Variant #0000321624 (NC_000010.10:g.76788618G>T, NM_012330.3:c.4036G>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.76788618G>T
DNA change (hg38) g.75028860G>T
Published as KAT6B(NM_001256468.1):c.3487G>T (p.(Asp1163Tyr))
ISCN -
DB-ID KAT6B_000065
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) 0.0017 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 ?/. - c.3487G>T r.(?) p.(Asp1163Tyr)
KAT6B NM_001256469.1 ?/. - c.3160G>T r.(?) p.(Asp1054Tyr)
KAT6B NM_012330.3 ?/. - c.4036G>T r.(?) p.(Asp1346Tyr)


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