Variant #0001044579 (NC_000003.11:g.145828163_145828182del, NM_182943.2:c.392_411del (PLOD2))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145828163_145828182del
DNA change (hg38) -
Published as -
ISCN -
DB-ID PLOD2_000069
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs753848468
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-05-07 22:20:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLOD2 NM_182943.2 +?/. - c.392_411del r.(?) p.(Lys131IlefsTer11)


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