Variant #0000998511 (NC_000010.10:g.76780376C>T, NM_012330.3:c.2666C>T (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.76780376C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID KAT6B_000214
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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 ?/. - c.2117C>T r.(?) p.(Ser706Phe)
KAT6B NM_001256469.1 ?/. - c.1790C>T r.(?) p.(Ser597Phe)
KAT6B NM_012330.3 ?/. - c.2666C>T r.(?) p.(Ser889Phe)


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