| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.225937602G>A | CA118943 | LEFTY2 | c.940C>T (p.Arg314Ter) c.838C>T (p.Arg280Ter) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 1 | g.225937602G>C | CA345013025 | LEFTY2 | c.940C>G (p.Arg314Gly) c.838C>G (p.Arg280Gly) | gnomAD v4 |
| 1 | g.225937602G= | CA1141581384 | LEFTY2 | c.940C= (p.Arg314=) c.838C= (p.Arg280=) | |
| 1 | g.225937602G>T | CA423731154 | LEFTY2 | c.940C>A (p.Arg314=) c.838C>A (p.Arg280=) | |
| 1 | g.225937603C>A | CA423731155 | LEFTY2 | c.939G>T (p.Pro313=) c.837G>T (p.Pro279=) | gnomAD v4 |
| 1 | g.225937603C= | CA1143392544 | LEFTY2 | c.939G= (p.Pro313=) c.837G= (p.Pro279=) | |
| 1 | g.225937603C>G | CA423731156 | LEFTY2 | c.939G>C (p.Pro313=) c.837G>C (p.Pro279=) | gnomAD v4 |
| 1 | g.225937603C>T | CA1420444 | LEFTY2 | c.939G>A (p.Pro313=) c.837G>A (p.Pro279=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.225937604G>A | CA1420445 | LEFTY2 | c.938C>T (p.Pro313Leu) c.836C>T (p.Pro279Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.225937604G>C | CA345013026 | LEFTY2 | c.938C>G (p.Pro313Arg) c.836C>G (p.Pro279Arg) | |
| 1 | g.225937604G= | CA1224682851 | LEFTY2 | c.938C= (p.Pro313=) c.836C= (p.Pro279=) | |
| 1 | g.225937604G>T | CA345013027 | LEFTY2 | c.938C>A (p.Pro313Gln) c.836C>A (p.Pro279Gln) | |
| 1 | g.225937605G>A | CA345013028 | LEFTY2 | c.937C>T (p.Pro313Ser) c.835C>T (p.Pro279Ser) | |
| 1 | g.225937605G>C | CA345013029 | LEFTY2 | c.937C>G (p.Pro313Ala) c.835C>G (p.Pro279Ala) | |
| 1 | g.225937605G>T | CA345013030 | LEFTY2 | c.937C>A (p.Pro313Thr) c.835C>A (p.Pro279Thr) | |
| 1 | g.225937606C>A | CA423731157 | LEFTY2 | c.936G>T (p.Gly312=) c.834G>T (p.Gly278=) | |
| 1 | g.225937606C>G | CA423731158 | LEFTY2 | c.936G>C (p.Gly312=) c.834G>C (p.Gly278=) | |
| 1 | g.225937606C>T | CA423731159 | LEFTY2 | c.936G>A (p.Gly312=) c.834G>A (p.Gly278=) | |
| 1 | g.225937607C>A | CA345013031 | LEFTY2 | c.935G>T (p.Gly312Val) c.833G>T (p.Gly278Val) | dbSNP |
| 1 | g.225937607C= | CA1224682854 | LEFTY2 | c.935G= (p.Gly312=) c.833G= (p.Gly278=) | |
| 1 | g.225937607C>G | CA345013032 | LEFTY2 | c.935G>C (p.Gly312Ala) c.833G>C (p.Gly278Ala) | |
| 1 | g.225937607C>T | CA345013033 | LEFTY2 | c.935G>A (p.Gly312Glu) c.833G>A (p.Gly278Glu) | |
| 1 | g.225937608C>A | CA345013034 | LEFTY2 | c.934G>T (p.Gly312Trp) c.832G>T (p.Gly278Trp) | gnomAD v4 |
| 1 | g.225937608C>G | CA345013035 | LEFTY2 | c.934G>C (p.Gly312Arg) c.832G>C (p.Gly278Arg) | |
| 1 | g.225937608C>T | CA345013036 | LEFTY2 | c.934G>A (p.Gly312Arg) c.832G>A (p.Gly278Arg) | COSMIC |
| 1 | g.225937609C>A | CA423731160 | LEFTY2 | c.933G>T (p.Leu311=) c.831G>T (p.Leu277=) | |
| 1 | g.225937609C>G | CA423731161 | LEFTY2 | c.933G>C (p.Leu311=) c.831G>C (p.Leu277=) | |
| 1 | g.225937609C>T | CA423731162 | LEFTY2 | c.933G>A (p.Leu311=) c.831G>A (p.Leu277=) | gnomAD v4 |
| 1 | g.225937610A>C | CA345013039 | LEFTY2 | c.932T>G (p.Leu311Arg) c.830T>G (p.Leu277Arg) | |
| 1 | g.225937610A>G | CA345013038 | LEFTY2 | c.932T>C (p.Leu311Pro) c.830T>C (p.Leu277Pro) | |
| 1 | g.225937610A>T | CA345013037 | LEFTY2 | c.932T>A (p.Leu311Gln) c.830T>A (p.Leu277Gln) | |
| 1 | g.225937611G>A | CA423731163 | LEFTY2 | c.931C>T (p.Leu311=) c.829C>T (p.Leu277=) | |
| 1 | g.225937611G>C | CA345013040 | LEFTY2 | c.931C>G (p.Leu311Val) c.829C>G (p.Leu277Val) | |
| 1 | g.225937611G>T | CA345013041 | LEFTY2 | c.931C>A (p.Leu311Met) c.829C>A (p.Leu277Met) | |
| 1 | g.225937612A>C | CA345013042 | LEFTY2 | c.930T>G (p.Phe310Leu) c.828T>G (p.Phe276Leu) | gnomAD v4 |
| 1 | g.225937612A>G | CA423731164 | LEFTY2 | c.930T>C (p.Phe310=) c.828T>C (p.Phe276=) | |
| 1 | g.225937612A>T | CA345013043 | LEFTY2 | c.930T>A (p.Phe310Leu) c.828T>A (p.Phe276Leu) | |
| 1 | g.225937613A>C | CA345013044 | LEFTY2 | c.929T>G (p.Phe310Cys) c.827T>G (p.Phe276Cys) | |
| 1 | g.225937613A>G | CA345013045 | LEFTY2 | c.929T>C (p.Phe310Ser) c.827T>C (p.Phe276Ser) | |
| 1 | g.225937613A>T | CA345013046 | LEFTY2 | c.929T>A (p.Phe310Tyr) c.827T>A (p.Phe276Tyr) | |
| 1 | g.225937614A>C | CA345013047 | LEFTY2 | c.928T>G (p.Phe310Val) c.826T>G (p.Phe276Val) | |
| 1 | g.225937614A>G | CA345013048 | LEFTY2 | c.928T>C (p.Phe310Leu) c.826T>C (p.Phe276Leu) | |
| 1 | g.225937614A>T | CA345013049 | LEFTY2 | c.928T>A (p.Phe310Ile) c.826T>A (p.Phe276Ile) | |
| 1 | g.225937615T>A | CA423731165 | LEFTY2 | c.927A>T (p.Pro309=) c.825A>T (p.Pro275=) | |
| 1 | g.225937615T>C | CA423731167 | LEFTY2 | c.927A>G (p.Pro309=) c.825A>G (p.Pro275=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.225937615T>G | CA423731166 | LEFTY2 | c.927A>C (p.Pro309=) c.825A>C (p.Pro275=) | |
| 1 | g.225937615T= | CA1224682855 | LEFTY2 | c.927A= (p.Pro309=) c.825A= (p.Pro275=) | |
| 1 | g.225937616G>A | CA345013050 | LEFTY2 | c.926C>T (p.Pro309Leu) c.824C>T (p.Pro275Leu) | gnomAD v4 |
| 1 | g.225937616G>C | CA1420446 | LEFTY2 | c.926C>G (p.Pro309Arg) c.824C>G (p.Pro275Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.225937616G= | CA1224682856 | LEFTY2 | c.926C= (p.Pro309=) c.824C= (p.Pro275=) |