Variant #0000668772 (NC_000022.10:g.41924482G>A, NC_000022.10(NM_001098.2):c.2209-1G>A (ACO2))
| Chromosome |
22 |
| 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.41924482G>A |
| DNA change (hg38) |
g.41528478G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ACO2_000100 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Marc Ferre |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2020-06-22 19:32:42 +02:00 (CEST) |
| Date last edited |
2020-08-25 21:30:19 +02:00 (CEST) |

Variant on transcripts
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