Variant #0000301077 (NC_000019.9:g.50369787T>C, NC_000019.9(NM_007254.3):c.152-85A>G (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.50369787T>C
DNA change (hg38) g.49866530T>C
Published as PNKP(NM_007254.4):c.152-85A>G
ISCN -
DB-ID PNKP_000041
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) 0.01466 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +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.152-85A>G r.(=) p.(=)
TBC1D17 NM_024682.2 -/. - c.-11194T>C r.(?) p.(=)
AKT1S1 NM_032375.4 -/. - c.*3387A>G r.(=) p.(=)


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