Variant #0000931665 (NC_000008.10:g.41834793G>A, NM_006766.3:c.1096C>T (KAT6A))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41834793G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID KAT6A_000057 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1564034820
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-08-01 11:38:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT6A NM_006766.3 +/. - c.1096C>T r.(?) p.(Arg366Ter)


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