Variant #0000656365 (NC_000009.11:g.449874G>C, NM_203447.3:c.5908G>C (DOCK8))

Chromosome 9
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.449874G>C
DNA change (hg38) g.449874G>C
Published as DOCK8(NM_203447.3):c.5908G>C (p.A1970P)
ISCN -
DB-ID C9orf66_000065 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) 0.06171 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C9orf66 NM_152569.2 -/. - c.-234478C>G r.(?) p.(=)
DOCK8 NM_203447.3 -/. - c.5908G>C r.(?) p.(Ala1970Pro)


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