Variant #0001026081 (NC_000011.9:g.76827269C>T, NC_000011.9(NM_004055.4):c.894-3C>T (CAPN5))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76827269C>T
DNA change (hg38) -
Published as CAPN5(NM_004055.4):c.894-3C>T, CAPN5(NM_004055.5):c.894-3C>T
ISCN -
DB-ID CAPN5_000026 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00134 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAPN5 NM_004055.4 -?/. - c.894-3C>T r.spl? p.?
OMP NM_006189.1 -?/. - c.*12892C>T r.(=) p.(=)


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