Variant #0000678914 (NC_000010.10:g.76744999G>A, NM_012330.3:c.2535G>A (KAT6B))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.76744999G>A
DNA change (hg38) -
Published as KAT6B(NM_012330.4):c.2535G>A (p.K845=)
ISCN -
DB-ID KAT6B_000167
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 +?/. - c.1986G>A r.(?) p.(Lys662=)
KAT6B NM_001256469.1 +?/. - c.1659G>A r.(?) p.(Lys553=)
KAT6B NM_012330.3 +?/. - c.2535G>A r.(?) p.(Lys845=)


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