Variant #0000567390 (NC_000019.9:g.40903448G>A, PRX(NM_181882.2):c.811C>T)

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.40903448G>A
DNA change (hg38) g.40397541G>A
Published as PRX(NM_181882.3):c.811C>T (p.P271S)
ISCN -
DB-ID PRX_000092
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRX NM_020956.2 ?/. - c.*1016C>T r.(=) p.(=)
PRX NM_181882.2 ?/. - c.811C>T r.(?) p.(Pro271Ser)