Variant #0000001700 (NC_000014.8:g.103395855C>T, NM_030943.3:c.742C>T (AMN))

Chromosome 14
Allele Paternal (confirmed)
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.103395855C>T
DNA change (hg38) g.102929518C>T
Published as -
ISCN -
DB-ID AMN_000009
Variant remarks 2 Turkish siblings with MGA1
Reference PubMed: Namour et al. 2011
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 2012-09-07 10:17:34 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMN NM_030943.3 +/+ 07 c.742C>T r.(742c>u) p.(Gln248*)


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