Variant #0000255015 (NC_000009.11:g.215387A>G, NC_000009.11(NM_203447.3):c.53+358A>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.215387A>G
DNA change (hg38) g.215387A>G
Published as C9orf66(NM_152569.2):c.10T>C (p.S4P)
ISCN -
DB-ID C9orf66_000002
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) 3.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +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.10T>C r.(?) p.(Ser4Pro)
DOCK8 NM_203447.3 -?/. - c.53+358A>G r.(=) p.(=)


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