Variant #0000690515 (NC_000009.11:g.271626G>T, NC_000009.11(NM_203447.3):c.54-1G>T (DOCK8))

Chromosome 9
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.271626G>T
DNA change (hg38) -
Published as DOCK8(NM_203447.3):c.54-1G>T, DOCK8(NM_203447.4):c.54-1G>T
ISCN -
DB-ID DOCK8_000003 See all 3 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) 0.00027 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C9orf66 NM_152569.2 +?/. - c.-56230C>A r.(?) p.(=)
DOCK8 NM_203447.3 +?/. - c.54-1G>T r.spl? p.?


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