Variant #0000163472 (NC_000003.11:g.53707831_53707832insGGG, NM_000720.3:c.1208_1209insGGG (CACNA1D))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.53707831_53707832insGGG
DNA change (hg38) g.53673804_53673805insGGG
Published as -
ISCN -
DB-ID CACNA1D_000008 See all 5 reported entries
Variant remarks cDNA expression cloning showed nonconducting calcium channels with abnormal voltage-dependent gating
Reference PubMed: Baig 2011, Journal: Baig 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-03-05 10:51:21 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +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 +/. 8 c.1208_1209insGGG r.(?) p.Gly403dup


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