Variant #0001041075 (NC_000016.9:g.31141816C>T, NM_032188.2:c.1046C>T (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.31141816C>T
DNA change (hg38) -
Published as KAT8(NM_182958.4):c.1046C>T (p.P349L)
ISCN -
DB-ID KAT8_000008
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +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     
PRSS8 NM_002773.3 ?/. - c.*1514G>A r.(=) p.(=)
KAT8 NM_032188.2 ?/. - c.1046C>T r.(?) p.(Pro349Leu)


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