Variant #0000001713 (NC_000014.8:g.103395776G>A, NM_030943.3:c.663G>A (AMN))

Chromosome 14
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.103395776G>A
DNA change (hg38) g.102929439G>A
Published as -
ISCN -
DB-ID AMN_000014
Variant remarks 1 Thai MGA1 patient (hom)
Reference PubMed: Densupsoontorn et al. 2012
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 2012-09-10 13:33:16 +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     
AMN NM_030943.3 +/+ 06 c.663G>A r.(663g>a) p.(Trp221*)


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