Variant #0000682356 (NC_000023.10:g.24197693_24197701dup, NM_003410.3:c.452_460dup (ZFX))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24197693_24197701dup
DNA change (hg38) -
Published as ZFX(NM_001178084.1):c.429_430insGTTGGACAT (p.(Asp143_Val144insValGlyHis))
ISCN -
DB-ID ZFX_000017
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZFX NM_003410.3 -?/. - c.452_460dup r.(?) p.(Gly151_Val153dup)


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