Variant #0000876843 (NC_000015.9:g.42695076C>T, NM_000070.2:c.1621C>T (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.42695076C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CAPN3_000129 See all 32 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs142004418
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-08-19 11:45:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAPN3 NM_000070.2 +?/. - c.1621C>T r.(?) p.(Arg541Trp)


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