Variant #0000993820 (NC_000003.11:g.53694320_53694322del, NC_000003.11(NM_000720.3):c.766+18_766+20del (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.53694320_53694322del
DNA change (hg38) -
Published as CACNA1D(NM_000720.4):c.766+18_766+20delCCT
ISCN -
DB-ID CACNA1D_000183
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:16:32 +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.766+18_766+20del r.(=) p.(=)
CACNA1D NM_001128840.2 -?/. - c.766+18_766+20del r.(=) p.(=)


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