Variant #0000352559 (NC_000001.10:g.46659284dup, NM_001243766.1:c.982dup (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.46659284dup
DNA change (hg38) g.46193612dup
Published as 1077insG
ISCN -
DB-ID POMGNT1_000017 See all 3 reported entries
Variant remarks 1 Japan MDDGA3 (MEB) patient (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 2020-06-04 14:00:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMGNT1 NM_001243766.1 +/+? 11 c.982dup r.(982dup) p.(Val328Glyfs*11)


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