Variant #0000894994 (NC_000019.9:g.40903719C>T, PRX(NM_181882.2):c.540G>A)

Chromosome 19
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.40903719C>T
DNA change (hg38) -
Published as PRX(NM_181882.2):c.540G>A (p.P180=)
ISCN -
DB-ID PRX_000117
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) 0.00046 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRX NM_020956.2 -?/. - c.*745G>A r.(=) p.(=)
PRX NM_181882.2 -?/. - c.540G>A r.(?) p.(Pro180=)