Variant #0000001718 (NC_000014.8:g.103396459_103396473del, NC_000014.8(NM_030943.3):c.1006+36_1007-29del (AMN))

Chromosome 14
Allele Unknown
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.103396459_103396473del
DNA change (hg38) g.102930122_102930136del
Published as c.1006+36_50del15bp
ISCN -
DB-ID AMN_000019
Variant remarks 1 Belgian MGA1 family (com-het)
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 14:25:13 +02:00 (CEST)
Date last edited 2020-07-06 09:08:21 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMN NM_030943.3 +?/+? i09 c.1006+36_1007-29del r.? p.?


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