Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_000069.3(CACNA1S):c.2854-2A>C | CACNA1S | Likely pathogenic | 1 | 201031644 | 201031644 | T | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000540.3(RYR1):c.11608+2T>C | RYR1 | Likely pathogenic | 19 | 39027409 | 39027409 | T | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000540.3(RYR1):c.7615-1G>T | RYR1 | Likely pathogenic | 19 | 38993146 | 38993146 | G | T | criteria provided, single submitter | - |
Deletion | NC_000019.10:g.(?_38502501)_(38502976_?)del | RYR1 | Pathogenic | 19 | 38993141 | 38993616 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_000540.3(RYR1):c.10687-2A>G | RYR1 | Likely pathogenic | 19 | 39018285 | 39018285 | A | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000540.3(RYR1):c.14129+1G>T | RYR1 | Likely pathogenic | 19 | 39063948 | 39063948 | G | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000540.3(RYR1):c.2290C>T (p.Gln764Ter) | RYR1 | Pathogenic/Likely pathogenic | 19 | 38949908 | 38949908 | C | T | criteria provided, multiple submitters, no conflicts | - |