_022552.4 +?/. - c.855+1G>A r.(?) p.(?)


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