Variant #0000608821 (NC_000003.11:g.53694181A>G, NM_000720.3:c.645A>G (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.53694181A>G
DNA change (hg38) g.53660154A>G
Published as -
ISCN -
DB-ID CACNA1D_000134
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) 9.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-15 11:04:37 +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.645A>G r.(?) p.(Glu215=)
CACNA1D NM_001128840.2 -?/. - c.645A>G r.(?) p.(Glu215=)


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