Variant #0000866764 (NC_000022.10:g.29083961C>A, NM_007194.3:c.1556G>T (CHEK2))

Chromosome 22
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.29083961C>A
DNA change (hg38) -
Published as CHEK2(NM_001005735.1):c.1685G>T (p.(Arg562Leu)), CHEK2(NM_007194.4):c.1556G>T (p.Arg519Leu, p.R519L)
ISCN -
DB-ID CHEK2_000036 See all 9 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHEK2 NM_007194.3 ?/. - c.1556G>T r.(?) p.(Arg519Leu)


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