Variant #0000951581 (NC_000022.10:g.29130652G>A, NM_007194.3:c.58C>T (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.29130652G>A |
DNA change (hg38) |
- |
Published as |
CHEK2(NM_001005735.1):c.58C>T (p.(Gln20Ter)), CHEK2(NM_007194.4):c.58C>T (p.Q20*) |
ISCN |
- |
DB-ID |
CHEK2_000005 See all 6 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) |
0.00015 View details |
Owner |
VKGL-NL_NKI |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_NKI |
Date created |
2023-11-27 17:35:39 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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