Variant #0001043117 (NC_000019.9:g.50367023G>A, NC_000019.9(NM_007254.3):c.745-6C>T (PNKP))

Chromosome 19
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.50367023G>A
DNA change (hg38) -
Published as PNKP(NM_007254.4):c.745-6C>T
ISCN -
DB-ID PNKP_000101
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 2025-05-05 21:14:00 +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     
PNKP NM_007254.3 -?/. - c.745-6C>T r.(=) p.(=)
PTOV1 NM_017432.3 -?/. - c.*3487G>A r.(=) p.(=)


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