Variant #0000949806 (NC_000011.9:g.76831868G>A, NM_004055.4:c.1400G>A (CAPN5))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.76831868G>A
DNA change (hg38) -
Published as CAPN5(NM_004055.5):c.1400G>A (p.R467H)
ISCN -
DB-ID CAPN5_000072
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) 2.0E-5 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 2023-11-27 17:35:39 +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.1400G>A r.(?) p.(Arg467His)
OMP NM_006189.1 ?/. - c.*17491G>A r.(=) p.(=)


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