Variant #0000322558 (NC_000011.9:g.119535697_119535702dup, NM_002855.4:c.1328_1333dup (PVRL1))

Chromosome 11
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.119535697_119535702dup
DNA change (hg38) g.119664987_119664992dup
Published as NECTIN1(NM_002855.5):c.1328_1333dup (p.(Glu443_Glu444dup)), NECTIN1(NM_002855.5):c.1328_1333dupAGGAGG (p.E443_E444dup)
ISCN -
DB-ID PVRL1_000003 See all 2 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PVRL1 NM_002855.4 ?/. - c.1328_1333dup r.(?) p.(Glu443_Glu444dup)


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