Variant #0000001555 (NC_000003.11:g.49459656C>A, NM_000481.3:c.139G>T (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.49459656C>A
DNA change (hg38) g.49422223C>A
Published as -
ISCN -
DB-ID AMT_000008
Variant remarks 1 Caucasian GCE family (P34; het)
Reference PubMed: Kure et al. 2006
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 No license selected
Created by Anne Polvi
Date created 2012-08-31 09:06:58 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMT NM_000481.3 +/+ 2 c.139G>T r.(139g>u) p.(Gly47Trp)


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