Variant #0000001709 (NC_000014.8:g.103394851del, NC_000014.8(NM_030943.3):c.295+1del (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.103394851del
DNA change (hg38) g.102928514del
Published as p.Gly98fs
ISCN -
DB-ID AMN_000010
Variant remarks 1 Yemen MGA1 family (hom)
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 13:06:24 +02:00 (CEST)
Date last edited 2020-07-06 09:08:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMN NM_030943.3 +/+ 04 c.295+1del r.(?) p.(Gly99Alafs*100)


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