Variant #0000565550 (NC_000019.9:g.10292756G>A, NC_000019.9(NM_001379.2):c.81-3C>T (DNMT1))

Chromosome 19
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.10292756G>A
DNA change (hg38) g.10182080G>A
Published as DNMT1(NM_001130823.1):c.81-3C>T (p.?), DNMT1(NM_001379.3):c.81-3C>T
ISCN -
DB-ID DNMT1_000086 See all 2 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) 0.00035 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 11:45:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNMT1 NM_001379.2 -?/. - c.81-3C>T r.spl? p.?


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