Variant #0000571665 (NC_000022.10:g.29090054G>A, NM_007194.3:c.1427C>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.29090054G>A |
| DNA change (hg38) |
g.28694066G>A |
| Published as |
CHEK2(NM_001005735.1):c.1556C>T (p.(Thr519Met)), CHEK2(NM_007194.4):c.1427C>T (p.T476M, p.Thr476Met) |
| ISCN |
- |
| DB-ID |
CHEK2_000009 See all 14 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) |
0.00034 View details |
| Owner |
VKGL-NL_NKI |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_NKI |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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