Variant #0000696742 (NC_000015.9:g.42680003C>T, NM_000070.2:c.551C>T (CAPN3))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.42680003C>T
DNA change (hg38) g.42387805C>T
Published as -
ISCN -
DB-ID CAPN3_000030 See all 16 reported entries
Variant remarks expression cloning mini-gene splicing assay affects splicing
Reference PubMed: Dionnet 2020
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0023 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 2020-10-03 15:24:59 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAPN3 NM_000070.2 ?/. 4 c.551C>T r.499_632del p.(fs)


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