Variant #0000320139 (NC_000016.9:g.72991711_72991731del, NM_006885.3:c.2328_2348del (ZFHX3))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.72991711_72991731del
DNA change (hg38) g.72957812_72957832del
Published as ZFHX3(NM_006885.3):c.2328_2348delGGTGGCTGCGGCGGCGGCGGC (p.V777_A783del)
ISCN -
DB-ID ZFHX3_000041
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ZFHX3 NM_006885.3 -?/. - c.2328_2348del - r.(?) p.(Val777_Ala783del)


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