Variant #0000001699 (NC_000014.8:g.103395814G>T, NM_030943.3:c.701G>T (AMN))

Chromosome 14
Allele Maternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.103395814G>T
DNA change (hg38) g.102929477G>T
Published as -
ISCN -
DB-ID AMN_000008
Variant remarks 1 English–Israeli (Jewish Ashkenazi) MGA1 patient (com-het)
Reference PubMed: Luder et al. 2007
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 10:01:42 +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.701G>T r.(701g>u) p.(Cys234Phe)


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