Variant #0000573023 (NC_000023.10:g.110653568_110653569delinsG, NM_000555.3:c.301_302delinsC (DCX))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.110653568_110653569delinsG
DNA change (hg38) g.111410340_111410341delinsG
Published as DCX(NM_178153.2):c.58_59delGGinsC (p.G20Pfs*4)
ISCN -
DB-ID DCX_000045
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 2020-07-21 08:55:57 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DCX NM_000555.3 +/. - c.301_302delinsC r.(?) p.(Gly101ProfsTer4)


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