Variant #0000563358 (NC_000017.10:g.7752258G>A, KDM6B(NM_001080424.1):c.2652G>A)

Chromosome 17
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.7752258G>A
DNA change (hg38) g.7848940G>A
Published as KDM6B(NM_001080424.2):c.2652G>A (p.A884=)
ISCN -
DB-ID KDM6B_000052
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDM6B NM_001080424.1 -?/. - c.2652G>A r.(?) p.(Ala884=)