Variant #0000320394 (NC_000002.11:g.1748227T>C, NM_012293.1:c.1A>G (PXDN))

Chromosome 2
Allele Maternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1748227T>C
DNA change (hg38) g.1744455T>C
Published as -
ISCN -
DB-ID PXDN_000029
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Celia Zazo-Seco
Database submission license No license selected
Created by Celia Zazo-Seco
Date created 2018-01-17 15:08:42 +01:00 (CET)
Date last edited 2020-06-06 17:52:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PXDN NM_012293.1 +?/. - c.1A>G r.(?) p.(Met1?)



Screenings

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