| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.1414744A= | CA1522628366 | SLC6A3 | c.1103T= (p.Leu368=) n.553T= | |
| 5 | g.1414744A>C | CA359083062 | SLC6A3 | c.1103T>G (p.Leu368Arg) n.553T>G | gnomAD v4 |
| 5 | g.1414744A>G | CA359083060 | SLC6A3 | c.1103T>C (p.Leu368Pro) n.553T>C | |
| 5 | g.1414744A>T | CA126861 | SLC6A3 | c.1103T>A (p.Leu368Gln) n.553T>A | ClinVar dbSNP |
| 5 | g.1414745G>A | CA3186158 | SLC6A3 | c.1102C>T (p.Leu368=) n.552C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.1414745G>C | CA359083066 | SLC6A3 | c.1102C>G (p.Leu368Val) n.552C>G | |
| 5 | g.1414745G= | CA1522628369 | SLC6A3 | c.1102C= (p.Leu368=) n.552C= | |
| 5 | g.1414745G>T | CA359083068 | SLC6A3 | c.1102C>A (p.Leu368Met) n.552C>A | gnomAD v4 |
| 5 | g.1414746G>A | CA443020862 | SLC6A3 | c.1101C>T (p.Phe367=) n.551C>T | |
| 5 | g.1414746G>C | CA359083070 | SLC6A3 | c.1101C>G (p.Phe367Leu) n.551C>G | |
| 5 | g.1414746G>T | CA359083072 | SLC6A3 | c.1101C>A (p.Phe367Leu) n.551C>A | |
| 5 | g.1414747A>C | CA359083074 | SLC6A3 | c.1100T>G (p.Phe367Cys) n.550T>G | |
| 5 | g.1414747A>G | CA359083076 | SLC6A3 | c.1100T>C (p.Phe367Ser) n.550T>C | |
| 5 | g.1414747A>T | CA359083078 | SLC6A3 | c.1100T>A (p.Phe367Tyr) n.550T>A | |
| 5 | g.1414748A>C | CA359083082 | SLC6A3 | c.1099T>G (p.Phe367Val) n.549T>G | |
| 5 | g.1414748A>G | CA359083084 | SLC6A3 | c.1099T>C (p.Phe367Leu) n.549T>C | gnomAD v4 |
| 5 | g.1414748A>T | CA359083087 | SLC6A3 | c.1099T>A (p.Phe367Ile) n.549T>A | |
| 5 | g.1414749G>A | CA443020863 | SLC6A3 | c.1098C>T (p.Ser366=) n.548C>T | dbSNP |
| 5 | g.1414749G>C | CA443020864 | SLC6A3 | c.1098C>G (p.Ser366=) n.548C>G | |
| 5 | g.1414749G= | CA1522628376 | SLC6A3 | c.1098C= (p.Ser366=) n.548C= | |
| 5 | g.1414749G>T | CA443020865 | SLC6A3 | c.1098C>A (p.Ser366=) n.548C>A | |
| 5 | g.1414750G>A | CA359083095 | SLC6A3 | c.1097C>T (p.Ser366Phe) n.547C>T | |
| 5 | g.1414750G>C | CA359083093 | SLC6A3 | c.1097C>G (p.Ser366Cys) n.547C>G | |
| 5 | g.1414750G>T | CA359083090 | SLC6A3 | c.1097C>A (p.Ser366Tyr) n.547C>A | |
| 5 | g.1414751A>C | CA359083098 | SLC6A3 | c.1096T>G (p.Ser366Ala) n.546T>G | |
| 5 | g.1414751A>G | CA359083100 | SLC6A3 | c.1096T>C (p.Ser366Pro) n.546T>C | |
| 5 | g.1414751A>T | CA359083102 | SLC6A3 | c.1096T>A (p.Ser366Thr) n.546T>A | |
| 5 | g.1414752G>A | CA443020866 | SLC6A3 | c.1095C>T (p.Phe365=) n.545C>T | |
| 5 | g.1414752G>C | CA359083106 | SLC6A3 | c.1095C>G (p.Phe365Leu) n.545C>G | |
| 5 | g.1414752G>T | CA359083109 | SLC6A3 | c.1095C>A (p.Phe365Leu) n.545C>A | |
| 5 | g.1414753A>C | CA359083116 | SLC6A3 | c.1094T>G (p.Phe365Cys) n.544T>G | |
| 5 | g.1414753A>G | CA359083114 | SLC6A3 | c.1094T>C (p.Phe365Ser) n.544T>C | |
| 5 | g.1414753A>T | CA359083112 | SLC6A3 | c.1094T>A (p.Phe365Tyr) n.544T>A | |
| 5 | g.1414754A>C | CA359083120 | SLC6A3 | c.1093T>G (p.Phe365Val) n.543T>G | |
| 5 | g.1414754A>G | CA359083122 | SLC6A3 | c.1093T>C (p.Phe365Leu) n.543T>C | |
| 5 | g.1414754A>T | CA359083125 | SLC6A3 | c.1093T>A (p.Phe365Ile) n.543T>A | |
| 5 | g.1414755G>A | CA443020868 | SLC6A3 | c.1092C>T (p.Val364=) n.542C>T | gnomAD v4 |
| 5 | g.1414755G>C | CA443020869 | SLC6A3 | c.1092C>G (p.Val364=) n.542C>G | gnomAD v4 |
| 5 | g.1414755G= | CA1522628379 | SLC6A3 | c.1092C= (p.Val364=) n.542C= | |
| 5 | g.1414755G>T | CA443020870 | SLC6A3 | c.1092C>A (p.Val364=) n.542C>A | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.1414756A>C | CA359083129 | SLC6A3 | c.1091T>G (p.Val364Gly) n.541T>G | |
| 5 | g.1414756A>G | CA359083132 | SLC6A3 | c.1091T>C (p.Val364Ala) n.541T>C | |
| 5 | g.1414756A>T | CA359083136 | SLC6A3 | c.1091T>A (p.Val364Asp) n.541T>A | |
| 5 | g.1414757C>A | CA359083140 | SLC6A3 | c.1090G>T (p.Val364Phe) n.540G>T | |
| 5 | g.1414757C= | CA1522628383 | SLC6A3 | c.1090G= (p.Val364=) n.540G= | |
| 5 | g.1414757C>G | CA359083145 | SLC6A3 | c.1090G>C (p.Val364Leu) n.540G>C | dbSNP |
| 5 | g.1414757C>T | CA3186159 | SLC6A3 | c.1090G>A (p.Val364Ile) n.540G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.1414758G>A | CA3186160 | SLC6A3 | c.1089C>T (p.Val363=) n.539C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.1414758G>C | CA443020871 | SLC6A3 | c.1089C>G (p.Val363=) n.539C>G | |
| 5 | g.1414758G= | CA1522628388 | SLC6A3 | c.1089C= (p.Val363=) n.539C= |