Variant #0000915227 (NC_000019.9:g.40901711G>C, NM_181882.2:c.2548C>G (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.40901711G>C
DNA change (hg38) -
Published as PRX(NM_181882.2):c.2548C>G (p.P850A), PRX(NM_181882.3):c.2548C>G (p.P850A)
ISCN -
DB-ID PRX_000024 See all 3 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) 0.00051 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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.*2753C>G r.(=) p.(=)
PRX NM_181882.2 ?/. - c.2548C>G r.(?) p.(Pro850Ala)


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