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) |

Variant on transcripts
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