Variant #0000675530 (NC_000001.10:g.1653047G>C, NM_024011.2:c.215C>G (CDK11A))
| Chromosome |
1 |
| 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.1653047G>C |
| DNA change (hg38) |
- |
| Published as |
CDK11A(NM_001313896.1):c.215C>G (p.S72*), CDK11B(NM_001787.2):c.215C>G (p.S72C), CDK11B(NM_033487.2):c.-288C>G, CDK11B(NM_033489.2):c.113C>G (p.S38C) |
| ISCN |
- |
| DB-ID |
CDK11A_000011 |
| 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) |
1.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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