Variant #0000438152 (NC_000019.9:g.13482558C>T, NM_001127221.1:c.575G>A (CACNA1A))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.13482558C>T
DNA change (hg38) g.13371744C>T
Published as -
ISCN -
DB-ID CACNA1A_000002 See all 15 reported entries
Variant remarks tested expression in vitro/in vivo
Reference {PMID15699344:Cao 2005}
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Paola Carrera
Database submission license No license selected
Created by Paola Carrera
Date created 2008-06-18 23:00:08 +02:00 (CEST)
Date last edited 2020-07-15 15:15:34 +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 +?/+? 4 c.575G>A - r.(?) p.(Arg192Gln) -


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