Variant #0000659077 (NC_000023.10:g.128977658_128977659dup, ZDHHC9(NM_016032.3):c.-204+16_-204+17dup)

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.128977658_128977659dup
DNA change (hg38) g.129843682_129843683dup
Published as ZDHHC9(NM_016032.4):c.-204+16_-204+17dupGG
ISCN -
DB-ID ZDHHC9_000028
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZDHHC9 NM_016032.3 ?/. - c.-204+16_-204+17dup r.(=) p.(=)