Variant #0001004429 (NC_000019.9:g.14578752A>G, NM_002741.3:c.1949A>G (PKN1))

Chromosome 19
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.14578752A>G
DNA change (hg38) -
Published as PKN1(NM_002741.3):c.1949A>G (p.(Asp650Gly))
ISCN -
DB-ID PKN1_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) 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 2024-08-28 13:16:32 +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     
PTGER1 NM_000955.2 ?/. - c.*4620T>C r.(=) p.(=)
PKN1 NM_002741.3 ?/. - c.1949A>G r.(?) p.(Asp650Gly)


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