Variant #0000808988 (NC_000019.9:g.50368450G>T, NM_007254.3:c.432C>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.50368450G>T
DNA change (hg38) -
Published as PNKP(NM_007254.3):c.432C>A (p.N144K)
ISCN -
DB-ID AKT1S1_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNKP NM_007254.3 -?/. - c.432C>A r.(?) p.(Asn144Lys)
PTOV1 NM_017432.3 -?/. - c.*4914G>T r.(=) p.(=)
TBC1D17 NM_024682.2 -?/. - c.-12531G>T r.(?) p.(=)
AKT1S1 NM_032375.4 -?/. - c.*4724C>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.