Variant #0000810253 (NC_000023.10:g.24226393_24226395dup, NM_003410.3:c.999_1001dup (ZFX))

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.24226393_24226395dup
DNA change (hg38) -
Published as ZFX(NM_001178085.1):c.999_1001dupTGC (p.A341dup), ZFX(NM_001330327.1):c.1116_1118dupTGC (p.A380dup), ZFX(NM_003410.4):c.999_1001dup (p.(Ala341dup))
ISCN -
DB-ID ZFX_000021 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) 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZFX NM_003410.3 ?/. - c.999_1001dup r.(?) p.(Ala341dup)


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