Variant #0000333519 (NC_000023.10:g.25025374_25025376dup, NM_139058.2:c.1318_1320dup (ARX))

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.25025374_25025376dup
DNA change (hg38) g.25007257_25007259dup
Published as ARX(NM_139058.2):c.1318_1320dupGCC (p.A440dup), ARX(NM_139058.2):c.1320_1321insGCC (p.(Ala440dup)), ARX(NM_139058.3):c.1318_1320dupGCC (p.A440dup)
ISCN -
DB-ID ARX_000030 See all 3 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
ARX NM_139058.2 -?/. - c.1318_1320dup r.(?) p.(Ala440dup)


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