Variant #0000568071 (NC_000019.9:g.50367493C>T, NM_007254.3:c.579G>A (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.50367493C>T
DNA change (hg38) g.49864236C>T
Published as PNKP(NM_007254.3):c.579G>A (p.R193=), PNKP(NM_007254.4):c.579G>A (p.(Arg193=), p.R193=)
ISCN -
DB-ID PNKP_000031 See all 3 reported entries
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) 0.00437 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNKP NM_007254.3 -?/. - c.579G>A r.(?) p.(Arg193=)
PTOV1 NM_017432.3 -?/. - c.*3957C>T r.(=) p.(=)
TBC1D17 NM_024682.2 -?/. - c.-13488C>T r.(?) p.(=)
AKT1S1 NM_032375.4 -?/. - c.*5681G>A r.(=) p.(=)


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