Variant #0000656562 (NC_000010.10:g.76735658T>G, NM_012330.3:c.1563T>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.76735658T>G
DNA change (hg38) g.74975900T>G
Published as KAT6B(NM_012330.4):c.1563T>G (p.S521R)
ISCN -
DB-ID KAT6B_000161
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 ?/. - c.1444+119T>G r.(=) p.(=)
KAT6B NM_001256469.1 ?/. - c.1117+446T>G r.(=) p.(=)
KAT6B NM_012330.3 ?/. - c.1563T>G r.(?) p.(Ser521Arg)


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