Variant #0000540980 (NC_000010.10:g.76781881A>G, NM_012330.3:c.3264A>G (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.76781881A>G
DNA change (hg38) g.75022123A>G
Published as KAT6B(NM_012330.3):c.3264A>G (p.E1088=)
ISCN -
DB-ID KAT6B_000124
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 2020-06-28 14:06:17 +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.2715A>G r.(?) p.(Glu905=)
KAT6B NM_001256469.1 -?/. - c.2388A>G r.(?) p.(Glu796=)
KAT6B NM_012330.3 -?/. - c.3264A>G r.(?) p.(Glu1088=)


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