Variant #0001075620 (NC_000015.9:g.42691829G>A, NM_000070.2:c.1333 G>A (CAPN3))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42691829G>A
DNA change (hg38) g.42399631G>A
Published as -
ISCN -
DB-ID CAPN3_000094 See all 35 reported entries
Variant remarks ACMG PM3_str, PP4_str, PM1, PM2, PP3; no effect on splicing in a minigene splicing assay
Reference PubMed: Dionnet 2020
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2026-04-28 09:52:51 +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     
CAPN3 NM_000070.2 +/. 10 c.1333 G>A r.(1333 G>A) p.(Gly445Arg)


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