Variant #0001008367 (NC_000023.10:g.128975773_128975774del, NM_016032.3:c.150_151del (ZDHHC9))

Chromosome X
Allele Unknown
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.128975773_128975774del
DNA change (hg38) -
Published as -
ISCN -
DB-ID ZDHHC9_000041
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-09-16 16:15:01 +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     
ZDHHC9 NM_016032.3 +?/. - c.150_151del r.(?) p.(Phe52LeufsTer4)


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