Variant #0000997836 (NC_000009.11:g.328062T>C, NM_203447.3:c.935T>C (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.328062T>C
DNA change (hg38) -
Published as DOCK8(NM_203447.3):c.935T>C (p.(Ile312Thr))
ISCN -
DB-ID C9orf66_000126
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
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.-112666A>G r.(?) p.(=)
DOCK8 NM_203447.3 ?/. - c.935T>C r.(?) p.(Phe312Ser)


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