Variant #0001019158 (NC_000015.9:g.42704505T>C, NM_000070.2:c.*534T>C (CAPN3))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.42704505T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID CAPN3_000940 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs772498665
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-12-18 12:39:14 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAPN3 NM_000070.2 ?/. - c.*534T>C r.(?) p.(?)


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