Variant #0001034097 (NC_000003.11:g.53764497C>A, NM_000720.3:c.2310C>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.53764497C>A
DNA change (hg38) -
Published as CACNA1D(NM_000720.4):c.2310C>A (p.I770=), CACNA1D(NM_001128840.3):c.2250C>A (p.(Ile750=))
ISCN -
DB-ID CACNA1D_000047 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) 0.00028 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1D NM_000720.3 ?/. - c.2310C>A r.(?) p.(Ile770=)
CACNA1D NM_001128840.2 ?/. - c.2250C>A r.(?) p.(Ile750=)


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