Variant #0000264027 (NC_000003.11:g.53757498C>T, NM_000720.3:c.1764C>T (CACNA1D))

Chromosome 3
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.53757498C>T
DNA change (hg38) g.53723471C>T
Published as CACNA1D(NM_000720.4):c.1764C>T (p.C588=)
ISCN -
DB-ID CACNA1D_000039
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) 5.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1D NM_000720.3 -?/. - c.1764C>T r.(?) p.(Cys588=)
CACNA1D NM_001128840.2 -?/. - c.1704C>T r.(?) p.(Cys568=)


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