Variant #0000532813 (NC_000007.13:g.82763802_82763803del, NM_033026.5:c.3064_3065del (PCLO))

Chromosome 7
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.82763802_82763803del
DNA change (hg38) g.83134486_83134487del
Published as PCLO(NM_033026.6):c.3064_3065delGA (p.E1022Nfs*9)
ISCN -
DB-ID PCLO_000045
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCLO NM_033026.5 ?/. - c.3064_3065del r.(?) p.(Glu1022AsnfsTer9)


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