Variant #0000352563 (NC_000001.10:g.46660575del, NM_001243766.1:c.593del (POMGNT1))

Chromosome 1
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46660575del
DNA change (hg38) g.46194903del
Published as 593delG
ISCN -
DB-ID POMGNT1_000051 See all 3 reported entries
Variant remarks 1 American and 1 German MDDGA3 (MEB) patient (both com-het)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2013-01-31 14:09:45 +01:00 (CET)
Date last edited 2018-01-19 19:56:48 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMGNT1 NM_001243766.1 +/+? 7 c.593del r.(593del) p.(Ser198Thrfs*43)


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