Variant #0000562100 (NC_000017.10:g.46023295C>G, NM_018129.3:c.486C>G (PNPO))

Chromosome 17
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.46023295C>G
DNA change (hg38) g.47945929C>G
Published as PNPO(NM_018129.4):c.486C>G (p.P162=)
ISCN -
DB-ID PNPO_000015
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) 0.0056 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
SP2 NM_003110.5 -/. - c.*18105C>G r.(=) p.(=)
PNPO NM_018129.3 -/. - c.486C>G r.(?) p.(Pro162=)


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