Variant #0000540988 (NC_000010.10:g.76788656_76788661del, NM_012330.3:c.4074_4079del (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.76788656_76788661del
DNA change (hg38) g.75028898_75028903del
Published as KAT6B(NM_012330.4):c.4074_4079delGGAGGA (p.E1367_E1368del)
ISCN -
DB-ID KAT6B_000037 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.3525_3530del r.(?) p.(Glu1184_Glu1185del)
KAT6B NM_001256469.1 -?/. - c.3198_3203del r.(?) p.(Glu1075_Glu1076del)
KAT6B NM_012330.3 -?/. - c.4074_4079del r.(?) p.(Glu1367_Glu1368del)


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