Variant #0000681485 (NC_000019.9:g.50365981C>T, NM_007254.3:c.831G>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.50365981C>T
DNA change (hg38) -
Published as PNKP(NM_007254.3):c.831G>A (p.T277=), PNKP(NM_007254.4):c.831G>A (p.T277=)
ISCN -
DB-ID PNKP_000022 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) 0.00128 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.831G>A r.(?) p.(Thr277=)
PTOV1 NM_017432.3 -?/. - c.*2445C>T r.(=) p.(=)


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