Variant #0000038934 (NC_000010.10:g.76789493_76789503del, NM_012330.3:c.4911_4921del (KAT6B))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.76789493_76789503del
DNA change (hg38) g.75029735_75029745del
Published as -
ISCN -
DB-ID KAT6B_000015 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jill Clayton-Smith
Database submission license No license selected
Created by Jill Clayton-Smith
Date created 2014-07-17 18:54:16 +02:00 (CEST)
Date last edited 2014-07-19 15:37:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6B NM_012330.3 +?/. 18 c.4911_4921del r.(?) p.(Val1638Alafs*27)



Screenings

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