Variant #0000001696 (NC_000014.8:g.103396826dup, NM_030943.3:c.1253dup (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.103396826dup
DNA change (hg38) g.102930489dup
Published as c.1253_1254insA
ISCN -
DB-ID AMN_000005
Variant remarks 1 Belgian MGA1 family (het)
Reference PubMed: Tanner et al. 2004
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 09:11:09 +02:00 (CEST)
Date last edited 2020-07-06 09:08:29 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMN NM_030943.3 +/+ 11 c.1253dup r.(?) p.(Leu419AlafsTer?)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.