Variant #0001055560 (NC_000016.9:g.31141487T>C, NC_000016.9(NM_032188.2):c.912+9T>C (KAT8))

Chromosome 16
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.31141487T>C
DNA change (hg38) -
Published as KAT8(NM_032188.3):c.912+9T>C
ISCN -
DB-ID KAT8_000012
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) 0 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 2025-11-01 13:22:20 +01:00 (CET)
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.*1843A>G r.(=) p.(=)
KAT8 NM_032188.2 -?/. - c.912+9T>C r.(=) p.(=)


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