Variant #0000993824 (NC_000003.11:g.53760991G>C, NM_000720.3:c.2246G>C (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.53760991G>C
DNA change (hg38) -
Published as CACNA1D(NM_001128840.2):c.2186G>C (p.(Cys729Ser))
ISCN -
DB-ID CACNA1D_000186
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1D NM_000720.3 ?/. - c.2246G>C r.(?) p.(Cys749Ser)
CACNA1D NM_001128840.2 ?/. - c.2186G>C r.(?) p.(Cys729Ser)


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