Variant #0000866232 (NC_000019.9:g.50367593G>C, NM_007254.3:c.566C>G (PNKP))

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.50367593G>C
DNA change (hg38) -
Published as PNKP(NM_007254.3):c.566C>G (p.P189R)
ISCN -
DB-ID PNKP_000093
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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.566C>G r.(?) p.(Pro189Arg)
PTOV1 NM_017432.3 ?/. - c.*4057G>C r.(=) p.(=)
TBC1D17 NM_024682.2 ?/. - c.-13388G>C r.(?) p.(=)


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