Variant #0000520420 (NC_000003.11:g.53736832G>A, NM_000720.3:c.1385G>A (CACNA1D))

Chromosome 3
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.53736832G>A
DNA change (hg38) g.53702805G>A
Published as CACNA1D(NM_000720.3):c.1385G>A (p.R462Q), CACNA1D(NM_001128840.3):c.1385G>A (p.(Arg462Gln))
ISCN -
DB-ID CACNA1D_000103 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) 6.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1D NM_000720.3 ?/. - c.1385G>A r.(?) p.(Arg462Gln)
CACNA1D NM_001128840.2 ?/. - c.1385G>A r.(?) p.(Arg462Gln)


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