Variant #0000269705 (NC_000011.9:g.64956204C>T, NM_005186.3:c.1152C>T (CAPN1))

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.64956204C>T
DNA change (hg38) g.65188733C>T
Published as CAPN1(NM_001198868.1):c.1152C>T (p.C384=), CAPN1(NM_005186.4):c.1152C>T (p.C384=)
ISCN -
DB-ID CAPN1_000007 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) 0.00238 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAPN1 NM_005186.3 -/. - c.1152C>T r.(?) p.(Cys384=)


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