Variant #0000681219 (NC_000019.9:g.10279007G>A, NM_001379.2:c.754C>T (DNMT1))

Chromosome 19
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.10279007G>A
DNA change (hg38) -
Published as DNMT1(NM_001130823.1):c.802C>T (p.(Pro268Ser)), DNMT1(NM_001130823.3):c.802C>T (p.P268S)
ISCN -
DB-ID DNMT1_000080 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) Retrieve
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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNMT1 NM_001379.2 ?/. - c.754C>T r.(?) p.(Pro252Ser)


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