Variant #0000573448 (NC_000023.10:g.128977665T>C, ZDHHC9(NM_016032.3):c.-204+7A>G)

Chromosome X
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.128977665T>C
DNA change (hg38) g.129843689T>C
Published as ZDHHC9(NM_001008222.2):c.-566A>G (p.(=))
ISCN -
DB-ID ZDHHC9_000025
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) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZDHHC9 NM_016032.3 -?/. - c.-204+7A>G r.(=) p.(=)