Variant #0000979155 (NC_000010.10:g.76780901G>A, NM_012330.3:c.2879G>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.76780901G>A
DNA change (hg38) -
Published as KAT6B(NM_012330.4):c.2879G>A (p.(Arg960Gln))
ISCN -
DB-ID KAT6B_000206
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 ?/. - c.2330G>A r.(?) p.(Arg777Gln)
KAT6B NM_001256469.1 ?/. - c.2003G>A r.(?) p.(Arg668Gln)
KAT6B NM_012330.3 ?/. - c.2879G>A r.(?) p.(Arg960Gln)


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