Variant #0000998508 (NC_000010.10:g.76719732G>A, NM_012330.3:c.626G>A (KAT6B))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.76719732G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID KAT6B_000211
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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 ?/. - c.626G>A r.(?) p.(Arg209His)
KAT6B NM_001256469.1 ?/. - c.626G>A r.(?) p.(Arg209His)
KAT6B NM_012330.3 ?/. - c.626G>A r.(?) p.(Arg209His)


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