Variant #0000612144 (NC_000009.11:g.439392A>G, NC_000009.11(NM_203447.3):c.5223+4A>G (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.439392A>G
DNA change (hg38) g.439392A>G
Published as DOCK8(NM_203447.3):c.5223+4A>G
ISCN -
DB-ID C9orf66_000056
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) 0.00064 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-25 12:01:34 +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.-223996T>C r.(?) p.(=)
DOCK8 NM_203447.3 ?/. - c.5223+4A>G r.spl? p.?


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