Variant #0000569369 (NC_000020.10:g.31383232C>T, NM_006892.3:c.1144C>T (DNMT3B))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31383232C>T
DNA change (hg38) g.32795426C>T
Published as DNMT3B(NM_006892.3):c.1144C>T (p.R382C), DNMT3B(NM_006892.4):c.1144C>T (p.(Arg382Cys))
ISCN -
DB-ID DNMT3B_000070 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) 0.00053 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNMT3B NM_006892.3 ?/. - c.1144C>T r.(?) p.(Arg382Cys)


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