Variant #0000352568 (NC_000001.10:g.46663473dup, NM_001243766.1:c.25dup (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.46663473dup
DNA change (hg38) g.46197801dup
Published as 25_26insC
ISCN -
DB-ID POMGNT1_000052 See all 2 reported entries
Variant remarks 1 German 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 14:03:52 +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 +/+? 2 c.25dup r.(25dup) p.(Leu9Profs*20)


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