Variant #0000275450 (NC_000020.10:g.31387951C>T, NC_000020.10(NM_006892.3):c.1760-8C>T (DNMT3B))

Chromosome 20
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.31387951C>T
DNA change (hg38) g.32800145C>T
Published as DNMT3B(NM_001207055.1):c.1574-8C>T (p.(=)), DNMT3B(NM_006892.3):c.1760-8C>T
ISCN -
DB-ID DNMT3B_000052 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) 0.00515 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNMT3B NM_006892.3 -?/. - c.1760-8C>T r.(=) p.(=)


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