Variant #0000690428 (NC_000009.11:g.131483793G>C, NM_013355.3:c.*908G>C (PKN3))

Chromosome 9
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.131483793G>C
DNA change (hg38) -
Published as ZDHHC12(NM_001318016.1):c.499C>G (p.P167A)
ISCN -
DB-ID PKN3_000009
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKN3 NM_013355.3 ?/. - c.*908G>C r.(=) p.(=)
ZDHHC12 NM_032799.4 ?/. - c.483-12C>G r.(=) p.(=)


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