Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.136674767_136674769del | CA2692654222 | AGPAT2 | c.629_631del (p.Phe210del) c.533_535del (p.Phe178del) n.557_559del | gnomAD v4 |
9 | g.136674773_136674775del | CA5342901 | AGPAT2 | c.626_628del (p.Ser209del) c.530_532del (p.Ser177del) n.554_556del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674769G>A | CA467738176 | AGPAT2 | c.627C>T (p.Ser209=) c.531C>T (p.Ser177=) n.555C>T | gnomAD v4 |
9 | g.136674769G>C | CA467738171 | AGPAT2 | c.627C>G (p.Ser209=) c.531C>G (p.Ser177=) n.555C>G | gnomAD v4 |
9 | g.136674769G>T | CA467738173 | AGPAT2 | c.627C>A (p.Ser209=) c.531C>A (p.Ser177=) n.555C>A | gnomAD v4 |
9 | g.136674770G>A | CA375578575 | AGPAT2 | c.626C>T (p.Ser209Phe) c.530C>T (p.Ser177Phe) n.554C>T | gnomAD v4 |
9 | g.136674770G>C | CA375578565 | AGPAT2 | c.626C>G (p.Ser209Cys) c.530C>G (p.Ser177Cys) n.554C>G | |
9 | g.136674770G>T | CA5342903 | AGPAT2 | c.626C>A (p.Ser209Tyr) c.530C>A (p.Ser177Tyr) n.554C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674772_136674776del | CA913189691 | AGPAT2 | c.622_626del (p.Ser208LeufsTer?) c.526_530del (p.Ser176LeufsTer?) n.550_554del | ClinVar dbSNP |
9 | g.136674771A>C | CA375578591 | AGPAT2 | c.625T>G (p.Ser209Ala) c.529T>G (p.Ser177Ala) n.553T>G | |
9 | g.136674771A>G | CA375578593 | AGPAT2 | c.625T>C (p.Ser209Pro) c.529T>C (p.Ser177Pro) n.553T>C | gnomAD v4 |
9 | g.136674771A>T | CA375578596 | AGPAT2 | c.625T>A (p.Ser209Thr) c.529T>A (p.Ser177Thr) n.553T>A | |
9 | g.136674772G>A | CA467738195 | AGPAT2 | c.624C>T (p.Ser208=) c.528C>T (p.Ser176=) n.552C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136674772G>C | CA467738199 | AGPAT2 | c.624C>G (p.Ser208=) c.528C>G (p.Ser176=) n.552C>G | gnomAD v4 |
9 | g.136674772G>T | CA467738197 | AGPAT2 | c.624C>A (p.Ser208=) c.528C>A (p.Ser176=) n.552C>A | gnomAD v4 |
9 | g.136674773G>A | CA201627675 | AGPAT2 | c.623C>T (p.Ser208Phe) c.527C>T (p.Ser176Phe) n.551C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.136674773G>C | CA375578605 | AGPAT2 | c.623C>G (p.Ser208Cys) c.527C>G (p.Ser176Cys) n.551C>G | |
9 | g.136674773G>T | CA375578606 | AGPAT2 | c.623C>A (p.Ser208Tyr) c.527C>A (p.Ser176Tyr) n.551C>A | |
9 | g.136674774A>C | CA375578610 | AGPAT2 | c.622T>G (p.Ser208Ala) c.526T>G (p.Ser176Ala) n.550T>G | |
9 | g.136674774A>G | CA5342904 | AGPAT2 | c.622T>C (p.Ser208Pro) c.526T>C (p.Ser176Pro) n.550T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674774A>T | CA375578608 | AGPAT2 | c.622T>A (p.Ser208Thr) c.526T>A (p.Ser176Thr) n.550T>A | gnomAD v4 |
9 | g.136674775G>A | CA467738219 | AGPAT2 | c.621C>T (p.Phe207=) c.525C>T (p.Phe175=) n.549C>T | ClinVar gnomAD v4 |
9 | g.136674775G>C | CA375578613 | AGPAT2 | c.621C>G (p.Phe207Leu) c.525C>G (p.Phe175Leu) n.549C>G | gnomAD v4 |
9 | g.136674775G>T | CA375578614 | AGPAT2 | c.621C>A (p.Phe207Leu) c.525C>A (p.Phe175Leu) n.549C>A | |
9 | g.136674779_136674782del | CA591183731 | AGPAT2 | c.618_621del (p.Phe207ProfsTer?) c.522_525del (p.Phe175ProfsTer?) n.546_549del | gnomAD v2 gnomAD v4 |
9 | g.136674776A>C | CA375578617 | AGPAT2 | c.620T>G (p.Phe207Cys) c.524T>G (p.Phe175Cys) n.548T>G | |
9 | g.136674776A>G | CA375578618 | AGPAT2 | c.620T>C (p.Phe207Ser) c.524T>C (p.Phe175Ser) n.548T>C | gnomAD v4 |
9 | g.136674776A>T | CA375578622 | AGPAT2 | c.620T>A (p.Phe207Tyr) c.524T>A (p.Phe175Tyr) n.548T>A | |
9 | g.136674777del | CA2692654224 | AGPAT2 | c.620del (p.Phe207SerfsTer?) c.524del (p.Phe175SerfsTer?) n.548del | gnomAD v4 |
9 | g.136674777A>C | CA375578630 | AGPAT2 | c.619T>G (p.Phe207Val) c.523T>G (p.Phe175Val) n.547T>G | |
9 | g.136674777A>G | CA375578628 | AGPAT2 | c.619T>C (p.Phe207Leu) c.523T>C (p.Phe175Leu) n.547T>C | gnomAD v4 |
9 | g.136674777A>T | CA375578629 | AGPAT2 | c.619T>A (p.Phe207Ile) c.523T>A (p.Phe175Ile) n.547T>A | gnomAD v4 |
9 | g.136674778G>A | CA5342905 | AGPAT2 | c.618C>T (p.Ser206=) c.522C>T (p.Ser174=) n.546C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674778G>C | CA467738236 | AGPAT2 | c.618C>G (p.Ser206=) c.522C>G (p.Ser174=) n.546C>G | |
9 | g.136674778G>T | CA467738238 | AGPAT2 | c.618C>A (p.Ser206=) c.522C>A (p.Ser174=) n.546C>A | |
9 | g.136674779G>A | CA5342906 | AGPAT2 | c.617C>T (p.Ser206Phe) c.521C>T (p.Ser174Phe) n.545C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674779G>C | CA375578635 | AGPAT2 | c.617C>G (p.Ser206Cys) c.521C>G (p.Ser174Cys) n.545C>G | |
9 | g.136674779G>T | CA375578636 | AGPAT2 | c.617C>A (p.Ser206Tyr) c.521C>A (p.Ser174Tyr) n.545C>A | |
9 | g.136674780A>C | CA375578637 | AGPAT2 | c.616T>G (p.Ser206Ala) c.520T>G (p.Ser174Ala) n.544T>G | |
9 | g.136674780A>G | CA375578646 | AGPAT2 | c.616T>C (p.Ser206Pro) c.520T>C (p.Ser174Pro) n.544T>C | gnomAD v4 |
9 | g.136674780A>T | CA375578650 | AGPAT2 | c.616T>A (p.Ser206Thr) c.520T>A (p.Ser174Thr) n.544T>A | |
9 | g.136674781A>C | CA467738254 | AGPAT2 | c.615T>G (p.Ser205=) c.519T>G (p.Ser173=) n.543T>G | |
9 | g.136674781A>G | CA467738256 | AGPAT2 | c.615T>C (p.Ser205=) c.519T>C (p.Ser173=) n.543T>C | gnomAD v4 |
9 | g.136674781A>T | CA467738259 | AGPAT2 | c.615T>A (p.Ser205=) c.519T>A (p.Ser173=) n.543T>A | gnomAD v4 |
9 | g.136674782G>A | CA375578653 | AGPAT2 | c.614C>T (p.Ser205Phe) c.518C>T (p.Ser173Phe) n.542C>T | gnomAD v4 |
9 | g.136674782G>C | CA375578654 | AGPAT2 | c.614C>G (p.Ser205Cys) c.518C>G (p.Ser173Cys) n.542C>G | |
9 | g.136674782G>T | CA375578655 | AGPAT2 | c.614C>A (p.Ser205Tyr) c.518C>A (p.Ser173Tyr) n.542C>A | |
9 | g.136674783A>C | CA375578656 | AGPAT2 | c.613T>G (p.Ser205Ala) c.517T>G (p.Ser173Ala) n.541T>G | |
9 | g.136674783A>G | CA375578657 | AGPAT2 | c.613T>C (p.Ser205Pro) c.517T>C (p.Ser173Pro) n.541T>C | gnomAD v4 |
9 | g.136674783A>T | CA375578658 | AGPAT2 | c.613T>A (p.Ser205Thr) c.517T>A (p.Ser173Thr) n.541T>A |