Variant #0001016521 (NC_000015.9:g.42693989T>C, NM_000070.2:c.1505T>C (CAPN3))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42693989T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID CAPN3_000391 See all 15 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs148044781
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-11-05 15:54:01 +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.1505T>C r.(?) p.(Ile502Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.