Variant #0000949267 (NC_000009.11:g.312104G>A, NM_203447.3:c.679G>A (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.312104G>A
DNA change (hg38) -
Published as DOCK8(NM_001190458.1):c.475G>A (p.(Glu159Lys)), DOCK8(NM_203447.3):c.679G>A (p.E227K)
ISCN -
DB-ID DOCK8_000013 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) 0.00181 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C9orf66 NM_152569.2 -/. - c.-96708C>T r.(?) p.(=)
DOCK8 NM_203447.3 -/. - c.679G>A r.(?) p.(Glu227Lys)


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