Variant #0000953644 (NC_000019.9:g.13002214G>A, NC_000019.9(NM_000159.3):c.91+5G>A (GCDH))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
ACMG |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13002214G>A |
| DNA change (hg38) |
g.12891400G>A |
| Published as |
IVS1+5G>A |
| ISCN |
- |
| DB-ID |
GCDH_000277 See all 7 reported entries |
| Variant remarks |
ACMG/ACGS: PS1, PS4_Moderate, PM3, PP3, 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) |
0 View details |
| Owner |
Sabrina Oeser |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Sabrina Oeser |
| Date created |
2023-12-15 15:56:29 +01:00 (CET) |
| Date last edited |
2024-11-08 13:43:06 +01:00 (CET) |

Variant on transcripts
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