Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.41237956G>A | CA308533780 | AXL | c.796G>A (p.Asp266Asn) c.-9G>A (n.-9G>A) n.810G>A | dbSNP |
19 | g.41237956G>C | CA405991019 | AXL | c.796G>C (p.Asp266His) c.-9G>C (n.-9G>C) n.810G>C | dbSNP |
19 | g.41237956G= | CA9458081 | AXL | c.796G= (p.Asp266=) c.-9G= (n.-9G=) n.810G= | dbSNP |