Variant #0000536442 (NC_000009.11:g.131486320G>A, NM_013355.3:c.*3435G>A (PKN3))

Chromosome 9
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.131486320G>A
DNA change (hg38) g.128724041G>A
Published as ZDHHC12(NM_032799.4):c.53C>T (p.(Thr18Ile))
ISCN -
DB-ID PKN3_000006
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKN3 NM_013355.3 -?/. - c.*3435G>A r.(=) p.(=)
ZDHHC12 NM_032799.4 -?/. - c.53C>T r.(?) p.(Thr18Ile)


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