Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.156326222_156330699del | CA2837995531 | NR4A2 | c.-146_1264del c.-34_1393del c.-34_1468del c.-45_1173-15del c.-34_1379-15del c.-45_1279del c.-45_1190-15del c.32-511_1501del c.-13-689_1279del c.32-511_1426del c.32-511_1412-15del n.2205-511_3568-15del n.335_1730-15del n.335_1552-15del n.246-511_1609-15del | |
2 | g.156329671G>A | CA429727709 | NR4A2 | c.327C>T (p.Arg109=) c.387C>T (p.Arg129=) c.516C>T (p.Arg172=) c.208+243C>T c.549C>T (p.Arg183=) n.2722C>T n.884C>T n.706C>T n.763C>T | |
2 | g.156329671G>C | CA429727710 | NR4A2 | c.327C>G (p.Arg109=) c.387C>G (p.Arg129=) c.516C>G (p.Arg172=) c.208+243C>G c.549C>G (p.Arg183=) n.2722C>G n.884C>G n.706C>G n.763C>G | |
2 | g.156329671G>T | CA429727712 | NR4A2 | c.327C>A (p.Arg109=) c.387C>A (p.Arg129=) c.516C>A (p.Arg172=) c.208+243C>A c.549C>A (p.Arg183=) n.2722C>A n.884C>A n.706C>A n.763C>A | |
2 | g.156329672C>A | CA348682252 | NR4A2 | c.326G>T (p.Arg109Leu) c.386G>T (p.Arg129Leu) c.515G>T (p.Arg172Leu) c.208+242G>T c.548G>T (p.Arg183Leu) n.2721G>T n.883G>T n.705G>T n.762G>T | gnomAD v4 |
2 | g.156329672C>G | CA348682253 | NR4A2 | c.326G>C (p.Arg109Pro) c.386G>C (p.Arg129Pro) c.515G>C (p.Arg172Pro) c.208+242G>C c.548G>C (p.Arg183Pro) n.2721G>C n.883G>C n.705G>C n.762G>C | |
2 | g.156329672C>T | CA348682254 | NR4A2 | c.326G>A (p.Arg109His) c.386G>A (p.Arg129His) c.515G>A (p.Arg172His) c.208+242G>A c.548G>A (p.Arg183His) n.2721G>A n.883G>A n.705G>A n.762G>A | gnomAD v4 COSMIC COSMIC |
2 | g.156329673G>A | CA348682255 | NR4A2 | c.325C>T (p.Arg109Cys) c.385C>T (p.Arg129Cys) c.514C>T (p.Arg172Cys) c.208+241C>T c.547C>T (p.Arg183Cys) n.2720C>T n.882C>T n.704C>T n.761C>T | dbSNP gnomAD v3 gnomAD v4 |
2 | g.156329673G>C | CA348682256 | NR4A2 | c.325C>G (p.Arg109Gly) c.385C>G (p.Arg129Gly) c.514C>G (p.Arg172Gly) c.208+241C>G c.547C>G (p.Arg183Gly) n.2720C>G n.882C>G n.704C>G n.761C>G | |
2 | g.156329673G= | CA1300460549 | NR4A2 | c.325C= (p.Arg109=) c.385C= (p.Arg129=) c.514C= (p.Arg172=) c.208+241C= c.547C= (p.Arg183=) n.2720C= n.882C= n.704C= n.761C= | |
2 | g.156329673G>T | CA348682257 | NR4A2 | c.325C>A (p.Arg109Ser) c.385C>A (p.Arg129Ser) c.514C>A (p.Arg172Ser) c.208+241C>A c.547C>A (p.Arg183Ser) n.2720C>A n.882C>A n.704C>A n.761C>A | |
2 | g.156329674G>A | CA429727717 | NR4A2 | c.324C>T (p.Ser108=) c.384C>T (p.Ser128=) c.513C>T (p.Ser171=) c.208+240C>T c.546C>T (p.Ser182=) n.2719C>T n.881C>T n.703C>T n.760C>T | gnomAD v4 |
2 | g.156329674G>C | CA429727718 | NR4A2 | c.324C>G (p.Ser108=) c.384C>G (p.Ser128=) c.513C>G (p.Ser171=) c.208+240C>G c.546C>G (p.Ser182=) n.2719C>G n.881C>G n.703C>G n.760C>G | |
2 | g.156329674G>T | CA429727719 | NR4A2 | c.324C>A (p.Ser108=) c.384C>A (p.Ser128=) c.513C>A (p.Ser171=) c.208+240C>A c.546C>A (p.Ser182=) n.2719C>A n.881C>A n.703C>A n.760C>A | |
2 | g.156329675G>A | CA348682258 | NR4A2 | c.323C>T (p.Ser108Phe) c.383C>T (p.Ser128Phe) c.512C>T (p.Ser171Phe) c.208+239C>T c.545C>T (p.Ser182Phe) n.2718C>T n.880C>T n.702C>T n.759C>T | ClinVar |
2 | g.156329675G>C | CA348682259 | NR4A2 | c.323C>G (p.Ser108Cys) c.383C>G (p.Ser128Cys) c.512C>G (p.Ser171Cys) c.208+239C>G c.545C>G (p.Ser182Cys) n.2718C>G n.880C>G n.702C>G n.759C>G | |
2 | g.156329675G>T | CA348682260 | NR4A2 | c.323C>A (p.Ser108Tyr) c.383C>A (p.Ser128Tyr) c.512C>A (p.Ser171Tyr) c.208+239C>A c.545C>A (p.Ser182Tyr) n.2718C>A n.880C>A n.702C>A n.759C>A | |
2 | g.156329676A= | CA1300460550 | NR4A2 | c.322T= (p.Ser108=) c.382T= (p.Ser128=) c.511T= (p.Ser171=) c.208+238T= c.544T= (p.Ser182=) n.2717T= n.879T= n.701T= n.758T= | |
2 | g.156329676A>C | CA348682261 | NR4A2 | c.322T>G (p.Ser108Ala) c.382T>G (p.Ser128Ala) c.511T>G (p.Ser171Ala) c.208+238T>G c.544T>G (p.Ser182Ala) n.2717T>G n.879T>G n.701T>G n.758T>G | |
2 | g.156329676A>G | CA348682262 | NR4A2 | c.322T>C (p.Ser108Pro) c.382T>C (p.Ser128Pro) c.511T>C (p.Ser171Pro) c.208+238T>C c.544T>C (p.Ser182Pro) n.2717T>C n.879T>C n.701T>C n.758T>C | dbSNP |
2 | g.156329676A>T | CA348682263 | NR4A2 | c.322T>A (p.Ser108Thr) c.382T>A (p.Ser128Thr) c.511T>A (p.Ser171Thr) c.208+238T>A c.544T>A (p.Ser182Thr) n.2717T>A n.879T>A n.701T>A n.758T>A | |
2 | g.156329677G>A | CA1916437 | NR4A2 | c.321C>T (p.Val107=) c.381C>T (p.Val127=) c.510C>T (p.Val170=) c.208+237C>T c.543C>T (p.Val181=) n.2716C>T n.878C>T n.700C>T n.757C>T | dbSNP ExAC gnomAD v2 |
2 | g.156329677G>C | CA429727728 | NR4A2 | c.321C>G (p.Val107=) c.381C>G (p.Val127=) c.510C>G (p.Val170=) c.208+237C>G c.543C>G (p.Val181=) n.2716C>G n.878C>G n.700C>G n.757C>G | dbSNP |
2 | g.156329677G= | CA1300460551 | NR4A2 | c.321C= (p.Val107=) c.381C= (p.Val127=) c.510C= (p.Val170=) c.208+237C= c.543C= (p.Val181=) n.2716C= n.878C= n.700C= n.757C= | |
2 | g.156329677G>T | CA429727726 | NR4A2 | c.321C>A (p.Val107=) c.381C>A (p.Val127=) c.510C>A (p.Val170=) c.208+237C>A c.543C>A (p.Val181=) n.2716C>A n.878C>A n.700C>A n.757C>A | |
2 | g.156329678A>C | CA348682265 | NR4A2 | c.320T>G (p.Val107Gly) c.380T>G (p.Val127Gly) c.509T>G (p.Val170Gly) c.208+236T>G c.320T>G c.542T>G (p.Val181Gly) n.2715T>G n.877T>G n.699T>G n.756T>G | |
2 | g.156329678A>G | CA348682266 | NR4A2 | c.320T>C (p.Val107Ala) c.380T>C (p.Val127Ala) c.509T>C (p.Val170Ala) c.208+236T>C c.320T>C c.542T>C (p.Val181Ala) n.2715T>C n.877T>C n.699T>C n.756T>C | |
2 | g.156329678A>T | CA348682264 | NR4A2 | c.320T>A (p.Val107Asp) c.380T>A (p.Val127Asp) c.509T>A (p.Val170Asp) c.208+236T>A c.320T>A c.542T>A (p.Val181Asp) n.2715T>A n.877T>A n.699T>A n.756T>A | |
2 | g.156329679C>A | CA348682268 | NR4A2 | c.319G>T (p.Val107Phe) c.379G>T (p.Val127Phe) c.508G>T (p.Val170Phe) c.208+235G>T c.319G>T c.541G>T (p.Val181Phe) n.2714G>T n.876G>T n.698G>T n.755G>T | |
2 | g.156329679C>G | CA348682267 | NR4A2 | c.319G>C (p.Val107Leu) c.379G>C (p.Val127Leu) c.508G>C (p.Val170Leu) c.208+235G>C c.319G>C c.541G>C (p.Val181Leu) n.2714G>C n.876G>C n.698G>C n.755G>C | |
2 | g.156329679C>T | CA348682269 | NR4A2 | c.319G>A (p.Val107Ile) c.379G>A (p.Val127Ile) c.508G>A (p.Val170Ile) c.208+235G>A c.319G>A c.541G>A (p.Val181Ile) n.2714G>A n.876G>A n.698G>A n.755G>A | |
2 | g.156329680T>A | CA429727732 | NR4A2 | c.318A>T (p.Pro106=) c.378A>T (p.Pro126=) c.507A>T (p.Pro169=) c.208+234A>T c.540A>T (p.Pro180=) n.2713A>T n.875A>T n.697A>T n.754A>T | |
2 | g.156329680T>C | CA429727733 | NR4A2 | c.318A>G (p.Pro106=) c.378A>G (p.Pro126=) c.507A>G (p.Pro169=) c.208+234A>G c.540A>G (p.Pro180=) n.2713A>G n.875A>G n.697A>G n.754A>G | |
2 | g.156329680T>G | CA429727734 | NR4A2 | c.318A>C (p.Pro106=) c.378A>C (p.Pro126=) c.507A>C (p.Pro169=) c.208+234A>C c.540A>C (p.Pro180=) n.2713A>C n.875A>C n.697A>C n.754A>C | gnomAD v4 |
2 | g.156329681G>A | CA348682270 | NR4A2 | c.317C>T (p.Pro106Leu) c.377C>T (p.Pro126Leu) c.506C>T (p.Pro169Leu) c.208+233C>T c.539C>T (p.Pro180Leu) n.2712C>T n.874C>T n.696C>T n.753C>T | |
2 | g.156329681G>C | CA348682272 | NR4A2 | c.317C>G (p.Pro106Arg) c.377C>G (p.Pro126Arg) c.506C>G (p.Pro169Arg) c.208+233C>G c.539C>G (p.Pro180Arg) n.2712C>G n.874C>G n.696C>G n.753C>G | |
2 | g.156329681G>T | CA348682271 | NR4A2 | c.317C>A (p.Pro106Gln) c.377C>A (p.Pro126Gln) c.506C>A (p.Pro169Gln) c.208+233C>A c.539C>A (p.Pro180Gln) n.2712C>A n.874C>A n.696C>A n.753C>A | |
2 | g.156329682G>A | CA348682273 | NR4A2 | c.316C>T (p.Pro106Ser) c.376C>T (p.Pro126Ser) c.505C>T (p.Pro169Ser) c.208+232C>T c.538C>T (p.Pro180Ser) n.2711C>T n.873C>T n.695C>T n.752C>T | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329682G>C | CA1916438 | NR4A2 | c.316C>G (p.Pro106Ala) c.376C>G (p.Pro126Ala) c.505C>G (p.Pro169Ala) c.208+232C>G c.538C>G (p.Pro180Ala) n.2711C>G n.873C>G n.695C>G n.752C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.156329682G= | CA1300460552 | NR4A2 | c.316C= (p.Pro106=) c.376C= (p.Pro126=) c.505C= (p.Pro169=) c.208+232C= c.538C= (p.Pro180=) n.2711C= n.873C= n.695C= n.752C= | |
2 | g.156329682G>T | CA348682274 | NR4A2 | c.316C>A (p.Pro106Thr) c.376C>A (p.Pro126Thr) c.505C>A (p.Pro169Thr) c.208+232C>A c.538C>A (p.Pro180Thr) n.2711C>A n.873C>A n.695C>A n.752C>A | |
2 | g.156329683C>A | CA429727740 | NR4A2 | c.315G>T (p.Thr105=) c.375G>T (p.Thr125=) c.504G>T (p.Thr168=) c.208+231G>T c.537G>T (p.Thr179=) n.2710G>T n.872G>T n.694G>T n.751G>T | |
2 | g.156329683C= | CA1300460553 | NR4A2 | c.315G= (p.Thr105=) c.375G= (p.Thr125=) c.504G= (p.Thr168=) c.208+231G= c.537G= (p.Thr179=) n.2710G= n.872G= n.694G= n.751G= | |
2 | g.156329683C>G | CA429727743 | NR4A2 | c.315G>C (p.Thr105=) c.375G>C (p.Thr125=) c.504G>C (p.Thr168=) c.208+231G>C c.537G>C (p.Thr179=) n.2710G>C n.872G>C n.694G>C n.751G>C | dbSNP |
2 | g.156329683C>T | CA1916439 | NR4A2 | c.315G>A (p.Thr105=) c.375G>A (p.Thr125=) c.504G>A (p.Thr168=) c.208+231G>A c.537G>A (p.Thr179=) n.2710G>A n.872G>A n.694G>A n.751G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
2 | g.156329684G>A | CA348682275 | NR4A2 | c.314C>T (p.Thr105Met) c.374C>T (p.Thr125Met) c.503C>T (p.Thr168Met) c.208+230C>T c.536C>T (p.Thr179Met) n.2709C>T n.871C>T n.693C>T n.750C>T | gnomAD v4 |
2 | g.156329684G>C | CA348682276 | NR4A2 | c.314C>G (p.Thr105Arg) c.374C>G (p.Thr125Arg) c.503C>G (p.Thr168Arg) c.208+230C>G c.536C>G (p.Thr179Arg) n.2709C>G n.871C>G n.693C>G n.750C>G | |
2 | g.156329684G>T | CA348682277 | NR4A2 | c.314C>A (p.Thr105Lys) c.374C>A (p.Thr125Lys) c.503C>A (p.Thr168Lys) c.208+230C>A c.536C>A (p.Thr179Lys) n.2709C>A n.871C>A n.693C>A n.750C>A | gnomAD v4 |
2 | g.156329685T>A | CA348682278 | NR4A2 | c.313A>T (p.Thr105Ser) c.373A>T (p.Thr125Ser) c.502A>T (p.Thr168Ser) c.208+229A>T c.535A>T (p.Thr179Ser) n.2708A>T n.870A>T n.692A>T n.749A>T | gnomAD v4 |
2 | g.156329685T>C | CA348682279 | NR4A2 | c.313A>G (p.Thr105Ala) c.373A>G (p.Thr125Ala) c.502A>G (p.Thr168Ala) c.208+229A>G c.535A>G (p.Thr179Ala) n.2708A>G n.870A>G n.692A>G n.749A>G | |
2 | g.156329685T>G | CA348682280 | NR4A2 | c.313A>C (p.Thr105Pro) c.373A>C (p.Thr125Pro) c.502A>C (p.Thr168Pro) c.208+229A>C c.535A>C (p.Thr179Pro) n.2708A>C n.870A>C n.692A>C n.749A>C | dbSNP |
2 | g.156329685T= | CA1300460554 | NR4A2 | c.313A= (p.Thr105=) c.373A= (p.Thr125=) c.502A= (p.Thr168=) c.208+229A= c.535A= (p.Thr179=) n.2708A= n.870A= n.692A= n.749A= | |
2 | g.156329686T>A | CA348682281 | NR4A2 | c.312A>T (p.Lys104Asn) c.372A>T (p.Lys124Asn) c.501A>T (p.Lys167Asn) c.208+228A>T c.534A>T (p.Lys178Asn) n.2707A>T n.869A>T n.691A>T n.748A>T | |
2 | g.156329686T>C | CA429727747 | NR4A2 | c.312A>G (p.Lys104=) c.372A>G (p.Lys124=) c.501A>G (p.Lys167=) c.208+228A>G c.534A>G (p.Lys178=) n.2707A>G n.869A>G n.691A>G n.748A>G | |
2 | g.156329686T>G | CA348682282 | NR4A2 | c.312A>C (p.Lys104Asn) c.372A>C (p.Lys124Asn) c.501A>C (p.Lys167Asn) c.208+228A>C c.534A>C (p.Lys178Asn) n.2707A>C n.869A>C n.691A>C n.748A>C | |
2 | g.156329687T>A | CA348682283 | NR4A2 | c.311A>T (p.Lys104Ile) c.371A>T (p.Lys124Ile) c.500A>T (p.Lys167Ile) c.208+227A>T c.533A>T (p.Lys178Ile) n.2706A>T n.868A>T n.690A>T n.747A>T | |
2 | g.156329687T>C | CA348682284 | NR4A2 | c.311A>G (p.Lys104Arg) c.371A>G (p.Lys124Arg) c.500A>G (p.Lys167Arg) c.208+227A>G c.533A>G (p.Lys178Arg) n.2706A>G n.868A>G n.690A>G n.747A>G | |
2 | g.156329687T>G | CA348682285 | NR4A2 | c.311A>C (p.Lys104Thr) c.371A>C (p.Lys124Thr) c.500A>C (p.Lys167Thr) c.208+227A>C c.533A>C (p.Lys178Thr) n.2706A>C n.868A>C n.690A>C n.747A>C | |
2 | g.156329688T>A | CA348682286 | NR4A2 | c.310A>T (p.Lys104Ter) c.370A>T (p.Lys124Ter) c.499A>T (p.Lys167Ter) c.208+226A>T c.532A>T (p.Lys178Ter) n.2705A>T n.867A>T n.689A>T n.746A>T | |
2 | g.156329688T>C | CA348682288 | NR4A2 | c.310A>G (p.Lys104Glu) c.370A>G (p.Lys124Glu) c.499A>G (p.Lys167Glu) c.208+226A>G c.532A>G (p.Lys178Glu) n.2705A>G n.867A>G n.689A>G n.746A>G | |
2 | g.156329688T>G | CA348682287 | NR4A2 | c.310A>C (p.Lys104Gln) c.370A>C (p.Lys124Gln) c.499A>C (p.Lys167Gln) c.208+226A>C c.532A>C (p.Lys178Gln) n.2705A>C n.867A>C n.689A>C n.746A>C | |
2 | g.156329689C>A | CA348682289 | NR4A2 | c.309G>T (p.Arg103Ser) c.369G>T (p.Arg123Ser) c.498G>T (p.Arg166Ser) c.208+225G>T c.531G>T (p.Arg177Ser) n.2704G>T n.866G>T n.688G>T n.745G>T | |
2 | g.156329689C= | CA1300460555 | NR4A2 | c.309G= (p.Arg103=) c.369G= (p.Arg123=) c.498G= (p.Arg166=) c.208+225G= c.531G= (p.Arg177=) n.2704G= n.866G= n.688G= n.745G= | |
2 | g.156329689C>G | CA348682290 | NR4A2 | c.309G>C (p.Arg103Ser) c.369G>C (p.Arg123Ser) c.498G>C (p.Arg166Ser) c.208+225G>C c.531G>C (p.Arg177Ser) n.2704G>C n.866G>C n.688G>C n.745G>C | |
2 | g.156329689C>T | CA59155128 | NR4A2 | c.309G>A (p.Arg103=) c.369G>A (p.Arg123=) c.498G>A (p.Arg166=) c.208+225G>A c.531G>A (p.Arg177=) n.2704G>A n.866G>A n.688G>A n.745G>A | dbSNP gnomAD v3 gnomAD v4 |
2 | g.156329690C>A | CA348682291 | NR4A2 | c.308G>T (p.Arg103Met) c.368G>T (p.Arg123Met) c.497G>T (p.Arg166Met) c.208+224G>T c.530G>T (p.Arg177Met) n.2703G>T n.865G>T n.687G>T n.744G>T | |
2 | g.156329690C= | CA1300460556 | NR4A2 | c.308G= (p.Arg103=) c.368G= (p.Arg123=) c.497G= (p.Arg166=) c.208+224G= c.530G= (p.Arg177=) n.2703G= n.865G= n.687G= n.744G= | |
2 | g.156329690C>G | CA348682292 | NR4A2 | c.308G>C (p.Arg103Thr) c.368G>C (p.Arg123Thr) c.497G>C (p.Arg166Thr) c.208+224G>C c.530G>C (p.Arg177Thr) n.2703G>C n.865G>C n.687G>C n.744G>C | |
2 | g.156329690C>T | CA348682293 | NR4A2 | c.308G>A (p.Arg103Lys) c.368G>A (p.Arg123Lys) c.497G>A (p.Arg166Lys) c.208+224G>A c.530G>A (p.Arg177Lys) n.2703G>A n.865G>A n.687G>A n.744G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329691T>A | CA348682294 | NR4A2 | c.307A>T (p.Arg103Trp) c.367A>T (p.Arg123Trp) c.496A>T (p.Arg166Trp) c.208+223A>T c.529A>T (p.Arg177Trp) n.2702A>T n.864A>T n.686A>T n.743A>T | |
2 | g.156329691T>C | CA348682295 | NR4A2 | c.307A>G (p.Arg103Gly) c.367A>G (p.Arg123Gly) c.496A>G (p.Arg166Gly) c.208+223A>G c.529A>G (p.Arg177Gly) n.2702A>G n.864A>G n.686A>G n.743A>G | |
2 | g.156329691T>G | CA429727754 | NR4A2 | c.307A>C (p.Arg103=) c.367A>C (p.Arg123=) c.496A>C (p.Arg166=) c.208+223A>C c.529A>C (p.Arg177=) n.2702A>C n.864A>C n.686A>C n.743A>C | |
2 | g.156329692C>A | CA348682296 | NR4A2 | c.306G>T (p.Gln102His) c.366G>T (p.Gln122His) c.495G>T (p.Gln165His) c.208+222G>T c.528G>T (p.Gln176His) n.2701G>T n.863G>T n.685G>T n.742G>T | |
2 | g.156329692C>G | CA348682297 | NR4A2 | c.306G>C (p.Gln102His) c.366G>C (p.Gln122His) c.495G>C (p.Gln165His) c.208+222G>C c.528G>C (p.Gln176His) n.2701G>C n.863G>C n.685G>C n.742G>C | gnomAD v4 |
2 | g.156329692C>T | CA429727755 | NR4A2 | c.306G>A (p.Gln102=) c.366G>A (p.Gln122=) c.495G>A (p.Gln165=) c.208+222G>A c.528G>A (p.Gln176=) n.2701G>A n.863G>A n.685G>A n.742G>A | |
2 | g.156329693T>A | CA348682298 | NR4A2 | c.305A>T (p.Gln102Leu) c.365A>T (p.Gln122Leu) c.494A>T (p.Gln165Leu) c.208+221A>T c.527A>T (p.Gln176Leu) n.2700A>T n.862A>T n.684A>T n.741A>T | |
2 | g.156329693T>C | CA1916440 | NR4A2 | c.305A>G (p.Gln102Arg) c.365A>G (p.Gln122Arg) c.494A>G (p.Gln165Arg) c.208+221A>G c.527A>G (p.Gln176Arg) n.2700A>G n.862A>G n.684A>G n.741A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329693T>G | CA1916441 | NR4A2 | c.305A>C (p.Gln102Pro) c.365A>C (p.Gln122Pro) c.494A>C (p.Gln165Pro) c.208+221A>C c.527A>C (p.Gln176Pro) n.2700A>C n.862A>C n.684A>C n.741A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.156329693T= | CA1300460557 | NR4A2 | c.305A= (p.Gln102=) c.365A= (p.Gln122=) c.494A= (p.Gln165=) c.208+221A= c.527A= (p.Gln176=) n.2700A= n.862A= n.684A= n.741A= | |
2 | g.156329694G>A | CA348682299 | NR4A2 | c.304C>T (p.Gln102Ter) c.364C>T (p.Gln122Ter) c.493C>T (p.Gln165Ter) c.208+220C>T c.526C>T (p.Gln176Ter) n.2699C>T n.861C>T n.683C>T n.740C>T | |
2 | g.156329694G>C | CA348682300 | NR4A2 | c.304C>G (p.Gln102Glu) c.364C>G (p.Gln122Glu) c.493C>G (p.Gln165Glu) c.208+220C>G c.526C>G (p.Gln176Glu) n.2699C>G n.861C>G n.683C>G n.740C>G | gnomAD v4 |
2 | g.156329694G>T | CA348682301 | NR4A2 | c.304C>A (p.Gln102Lys) c.364C>A (p.Gln122Lys) c.493C>A (p.Gln165Lys) c.208+220C>A c.526C>A (p.Gln176Lys) n.2699C>A n.861C>A n.683C>A n.740C>A | gnomAD v4 |
2 | g.156329695C>A | CA348682302 | NR4A2 | c.303G>T (p.Glu101Asp) c.363G>T (p.Glu121Asp) c.492G>T (p.Glu164Asp) c.208+219G>T c.525G>T (p.Glu175Asp) n.2698G>T n.860G>T n.682G>T n.739G>T | |
2 | g.156329695C= | CA1300460558 | NR4A2 | c.303G= (p.Glu101=) c.363G= (p.Glu121=) c.492G= (p.Glu164=) c.208+219G= c.525G= (p.Glu175=) n.2698G= n.860G= n.682G= n.739G= | |
2 | g.156329695C>G | CA348682303 | NR4A2 | c.303G>C (p.Glu101Asp) c.363G>C (p.Glu121Asp) c.492G>C (p.Glu164Asp) c.208+219G>C c.525G>C (p.Glu175Asp) n.2698G>C n.860G>C n.682G>C n.739G>C | gnomAD v4 |
2 | g.156329695C>T | CA59155129 | NR4A2 | c.303G>A (p.Glu101=) c.363G>A (p.Glu121=) c.492G>A (p.Glu164=) c.208+219G>A c.525G>A (p.Glu175=) n.2698G>A n.860G>A n.682G>A n.739G>A | dbSNP gnomAD v4 |
2 | g.156329696T>A | CA348682304 | NR4A2 | c.302A>T (p.Glu101Val) c.362A>T (p.Glu121Val) c.491A>T (p.Glu164Val) c.208+218A>T c.524A>T (p.Glu175Val) n.2697A>T n.859A>T n.681A>T n.738A>T | |
2 | g.156329696T>C | CA348682305 | NR4A2 | c.302A>G (p.Glu101Gly) c.362A>G (p.Glu121Gly) c.491A>G (p.Glu164Gly) c.208+218A>G c.524A>G (p.Glu175Gly) n.2697A>G n.859A>G n.681A>G n.738A>G | dbSNP |
2 | g.156329696T>G | CA348682306 | NR4A2 | c.302A>C (p.Glu101Ala) c.362A>C (p.Glu121Ala) c.491A>C (p.Glu164Ala) c.208+218A>C c.524A>C (p.Glu175Ala) n.2697A>C n.859A>C n.681A>C n.738A>C | |
2 | g.156329696T= | CA1300460559 | NR4A2 | c.302A= (p.Glu101=) c.362A= (p.Glu121=) c.491A= (p.Glu164=) c.208+218A= c.524A= (p.Glu175=) n.2697A= n.859A= n.681A= n.738A= | |
2 | g.156329697C>A | CA348682307 | NR4A2 | c.301G>T (p.Glu101Ter) c.361G>T (p.Glu121Ter) c.490G>T (p.Glu164Ter) c.208+217G>T c.523G>T (p.Glu175Ter) n.2696G>T n.858G>T n.680G>T n.737G>T | |
2 | g.156329697C>G | CA348682308 | NR4A2 | c.301G>C (p.Glu101Gln) c.361G>C (p.Glu121Gln) c.490G>C (p.Glu164Gln) c.208+217G>C c.523G>C (p.Glu175Gln) n.2696G>C n.858G>C n.680G>C n.737G>C | gnomAD v4 |
2 | g.156329697C>T | CA348682309 | NR4A2 | c.301G>A (p.Glu101Lys) c.361G>A (p.Glu121Lys) c.490G>A (p.Glu164Lys) c.208+217G>A c.523G>A (p.Glu175Lys) n.2696G>A n.858G>A n.680G>A n.737G>A | COSMIC COSMIC |
2 | g.156329698G>A | CA429727766 | NR4A2 | c.300C>T (p.Ile100=) c.360C>T (p.Ile120=) c.489C>T (p.Ile163=) c.208+216C>T c.522C>T (p.Ile174=) n.2695C>T n.857C>T n.679C>T n.736C>T | |
2 | g.156329698G>C | CA348682310 | NR4A2 | c.300C>G (p.Ile100Met) c.360C>G (p.Ile120Met) c.489C>G (p.Ile163Met) c.208+216C>G c.522C>G (p.Ile174Met) n.2695C>G n.857C>G n.679C>G n.736C>G | |
2 | g.156329698G= | CA1300460560 | NR4A2 | c.300C= (p.Ile100=) c.360C= (p.Ile120=) c.489C= (p.Ile163=) c.208+216C= c.522C= (p.Ile174=) n.2695C= n.857C= n.679C= n.736C= | |
2 | g.156329698G>T | CA1916442 | NR4A2 | c.300C>A (p.Ile100=) c.360C>A (p.Ile120=) c.489C>A (p.Ile163=) c.208+216C>A c.522C>A (p.Ile174=) n.2695C>A n.857C>A n.679C>A n.736C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329699A>C | CA348682311 | NR4A2 | c.299T>G (p.Ile100Ser) c.359T>G (p.Ile120Ser) c.488T>G (p.Ile163Ser) c.208+215T>G c.521T>G (p.Ile174Ser) n.2694T>G n.856T>G n.678T>G n.735T>G | |
2 | g.156329699A>G | CA348682312 | NR4A2 | c.299T>C (p.Ile100Thr) c.359T>C (p.Ile120Thr) c.488T>C (p.Ile163Thr) c.208+215T>C c.521T>C (p.Ile174Thr) n.2694T>C n.856T>C n.678T>C n.735T>C | gnomAD v4 |
2 | g.156329699A>T | CA348682313 | NR4A2 | c.299T>A (p.Ile100Asn) c.359T>A (p.Ile120Asn) c.488T>A (p.Ile163Asn) c.208+215T>A c.521T>A (p.Ile174Asn) n.2694T>A n.856T>A n.678T>A n.735T>A | |
2 | g.156329700T>A | CA348682314 | NR4A2 | c.298A>T (p.Ile100Phe) c.358A>T (p.Ile120Phe) c.487A>T (p.Ile163Phe) c.208+214A>T c.520A>T (p.Ile174Phe) n.2693A>T n.855A>T n.677A>T n.734A>T | |
2 | g.156329700T>C | CA348682315 | NR4A2 | c.298A>G (p.Ile100Val) c.358A>G (p.Ile120Val) c.487A>G (p.Ile163Val) c.208+214A>G c.520A>G (p.Ile174Val) n.2693A>G n.855A>G n.677A>G n.734A>G | |
2 | g.156329700T>G | CA348682316 | NR4A2 | c.298A>C (p.Ile100Leu) c.358A>C (p.Ile120Leu) c.487A>C (p.Ile163Leu) c.208+214A>C c.520A>C (p.Ile174Leu) n.2693A>C n.855A>C n.677A>C n.734A>C | |
2 | g.156329701C>A | CA348682317 | NR4A2 | c.297G>T (p.Met99Ile) c.357G>T (p.Met119Ile) c.486G>T (p.Met162Ile) c.208+213G>T c.519G>T (p.Met173Ile) n.2692G>T n.854G>T n.676G>T n.733G>T | gnomAD v4 |
2 | g.156329701C>G | CA348682318 | NR4A2 | c.297G>C (p.Met99Ile) c.357G>C (p.Met119Ile) c.486G>C (p.Met162Ile) c.208+213G>C c.519G>C (p.Met173Ile) n.2692G>C n.854G>C n.676G>C n.733G>C | |
2 | g.156329701C>T | CA348682319 | NR4A2 | c.297G>A (p.Met99Ile) c.357G>A (p.Met119Ile) c.486G>A (p.Met162Ile) c.208+213G>A c.519G>A (p.Met173Ile) n.2692G>A n.854G>A n.676G>A n.733G>A | COSMIC COSMIC |
2 | g.156329702A= | CA1300460561 | NR4A2 | c.296T= (p.Met99=) c.356T= (p.Met119=) c.485T= (p.Met162=) c.208+212T= c.518T= (p.Met173=) n.2691T= n.853T= n.675T= n.732T= | |
2 | g.156329702A>C | CA348682320 | NR4A2 | c.296T>G (p.Met99Arg) c.356T>G (p.Met119Arg) c.485T>G (p.Met162Arg) c.208+212T>G c.518T>G (p.Met173Arg) n.2691T>G n.853T>G n.675T>G n.732T>G | gnomAD v4 |
2 | g.156329702A>G | CA348682321 | NR4A2 | c.296T>C (p.Met99Thr) c.356T>C (p.Met119Thr) c.485T>C (p.Met162Thr) c.208+212T>C c.518T>C (p.Met173Thr) n.2691T>C n.853T>C n.675T>C n.732T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329702A>T | CA348682322 | NR4A2 | c.296T>A (p.Met99Lys) c.356T>A (p.Met119Lys) c.485T>A (p.Met162Lys) c.208+212T>A c.518T>A (p.Met173Lys) n.2691T>A n.853T>A n.675T>A n.732T>A | gnomAD v4 |
2 | g.156329703T>A | CA348682324 | NR4A2 | c.295A>T (p.Met99Leu) c.355A>T (p.Met119Leu) c.484A>T (p.Met162Leu) c.208+211A>T c.517A>T (p.Met173Leu) n.2690A>T n.852A>T n.674A>T n.731A>T | |
2 | g.156329703T>C | CA348682325 | NR4A2 | c.295A>G (p.Met99Val) c.355A>G (p.Met119Val) c.484A>G (p.Met162Val) c.208+211A>G c.517A>G (p.Met173Val) n.2690A>G n.852A>G n.674A>G n.731A>G | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329703T>G | CA348682323 | NR4A2 | c.295A>C (p.Met99Leu) c.355A>C (p.Met119Leu) c.484A>C (p.Met162Leu) c.208+211A>C c.517A>C (p.Met173Leu) n.2690A>C n.852A>C n.674A>C n.731A>C | |
2 | g.156329703T= | CA1300460562 | NR4A2 | c.295A= (p.Met99=) c.355A= (p.Met119=) c.484A= (p.Met162=) c.208+211A= c.517A= (p.Met173=) n.2690A= n.852A= n.674A= n.731A= | |
2 | g.156329704G>A | CA429727777 | NR4A2 | c.294C>T (p.His98=) c.354C>T (p.His118=) c.483C>T (p.His161=) c.208+210C>T c.516C>T (p.His172=) n.2689C>T n.851C>T n.673C>T n.730C>T | |
2 | g.156329704G>C | CA348682327 | NR4A2 | c.294C>G (p.His98Gln) c.354C>G (p.His118Gln) c.483C>G (p.His161Gln) c.208+210C>G c.516C>G (p.His172Gln) n.2689C>G n.851C>G n.673C>G n.730C>G | |
2 | g.156329704G>T | CA348682326 | NR4A2 | c.294C>A (p.His98Gln) c.354C>A (p.His118Gln) c.483C>A (p.His161Gln) c.208+210C>A c.516C>A (p.His172Gln) n.2689C>A n.851C>A n.673C>A n.730C>A | |
2 | g.156329705T>A | CA348682328 | NR4A2 | c.293A>T (p.His98Leu) c.353A>T (p.His118Leu) c.482A>T (p.His161Leu) c.208+209A>T c.515A>T (p.His172Leu) n.2688A>T n.850A>T n.672A>T n.729A>T | gnomAD v4 |
2 | g.156329705T>C | CA348682329 | NR4A2 | c.293A>G (p.His98Arg) c.353A>G (p.His118Arg) c.482A>G (p.His161Arg) c.208+209A>G c.515A>G (p.His172Arg) n.2688A>G n.850A>G n.672A>G n.729A>G | |
2 | g.156329705T>G | CA348682330 | NR4A2 | c.293A>C (p.His98Pro) c.353A>C (p.His118Pro) c.482A>C (p.His161Pro) c.208+209A>C c.515A>C (p.His172Pro) n.2688A>C n.850A>C n.672A>C n.729A>C | |
2 | g.156329706G>A | CA348682331 | NR4A2 | c.292C>T (p.His98Tyr) c.352C>T (p.His118Tyr) c.481C>T (p.His161Tyr) c.208+208C>T c.514C>T (p.His172Tyr) n.2687C>T n.849C>T n.671C>T n.728C>T | gnomAD v4 |
2 | g.156329706G>C | CA348682332 | NR4A2 | c.292C>G (p.His98Asp) c.352C>G (p.His118Asp) c.481C>G (p.His161Asp) c.208+208C>G c.514C>G (p.His172Asp) n.2687C>G n.849C>G n.671C>G n.728C>G | |
2 | g.156329706G>T | CA348682333 | NR4A2 | c.292C>A (p.His98Asn) c.352C>A (p.His118Asn) c.481C>A (p.His161Asn) c.208+208C>A c.514C>A (p.His172Asn) n.2687C>A n.849C>A n.671C>A n.728C>A | |
2 | g.156329707C>A | CA429727780 | NR4A2 | c.291G>T (p.Thr97=) c.351G>T (p.Thr117=) c.480G>T (p.Thr160=) c.208+207G>T c.513G>T (p.Thr171=) n.2686G>T n.848G>T n.670G>T n.727G>T | |
2 | g.156329707C= | CA1300460563 | NR4A2 | c.291G= (p.Thr97=) c.351G= (p.Thr117=) c.480G= (p.Thr160=) c.208+207G= c.513G= (p.Thr171=) n.2686G= n.848G= n.670G= n.727G= | |
2 | g.156329707C>G | CA429727781 | NR4A2 | c.291G>C (p.Thr97=) c.351G>C (p.Thr117=) c.480G>C (p.Thr160=) c.208+207G>C c.513G>C (p.Thr171=) n.2686G>C n.848G>C n.670G>C n.727G>C | |
2 | g.156329707C>T | CA429727782 | NR4A2 | c.291G>A (p.Thr97=) c.351G>A (p.Thr117=) c.480G>A (p.Thr160=) c.208+207G>A c.513G>A (p.Thr171=) n.2686G>A n.848G>A n.670G>A n.727G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329708G>A | CA1916443 | NR4A2 | c.290C>T (p.Thr97Met) c.350C>T (p.Thr117Met) c.479C>T (p.Thr160Met) c.208+206C>T c.512C>T (p.Thr171Met) n.2685C>T n.847C>T n.669C>T n.726C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.156329708G>C | CA348682334 | NR4A2 | c.290C>G (p.Thr97Arg) c.350C>G (p.Thr117Arg) c.479C>G (p.Thr160Arg) c.208+206C>G c.512C>G (p.Thr171Arg) n.2685C>G n.847C>G n.669C>G n.726C>G | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329708G= | CA1300460564 | NR4A2 | c.290C= (p.Thr97=) c.350C= (p.Thr117=) c.479C= (p.Thr160=) c.208+206C= c.512C= (p.Thr171=) n.2685C= n.847C= n.669C= n.726C= | |
2 | g.156329708G>T | CA348682335 | NR4A2 | c.290C>A (p.Thr97Lys) c.350C>A (p.Thr117Lys) c.479C>A (p.Thr160Lys) c.208+206C>A c.512C>A (p.Thr171Lys) n.2685C>A n.847C>A n.669C>A n.726C>A | |
2 | g.156329709T>A | CA348682336 | NR4A2 | c.289A>T (p.Thr97Ser) c.349A>T (p.Thr117Ser) c.478A>T (p.Thr160Ser) c.208+205A>T c.511A>T (p.Thr171Ser) n.2684A>T n.846A>T n.668A>T n.725A>T | |
2 | g.156329709T>C | CA1916444 | NR4A2 | c.289A>G (p.Thr97Ala) c.349A>G (p.Thr117Ala) c.478A>G (p.Thr160Ala) c.208+205A>G c.511A>G (p.Thr171Ala) n.2684A>G n.846A>G n.668A>G n.725A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329709T>G | CA348682337 | NR4A2 | c.289A>C (p.Thr97Pro) c.349A>C (p.Thr117Pro) c.478A>C (p.Thr160Pro) c.208+205A>C c.511A>C (p.Thr171Pro) n.2684A>C n.846A>C n.668A>C n.725A>C | |
2 | g.156329709T= | CA1300460565 | NR4A2 | c.289A= (p.Thr97=) c.349A= (p.Thr117=) c.478A= (p.Thr160=) c.208+205A= c.511A= (p.Thr171=) n.2684A= n.846A= n.668A= n.725A= | |
2 | g.156329710A= | CA1300460566 | NR4A2 | c.288T= (p.Thr96=) c.348T= (p.Thr116=) c.477T= (p.Thr159=) c.208+204T= c.510T= (p.Thr170=) n.2683T= n.845T= n.667T= n.724T= | |
2 | g.156329710A>C | CA429727785 | NR4A2 | c.288T>G (p.Thr96=) c.348T>G (p.Thr116=) c.477T>G (p.Thr159=) c.208+204T>G c.510T>G (p.Thr170=) n.2683T>G n.845T>G n.667T>G n.724T>G | |
2 | g.156329710A>G | CA429727786 | NR4A2 | c.288T>C (p.Thr96=) c.348T>C (p.Thr116=) c.477T>C (p.Thr159=) c.208+204T>C c.510T>C (p.Thr170=) n.2683T>C n.845T>C n.667T>C n.724T>C | gnomAD v3 gnomAD v4 |
2 | g.156329710A>T | CA429727787 | NR4A2 | c.288T>A (p.Thr96=) c.348T>A (p.Thr116=) c.477T>A (p.Thr159=) c.208+204T>A c.510T>A (p.Thr170=) n.2683T>A n.845T>A n.667T>A n.724T>A | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329711G>A | CA348682340 | NR4A2 | c.287C>T (p.Thr96Ile) c.347C>T (p.Thr116Ile) c.476C>T (p.Thr159Ile) c.208+203C>T c.509C>T (p.Thr170Ile) n.2682C>T n.844C>T n.666C>T n.723C>T | |
2 | g.156329711G>C | CA348682338 | NR4A2 | c.287C>G (p.Thr96Ser) c.347C>G (p.Thr116Ser) c.476C>G (p.Thr159Ser) c.208+203C>G c.509C>G (p.Thr170Ser) n.2682C>G n.844C>G n.666C>G n.723C>G | |
2 | g.156329711G>T | CA348682339 | NR4A2 | c.287C>A (p.Thr96Asn) c.347C>A (p.Thr116Asn) c.476C>A (p.Thr159Asn) c.208+203C>A c.509C>A (p.Thr170Asn) n.2682C>A n.844C>A n.666C>A n.723C>A | gnomAD v4 |
2 | g.156329712T>A | CA348682341 | NR4A2 | c.286A>T (p.Thr96Ser) c.346A>T (p.Thr116Ser) c.475A>T (p.Thr159Ser) c.208+202A>T c.508A>T (p.Thr170Ser) n.2681A>T n.843A>T n.665A>T n.722A>T | |
2 | g.156329712T>C | CA348682342 | NR4A2 | c.286A>G (p.Thr96Ala) c.346A>G (p.Thr116Ala) c.475A>G (p.Thr159Ala) c.208+202A>G c.508A>G (p.Thr170Ala) n.2681A>G n.843A>G n.665A>G n.722A>G | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329712T>G | CA348682343 | NR4A2 | c.286A>C (p.Thr96Pro) c.346A>C (p.Thr116Pro) c.475A>C (p.Thr159Pro) c.208+202A>C c.508A>C (p.Thr170Pro) n.2681A>C n.843A>C n.665A>C n.722A>C | |
2 | g.156329712T= | CA1300460567 | NR4A2 | c.286A= (p.Thr96=) c.346A= (p.Thr116=) c.475A= (p.Thr159=) c.208+202A= c.508A= (p.Thr170=) n.2681A= n.843A= n.665A= n.722A= | |
2 | g.156329713G>A | CA1916445 | NR4A2 | c.285C>T (p.Ala95=) c.345C>T (p.Ala115=) c.474C>T (p.Ala158=) c.208+201C>T c.507C>T (p.Ala169=) n.2680C>T n.842C>T n.664C>T n.721C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.156329713G>C | CA429727793 | NR4A2 | c.285C>G (p.Ala95=) c.345C>G (p.Ala115=) c.474C>G (p.Ala158=) c.208+201C>G c.507C>G (p.Ala169=) n.2680C>G n.842C>G n.664C>G n.721C>G | |
2 | g.156329713G= | CA1300460568 | NR4A2 | c.285C= (p.Ala95=) c.345C= (p.Ala115=) c.474C= (p.Ala158=) c.208+201C= c.507C= (p.Ala169=) n.2680C= n.842C= n.664C= n.721C= | |
2 | g.156329713G>T | CA429727794 | NR4A2 | c.285C>A (p.Ala95=) c.345C>A (p.Ala115=) c.474C>A (p.Ala158=) c.208+201C>A c.507C>A (p.Ala169=) n.2680C>A n.842C>A n.664C>A n.721C>A | |
2 | g.156329714G>A | CA348682344 | NR4A2 | c.284C>T (p.Ala95Val) c.344C>T (p.Ala115Val) c.473C>T (p.Ala158Val) c.208+200C>T c.506C>T (p.Ala169Val) n.2679C>T n.841C>T n.663C>T n.720C>T | |
2 | g.156329714G>C | CA348682345 | NR4A2 | c.284C>G (p.Ala95Gly) c.344C>G (p.Ala115Gly) c.473C>G (p.Ala158Gly) c.208+200C>G c.506C>G (p.Ala169Gly) n.2679C>G n.841C>G n.663C>G n.720C>G | |
2 | g.156329714G>T | CA348682346 | NR4A2 | c.284C>A (p.Ala95Asp) c.344C>A (p.Ala115Asp) c.473C>A (p.Ala158Asp) c.208+200C>A c.506C>A (p.Ala169Asp) n.2679C>A n.841C>A n.663C>A n.720C>A | |
2 | g.156329714_156329717delinsGCCA | CA1300460569 | NR4A2 | c.281_284delinsTGGC (p.Val94=) c.341_344delinsTGGC (p.Val114=) c.470_473delinsTGGC (p.Val157=) c.208+197_208+200delinsTGGC c.503_506delinsTGGC (p.Val168=) n.2676_2679delinsTGGC n.838_841delinsTGGC n.660_663delinsTGGC n.717_720delinsTGGC | |
2 | g.156329715C>A | CA348682347 | NR4A2 | c.283G>T (p.Ala95Ser) c.343G>T (p.Ala115Ser) c.472G>T (p.Ala158Ser) c.208+199G>T c.505G>T (p.Ala169Ser) n.2678G>T n.840G>T n.662G>T n.719G>T | gnomAD v4 |
2 | g.156329715C>G | CA348682348 | NR4A2 | c.283G>C (p.Ala95Pro) c.343G>C (p.Ala115Pro) c.472G>C (p.Ala158Pro) c.208+199G>C c.505G>C (p.Ala169Pro) n.2678G>C n.840G>C n.662G>C n.719G>C | |
2 | g.156329715C>T | CA348682349 | NR4A2 | c.283G>A (p.Ala95Thr) c.343G>A (p.Ala115Thr) c.472G>A (p.Ala158Thr) c.208+199G>A c.505G>A (p.Ala169Thr) n.2678G>A n.840G>A n.662G>A n.719G>A | gnomAD v4 |
2 | g.156329716_156329718del | CA537508954 | NR4A2 | c.281_283del (p.Val94del) c.341_343del (p.Val114del) c.470_472del (p.Val157del) c.208+197_208+199del c.503_505del (p.Val168del) n.2676_2678del n.838_840del n.660_662del n.717_719del | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329716C>A | CA1916446 | NR4A2 | c.282G>T (p.Val94=) c.342G>T (p.Val114=) c.471G>T (p.Val157=) c.208+198G>T c.504G>T (p.Val168=) n.2677G>T n.839G>T n.661G>T n.718G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.156329716C= | CA1300460570 | NR4A2 | c.282G= (p.Val94=) c.342G= (p.Val114=) c.471G= (p.Val157=) c.208+198G= c.504G= (p.Val168=) n.2677G= n.839G= n.661G= n.718G= | |
2 | g.156329716C>G | CA429727795 | NR4A2 | c.282G>C (p.Val94=) c.342G>C (p.Val114=) c.471G>C (p.Val157=) c.208+198G>C c.504G>C (p.Val168=) n.2677G>C n.839G>C n.661G>C n.718G>C | |
2 | g.156329716C>T | CA429727797 | NR4A2 | c.282G>A (p.Val94=) c.342G>A (p.Val114=) c.471G>A (p.Val157=) c.208+198G>A c.504G>A (p.Val168=) n.2677G>A n.839G>A n.661G>A n.718G>A | dbSNP gnomAD v3 gnomAD v4 |
2 | g.156329717A>C | CA348682352 | NR4A2 | c.281T>G (p.Val94Gly) c.341T>G (p.Val114Gly) c.470T>G (p.Val157Gly) c.208+197T>G c.503T>G (p.Val168Gly) n.2676T>G n.838T>G n.660T>G n.717T>G | |
2 | g.156329717A>G | CA348682351 | NR4A2 | c.281T>C (p.Val94Ala) c.341T>C (p.Val114Ala) c.470T>C (p.Val157Ala) c.208+197T>C c.503T>C (p.Val168Ala) n.2676T>C n.838T>C n.660T>C n.717T>C | |
2 | g.156329717A>T | CA348682350 | NR4A2 | c.281T>A (p.Val94Glu) c.341T>A (p.Val114Glu) c.470T>A (p.Val157Glu) c.208+197T>A c.503T>A (p.Val168Glu) n.2676T>A n.838T>A n.660T>A n.717T>A | |
2 | g.156329718C>A | CA348682353 | NR4A2 | c.280G>T (p.Val94Leu) c.340G>T (p.Val114Leu) c.469G>T (p.Val157Leu) c.208+196G>T c.502G>T (p.Val168Leu) n.2675G>T n.837G>T n.659G>T n.716G>T | |
2 | g.156329718C>G | CA348682354 | NR4A2 | c.280G>C (p.Val94Leu) c.340G>C (p.Val114Leu) c.469G>C (p.Val157Leu) c.208+196G>C c.502G>C (p.Val168Leu) n.2675G>C n.837G>C n.659G>C n.716G>C | |
2 | g.156329718C>T | CA348682355 | NR4A2 | c.280G>A (p.Val94Met) c.340G>A (p.Val114Met) c.469G>A (p.Val157Met) c.208+196G>A c.502G>A (p.Val168Met) n.2675G>A n.837G>A n.659G>A n.716G>A | gnomAD v4 |
2 | g.156329719G>A | CA429727803 | NR4A2 | c.279C>T (p.Tyr93=) c.339C>T (p.Tyr113=) c.468C>T (p.Tyr156=) c.208+195C>T c.501C>T (p.Tyr167=) n.2674C>T n.836C>T n.658C>T n.715C>T | gnomAD v4 |
2 | g.156329719G>C | CA348682356 | NR4A2 | c.279C>G (p.Tyr93Ter) c.339C>G (p.Tyr113Ter) c.468C>G (p.Tyr156Ter) c.208+195C>G c.501C>G (p.Tyr167Ter) n.2674C>G n.836C>G n.658C>G n.715C>G | |
2 | g.156329719G>T | CA348682357 | NR4A2 | c.279C>A (p.Tyr93Ter) c.339C>A (p.Tyr113Ter) c.468C>A (p.Tyr156Ter) c.208+195C>A c.501C>A (p.Tyr167Ter) n.2674C>A n.836C>A n.658C>A n.715C>A | |
2 | g.156329720T>A | CA1916447 | NR4A2 | c.278A>T (p.Tyr93Phe) c.338A>T (p.Tyr113Phe) c.467A>T (p.Tyr156Phe) c.208+194A>T c.500A>T (p.Tyr167Phe) n.2673A>T n.835A>T n.657A>T n.714A>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329720T>C | CA348682358 | NR4A2 | c.278A>G (p.Tyr93Cys) c.338A>G (p.Tyr113Cys) c.467A>G (p.Tyr156Cys) c.208+194A>G c.500A>G (p.Tyr167Cys) n.2673A>G n.835A>G n.657A>G n.714A>G | gnomAD v4 |
2 | g.156329720T>G | CA348682359 | NR4A2 | c.278A>C (p.Tyr93Ser) c.338A>C (p.Tyr113Ser) c.467A>C (p.Tyr156Ser) c.208+194A>C c.500A>C (p.Tyr167Ser) n.2673A>C n.835A>C n.657A>C n.714A>C | |
2 | g.156329720T= | CA1300460571 | NR4A2 | c.278A= (p.Tyr93=) c.338A= (p.Tyr113=) c.467A= (p.Tyr156=) c.208+194A= c.500A= (p.Tyr167=) n.2673A= n.835A= n.657A= n.714A= | |
2 | g.156329721A= | CA1300460572 | NR4A2 | c.277T= (p.Tyr93=) c.337T= (p.Tyr113=) c.466T= (p.Tyr156=) c.208+193T= c.499T= (p.Tyr167=) n.2672T= n.834T= n.656T= n.713T= | |
2 | g.156329721A>C | CA348682360 | NR4A2 | c.277T>G (p.Tyr93Asp) c.337T>G (p.Tyr113Asp) c.466T>G (p.Tyr156Asp) c.208+193T>G c.499T>G (p.Tyr167Asp) n.2672T>G n.834T>G n.656T>G n.713T>G | |
2 | g.156329721A>G | CA348682361 | NR4A2 | c.277T>C (p.Tyr93His) c.337T>C (p.Tyr113His) c.466T>C (p.Tyr156His) c.208+193T>C c.499T>C (p.Tyr167His) n.2672T>C n.834T>C n.656T>C n.713T>C | dbSNP gnomAD v3 gnomAD v4 |
2 | g.156329721A>T | CA348682362 | NR4A2 | c.277T>A (p.Tyr93Asn) c.337T>A (p.Tyr113Asn) c.466T>A (p.Tyr156Asn) c.208+193T>A c.499T>A (p.Tyr167Asn) n.2672T>A n.834T>A n.656T>A n.713T>A | |
2 | g.156329722G>A | CA429727806 | NR4A2 | c.276C>T (p.Asn92=) c.336C>T (p.Asn112=) c.465C>T (p.Asn155=) c.208+192C>T c.498C>T (p.Asn166=) n.2671C>T n.833C>T n.655C>T n.712C>T | |
2 | g.156329722G>C | CA348682363 | NR4A2 | c.276C>G (p.Asn92Lys) c.336C>G (p.Asn112Lys) c.465C>G (p.Asn155Lys) c.208+192C>G c.498C>G (p.Asn166Lys) n.2671C>G n.833C>G n.655C>G n.712C>G | |
2 | g.156329722G>T | CA348682364 | NR4A2 | c.276C>A (p.Asn92Lys) c.336C>A (p.Asn112Lys) c.465C>A (p.Asn155Lys) c.208+192C>A c.498C>A (p.Asn166Lys) n.2671C>A n.833C>A n.655C>A n.712C>A | |
2 | g.156329723T>A | CA348682367 | NR4A2 | c.275A>T (p.Asn92Ile) c.335A>T (p.Asn112Ile) c.464A>T (p.Asn155Ile) c.208+191A>T c.497A>T (p.Asn166Ile) n.2670A>T n.832A>T n.654A>T n.711A>T | |
2 | g.156329723T>C | CA348682365 | NR4A2 | c.275A>G (p.Asn92Ser) c.335A>G (p.Asn112Ser) c.464A>G (p.Asn155Ser) c.208+191A>G c.497A>G (p.Asn166Ser) n.2670A>G n.832A>G n.654A>G n.711A>G | |
2 | g.156329723T>G | CA348682366 | NR4A2 | c.275A>C (p.Asn92Thr) c.335A>C (p.Asn112Thr) c.464A>C (p.Asn155Thr) c.208+191A>C c.497A>C (p.Asn166Thr) n.2670A>C n.832A>C n.654A>C n.711A>C | |
2 | g.156329724T>A | CA348682368 | NR4A2 | c.274A>T (p.Asn92Tyr) c.334A>T (p.Asn112Tyr) c.463A>T (p.Asn155Tyr) c.208+190A>T c.496A>T (p.Asn166Tyr) n.2669A>T n.831A>T n.653A>T n.710A>T | gnomAD v4 |
2 | g.156329724T>C | CA348682369 | NR4A2 | c.274A>G (p.Asn92Asp) c.334A>G (p.Asn112Asp) c.463A>G (p.Asn155Asp) c.208+190A>G c.496A>G (p.Asn166Asp) n.2669A>G n.831A>G n.653A>G n.710A>G | |
2 | g.156329724T>G | CA348682370 | NR4A2 | c.274A>C (p.Asn92His) c.334A>C (p.Asn112His) c.463A>C (p.Asn155His) c.208+190A>C c.496A>C (p.Asn166His) n.2669A>C n.831A>C n.653A>C n.710A>C | |
2 | g.156329725C>A | CA348682371 | NR4A2 | c.273G>T (p.Gln91His) c.333G>T (p.Gln111His) c.462G>T (p.Gln154His) c.208+189G>T c.495G>T (p.Gln165His) n.2668G>T n.830G>T n.652G>T n.709G>T | |
2 | g.156329725C= | CA1300460573 | NR4A2 | c.273G= (p.Gln91=) c.333G= (p.Gln111=) c.462G= (p.Gln154=) c.208+189G= c.495G= (p.Gln165=) n.2668G= n.830G= n.652G= n.709G= | |
2 | g.156329725C>G | CA348682372 | NR4A2 | c.273G>C (p.Gln91His) c.333G>C (p.Gln111His) c.462G>C (p.Gln154His) c.208+189G>C c.495G>C (p.Gln165His) n.2668G>C n.830G>C n.652G>C n.709G>C | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329725C>T | CA429727808 | NR4A2 | c.273G>A (p.Gln91=) c.333G>A (p.Gln111=) c.462G>A (p.Gln154=) c.208+189G>A c.495G>A (p.Gln165=) n.2668G>A n.830G>A n.652G>A n.709G>A | COSMIC COSMIC |
2 | g.156329726T>A | CA348682373 | NR4A2 | c.272A>T (p.Gln91Leu) c.332A>T (p.Gln111Leu) c.461A>T (p.Gln154Leu) c.208+188A>T c.494A>T (p.Gln165Leu) n.2667A>T n.829A>T n.651A>T n.708A>T | |
2 | g.156329726T>C | CA348682374 | NR4A2 | c.272A>G (p.Gln91Arg) c.332A>G (p.Gln111Arg) c.461A>G (p.Gln154Arg) c.208+188A>G c.494A>G (p.Gln165Arg) n.2667A>G n.829A>G n.651A>G n.708A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329726T>G | CA348682375 | NR4A2 | c.272A>C (p.Gln91Pro) c.332A>C (p.Gln111Pro) c.461A>C (p.Gln154Pro) c.208+188A>C c.494A>C (p.Gln165Pro) n.2667A>C n.829A>C n.651A>C n.708A>C | |
2 | g.156329726T= | CA1300460574 | NR4A2 | c.272A= (p.Gln91=) c.332A= (p.Gln111=) c.461A= (p.Gln154=) c.208+188A= c.494A= (p.Gln165=) n.2667A= n.829A= n.651A= n.708A= | |
2 | g.156329727G>A | CA348682376 | NR4A2 | c.271C>T (p.Gln91Ter) c.331C>T (p.Gln111Ter) c.460C>T (p.Gln154Ter) c.208+187C>T c.493C>T (p.Gln165Ter) n.2666C>T n.828C>T n.650C>T n.707C>T | |
2 | g.156329727G>C | CA1916448 | NR4A2 | c.271C>G (p.Gln91Glu) c.331C>G (p.Gln111Glu) c.460C>G (p.Gln154Glu) c.208+187C>G c.493C>G (p.Gln165Glu) n.2666C>G n.828C>G n.650C>G n.707C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329727G= | CA1300460575 | NR4A2 | c.271C= (p.Gln91=) c.331C= (p.Gln111=) c.460C= (p.Gln154=) c.208+187C= c.493C= (p.Gln165=) n.2666C= n.828C= n.650C= n.707C= | |
2 | g.156329727G>T | CA348682377 | NR4A2 | c.271C>A (p.Gln91Lys) c.331C>A (p.Gln111Lys) c.460C>A (p.Gln154Lys) c.208+187C>A c.493C>A (p.Gln165Lys) n.2666C>A n.828C>A n.650C>A n.707C>A | |
2 | g.156329728G>A | CA429727815 | NR4A2 | c.270C>T (p.His90=) c.330C>T (p.His110=) c.459C>T (p.His153=) c.208+186C>T c.492C>T (p.His164=) n.2665C>T n.827C>T n.649C>T n.706C>T | |
2 | g.156329728G>C | CA348682378 | NR4A2 | c.270C>G (p.His90Gln) c.330C>G (p.His110Gln) c.459C>G (p.His153Gln) c.208+186C>G c.492C>G (p.His164Gln) n.2665C>G n.827C>G n.649C>G n.706C>G | |
2 | g.156329728G>T | CA348682379 | NR4A2 | c.270C>A (p.His90Gln) c.330C>A (p.His110Gln) c.459C>A (p.His153Gln) c.208+186C>A c.492C>A (p.His164Gln) n.2665C>A n.827C>A n.649C>A n.706C>A | |
2 | g.156329729T>A | CA348682381 | NR4A2 | c.269A>T (p.His90Leu) c.329A>T (p.His110Leu) c.458A>T (p.His153Leu) c.208+185A>T c.491A>T (p.His164Leu) n.2664A>T n.826A>T n.648A>T n.705A>T | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329729T>C | CA348682382 | NR4A2 | c.269A>G (p.His90Arg) c.329A>G (p.His110Arg) c.458A>G (p.His153Arg) c.208+185A>G c.491A>G (p.His164Arg) n.2664A>G n.826A>G n.648A>G n.705A>G | |
2 | g.156329729T>G | CA348682380 | NR4A2 | c.269A>C (p.His90Pro) c.329A>C (p.His110Pro) c.458A>C (p.His153Pro) c.208+185A>C c.491A>C (p.His164Pro) n.2664A>C n.826A>C n.648A>C n.705A>C | dbSNP |
2 | g.156329729T= | CA1300460576 | NR4A2 | c.269A= (p.His90=) c.329A= (p.His110=) c.458A= (p.His153=) c.208+185A= c.491A= (p.His164=) n.2664A= n.826A= n.648A= n.705A= | |
2 | g.156329730G>A | CA348682384 | NR4A2 | c.268C>T (p.His90Tyr) c.328C>T (p.His110Tyr) c.457C>T (p.His153Tyr) c.208+184C>T c.490C>T (p.His164Tyr) n.2663C>T n.825C>T n.647C>T n.704C>T | gnomAD v4 |
2 | g.156329730G>C | CA348682383 | NR4A2 | c.268C>G (p.His90Asp) c.328C>G (p.His110Asp) c.457C>G (p.His153Asp) c.208+184C>G c.490C>G (p.His164Asp) n.2663C>G n.825C>G n.647C>G n.704C>G | |
2 | g.156329730G>T | CA348682385 | NR4A2 | c.268C>A (p.His90Asn) c.328C>A (p.His110Asn) c.457C>A (p.His153Asn) c.208+184C>A c.490C>A (p.His164Asn) n.2663C>A n.825C>A n.647C>A n.704C>A | |
2 | g.156329731G>A | CA429727969 | NR4A2 | c.267C>T (p.Phe89=) c.327C>T (p.Phe109=) c.456C>T (p.Phe152=) c.208+183C>T c.489C>T (p.Phe163=) n.2662C>T n.824C>T n.646C>T n.703C>T | dbSNP gnomAD v4 |
2 | g.156329731G>C | CA348682386 | NR4A2 | c.267C>G (p.Phe89Leu) c.327C>G (p.Phe109Leu) c.456C>G (p.Phe152Leu) c.208+183C>G c.489C>G (p.Phe163Leu) n.2662C>G n.824C>G n.646C>G n.703C>G | |
2 | g.156329731G= | CA1300460577 | NR4A2 | c.267C= (p.Phe89=) c.327C= (p.Phe109=) c.456C= (p.Phe152=) c.208+183C= c.489C= (p.Phe163=) n.2662C= n.824C= n.646C= n.703C= | |
2 | g.156329731G>T | CA348682387 | NR4A2 | c.267C>A (p.Phe89Leu) c.327C>A (p.Phe109Leu) c.456C>A (p.Phe152Leu) c.208+183C>A c.489C>A (p.Phe163Leu) n.2662C>A n.824C>A n.646C>A n.703C>A | |
2 | g.156329732A>C | CA348682388 | NR4A2 | c.266T>G (p.Phe89Cys) c.326T>G (p.Phe109Cys) c.455T>G (p.Phe152Cys) c.208+182T>G c.488T>G (p.Phe163Cys) n.2661T>G n.823T>G n.645T>G n.702T>G | |
2 | g.156329732A>G | CA348682389 | NR4A2 | c.266T>C (p.Phe89Ser) c.326T>C (p.Phe109Ser) c.455T>C (p.Phe152Ser) c.208+182T>C c.488T>C (p.Phe163Ser) n.2661T>C n.823T>C n.645T>C n.702T>C | |
2 | g.156329732A>T | CA348682390 | NR4A2 | c.266T>A (p.Phe89Tyr) c.326T>A (p.Phe109Tyr) c.455T>A (p.Phe152Tyr) c.208+182T>A c.488T>A (p.Phe163Tyr) n.2661T>A n.823T>A n.645T>A n.702T>A | |
2 | g.156329733A= | CA1300460578 | NR4A2 | c.265T= (p.Phe89=) c.325T= (p.Phe109=) c.454T= (p.Phe152=) c.208+181T= c.487T= (p.Phe163=) n.2660T= n.822T= n.644T= n.701T= | |
2 | g.156329733A>C | CA348682391 | NR4A2 | c.265T>G (p.Phe89Val) c.325T>G (p.Phe109Val) c.454T>G (p.Phe152Val) c.208+181T>G c.487T>G (p.Phe163Val) n.2660T>G n.822T>G n.644T>G n.701T>G | |
2 | g.156329733A>G | CA348682392 | NR4A2 | c.265T>C (p.Phe89Leu) c.325T>C (p.Phe109Leu) c.454T>C (p.Phe152Leu) c.208+181T>C c.487T>C (p.Phe163Leu) n.2660T>C n.822T>C n.644T>C n.701T>C | gnomAD v4 |
2 | g.156329733A>T | CA59155130 | NR4A2 | c.265T>A (p.Phe89Ile) c.325T>A (p.Phe109Ile) c.454T>A (p.Phe152Ile) c.208+181T>A c.487T>A (p.Phe163Ile) n.2660T>A n.822T>A n.644T>A n.701T>A | dbSNP gnomAD v4 |
2 | g.156329734G>A | CA1916449 | NR4A2 | c.264C>T (p.Asn88=) c.324C>T (p.Asn108=) c.453C>T (p.Asn151=) c.208+180C>T c.486C>T (p.Asn162=) n.2659C>T n.821C>T n.643C>T n.700C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.156329734G>C | CA348682393 | NR4A2 | c.264C>G (p.Asn88Lys) c.324C>G (p.Asn108Lys) c.453C>G (p.Asn151Lys) c.208+180C>G c.486C>G (p.Asn162Lys) n.2659C>G n.821C>G n.643C>G n.700C>G | gnomAD v4 |
2 | g.156329734G= | CA1300460579 | NR4A2 | c.264C= (p.Asn88=) c.324C= (p.Asn108=) c.453C= (p.Asn151=) c.208+180C= c.486C= (p.Asn162=) n.2659C= n.821C= n.643C= n.700C= | |
2 | g.156329734G>T | CA348682394 | NR4A2 | c.264C>A (p.Asn88Lys) c.324C>A (p.Asn108Lys) c.453C>A (p.Asn151Lys) c.208+180C>A c.486C>A (p.Asn162Lys) n.2659C>A n.821C>A n.643C>A n.700C>A | |
2 | g.156329735T>A | CA348682397 | NR4A2 | c.263A>T (p.Asn88Ile) c.323A>T (p.Asn108Ile) c.452A>T (p.Asn151Ile) c.208+179A>T c.485A>T (p.Asn162Ile) n.2658A>T n.820A>T n.642A>T n.699A>T | |
2 | g.156329735T>C | CA348682396 | NR4A2 | c.263A>G (p.Asn88Ser) c.323A>G (p.Asn108Ser) c.452A>G (p.Asn151Ser) c.208+179A>G c.485A>G (p.Asn162Ser) n.2658A>G n.820A>G n.642A>G n.699A>G | COSMIC COSMIC |
2 | g.156329735T>G | CA348682395 | NR4A2 | c.263A>C (p.Asn88Thr) c.323A>C (p.Asn108Thr) c.452A>C (p.Asn151Thr) c.208+179A>C c.485A>C (p.Asn162Thr) n.2658A>C n.820A>C n.642A>C n.699A>C | |
2 | g.156329736dup | CA2842004114 | NR4A2 | c.263dup (p.Asn88LysfsTer29) c.323dup (p.Asn108LysfsTer29) c.452dup (p.Asn151LysfsTer29) c.208+179dup c.263dup (p.Asn88LysfsTer?) c.485dup (p.Asn162LysfsTer29) n.2658dup n.820dup n.642dup n.699dup | |
2 | g.156329736T>A | CA348682398 | NR4A2 | c.262A>T (p.Asn88Tyr) c.322A>T (p.Asn108Tyr) c.451A>T (p.Asn151Tyr) c.208+178A>T c.484A>T (p.Asn162Tyr) n.2657A>T n.819A>T n.641A>T n.698A>T | |
2 | g.156329736T>C | CA348682399 | NR4A2 | c.262A>G (p.Asn88Asp) c.322A>G (p.Asn108Asp) c.451A>G (p.Asn151Asp) c.208+178A>G c.484A>G (p.Asn162Asp) n.2657A>G n.819A>G n.641A>G n.698A>G | gnomAD v4 |
2 | g.156329736T>G | CA348682400 | NR4A2 | c.262A>C (p.Asn88His) c.322A>C (p.Asn108His) c.451A>C (p.Asn151His) c.208+178A>C c.484A>C (p.Asn162His) n.2657A>C n.819A>C n.641A>C n.698A>C | |
2 | g.156329737G>A | CA429727979 | NR4A2 | c.261C>T (p.His87=) c.321C>T (p.His107=) c.450C>T (p.His150=) c.208+177C>T c.483C>T (p.His161=) n.2656C>T n.818C>T n.640C>T n.697C>T | |
2 | g.156329737G>C | CA348682401 | NR4A2 | c.261C>G (p.His87Gln) c.321C>G (p.His107Gln) c.450C>G (p.His150Gln) c.208+177C>G c.483C>G (p.His161Gln) n.2656C>G n.818C>G n.640C>G n.697C>G | |
2 | g.156329737G>T | CA348682402 | NR4A2 | c.261C>A (p.His87Gln) c.321C>A (p.His107Gln) c.450C>A (p.His150Gln) c.208+177C>A c.483C>A (p.His161Gln) n.2656C>A n.818C>A n.640C>A n.697C>A | |
2 | g.156329738T>A | CA348682403 | NR4A2 | c.260A>T (p.His87Leu) c.320A>T (p.His107Leu) c.449A>T (p.His150Leu) c.208+176A>T c.482A>T (p.His161Leu) n.2655A>T n.817A>T n.639A>T n.696A>T | |
2 | g.156329738T>C | CA348682404 | NR4A2 | c.260A>G (p.His87Arg) c.320A>G (p.His107Arg) c.449A>G (p.His150Arg) c.208+176A>G c.482A>G (p.His161Arg) n.2655A>G n.817A>G n.639A>G n.696A>G | |
2 | g.156329738T>G | CA348682405 | NR4A2 | c.260A>C (p.His87Pro) c.320A>C (p.His107Pro) c.449A>C (p.His150Pro) c.208+176A>C c.482A>C (p.His161Pro) n.2655A>C n.817A>C n.639A>C n.696A>C | gnomAD v4 |
2 | g.156329739G>A | CA348682406 | NR4A2 | c.259C>T (p.His87Tyr) c.319C>T (p.His107Tyr) c.448C>T (p.His150Tyr) c.208+175C>T c.481C>T (p.His161Tyr) n.2654C>T n.816C>T n.638C>T n.695C>T | gnomAD v4 |
2 | g.156329739G>C | CA348682407 | NR4A2 | c.259C>G (p.His87Asp) c.319C>G (p.His107Asp) c.448C>G (p.His150Asp) c.208+175C>G c.481C>G (p.His161Asp) n.2654C>G n.816C>G n.638C>G n.695C>G | |
2 | g.156329739G>T | CA348682408 | NR4A2 | c.259C>A (p.His87Asn) c.319C>A (p.His107Asn) c.448C>A (p.His150Asn) c.208+175C>A c.481C>A (p.His161Asn) n.2654C>A n.816C>A n.638C>A n.695C>A | |
2 | g.156329740G>A | CA1916450 | NR4A2 | c.258C>T (p.Leu86=) c.318C>T (p.Leu106=) c.447C>T (p.Leu149=) c.208+174C>T c.480C>T (p.Leu160=) n.2653C>T n.815C>T n.637C>T n.694C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329740G>C | CA429727990 | NR4A2 | c.258C>G (p.Leu86=) c.318C>G (p.Leu106=) c.447C>G (p.Leu149=) c.208+174C>G c.480C>G (p.Leu160=) n.2653C>G n.815C>G n.637C>G n.694C>G | |
2 | g.156329740G= | CA1300460580 | NR4A2 | c.258C= (p.Leu86=) c.318C= (p.Leu106=) c.447C= (p.Leu149=) c.208+174C= c.480C= (p.Leu160=) n.2653C= n.815C= n.637C= n.694C= | |
2 | g.156329740G>T | CA429727987 | NR4A2 | c.258C>A (p.Leu86=) c.318C>A (p.Leu106=) c.447C>A (p.Leu149=) c.208+174C>A c.480C>A (p.Leu160=) n.2653C>A n.815C>A n.637C>A n.694C>A | |
2 | g.156329741A>C | CA348682410 | NR4A2 | c.257T>G (p.Leu86Arg) c.317T>G (p.Leu106Arg) c.446T>G (p.Leu149Arg) c.208+173T>G c.479T>G (p.Leu160Arg) n.2652T>G n.814T>G n.636T>G n.693T>G | |
2 | g.156329741A>G | CA348682411 | NR4A2 | c.257T>C (p.Leu86Pro) c.317T>C (p.Leu106Pro) c.446T>C (p.Leu149Pro) c.208+173T>C c.479T>C (p.Leu160Pro) n.2652T>C n.814T>C n.636T>C n.693T>C | |
2 | g.156329741A>T | CA348682409 | NR4A2 | c.257T>A (p.Leu86His) c.317T>A (p.Leu106His) c.446T>A (p.Leu149His) c.208+173T>A c.479T>A (p.Leu160His) n.2652T>A n.814T>A n.636T>A n.693T>A | |
2 | g.156329742G>A | CA348682412 | NR4A2 | c.256C>T (p.Leu86Phe) c.316C>T (p.Leu106Phe) c.445C>T (p.Leu149Phe) c.208+172C>T c.478C>T (p.Leu160Phe) n.2651C>T n.813C>T n.635C>T n.692C>T | |
2 | g.156329742G>C | CA348682413 | NR4A2 | c.256C>G (p.Leu86Val) c.316C>G (p.Leu106Val) c.445C>G (p.Leu149Val) c.208+172C>G c.478C>G (p.Leu160Val) n.2651C>G n.813C>G n.635C>G n.692C>G | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329742G= | CA1300460581 | NR4A2 | c.256C= (p.Leu86=) c.316C= (p.Leu106=) c.445C= (p.Leu149=) c.208+172C= c.478C= (p.Leu160=) n.2651C= n.813C= n.635C= n.692C= | |
2 | g.156329742G>T | CA348682414 | NR4A2 | c.256C>A (p.Leu86Ile) c.316C>A (p.Leu106Ile) c.445C>A (p.Leu149Ile) c.208+172C>A c.478C>A (p.Leu160Ile) n.2651C>A n.813C>A n.635C>A n.692C>A | gnomAD v4 |
2 | g.156329743A>C | CA429728005 | NR4A2 | c.255T>G (p.Ser85=) c.315T>G (p.Ser105=) c.444T>G (p.Ser148=) c.208+171T>G c.477T>G (p.Ser159=) n.2650T>G n.812T>G n.634T>G n.691T>G | |
2 | g.156329743A>G | CA429728004 | NR4A2 | c.255T>C (p.Ser85=) c.315T>C (p.Ser105=) c.444T>C (p.Ser148=) c.208+171T>C c.477T>C (p.Ser159=) n.2650T>C n.812T>C n.634T>C n.691T>C | gnomAD v3 gnomAD v4 |
2 | g.156329743A>T | CA429728003 | NR4A2 | c.255T>A (p.Ser85=) c.315T>A (p.Ser105=) c.444T>A (p.Ser148=) c.208+171T>A c.477T>A (p.Ser159=) n.2650T>A n.812T>A n.634T>A n.691T>A | |
2 | g.156329744G>A | CA348682415 | NR4A2 | c.254C>T (p.Ser85Phe) c.314C>T (p.Ser105Phe) c.443C>T (p.Ser148Phe) c.208+170C>T c.476C>T (p.Ser159Phe) n.2649C>T n.811C>T n.633C>T n.690C>T | dbSNP gnomAD v4 |
2 | g.156329744G>C | CA348682416 | NR4A2 | c.254C>G (p.Ser85Cys) c.314C>G (p.Ser105Cys) c.443C>G (p.Ser148Cys) c.208+170C>G c.476C>G (p.Ser159Cys) n.2649C>G n.811C>G n.633C>G n.690C>G | COSMIC COSMIC |
2 | g.156329744G= | CA1300460582 | NR4A2 | c.254C= (p.Ser85=) c.314C= (p.Ser105=) c.443C= (p.Ser148=) c.208+170C= c.476C= (p.Ser159=) n.2649C= n.811C= n.633C= n.690C= | |
2 | g.156329744G>T | CA348682417 | NR4A2 | c.254C>A (p.Ser85Tyr) c.314C>A (p.Ser105Tyr) c.443C>A (p.Ser148Tyr) c.208+170C>A c.476C>A (p.Ser159Tyr) n.2649C>A n.811C>A n.633C>A n.690C>A | gnomAD v4 |
2 | g.156329745A>C | CA348682418 | NR4A2 | c.253T>G (p.Ser85Ala) c.313T>G (p.Ser105Ala) c.442T>G (p.Ser148Ala) c.208+169T>G c.475T>G (p.Ser159Ala) n.2648T>G n.810T>G n.632T>G n.689T>G | |
2 | g.156329745A>G | CA348682419 | NR4A2 | c.253T>C (p.Ser85Pro) c.313T>C (p.Ser105Pro) c.442T>C (p.Ser148Pro) c.208+169T>C c.475T>C (p.Ser159Pro) n.2648T>C n.810T>C n.632T>C n.689T>C | |
2 | g.156329745A>T | CA348682420 | NR4A2 | c.253T>A (p.Ser85Thr) c.313T>A (p.Ser105Thr) c.442T>A (p.Ser148Thr) c.208+169T>A c.475T>A (p.Ser159Thr) n.2648T>A n.810T>A n.632T>A n.689T>A | |
2 | g.156329746T>A | CA429728013 | NR4A2 | c.252A>T (p.Gly84=) c.312A>T (p.Gly104=) c.441A>T (p.Gly147=) c.208+168A>T c.474A>T (p.Gly158=) n.2647A>T n.809A>T n.631A>T n.688A>T | |
2 | g.156329746T>C | CA429728016 | NR4A2 | c.252A>G (p.Gly84=) c.312A>G (p.Gly104=) c.441A>G (p.Gly147=) c.208+168A>G c.474A>G (p.Gly158=) n.2647A>G n.809A>G n.631A>G n.688A>G | dbSNP |
2 | g.156329746T>G | CA429728015 | NR4A2 | c.252A>C (p.Gly84=) c.312A>C (p.Gly104=) c.441A>C (p.Gly147=) c.208+168A>C c.474A>C (p.Gly158=) n.2647A>C n.809A>C n.631A>C n.688A>C | |
2 | g.156329747C>A | CA348682421 | NR4A2 | c.251G>T (p.Gly84Val) c.311G>T (p.Gly104Val) c.440G>T (p.Gly147Val) c.208+167G>T c.473G>T (p.Gly158Val) n.2646G>T n.808G>T n.630G>T n.687G>T | |
2 | g.156329747C>G | CA348682422 | NR4A2 | c.251G>C (p.Gly84Ala) c.311G>C (p.Gly104Ala) c.440G>C (p.Gly147Ala) c.208+167G>C c.473G>C (p.Gly158Ala) n.2646G>C n.808G>C n.630G>C n.687G>C | |
2 | g.156329747C>T | CA348682423 | NR4A2 | c.251G>A (p.Gly84Glu) c.311G>A (p.Gly104Glu) c.440G>A (p.Gly147Glu) c.208+167G>A c.473G>A (p.Gly158Glu) n.2646G>A n.808G>A n.630G>A n.687G>A | |
2 | g.156329748C>A | CA348682425 | NR4A2 | c.250G>T (p.Gly84Ter) c.310G>T (p.Gly104Ter) c.439G>T (p.Gly147Ter) c.208+166G>T c.472G>T (p.Gly158Ter) n.2645G>T n.807G>T n.629G>T n.686G>T | |
2 | g.156329748C>G | CA348682426 | NR4A2 | c.250G>C (p.Gly84Arg) c.310G>C (p.Gly104Arg) c.439G>C (p.Gly147Arg) c.208+166G>C c.472G>C (p.Gly158Arg) n.2645G>C n.807G>C n.629G>C n.686G>C | |
2 | g.156329748C>T | CA348682424 | NR4A2 | c.250G>A (p.Gly84Arg) c.310G>A (p.Gly104Arg) c.439G>A (p.Gly147Arg) c.208+166G>A c.472G>A (p.Gly158Arg) n.2645G>A n.807G>A n.629G>A n.686G>A | gnomAD v4 |
2 | g.156329749C>A | CA429728022 | NR4A2 | c.249G>T (p.Pro83=) c.309G>T (p.Pro103=) c.438G>T (p.Pro146=) c.208+165G>T c.471G>T (p.Pro157=) n.2644G>T n.806G>T n.628G>T n.685G>T | |
2 | g.156329749C>G | CA429728024 | NR4A2 | c.249G>C (p.Pro83=) c.309G>C (p.Pro103=) c.438G>C (p.Pro146=) c.208+165G>C c.471G>C (p.Pro157=) n.2644G>C n.806G>C n.628G>C n.685G>C | |
2 | g.156329749C>T | CA429728026 | NR4A2 | c.249G>A (p.Pro83=) c.309G>A (p.Pro103=) c.438G>A (p.Pro146=) c.208+165G>A c.471G>A (p.Pro157=) n.2644G>A n.806G>A n.628G>A n.685G>A | gnomAD v4 |
2 | g.156329750G>A | CA348682427 | NR4A2 | c.248C>T (p.Pro83Leu) c.308C>T (p.Pro103Leu) c.437C>T (p.Pro146Leu) c.208+164C>T c.470C>T (p.Pro157Leu) n.2643C>T n.805C>T n.627C>T n.684C>T | gnomAD v4 |
2 | g.156329750G>C | CA348682428 | NR4A2 | c.248C>G (p.Pro83Arg) c.308C>G (p.Pro103Arg) c.437C>G (p.Pro146Arg) c.208+164C>G c.470C>G (p.Pro157Arg) n.2643C>G n.805C>G n.627C>G n.684C>G | gnomAD v4 |
2 | g.156329750G>T | CA348682429 | NR4A2 | c.248C>A (p.Pro83Gln) c.308C>A (p.Pro103Gln) c.437C>A (p.Pro146Gln) c.208+164C>A c.470C>A (p.Pro157Gln) n.2643C>A n.805C>A n.627C>A n.684C>A | |
2 | g.156329751G>A | CA1916452 | NR4A2 | c.247C>T (p.Pro83Ser) c.307C>T (p.Pro103Ser) c.436C>T (p.Pro146Ser) c.208+163C>T c.469C>T (p.Pro157Ser) n.2642C>T n.804C>T n.626C>T n.683C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329751G>C | CA348682430 | NR4A2 | c.247C>G (p.Pro83Ala) c.307C>G (p.Pro103Ala) c.436C>G (p.Pro146Ala) c.208+163C>G c.469C>G (p.Pro157Ala) n.2642C>G n.804C>G n.626C>G n.683C>G | |
2 | g.156329751G= | CA1300460583 | NR4A2 | c.247C= (p.Pro83=) c.307C= (p.Pro103=) c.436C= (p.Pro146=) c.208+163C= c.469C= (p.Pro157=) n.2642C= n.804C= n.626C= n.683C= | |
2 | g.156329751G>T | CA348682431 | NR4A2 | c.247C>A (p.Pro83Thr) c.307C>A (p.Pro103Thr) c.436C>A (p.Pro146Thr) c.208+163C>A c.469C>A (p.Pro157Thr) n.2642C>A n.804C>A n.626C>A n.683C>A | |
2 | g.156329752G>A | CA429728032 | NR4A2 | c.246C>T (p.Asp82=) c.306C>T (p.Asp102=) c.435C>T (p.Asp145=) c.208+162C>T c.468C>T (p.Asp156=) n.2641C>T n.803C>T n.625C>T n.682C>T | |
2 | g.156329752G>C | CA348682432 | NR4A2 | c.246C>G (p.Asp82Glu) c.306C>G (p.Asp102Glu) c.435C>G (p.Asp145Glu) c.208+162C>G c.468C>G (p.Asp156Glu) n.2641C>G n.803C>G n.625C>G n.682C>G | |
2 | g.156329752G>T | CA348682433 | NR4A2 | c.246C>A (p.Asp82Glu) c.306C>A (p.Asp102Glu) c.435C>A (p.Asp145Glu) c.208+162C>A c.468C>A (p.Asp156Glu) n.2641C>A n.803C>A n.625C>A n.682C>A | |
2 | g.156329755_156329757dup | CA1916451 | NR4A2 | c.244_246dup (p.Asp82_Pro83insAsp) c.304_306dup (p.Asp102_Pro103insAsp) c.433_435dup (p.Asp145_Pro146insAsp) c.208+160_208+162dup c.466_468dup (p.Asp156_Pro157insAsp) n.2639_2641dup n.801_803dup n.623_625dup n.680_682dup | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.156329753T>A | CA348682434 | NR4A2 | c.245A>T (p.Asp82Val) c.305A>T (p.Asp102Val) c.434A>T (p.Asp145Val) c.208+161A>T c.467A>T (p.Asp156Val) n.2640A>T n.802A>T n.624A>T n.681A>T | |
2 | g.156329753T>C | CA348682435 | NR4A2 | c.245A>G (p.Asp82Gly) c.305A>G (p.Asp102Gly) c.434A>G (p.Asp145Gly) c.208+161A>G c.467A>G (p.Asp156Gly) n.2640A>G n.802A>G n.624A>G n.681A>G | |
2 | g.156329753T>G | CA348682436 | NR4A2 | c.245A>C (p.Asp82Ala) c.305A>C (p.Asp102Ala) c.434A>C (p.Asp145Ala) c.208+161A>C c.467A>C (p.Asp156Ala) n.2640A>C n.802A>C n.624A>C n.681A>C | gnomAD v4 |
2 | g.156329754C>A | CA348682437 | NR4A2 | c.244G>T (p.Asp82Tyr) c.304G>T (p.Asp102Tyr) c.433G>T (p.Asp145Tyr) c.208+160G>T c.466G>T (p.Asp156Tyr) n.2639G>T n.801G>T n.623G>T n.680G>T | gnomAD v4 |
2 | g.156329754C>G | CA348682438 | NR4A2 | c.244G>C (p.Asp82His) c.304G>C (p.Asp102His) c.433G>C (p.Asp145His) c.208+160G>C c.466G>C (p.Asp156His) n.2639G>C n.801G>C n.623G>C n.680G>C | gnomAD v4 |
2 | g.156329754C>T | CA348682439 | NR4A2 | c.244G>A (p.Asp82Asn) c.304G>A (p.Asp102Asn) c.433G>A (p.Asp145Asn) c.208+160G>A c.466G>A (p.Asp156Asn) n.2639G>A n.801G>A n.623G>A n.680G>A | COSMIC COSMIC |
2 | g.156329755G>A | CA429728042 | NR4A2 | c.243C>T (p.Asp81=) c.303C>T (p.Asp101=) c.432C>T (p.Asp144=) c.208+159C>T c.465C>T (p.Asp155=) n.2638C>T n.800C>T n.622C>T n.679C>T | gnomAD v4 COSMIC COSMIC |
2 | g.156329755G>C | CA348682440 | NR4A2 | c.243C>G (p.Asp81Glu) c.303C>G (p.Asp101Glu) c.432C>G (p.Asp144Glu) c.208+159C>G c.465C>G (p.Asp155Glu) n.2638C>G n.800C>G n.622C>G n.679C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329755G= | CA1300460584 | NR4A2 | c.243C= (p.Asp81=) c.303C= (p.Asp101=) c.432C= (p.Asp144=) c.208+159C= c.465C= (p.Asp155=) n.2638C= n.800C= n.622C= n.679C= | |
2 | g.156329755G>T | CA348682441 | NR4A2 | c.243C>A (p.Asp81Glu) c.303C>A (p.Asp101Glu) c.432C>A (p.Asp144Glu) c.208+159C>A c.465C>A (p.Asp155Glu) n.2638C>A n.800C>A n.622C>A n.679C>A | |
2 | g.156329756T>A | CA348682442 | NR4A2 | c.242A>T (p.Asp81Val) c.302A>T (p.Asp101Val) c.431A>T (p.Asp144Val) c.208+158A>T c.464A>T (p.Asp155Val) n.2637A>T n.799A>T n.621A>T n.678A>T | |
2 | g.156329756T>C | CA348682444 | NR4A2 | c.242A>G (p.Asp81Gly) c.302A>G (p.Asp101Gly) c.431A>G (p.Asp144Gly) c.208+158A>G c.464A>G (p.Asp155Gly) n.2637A>G n.799A>G n.621A>G n.678A>G | |
2 | g.156329756T>G | CA348682443 | NR4A2 | c.242A>C (p.Asp81Ala) c.302A>C (p.Asp101Ala) c.431A>C (p.Asp144Ala) c.208+158A>C c.464A>C (p.Asp155Ala) n.2637A>C n.799A>C n.621A>C n.678A>C | |
2 | g.156329757C>A | CA348682445 | NR4A2 | c.241G>T (p.Asp81Tyr) c.301G>T (p.Asp101Tyr) c.430G>T (p.Asp144Tyr) c.208+157G>T c.463G>T (p.Asp155Tyr) n.2636G>T n.798G>T n.620G>T n.677G>T | |
2 | g.156329757C= | CA1300460585 | NR4A2 | c.241G= (p.Asp81=) c.301G= (p.Asp101=) c.430G= (p.Asp144=) c.208+157G= c.463G= (p.Asp155=) n.2636G= n.798G= n.620G= n.677G= | |
2 | g.156329757C>G | CA348682446 | NR4A2 | c.241G>C (p.Asp81His) c.301G>C (p.Asp101His) c.430G>C (p.Asp144His) c.208+157G>C c.463G>C (p.Asp155His) n.2636G>C n.798G>C n.620G>C n.677G>C | |
2 | g.156329757C>T | CA348682447 | NR4A2 | c.241G>A (p.Asp81Asn) c.301G>A (p.Asp101Asn) c.430G>A (p.Asp144Asn) c.208+157G>A c.463G>A (p.Asp155Asn) n.2636G>A n.798G>A n.620G>A n.677G>A | dbSNP gnomAD v3 gnomAD v4 |
2 | g.156329759del | CA645529279 | NR4A2 | c.241del (p.Asp81ThrfsTer19) c.301del (p.Asp101ThrfsTer19) c.430del (p.Asp144ThrfsTer19) c.208+157del c.463del (p.Asp155ThrfsTer19) n.2636del n.798del n.620del n.677del | COSMIC COSMIC |
2 | g.156329758C>A | CA348682448 | NR4A2 | c.240G>T (p.Trp80Cys) c.300G>T (p.Trp100Cys) c.429G>T (p.Trp143Cys) c.208+156G>T c.462G>T (p.Trp154Cys) n.2635G>T n.797G>T n.619G>T n.676G>T | |
2 | g.156329758C>G | CA348682449 | NR4A2 | c.240G>C (p.Trp80Cys) c.300G>C (p.Trp100Cys) c.429G>C (p.Trp143Cys) c.208+156G>C c.462G>C (p.Trp154Cys) n.2635G>C n.797G>C n.619G>C n.676G>C | |
2 | g.156329758C>T | CA348682450 | NR4A2 | c.240G>A (p.Trp80Ter) c.300G>A (p.Trp100Ter) c.429G>A (p.Trp143Ter) c.208+156G>A c.462G>A (p.Trp154Ter) n.2635G>A n.797G>A n.619G>A n.676G>A | |
2 | g.156329759C>A | CA348682451 | NR4A2 | c.239G>T (p.Trp80Leu) c.299G>T (p.Trp100Leu) c.428G>T (p.Trp143Leu) c.208+155G>T c.461G>T (p.Trp154Leu) n.2634G>T n.796G>T n.618G>T n.675G>T | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329759C= | CA1300460586 | NR4A2 | c.239G= (p.Trp80=) c.299G= (p.Trp100=) c.428G= (p.Trp143=) c.208+155G= c.461G= (p.Trp154=) n.2634G= n.796G= n.618G= n.675G= | |
2 | g.156329759C>G | CA348682452 | NR4A2 | c.239G>C (p.Trp80Ser) c.299G>C (p.Trp100Ser) c.428G>C (p.Trp143Ser) c.208+155G>C c.461G>C (p.Trp154Ser) n.2634G>C n.796G>C n.618G>C n.675G>C | |
2 | g.156329759C>T | CA348682453 | NR4A2 | c.239G>A (p.Trp80Ter) c.299G>A (p.Trp100Ter) c.428G>A (p.Trp143Ter) c.208+155G>A c.461G>A (p.Trp154Ter) n.2634G>A n.796G>A n.618G>A n.675G>A | |
2 | g.156329760A>C | CA348682454 | NR4A2 | c.238T>G (p.Trp80Gly) c.298T>G (p.Trp100Gly) c.427T>G (p.Trp143Gly) c.208+154T>G c.460T>G (p.Trp154Gly) n.2633T>G n.795T>G n.617T>G n.674T>G | |
2 | g.156329760A>G | CA348682455 | NR4A2 | c.238T>C (p.Trp80Arg) c.298T>C (p.Trp100Arg) c.427T>C (p.Trp143Arg) c.208+154T>C c.460T>C (p.Trp154Arg) n.2633T>C n.795T>C n.617T>C n.674T>C | |
2 | g.156329760A>T | CA348682456 | NR4A2 | c.238T>A (p.Trp80Arg) c.298T>A (p.Trp100Arg) c.427T>A (p.Trp143Arg) c.208+154T>A c.460T>A (p.Trp154Arg) n.2633T>A n.795T>A n.617T>A n.674T>A | |
2 | g.156329761C>A | CA348682459 | NR4A2 | c.237G>T (p.Met79Ile) c.297G>T (p.Met99Ile) c.426G>T (p.Met142Ile) c.208+153G>T c.459G>T (p.Met153Ile) n.2632G>T n.794G>T n.616G>T n.673G>T | |
2 | g.156329761C= | CA1300460587 | NR4A2 | c.237G= (p.Met79=) c.297G= (p.Met99=) c.426G= (p.Met142=) c.208+153G= c.459G= (p.Met153=) n.2632G= n.794G= n.616G= n.673G= | |
2 | g.156329761C>G | CA348682457 | NR4A2 | c.237G>C (p.Met79Ile) c.297G>C (p.Met99Ile) c.426G>C (p.Met142Ile) c.208+153G>C c.459G>C (p.Met153Ile) n.2632G>C n.794G>C n.616G>C n.673G>C | |
2 | g.156329761C>T | CA348682458 | NR4A2 | c.237G>A (p.Met79Ile) c.297G>A (p.Met99Ile) c.426G>A (p.Met142Ile) c.208+153G>A c.459G>A (p.Met153Ile) n.2632G>A n.794G>A n.616G>A n.673G>A | dbSNP gnomAD v2 gnomAD v4 |
2 | g.156329762A>C | CA348682460 | NR4A2 | c.236T>G (p.Met79Arg) c.296T>G (p.Met99Arg) c.425T>G (p.Met142Arg) c.208+152T>G c.458T>G (p.Met153Arg) n.2631T>G n.793T>G n.615T>G n.672T>G | |
2 | g.156329762A>G | CA348682461 | NR4A2 | c.236T>C (p.Met79Thr) c.296T>C (p.Met99Thr) c.425T>C (p.Met142Thr) c.208+152T>C c.458T>C (p.Met153Thr) n.2631T>C n.793T>C n.615T>C n.672T>C | gnomAD v4 |
2 | g.156329762A>T | CA348682462 | NR4A2 | c.236T>A (p.Met79Lys) c.296T>A (p.Met99Lys) c.425T>A (p.Met142Lys) c.208+152T>A c.458T>A (p.Met153Lys) n.2631T>A n.793T>A n.615T>A n.672T>A | |
2 | g.156329763T>A | CA348682463 | NR4A2 | c.235A>T (p.Met79Leu) c.295A>T (p.Met99Leu) c.424A>T (p.Met142Leu) c.208+151A>T c.457A>T (p.Met153Leu) n.2630A>T n.792A>T n.614A>T n.671A>T | dbSNP |
2 | g.156329763T>C | CA348682464 | NR4A2 | c.235A>G (p.Met79Val) c.295A>G (p.Met99Val) c.424A>G (p.Met142Val) c.208+151A>G c.457A>G (p.Met153Val) n.2630A>G n.792A>G n.614A>G n.671A>G | gnomAD v4 |
2 | g.156329763T>G | CA348682465 | NR4A2 | c.235A>C (p.Met79Leu) c.295A>C (p.Met99Leu) c.424A>C (p.Met142Leu) c.208+151A>C c.457A>C (p.Met153Leu) n.2630A>C n.792A>C n.614A>C n.671A>C | |
2 | g.156329763T= | CA1300460588 | NR4A2 | c.235A= (p.Met79=) c.295A= (p.Met99=) c.424A= (p.Met142=) c.208+151A= c.457A= (p.Met153=) n.2630A= n.792A= n.614A= n.671A= | |
2 | g.156329764G>A | CA429728056 | NR4A2 | c.234C>T (p.Pro78=) c.294C>T (p.Pro98=) c.423C>T (p.Pro141=) c.208+150C>T c.456C>T (p.Pro152=) n.2629C>T n.791C>T n.613C>T n.670C>T | |
2 | g.156329764G>C | CA429728058 | NR4A2 | c.234C>G (p.Pro78=) c.294C>G (p.Pro98=) c.423C>G (p.Pro141=) c.208+150C>G c.456C>G (p.Pro152=) n.2629C>G n.791C>G n.613C>G n.670C>G | |
2 | g.156329764G>T | CA429728059 | NR4A2 | c.234C>A (p.Pro78=) c.294C>A (p.Pro98=) c.423C>A (p.Pro141=) c.208+150C>A c.456C>A (p.Pro152=) n.2629C>A n.791C>A n.613C>A n.670C>A | |
2 | g.156329767dup | CA1300460589 | NR4A2 | c.234dup (p.Met79HisfsTer?) c.294dup (p.Met99HisfsTer?) c.423dup (p.Met142HisfsTer?) c.208+150dup c.456dup (p.Met153HisfsTer?) n.2629dup n.791dup n.613dup n.670dup | dbSNP |
2 | g.156329765G>A | CA348682466 | NR4A2 | c.233C>T (p.Pro78Leu) c.293C>T (p.Pro98Leu) c.422C>T (p.Pro141Leu) c.208+149C>T c.455C>T (p.Pro152Leu) n.2628C>T n.790C>T n.612C>T n.669C>T | |
2 | g.156329765G>C | CA348682467 | NR4A2 | c.233C>G (p.Pro78Arg) c.293C>G (p.Pro98Arg) c.422C>G (p.Pro141Arg) c.208+149C>G c.455C>G (p.Pro152Arg) n.2628C>G n.790C>G n.612C>G n.669C>G | |
2 | g.156329765G>T | CA348682468 | NR4A2 | c.233C>A (p.Pro78His) c.293C>A (p.Pro98His) c.422C>A (p.Pro141His) c.208+149C>A c.455C>A (p.Pro152His) n.2628C>A n.790C>A n.612C>A n.669C>A | |
2 | g.156329766G>A | CA348682469 | NR4A2 | c.232C>T (p.Pro78Ser) c.292C>T (p.Pro98Ser) c.421C>T (p.Pro141Ser) c.208+148C>T c.454C>T (p.Pro152Ser) n.2627C>T n.789C>T n.611C>T n.668C>T | dbSNP gnomAD v4 |
2 | g.156329766G>C | CA348682470 | NR4A2 | c.232C>G (p.Pro78Ala) c.292C>G (p.Pro98Ala) c.421C>G (p.Pro141Ala) c.208+148C>G c.454C>G (p.Pro152Ala) n.2627C>G n.789C>G n.611C>G n.668C>G | |
2 | g.156329766G= | CA1300460590 | NR4A2 | c.232C= (p.Pro78=) c.292C= (p.Pro98=) c.421C= (p.Pro141=) c.208+148C= c.454C= (p.Pro152=) n.2627C= n.789C= n.611C= n.668C= | |
2 | g.156329766G>T | CA348682471 | NR4A2 | c.232C>A (p.Pro78Thr) c.292C>A (p.Pro98Thr) c.421C>A (p.Pro141Thr) c.208+148C>A c.454C>A (p.Pro152Thr) n.2627C>A n.789C>A n.611C>A n.668C>A | |
2 | g.156329767G>A | CA429728066 | NR4A2 | c.231C>T (p.Ser77=) c.291C>T (p.Ser97=) c.420C>T (p.Ser140=) c.208+147C>T c.453C>T (p.Ser151=) n.2626C>T n.788C>T n.610C>T n.667C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329767G>C | CA348682472 | NR4A2 | c.231C>G (p.Ser77Arg) c.291C>G (p.Ser97Arg) c.420C>G (p.Ser140Arg) c.208+147C>G c.453C>G (p.Ser151Arg) n.2626C>G n.788C>G n.610C>G n.667C>G | |
2 | g.156329767G= | CA1300460591 | NR4A2 | c.231C= (p.Ser77=) c.291C= (p.Ser97=) c.420C= (p.Ser140=) c.208+147C= c.453C= (p.Ser151=) n.2626C= n.788C= n.610C= n.667C= | |
2 | g.156329767G>T | CA348682473 | NR4A2 | c.231C>A (p.Ser77Arg) c.291C>A (p.Ser97Arg) c.420C>A (p.Ser140Arg) c.208+147C>A c.453C>A (p.Ser151Arg) n.2626C>A n.788C>A n.610C>A n.667C>A | |
2 | g.156329768C>A | CA348682474 | NR4A2 | c.230G>T (p.Ser77Ile) c.290G>T (p.Ser97Ile) c.419G>T (p.Ser140Ile) c.208+146G>T c.452G>T (p.Ser151Ile) n.2625G>T n.787G>T n.609G>T n.666G>T | |
2 | g.156329768C= | CA1300460592 | NR4A2 | c.230G= (p.Ser77=) c.290G= (p.Ser97=) c.419G= (p.Ser140=) c.208+146G= c.452G= (p.Ser151=) n.2625G= n.787G= n.609G= n.666G= | |
2 | g.156329768C>G | CA1916453 | NR4A2 | c.230G>C (p.Ser77Thr) c.290G>C (p.Ser97Thr) c.419G>C (p.Ser140Thr) c.208+146G>C c.452G>C (p.Ser151Thr) n.2625G>C n.787G>C n.609G>C n.666G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.156329768C>T | CA348682475 | NR4A2 | c.230G>A (p.Ser77Asn) c.290G>A (p.Ser97Asn) c.419G>A (p.Ser140Asn) c.208+146G>A c.452G>A (p.Ser151Asn) n.2625G>A n.787G>A n.609G>A n.666G>A | |
2 | g.156329769T>A | CA348682476 | NR4A2 | c.229A>T (p.Ser77Cys) c.289A>T (p.Ser97Cys) c.418A>T (p.Ser140Cys) c.208+145A>T c.451A>T (p.Ser151Cys) n.2624A>T n.786A>T n.608A>T n.665A>T | |
2 | g.156329769T>C | CA348682477 | NR4A2 | c.229A>G (p.Ser77Gly) c.289A>G (p.Ser97Gly) c.418A>G (p.Ser140Gly) c.208+145A>G c.451A>G (p.Ser151Gly) n.2624A>G n.786A>G n.608A>G n.665A>G | |
2 | g.156329769T>G | CA348682478 | NR4A2 | c.229A>C (p.Ser77Arg) c.289A>C (p.Ser97Arg) c.418A>C (p.Ser140Arg) c.208+145A>C c.451A>C (p.Ser151Arg) n.2624A>C n.786A>C n.608A>C n.665A>C | |
2 | g.156329770G>A | CA1916454 | NR4A2 | c.228C>T (p.His76=) c.288C>T (p.His96=) c.417C>T (p.His139=) c.208+144C>T c.450C>T (p.His150=) n.2623C>T n.785C>T n.607C>T n.664C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.156329770G>C | CA348682479 | NR4A2 | c.228C>G (p.His76Gln) c.288C>G (p.His96Gln) c.417C>G (p.His139Gln) c.208+144C>G c.450C>G (p.His150Gln) n.2623C>G n.785C>G n.607C>G n.664C>G | |
2 | g.156329770G= | CA1300460593 | NR4A2 | c.228C= (p.His76=) c.288C= (p.His96=) c.417C= (p.His139=) c.208+144C= c.450C= (p.His150=) n.2623C= n.785C= n.607C= n.664C= | |
2 | g.156329770G>T | CA348682480 | NR4A2 | c.228C>A (p.His76Gln) c.288C>A (p.His96Gln) c.417C>A (p.His139Gln) c.208+144C>A c.450C>A (p.His150Gln) n.2623C>A n.785C>A n.607C>A n.664C>A | |
2 | g.156329771T>A | CA348682481 | NR4A2 | c.227A>T (p.His76Leu) c.287A>T (p.His96Leu) c.416A>T (p.His139Leu) c.208+143A>T c.449A>T (p.His150Leu) n.2622A>T n.784A>T n.606A>T n.663A>T | |
2 | g.156329771T>C | CA348682482 | NR4A2 | c.227A>G (p.His76Arg) c.287A>G (p.His96Arg) c.416A>G (p.His139Arg) c.208+143A>G c.449A>G (p.His150Arg) n.2622A>G n.784A>G n.606A>G n.663A>G | |
2 | g.156329771T>G | CA348682483 | NR4A2 | c.227A>C (p.His76Pro) c.287A>C (p.His96Pro) c.416A>C (p.His139Pro) c.208+143A>C c.449A>C (p.His150Pro) n.2622A>C n.784A>C n.606A>C n.663A>C |