Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.117403216C>T | CA3975861 | ROS1 | c.527G>A (p.Arg176Gln) c.500G>A (p.Arg167Gln) c.548-81822G>A (n.548-81822G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.117403216C>A | CA145987575 | ROS1 | c.527G>T (p.Arg176Leu) c.500G>T (p.Arg167Leu) c.548-81822G>T (n.548-81822G>T) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.117403216C>G | CA365446082 | ROS1 | c.527G>C (p.Arg176Pro) c.500G>C (p.Arg167Pro) c.548-81822G>C (n.548-81822G>C) | dbSNP |
6 | g.117403216C= | CA1657664669 | ROS1 | c.527G= (p.Arg176=) c.500G= (p.Arg167=) c.548-81822G= (n.548-81822G=) | dbSNP |