Variant #0000453857 (NC_000019.9:g.38931442T>C, NM_000540.2:c.103T>C (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.38931442T>C |
| DNA change (hg38) |
g.38440802T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
RYR1_000027 See all 5 reported entries |
| Variant remarks |
in vitro functional study shows altered ryanodine receptor function; EMHG RYR1 db (http://www.emhg.org/genetics/mutations-in-ryr1/) |
| Reference |
European MH Group genetic testing guidelines May 2005 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2009-11-01 22:02:20 +01:00 (CET) |
| Date last edited |
2020-07-15 17:49:12 +02:00 (CEST) |

Variant on transcripts
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