Variant #0000338739 (NC_000010.10:g.76732253A>G, NC_000010.10(NM_012330.3):c.929-12A>G (KAT6B))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76732253A>G
DNA change (hg38) g.74972495A>G
Published as -
ISCN -
DB-ID KAT6B_000080
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) 0.00778 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.929-12A>G r.(=) p.(=)
KAT6B NM_001256469.1 -/. - c.929-12A>G r.(=) p.(=)
KAT6B NM_012330.3 -/. - c.929-12A>G r.(=) p.(=)


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