Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.38446710G>A | CA024797 | RYR1 | c.742G>A (p.Gly248Arg) n.825G>A | ClinVar dbSNP gnomAD v4 COSMIC |
19 | g.38446710G>T | CA069619 | RYR1 | c.742G>T (p.Gly248Trp) n.825G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.38446710G>C | CA024799 | RYR1 | c.742G>C (p.Gly248Arg) n.825G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |