Variant #0000326369 (NC_000019.9:g.33076718T>C, PDCD5(NM_004708.3):c.167-4T>C)

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.33076718T>C
DNA change (hg38) g.32585812T>C
Published as PDCD5(NM_004708.3):c.167-4T>C (p.?)
ISCN -
DB-ID PDCD5_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license No license selected
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDCD5 NM_004708.3 ?/. - c.167-4T>C r.spl? p.?