Variant #0000332800 (NC_000009.11:g.131482243_131482250del, NM_013355.3:c.2323_2330del (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.131482243_131482250del
DNA change (hg38) g.128719964_128719971del
Published as PKN3(NM_013355.3):c.2323_2330del (p.(Asp775LeufsTer11))
ISCN -
DB-ID PKN3_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-25 18:51:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKN3 NM_013355.3 ?/. - c.2323_2330del r.(?) p.(Asp775LeufsTer11)
ZDHHC12 NM_032799.4 ?/. - c.*1210_*1217del r.(=) p.(=)


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