Variant #0000438148 (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 |
{PMID19847904:Eikermann-Haerter 2009} |
| 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 15:15:33 +02:00 (CEST) |

Variant on transcripts
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