Variant #0000580758 (NC_000023.10:g.153774272T>C, NM_000402.3:c.189A>G (G6PD))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.153774272T>C |
| DNA change (hg38) |
g.154546057T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
G6PD_000060 See all 3 reported entries |
| Variant remarks |
WHO classification-Class I: severe enzyme deficiency with chronic non-spherocytic haemolytic anaemia (CNSHA) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2019-08-05 12:03:10 +02:00 (CEST) |
| Date last edited |
2019-08-06 13:48:23 +02:00 (CEST) |

Variant on transcripts
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