Variant #0000852595 (NC_000010.10:g.76780463A>G, NM_012330.3:c.2753A>G (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.76780463A>G
DNA change (hg38) -
Published as KAT6B(NM_012330.4):c.2753A>G (p.H918R)
ISCN -
DB-ID KAT6B_000181
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +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.2204A>G r.(?) p.(His735Arg)
KAT6B NM_001256469.1 ?/. - c.1877A>G r.(?) p.(His626Arg)
KAT6B NM_012330.3 ?/. - c.2753A>G r.(?) p.(His918Arg)


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