Variant #0001049131 (NC_000012.11:g.12871135C>T, NM_004064.3:c.362C>T (CDKN1B))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.12871135C>T |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CDKN1B_000029 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs201685429 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
| Owner |
MobiDetails |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
MobiDetails |
| Date created |
2025-10-10 22:50:02 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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