Variant #0000001719 (NC_000014.8:g.103396509_103396516del, NM_030943.3:c.1014_1021del (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.103396509_103396516del
DNA change (hg38) g.102930172_102930179del
Published as -
ISCN -
DB-ID AMN_000020
Variant remarks 2 MGA1 families: 1 Guatemalan (Mayan)/USA and 1
Guatemala (Mayan)/Ireland origin
Reference PubMed: Tanner 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 14:31:12 +02:00 (CEST)
Date last edited 2020-07-06 09:08:22 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMN NM_030943.3 +/+ 09 c.1014_1021del r.(?) p.(Leu339ProfsTer?)


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