Variant #0000480226 (NC_000019.9:g.13007063G>C, NM_000159.3:c.680G>C (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.13007063G>C |
| DNA change (hg38) |
g.12896249G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GCDH_000021 See all 30 reported entries |
| Variant remarks |
ACMG/ACGS: PS4_Moderate, PM3_Very Strong, PP4_Moderate, PP3, PS3 (December 2023) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00018 View details |
| 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 12:43:48 +02:00 (CEST) |

Variant on transcripts
|