Variant #0000540979 (NC_000010.10:g.76781875A>C, NM_012330.3:c.3258A>C (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.76781875A>C
DNA change (hg38) g.75022117A>C
Published as KAT6B(NM_012330.3):c.3258A>C (p.E1086D)
ISCN -
DB-ID KAT6B_000123
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 -?/. - c.2709A>C r.(?) p.(Glu903Asp)
KAT6B NM_001256469.1 -?/. - c.2382A>C r.(?) p.(Glu794Asp)
KAT6B NM_012330.3 -?/. - c.3258A>C r.(?) p.(Glu1086Asp)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.