Variant #0000299153 (NC_000019.9:g.40901795C>T, NM_181882.2:c.2464G>A (PRX))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.40901795C>T
DNA change (hg38) g.40395888C>T
Published as PRX(NM_181882.3):c.2464G>A (p.E822K)
ISCN -
DB-ID PRX_000025
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) 9.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRX NM_020956.2 ?/. - c.*2669G>A r.(=) p.(=)
PRX NM_181882.2 ?/. - c.2464G>A r.(?) p.(Glu822Lys)


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