Variant #0000953642 (NC_000019.9:g.13002128A>T, NM_000159.3:c.10A>T (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.13002128A>T |
| DNA change (hg38) |
g.12891314A>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GCDH_000275 See all 2 reported entries |
| Variant remarks |
ACMG/ACGS: PVS1,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 12:21:20 +01:00 (CET) |
| Date last edited |
2024-11-12 13:34:06 +01:00 (CET) |

Variant on transcripts
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