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 28 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
|