Variant #0000544961 (NC_000011.9:g.64976831G>A, NM_005186.3:c.1767G>A (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.64976831G>A
DNA change (hg38) g.65209360G>A
Published as CAPN1(NM_001198868.1):c.1767G>A (p.S589=)
ISCN -
DB-ID SLC22A20_000002
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) 0.00144 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 18:04:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC22A20 NM_001004326.4 -/. - c.-4513G>A r.(?) p.(=)
CAPN1 NM_005186.3 -/. - c.1767G>A r.(?) p.(Ser589=)


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