Variant #0000001722 (NC_000014.8:g.103396969_103396970del, NM_030943.3:c.1314_1315del (AMN))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.103396969_103396970del |
| DNA change (hg38) |
g.102930632_102930633del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
AMN_000023 |
| Variant remarks |
2 European MGA1 families |
| Reference |
PubMed: Tanner et al. 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-09-10 14:43:14 +02:00 (CEST) |
| Date last edited |
2020-07-06 09:08:30 +02:00 (CEST) |

Variant on transcripts
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