Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.180603313C>T | CA3605613 | FLT4 | c.3971G>A (p.Arg1324Gln) n.671G>A c.4220G>A (p.Arg1407Gln) c.4202G>A (p.Arg1401Gln) c.*117G>A (n.*117G>A) c.3989G>A (p.Arg1330Gln) c.3911G>A (p.Arg1304Gln) c.3512G>A (p.Arg1171Gln) n.4257G>A c.3893G>A (p.Arg1298Gln) n.4461G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.180603313C>G | CA3605612 | FLT4 | c.3971G>C (p.Arg1324Pro) n.671G>C c.4220G>C (p.Arg1407Pro) c.4202G>C (p.Arg1401Pro) c.*117G>C (n.*117G>C) c.3989G>C (p.Arg1330Pro) c.3911G>C (p.Arg1304Pro) c.3512G>C (p.Arg1171Pro) n.4257G>C c.3893G>C (p.Arg1298Pro) n.4461G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.180603313C>A | CA3605611 | FLT4 | c.3971G>T (p.Arg1324Leu) n.671G>T c.4220G>T (p.Arg1407Leu) c.4202G>T (p.Arg1401Leu) c.*117G>T (n.*117G>T) c.3989G>T (p.Arg1330Leu) c.3911G>T (p.Arg1304Leu) c.3512G>T (p.Arg1171Leu) n.4257G>T c.3893G>T (p.Arg1298Leu) n.4461G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |