Variant #0000540976 (NC_000010.10:g.76781848_76781859del, NM_012330.3:c.3231_3242del (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.76781848_76781859del
DNA change (hg38) g.75022090_75022101del
Published as KAT6B(NM_001256468.1):c.2682_2693del (p.(Asp894_Glu897del)), KAT6B(NM_012330.4):c.3231_3242delCGAGGAGGAGGA (p.D1077_E1080del)
ISCN -
DB-ID KAT6B_000060 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_001256468.1 ?/. - c.2682_2693del r.(?) p.(Asp894_Glu897del)
KAT6B NM_001256469.1 ?/. - c.2355_2366del r.(?) p.(Asp785_Glu788del)
KAT6B NM_012330.3 ?/. - c.3231_3242del r.(?) p.(Asp1077_Glu1080del)


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