Variant #0000018001 (NC_000016.9:g.72832634dup, NC_000016.9(NM_006885.3):c.3968-6dup (ZFHX3))

Chromosome 16
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.72832634dup
DNA change (hg38) g.72798735dup
Published as -
ISCN -
DB-ID ZFHX3_000002
Variant remarks variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me.
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 1
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 Johan den Dunnen
Date created 2013-05-08 23:53:32 +02:00 (CEST)
Date last edited 2022-10-13 02:58:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ZFHX3 NM_006885.3 ?/? ? c.3968-6dup - r.(=) p.(=)



Screenings

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