Variant #0000273525 (NC_000022.10:g.29091857del, NM_007194.3:c.1100del (CHEK2))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29091857del
DNA change (hg38) g.28695869del
Published as CHEK2(NM_001005735.1):c.1229delC (p.(Thr410Metfs*15)), CHEK2(NM_007194.4):c.1100delC (p.T367Mfs*15)
ISCN -
DB-ID CHEK2_000001 See all 33 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) 0.00208 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 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     
CHEK2 NM_007194.3 +/. 11 c.1100del r.(?) p.(Thr367MetfsTer15)


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