Genomic variant #0000346902

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.76788961del
DNA change (hg38) -
Published as KAT6B:NM_012330.3:c.4379del (Leu1460*)
ISCN -
DB-ID KAT6B_000093
Variant remarks VKGL data sharing initiative Nederland; correct HGVS to be checked
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Nijmegen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
KAT6B NM_001256468.1 +/. - c.3830del pathogenic r.(?) p.(Leu1277*)
KAT6B NM_001256469.1 +/. - c.3503del pathogenic r.(?) p.(Leu1168*)
KAT6B NM_012330.3 +/. - c.4379del pathogenic r.(?) p.(Leu1460*)