Variant #0000538009 (NC_000009.11:g.340229C>G, NM_203447.3:c.1587C>G (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.340229C>G
DNA change (hg38) g.340229C>G
Published as DOCK8(NM_203447.3):c.1587C>G (p.P529=)
ISCN -
DB-ID C9orf66_000015
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) 0.00073 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C9orf66 NM_152569.2 -/. - c.-124833G>C r.(?) p.(=)
DOCK8 NM_203447.3 -/. - c.1587C>G r.(?) p.(Pro529=)


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