Variant #0000676597 (NC_000002.11:g.25470960G>A, NM_022552.4:c.801C>T (DNMT3A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.25470960G>A
DNA change (hg38) -
Published as DNMT3A(NM_001320893.1):c.345C>T (p.(Ser115=)), DNMT3A(NM_022552.5):c.801C>T (p.S267=), DNMT3A(NM_175629.2):c.801C>T (p.S267=)
ISCN -
DB-ID DNMT3A_000029 See all 3 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) 0.00248 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNMT3A NM_022552.4 -?/. - c.801C>T r.(?) p.(Ser267=)


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