Variant #0000617387 (NC_000019.9:g.13470494C>T, NM_001127221.1:c.904G>A (CACNA1A))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13470494C>T
DNA change (hg38) g.13359680C>T
Published as CACNA1A(NM_023035.2):c.904G>A (p.D302N), CACNA1A(NM_023035.3):c.904G>A (p.D302N)
ISCN -
DB-ID CACNA1A_000361 See all 3 reported entries
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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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.904G>A - r.(?) p.(Asp302Asn) -
CACNA1A NM_023035.2 +/. - c.904G>A - r.(?) p.(Asp302Asn) -


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