Variant #0000001699 (NC_000014.8:g.103395814G>T, NM_030943.3:c.701G>T (AMN))
| Chromosome |
14 |
| Allele |
Maternal (confirmed) |
| 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.103395814G>T |
| DNA change (hg38) |
g.102929477G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
AMN_000008 |
| Variant remarks |
1 English–Israeli (Jewish Ashkenazi) MGA1 patient (com-het) |
| Reference |
PubMed: Luder et al. 2007 |
| 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 |
2012-09-07 10:01:42 +02:00 (CEST) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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