Variant #0000001567 (NC_000003.11:g.49456715T>C, NM_000481.3:c.674A>G (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.49456715T>C
DNA change (hg38) g.49419282T>C
Published as -
ISCN -
DB-ID AMT_000020 See all 2 reported entries
Variant remarks 1 GCE patient
Reference PubMed: Toone et al. 2003
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 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-08-31 10:47:48 +02:00 (CEST)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMT NM_000481.3 +/+ 6 c.674A>G r.(674a>g) p.(Tyr225Cys)


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