Variant #0000270876 (NC_000009.11:g.312134G>A, NM_203447.3:c.709G>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.312134G>A
DNA change (hg38) g.312134G>A
Published as DOCK8(NM_001190458.1):c.505G>A (p.(Glu169Lys)), DOCK8(NM_203447.3):c.709G>A (p.E237K)
ISCN -
DB-ID DOCK8_000015 See all 4 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) 0.0283 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +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.-96738C>T r.(?) p.(=)
DOCK8 NM_203447.3 -/. - c.709G>A r.(?) p.(Glu237Lys)


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