Variant #0000934961 (NC_000008.10:g.19805844G>A, NM_000237.2:c.242G>A (LPL))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.19805844G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID LPL_000328
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs762007406
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 2023-10-13 15:25:01 +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     
LPL NM_000237.2 +/. - c.242G>A r.(?) p.(Gly81Asp)


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