Variant #0000290149 (NC_000023.10:g.44922890C>T, NM_021140.2:c.1751C>T (KDM6A))

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.44922890C>T
DNA change (hg38) g.45063645C>T
Published as KDM6A(NM_001291415.1):c.1907C>T (p.T636M), KDM6A(NM_001291415.2):c.1907C>T (p.(Thr584Met), p.T636M)
ISCN -
DB-ID KDM6A_000046 See all 4 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) 0.00083 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDM6A NM_021140.2 -?/. - c.1751C>T r.(?) p.(Thr584Met)


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