Variant #0000001720 (NC_000014.8:g.103396737C>T, NC_000014.8(NM_030943.3):c.1170-6C>T (AMN))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.103396737C>T |
| DNA change (hg38) |
g.102930400C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
AMN_000021 See all 3 reported entries |
| Variant remarks |
1 Finnish MGA1 family (het) |
| 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) |
0.00217 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-09-10 14:36:14 +02:00 (CEST) |
| Date last edited |
2020-07-06 09:08:28 +02:00 (CEST) |

Variant on transcripts
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