Variant #0000966483 (NC_000011.9:g.64976830C>T, NM_005186.3:c.1766C>T (CAPN1))

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.64976830C>T
DNA change (hg38) -
Published as CAPN1(NM_001198868.2):c.1766C>T (p.S589L), CAPN1(NM_005186.4):c.1766C>T (p.S589L)
ISCN -
DB-ID SLC22A20_000006
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +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     
SLC22A20 NM_001004326.4 ?/. - c.-4514C>T r.(?) p.(=)
CAPN1 NM_005186.3 ?/. - c.1766C>T r.(?) p.(Ser589Leu)


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