Variant #0000692748 (NC_000019.9:g.33792565C>A, NM_004364.3:c.756G>T (CEBPA))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.33792565C>A |
| DNA change (hg38) |
- |
| Published as |
CEBPA(NM_001285829.1):c.399G>T (p.(Ala133=)), CEBPA(NM_004364.3):c.756G>T (p.A252=), CEBPA(NM_004364.5):c.756G>T (p.A252=) |
| ISCN |
- |
| DB-ID |
CEBPA_000016 See all 3 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) |
0.00178 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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