Variant #0000613722 (NC_000011.9:g.76825363T>C, NM_004055.4:c.582T>C (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.76825363T>C
DNA change (hg38) g.77114317T>C
Published as CAPN5(NM_004055.4):c.582T>C (p.S194=), CAPN5(NM_004055.5):c.582T>C (p.S194=)
ISCN -
DB-ID CAPN5_000036 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) 0.00021 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAPN5 NM_004055.4 -?/. - c.582T>C r.(?) p.(Ser194=)
OMP NM_006189.1 -?/. - c.*10986T>C r.(=) p.(=)


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