Variant #0000926822 (NC_000019.9:g.13616743T>G, NC_000019.9(NM_001127221.1):c.293+3A>C (CACNA1A))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13616743T>G
DNA change (hg38) -
Published as CACNA1A(NM_001127221.1):c.293+3A>C (p.?)
ISCN -
DB-ID CACNA1A_000491
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     

P-domain     
CACNA1A NM_001127221.1 +?/. - c.293+3A>C - r.spl? p.? -
CACNA1A NM_023035.2 +?/. - c.293+3A>C - r.spl? p.? -


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