Variant #0000858634 (NC_000002.11:g.68385088C>G, NM_020143.2:c.22C>G (PNO1))

Chromosome 2
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.68385088C>G
DNA change (hg38) -
Published as PNO1(NM_001329916.1):c.22C>G (p.(Gln8Glu))
ISCN -
DB-ID PNO1_000003
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNO1 NM_020143.2 -?/. - c.22C>G r.(?) p.(Gln8Glu)
WDR92 NM_138458.3 -?/. - c.-513G>C r.(?) p.(=)


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