Variant #0000247008 (NC_000011.9:g.76796018A>C, NM_004055.4:c.86A>C (CAPN5))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76796018A>C
DNA change (hg38) g.77084972A>C
Published as CAPN5(NM_004055.5):c.86A>C (p.D29A)
ISCN -
DB-ID CAPN5_000005
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) 0.00208 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +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.86A>C r.(?) p.(Asp29Ala)
OMP NM_006189.1 -/. - c.-17868A>C r.(?) p.(=)


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