Variant #0000722479 (NC_000009.11:g.312088C>A, NM_203447.3:c.663C>A (DOCK8))

Chromosome 9
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.312088C>A
DNA change (hg38) -
Published as DOCK8(NM_203447.3):c.663C>A (p.D221E), DOCK8(NM_203447.4):c.663C>A (p.D221E)
ISCN -
DB-ID DOCK8_000012 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) 0.00174 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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.-96692G>T r.(?) p.(=)
DOCK8 NM_203447.3 ?/. - c.663C>A r.(?) p.(Asp221Glu)


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