Variant #0000568063 (NC_000019.9:g.50365782dup, NC_000019.9(NM_007254.3):c.936+17dup (PNKP))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50365782dup
DNA change (hg38) g.49862525dup
Published as PNKP(NM_007254.3):c.936+17dupC, PNKP(NM_007254.4):c.936+12delGinsGC, PNKP(NM_007254.4):c.936+17dupC
ISCN -
DB-ID PNKP_000020 See all 2 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNKP NM_007254.3 -/. - c.936+17dup r.(=) p.(=)
PTOV1 NM_017432.3 -/. - c.*2246dup r.(?) p.(=)


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