Variant #0000306003 (NC_000019.9:g.50365370G>A, NC_000019.9(NM_007254.3):c.1127-8C>T (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.50365370G>A
DNA change (hg38) g.49862113G>A
Published as PNKP(NM_007254.3):c.1127-8C>T (p.(=)), PNKP(NM_007254.4):c.1127-8C>T
ISCN -
DB-ID PNKP_000013 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) 0.00673 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 2025-02-07 18:57:27 +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.1127-8C>T r.(=) p.(=)
PTOV1 NM_017432.3 -/. - c.*1834G>A r.(=) p.(=)


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