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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