Variant #0000313129 (NC_000023.10:g.128957640T>C, ZDHHC9(NM_016032.3):c.487+15A>G)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.128957640T>C
DNA change (hg38) g.129823664T>C
Published as ZDHHC9(NM_001008222.3):c.487+15A>G
ISCN -
DB-ID ZDHHC9_000005 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.91131 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZDHHC9 NM_016032.3 -/. - c.487+15A>G r.(=) p.(=)