Variant #0000576942 (NC_000023.10:g.6451864_6451923del, NM_016379.3:c.478_537del (VCX3A))

Chromosome X
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.6451864_6451923del
DNA change (hg38) g.6533823_6533882del
Published as VCX3A(NM_016379.3):c.478_537del (p.(Val160_Glu179del)), VCX3A(NM_016379.4):c.478_537del (p.V160_E179del)
ISCN -
DB-ID VCX3A_000037 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) 0.00096 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VCX3A NM_016379.3 ?/. - c.478_537del r.(?) p.(Val160_Glu179del)


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