Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38603758C>T | CA015428 | SCN5A | c.1844G>A (p.Gly615Glu) c.1715G>A (p.Gly572Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38603758C= | CA1358584768 | SCN5A | c.1844G= (p.Gly615=) c.1715G= (p.Gly572=) | dbSNP |
3 | g.38603758C>G | CA352145937 | SCN5A | c.1844G>C (p.Gly615Ala) c.1715G>C (p.Gly572Ala) | dbSNP |