Variant #0000690784 (NC_000010.10:g.76788700_76788702dup, NM_012330.3:c.4118_4120dup (KAT6B))

Chromosome 10
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.76788700_76788702dup
DNA change (hg38) -
Published as KAT6B(NM_012330.4):c.4118_4120dupAAG (p.E1373dup)
ISCN -
DB-ID KAT6B_000170
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 -?/. - c.3569_3571dup r.(?) p.(Glu1190dup)
KAT6B NM_001256469.1 -?/. - c.3242_3244dup r.(?) p.(Glu1081dup)
KAT6B NM_012330.3 -?/. - c.4118_4120dup r.(?) p.(Glu1373dup)


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