Variant #0001014858 (NC_000011.9:g.64977890G>A, NM_005186.3:c.2026G>A (CAPN1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.64977890G>A
DNA change (hg38) -
Published as CAPN1(NM_001198868.2):c.2026G>A (p.V676I)
ISCN -
DB-ID SLC22A20_000008
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) 0.00232 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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC22A20 NM_001004326.4 -?/. - c.-3454G>A r.(?) p.(=)
CAPN1 NM_005186.3 -?/. - c.2026G>A r.(?) p.(Val676Ile)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.