Variant #0000998510 (NC_000010.10:g.76737164T>C, NM_012330.3:c.2084T>C (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.76737164T>C
DNA change (hg38) -
Published as KAT6B(NM_012330.3):c.2084T>C (p.(Val695Ala))
ISCN -
DB-ID KAT6B_000213
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
KAT6B NM_001256468.1 -?/. - c.1535T>C r.(?) p.(Val512Ala)
KAT6B NM_001256469.1 -?/. - c.1208T>C r.(?) p.(Val403Ala)
KAT6B NM_012330.3 -?/. - c.2084T>C r.(?) p.(Val695Ala)


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