Variant #0000538294 (NC_000009.11:g.451995_452003del, NC_000009.11(NM_203447.3):c.5962-16_5962-8del (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.451995_452003del
DNA change (hg38) g.451995_452003del
Published as DOCK8(NM_203447.3):c.5962-16_5962-8delTTTTTTTTC
ISCN -
DB-ID C9orf66_000043
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.-236607_-236599del r.(?) p.(=)
DOCK8 NM_203447.3 -?/. - c.5962-16_5962-8del r.(=) p.(=)


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