Variant #0000480375 (NC_000019.9:g.13002119A>G, NM_000159.3:c.1A>G (GCDH))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Effect unknown |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13002119A>G |
| DNA change (hg38) |
g.12891305A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GCDH_000197 See all 2 reported entries |
| Variant remarks |
ACMG/ACGS: PM3_Supporting, PP4, PVS1_Moderate, 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) |
Retrieve |
| Owner |
Isabelle Rinke |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2019-05-22 09:22:27 +02:00 (CEST) |
| Date last edited |
2024-10-24 14:57:59 +02:00 (CEST) |

Variant on transcripts
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