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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMT NM_000481.3 +/+ 7i c.878-1G>A r.spl? p.?


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