Variant #0000927322 (NC_000023.10:g.25031660_25031683del, NM_139058.2:c.441_464del (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.25031660_25031683del
DNA change (hg38) -
Published as ARX(NM_139058.2):c.441_464del (p.(Ala148_Ala155del)), ARX(NM_139058.3):c.441_464delAGCCGCGGCCGCGGCCGCCGCGGC (p.A148_A155del)
ISCN -
DB-ID ARX_000041 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARX NM_139058.2 -?/. - c.441_464del r.(?) p.(Ala148_Ala155del)


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