Variant #0001039756 (NC_000013.10:g.99582495C>T, NM_015296.2:c.263G>A (DOCK9))

Chromosome 13
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.99582495C>T
DNA change (hg38) -
Published as DOCK9(NM_001130048.1):c.260G>A (p.R87Q), DOCK9(NM_001366683.2):c.260G>A (p.(Arg87Gln))
ISCN -
DB-ID DOCK9_000005 See all 2 reported entries
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) 0.00116 View details
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     
DOCK9 NM_015296.2 ?/. - c.263G>A r.(?) p.(Arg88Gln)


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