Variant #0000326739 (NC_000019.9:g.50365061_50365077dup, NM_007254.3:c.1253_1269dup (PNKP))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.50365061_50365077dup
DNA change (hg38) g.49861804_49861820dup
Published as PNKP(NM_007254.3):c.1253_1269dupGGGTCGCCATCGACAAC (p.(Thr424fs)), PNKP(NM_007254.3):c.1253_1269dupGGGTCGCCATCGACAAC (p.T424Gfs*49), PNKP(NM_007254...)
ISCN -
DB-ID PNKP_000009 See all 5 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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.1253_1269dup r.(?) p.(Thr424GlyfsTer49)
PTOV1 NM_017432.3 +/. - c.*1525_*1541dup r.(=) p.(=)


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