Variant #0001066481 (NC_000016.9:g.31138664G>A, NM_032188.2:c.671G>A (KAT8))

Chromosome 16
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.31138664G>A
DNA change (hg38) -
Published as KAT8(NM_032188.3):c.671G>A (p.(Arg224His))
ISCN -
DB-ID chr16_007748
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRSS8 NM_002773.3 ?/. - c.*4666C>T r.(=) p.(=)
KAT8 NM_032188.2 ?/. - c.671G>A r.(?) p.(Arg224His)


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