Variant #0001056669 (NC_000019.9:g.40902115_40902116del, NM_181882.2:c.2145_2146del (PRX))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.40902115_40902116del
DNA change (hg38) -
Published as PRX(NM_181882.3):c.2145_2146del (p.(Cys715*))
ISCN -
DB-ID PRX_000125
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRX NM_020956.2 +?/. - c.*2350_*2351del r.(=) p.(=)
PRX NM_181882.2 +?/. - c.2145_2146del r.(?) p.(Cys715*)


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