Variant #0000696736 (NC_000015.9:g.42703124G>A, NM_000070.2:c.2306G>A (CAPN3))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.42703124G>A
DNA change (hg38) g.42410926G>A
Published as -
ISCN -
DB-ID CAPN3_000013 See all 50 reported entries
Variant remarks expression cloning mini-gene splicing assay mild effect on 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) 3.0E-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 2020-10-03 15:24:59 +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 +/. 22 c.2306G>A r.[2306g>a,2264_23805del] p.[(Arg769Gln,?)]


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