Variant #0000001691 (NC_000014.8:g.103389039del, NM_030943.3:c.14del (AMN))

Chromosome 14
Allele Both (homozygous)
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.103389039del
DNA change (hg38) g.102922702del
Published as -
ISCN -
DB-ID AMN_000001
Variant remarks 3 Norwegian MGA1 families.
Reference PubMed: Tanner et al. 2003
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/177 CON
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 08:29:52 +02:00 (CEST)
Date last edited 2020-07-06 09:08:01 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMN NM_030943.3 +/+ 01 c.14del r.14del p.Gly5Alafs*12


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