Variant #0000547104 (NC_000012.11:g.12871186_12871187insT, NM_004064.3:c.413_414insT (CDKN1B))
| Chromosome |
12 |
| 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.12871186_12871187insT |
| DNA change (hg38) |
g.12718252_12718253insT |
| Published as |
CDKN1B(NM_004064.5):c.413_414insT (p.D139Gfs*66) |
| ISCN |
- |
| DB-ID |
CDKN1B_000013 |
| 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_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
|