Variant #0000052385 (NC_000020.10:g.22496147_22773103del, NM_021784.4:c.-208187_*66341del (FOXA2))

Chromosome 20
Allele Paternal (confirmed)
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.22496147_22773103del
DNA change (hg38) g.22515509_22792465del
Published as CNV
ISCN -
DB-ID FOXA2_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ramakrishnan Rajagopalan
Database submission license No license selected
Created by Ramakrishnan Rajagopalan
Date created 2015-01-15 17:37:49 +01:00 (CET)
Date last edited 2015-01-16 16:16:35 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXA2 NM_021784.4 ?/. - c.-208187_*66341del r.0? p.0?



Screenings

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