Variant #0000953647 (NC_000019.9:g.13002684T>G, NM_000159.3:c.167T>G (GCDH))
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Classification method |
ACMG |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13002684T>G |
DNA change (hg38) |
g.12891870T>G |
Published as |
- |
ISCN |
- |
DB-ID |
GCDH_000280 See all 2 reported entries |
Variant remarks |
ACMG/ACGS: PM3_Supporting, PP3_Strong, 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 |
Sabrina Oeser |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Sabrina Oeser |
Date created |
2023-12-15 16:10:12 +01:00 (CET) |
Date last edited |
2024-11-11 13:54:46 +01:00 (CET) |

Variant on transcripts
|