Variant #0000537809 (NC_000009.11:g.215192C>G, NC_000009.11(NM_203447.3):c.53+163C>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.215192C>G
DNA change (hg38) g.215192C>G
Published as C9orf66(NM_152569.2):c.205G>C (p.A69P)
ISCN -
DB-ID C9orf66_000006
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_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 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.205G>C r.(?) p.(Ala69Pro)
DOCK8 NM_203447.3 ?/. - c.53+163C>G r.(=) p.(=)


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