Variant #0000001717 (NC_000014.8:g.103396439_103396453del, NC_000014.8(NM_030943.3):c.1006+16_1006+30del (AMN))

Chromosome 14
Allele Both (homozygous)
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.103396439_103396453del
DNA change (hg38) g.102930102_102930116del
Published as c.1006+16_30del15bp
ISCN -
DB-ID AMN_000018
Variant remarks 2 Jemen brothers (hom) with MGA1
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 14:20:15 +02:00 (CEST)
Date last edited 2020-07-06 09:08:20 +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+16_1006+30del r.(=) p.(=)


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