Variant #0000545767 (NC_000011.9:g.76826545A>G, NM_004055.4:c.804A>G (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.76826545A>G
DNA change (hg38) g.77115499A>G
Published as CAPN5(NM_004055.4):c.804A>G (p.L268=), CAPN5(NM_004055.5):c.804A>G (p.L268=)
ISCN -
DB-ID CAPN5_000009 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) 0.00297 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 2019-07-18 18:22:55 +02:00 (CEST)
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.804A>G r.(?) p.(Leu268=)
OMP NM_006189.1 -/. - c.*12168A>G r.(=) p.(=)


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