Variant #0001016736 (NC_000019.9:g.13002675C>G, NM_000159.3:c.158C>G (GCDH))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13002675C>G |
| DNA change (hg38) |
g.12891861C>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GCDH_000333 See all 2 reported entries |
| Variant remarks |
ACMG/ACGS: PM2_Supporting (November 2024) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Alexandra Tibelius |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Alexandra Tibelius |
| Date created |
2024-11-11 12:25:41 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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