Variant #0000321618 (NC_000010.10:g.76602877T>G, NM_012330.3:c.262T>G (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.76602877T>G
DNA change (hg38) g.74843119T>G
Published as KAT6B(NM_001256468.1):c.262T>G (p.(Phe88Val))
ISCN -
DB-ID KAT6B_000052
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 -?/. - c.262T>G r.(?) p.(Phe88Val)
KAT6B NM_001256469.1 -?/. - c.262T>G r.(?) p.(Phe88Val)
KAT6B NM_012330.3 -?/. - c.262T>G r.(?) p.(Phe88Val)


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