Variant #0001027499 (NC_000023.10:g.44920013T>C, NC_000023.10(NM_021140.2):c.1330-556T>C (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.44920013T>C
DNA change (hg38) -
Published as KDM6A(NM_001291415.1):c.1485+4T>C, KDM6A(NM_021140.4):c.1330-556T>C
ISCN -
DB-ID KDM6A_000095 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 2025-02-07 18:57:27 +01:00 (CET)
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.1330-556T>C r.(=) p.(=)


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