Variant #0001031524 (NC_000001.10:g.182856342_182856356del, NM_001357.4:c.3586_3600del (DHX9))

Chromosome 1
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.182856342_182856356del
DNA change (hg38) -
Published as DHX9(NM_001357.5):c.3586_3600del (p.(Ser1196_Gly1200del))
ISCN -
DB-ID DHX9_000023
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHX9 NM_001357.4 -?/. - c.3586_3600del r.(?) p.(Ser1196_Gly1200del)


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