Variant #0001017878 (NC_000019.9:g.13007757G>A, NM_000159.3:c.886G>A (GCDH))
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Probably does not affect function |
Classification method |
ACMG |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13007757G>A |
DNA change (hg38) |
g.12896943G>A |
Published as |
- |
ISCN |
- |
DB-ID |
GCDH_000186 See all 3 reported entries |
Variant remarks |
ACMG/ACGS: PP3_Strong, BS1, BP5 (December 2024) |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00049 View details |
Owner |
Alexandra Tibelius |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Alexandra Tibelius |
Date created |
2024-12-03 12:37:53 +01:00 (CET) |
Date last edited |
2024-12-03 12:38:53 +01:00 (CET) |

Variant on transcripts
|