Variant #0001065273 (NC_000010.10:g.76781913_76781914insGGAAGA, NM_012330.3:c.3296_3297insGGAAGA (KAT6B))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.76781913_76781914insGGAAGA
DNA change (hg38) -
Published as -
ISCN -
DB-ID KAT6B_000235
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 2026-01-20 18:57:21 +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     
KAT6B NM_001256468.1 ?/. - c.2747_2748insGGAAGA r.(?) p.(Glu920_Glu921dup)
KAT6B NM_001256469.1 ?/. - c.2420_2421insGGAAGA r.(?) p.(Glu811_Glu812dup)
KAT6B NM_012330.3 ?/. - c.3296_3297insGGAAGA r.(?) p.(Glu1103_Glu1104dup)


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