Variant #0000927370 (NC_000023.10:g.44732872_44732887dup, NM_021140.2:c.75_90dup (KDM6A))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44732872_44732887dup
DNA change (hg38) -
Published as KDM6A(NM_021140.4):c.75_90dupGGCGGCGGGAAAAGCG (p.S31Gfs*39)
ISCN -
DB-ID KDM6A_000147
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     
KDM6A NM_021140.2 +?/. - c.75_90dup r.(?) p.(Ser31Glyfs*39)


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