Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_000540.3(RYR1):c.463C>A (p.Gln155Lys) | RYR1 | Likely pathogenic | 19 | 38934827 | 38934827 | C | A | reviewed by expert panel | ClinGen:CA024451 |
single nucleotide variant | NM_000540.3(RYR1):c.325C>T (p.Arg109Trp) | RYR1 | Pathogenic/Likely pathogenic | 19 | 38934252 | 38934252 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA024392,UniProtKB:P21817#VAR_032910,OMIM:180901.0026 |
single nucleotide variant | NM_000540.3(RYR1):c.223C>T (p.Arg75Ter) | RYR1 | Pathogenic | 19 | 38933046 | 38933046 | C | T | criteria provided, single submitter | ClinGen:CA405674145 |
single nucleotide variant | NM_000540.3(RYR1):c.208C>T (p.Gln70Ter) | RYR1 | Pathogenic | 19 | 38933031 | 38933031 | C | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000540.3(RYR1):c.163C>T (p.Gln55Ter) | RYR1 | Pathogenic | 19 | 38931502 | 38931502 | C | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000540.3(RYR1):c.97A>G (p.Lys33Glu) | RYR1 | Likely pathogenic | 19 | 38931436 | 38931436 | A | G | reviewed by expert panel | ClinGen:CA025005,OMIM:180901.0038 |
single nucleotide variant | NM_000540.3(RYR1):c.38T>G (p.Leu13Arg) | RYR1 | Likely pathogenic | 19 | 38924507 | 38924507 | T | G | reviewed by expert panel | UniProtKB:P21817#VAR_058560,ClinGen:CA024414 |