Variant #0000275422 (NC_000019.9:g.10270756_10270757del, NC_000019.9(NM_001379.2):c.996-9_996-8del (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.10270756_10270757del
DNA change (hg38) g.10160080_10160081del
Published as DNMT1(NM_001130823.1):c.1044-9_1044-8del (p.(=)), DNMT1(NM_001130823.1):c.1044-9_1044-8delTT, DNMT1(NM_001130823.3):c.1044-9_1044-8delTT
ISCN -
DB-ID DNMT1_000030 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) Retrieve
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 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.996-9_996-8del r.(=) p.(=)


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