Variant #0000319563 (NC_000023.10:g.7811821_7811822del, NM_013452.2:c.385_386del (VCX))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7811821_7811822del
DNA change (hg38) g.7843780_7843781del
Published as VCX(NM_013452.2):c.385_386del (p.?), VCX(NM_013452.2):c.385_386delCA (p.Q129Gfs*?)
ISCN -
DB-ID VCX_000009 See all 2 reported entries
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) 0.00796 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 2020-07-17 18:05:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VCX NM_013452.2 -/. - c.385_386del r.(?) p.(Gln129GlyfsTer?)


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