Variant #0000480213 (NC_000019.9:g.13007748G>A, NM_000159.3:c.877G>A (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.13007748G>A |
DNA change (hg38) |
g.12896934G>A |
Published as |
- |
ISCN |
- |
DB-ID |
GCDH_000006 See all 57 reported entries |
Variant remarks |
ACMG/ACGS: PS4_Moderate, PM3_Very Strong, PP4, PP3_Strong, PS3_Supporting (December 2023) |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
6.0E-5 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 |
2024-12-02 11:59:59 +01:00 (CET) |

Variant on transcripts
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