Variant #0000540971 (NC_000010.10:g.76735758G>A, NM_012330.3:c.1663G>A (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.76735758G>A
DNA change (hg38) g.74976000G>A
Published as KAT6B(NM_012330.3):c.1663G>A (p.(Gly555Arg))
ISCN -
DB-ID KAT6B_000116
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) 0.00243 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.1444+219G>A r.(=) p.(=)
KAT6B NM_001256469.1 -?/. - c.1117+546G>A r.(=) p.(=)
KAT6B NM_012330.3 -?/. - c.1663G>A r.(?) p.(Gly555Arg)


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