Variant #0000001569 (NC_000003.11:g.49455407C>T, NC_000003.11(NM_000481.3):c.878-1G>A (AMT))
Chromosome |
3 |
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.49455407C>T |
DNA change (hg38) |
g.49417974C>T |
Published as |
IVS7-1G>A |
ISCN |
- |
DB-ID |
AMT_000022 See all 2 reported entries |
Variant remarks |
5 GCE patients |
Reference |
PubMed: Toone et al. 2001, PubMed: Toone et al. 2001 |
ClinVar ID |
- |
dbSNP ID |
rs181134220 |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
Owner |
Anne Polvi |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Anne Polvi |
Date created |
2012-08-31 10:55:51 +02:00 (CEST) |
Date last edited |
2020-06-15 10:00:04 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|