Variant #0000306017 (NC_000019.9:g.50367287C>T, NM_007254.3:c.678G>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.50367287C>T
DNA change (hg38) g.49864030C>T
Published as PNKP(NM_007254.3):c.678G>A (p.K226=)
ISCN -
DB-ID PNKP_000027
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) 0.00013 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 10:56:08 +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.678G>A r.(?) p.(Lys226=)
PTOV1 NM_017432.3 -?/. - c.*3751C>T r.(=) p.(=)


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