Variant #0000506330 (NC_000001.10:g.237656365C>T, NM_001035.2:c.1939C>T (RYR2))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.237656365C>T |
| DNA change (hg38) |
g.237493065C>T |
| Published as |
RYR2(NM_001035.2):c.1939C>T (p.R647C), RYR2(NM_001035.3):c.1939C>T (p.R647C) |
| ISCN |
- |
| DB-ID |
RYR2_000781 See all 7 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00015 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2019-12-04 14:54:23 +01:00 (CET) |

Variant on transcripts
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