Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.123642468G>C | CA10575989 | SCN3B | c.423C>G (p.Ile141Met) c.119C>G n.830C>G | ClinVar dbSNP gnomAD v4 COSMIC |
11 | g.123642468G>A | CA477241014 | SCN3B | c.423C>T (p.Ile141=) c.119C>T n.830C>T | ClinVar dbSNP gnomAD v4 |
11 | g.123642468G>T | CA477241017 | SCN3B | c.423C>A (p.Ile141=) c.119C>A n.830C>A | dbSNP gnomAD v4 |
11 | g.123642468G= | CA2005869708 | SCN3B | c.423C= (p.Ile141=) c.119C= n.830C= | dbSNP |