Variant #0000540967 (NC_000010.10:g.76603046A>C, NM_012330.3:c.431A>C (KAT6B))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.76603046A>C
DNA change (hg38) g.74843288A>C
Published as KAT6B(NM_001256468.1):c.431A>C (p.(Asn144Thr))
ISCN -
DB-ID KAT6B_000112
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.431A>C r.(?) p.(Asn144Thr)
KAT6B NM_001256469.1 ?/. - c.431A>C r.(?) p.(Asn144Thr)
KAT6B NM_012330.3 ?/. - c.431A>C r.(?) p.(Asn144Thr)


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