Variant #0000953710 (NC_000019.9:g.13007115_13007116del, NM_000159.3:c.732_733del (GCDH))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
ACMG |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13007115_13007116del |
| DNA change (hg38) |
g.12896301_12896302del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GCDH_000306 See all 2 reported entries |
| Variant remarks |
ACMG/ACGS: PM3_Supporting, PVS1, PM2_Supporting (December 2023) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Alexandra Tibelius |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Alexandra Tibelius |
| Date created |
2023-12-18 12:35:43 +01:00 (CET) |
| Date last edited |
2024-11-29 10:45:42 +01:00 (CET) |

Variant on transcripts
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