Variant #0001003217 (NC_000017.10:g.40273043C>A, NM_021078.2:c.280G>T (KAT2A))

Chromosome 17
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.40273043C>A
DNA change (hg38) -
Published as KAT2A(NM_021078.2):c.280G>T (p.(Val94Phe))
ISCN -
DB-ID HSPB9_000002
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 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     
RAB5C NM_004583.3 ?/. - c.*4758G>T r.(=) p.(=)
KAT2A NM_021078.2 ?/. - c.280G>T r.(?) p.(Val94Phe)
HSPB9 NM_033194.2 ?/. - c.-1826C>A r.(?) p.(=)


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