Variant #0000453866 (NC_000019.9:g.38990633G>A, NM_000540.2:c.7300G>A (RYR1))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.38990633G>A |
| DNA change (hg38) |
g.38499993G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
RYR1_000099 See all 30 reported entries |
| Variant remarks |
high affinity [3H]ryanodine binding enhanced sensitivity to Ca2+, caffeine and 4-chloro-m-cresol; reduced sensitivity to calmodulin |
| Reference |
PubMed: Richter 1997 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2010-03-06 21:30:45 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
|