Variant #0000622250 (NC_000009.11:g.289557G>A, NM_203447.3:c.380G>A (DOCK8))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.289557G>A
DNA change (hg38) g.289557G>A
Published as DOCK8(NM_203447.3):c.380G>A (p.R127H), DOCK8(NM_203447.4):c.380G>A (p.R127H)
ISCN -
DB-ID C9orf66_000009 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) 0.00198 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-74161C>T r.(?) p.(=)
DOCK8 NM_203447.3 -?/. - c.380G>A r.(?) p.(Arg127His)


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