Variant #0000656340 (NC_000009.11:g.312048A>G, NM_203447.3:c.623A>G (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.312048A>G
DNA change (hg38) g.312048A>G
Published as DOCK8(NM_203447.3):c.623A>G (p.K208R)
ISCN -
DB-ID C9orf66_000059
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) 2.0E-5 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 2020-03-23 16:13:27 +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.-96652T>C r.(?) p.(=)
DOCK8 NM_203447.3 -?/. - c.623A>G r.(?) p.(Lys208Arg)


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