Variant #0000870928 (NC_000010.10:g.104128551A>C, NM_004193.2:c.2932A>C (GBF1))
| Chromosome |
10 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.104128551A>C |
| DNA change (hg38) |
g.102368794A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GBF1_000008 |
| Variant remarks |
De novo variant |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Gianina Ravenscroft |
| Database submission license |
Creative Commons Attribution-NonCommercial 4.0 International |
| Created by |
Gianina Ravenscroft |
| Date created |
2022-06-22 17:19:28 +02:00 (CEST) |
| Date last edited |
2024-06-24 16:56:22 +02:00 (CEST) |

Variant on transcripts
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