Variant #0000438153 (NC_000019.9:g.13476262G>A, NM_001127221.1:c.653C>T (CACNA1A))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.13476262G>A
DNA change (hg38) g.13365448G>A
Published as -
ISCN -
DB-ID CACNA1A_000004 See all 15 reported entries
Variant remarks tested expression in vitro/in vivo
Reference PubMed: 15743764
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 15:15:28 +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 ?/? 5 c.653C>T - r.(?) p.(Ser218Leu) -


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