Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.8076228C>A | CA497759032 | ALOX12B | c.1479G>T (p.Leu493=) c.543G>T (p.Leu181=) n.426G>T n.863G>T | gnomAD v4 COSMIC COSMIC |
17 | g.8076228C>G | CA497759034 | ALOX12B | c.1479G>C (p.Leu493=) c.543G>C (p.Leu181=) n.426G>C n.863G>C | gnomAD v4 |
17 | g.8076228C>T | CA497759036 | ALOX12B | c.1479G>A (p.Leu493=) c.543G>A (p.Leu181=) n.426G>A n.863G>A | gnomAD v4 |
17 | g.8076229A>C | CA397990418 | ALOX12B | c.1478T>G (p.Leu493Arg) c.542T>G (p.Leu181Arg) n.425T>G n.862T>G | |
17 | g.8076229A>G | CA397990420 | ALOX12B | c.1478T>C (p.Leu493Pro) c.542T>C (p.Leu181Pro) n.425T>C n.862T>C | |
17 | g.8076229A>T | CA397990422 | ALOX12B | c.1478T>A (p.Leu493Gln) c.542T>A (p.Leu181Gln) n.425T>A n.862T>A | |
17 | g.8076230G>A | CA8367294 | ALOX12B | c.1477C>T (p.Leu493=) c.541C>T (p.Leu181=) n.424C>T n.861C>T | dbSNP ExAC gnomAD v3 gnomAD v4 |
17 | g.8076230G>C | CA397990425 | ALOX12B | c.1477C>G (p.Leu493Val) c.541C>G (p.Leu181Val) n.424C>G n.861C>G | |
17 | g.8076230G= | CA2246126391 | ALOX12B | c.1477C= (p.Leu493=) c.541C= (p.Leu181=) n.424C= n.861C= | |
17 | g.8076230G>T | CA397990427 | ALOX12B | c.1477C>A (p.Leu493Met) c.541C>A (p.Leu181Met) n.424C>A n.861C>A | COSMIC COSMIC |
17 | g.8076231G>A | CA497759046 | ALOX12B | c.1476C>T (p.Asp492=) c.540C>T (p.Asp180=) n.423C>T n.860C>T | |
17 | g.8076231G>C | CA397990429 | ALOX12B | c.1476C>G (p.Asp492Glu) c.540C>G (p.Asp180Glu) n.423C>G n.860C>G | |
17 | g.8076231G>T | CA397990431 | ALOX12B | c.1476C>A (p.Asp492Glu) c.540C>A (p.Asp180Glu) n.423C>A n.860C>A | |
17 | g.8076232T>A | CA397990433 | ALOX12B | c.1475A>T (p.Asp492Val) c.539A>T (p.Asp180Val) n.422A>T n.859A>T | |
17 | g.8076232T>C | CA397990435 | ALOX12B | c.1475A>G (p.Asp492Gly) c.539A>G (p.Asp180Gly) n.422A>G n.859A>G | |
17 | g.8076232T>G | CA397990437 | ALOX12B | c.1475A>C (p.Asp492Ala) c.539A>C (p.Asp180Ala) n.422A>C n.859A>C | |
17 | g.8076233C>A | CA397990442 | ALOX12B | c.1474G>T (p.Asp492Tyr) c.538G>T (p.Asp180Tyr) n.421G>T n.858G>T | dbSNP |
17 | g.8076233C= | CA2246126392 | ALOX12B | c.1474G= (p.Asp492=) c.538G= (p.Asp180=) n.421G= n.858G= | |
17 | g.8076233C>G | CA397990441 | ALOX12B | c.1474G>C (p.Asp492His) c.538G>C (p.Asp180His) n.421G>C n.858G>C | |
17 | g.8076233C>T | CA397990439 | ALOX12B | c.1474G>A (p.Asp492Asn) c.538G>A (p.Asp180Asn) n.421G>A n.858G>A | dbSNP gnomAD v4 |
17 | g.8076234C>A | CA397990444 | ALOX12B | c.1473G>T (p.Gln491His) c.537G>T (p.Gln179His) n.420G>T n.857G>T | |
17 | g.8076234C>G | CA397990445 | ALOX12B | c.1473G>C (p.Gln491His) c.537G>C (p.Gln179His) n.420G>C n.857G>C | |
17 | g.8076234C>T | CA497759064 | ALOX12B | c.1473G>A (p.Gln491=) c.537G>A (p.Gln179=) n.420G>A n.857G>A | |
17 | g.8076235T>A | CA397990449 | ALOX12B | c.1472A>T (p.Gln491Leu) c.536A>T (p.Gln179Leu) n.419A>T n.856A>T | |
17 | g.8076235T>C | CA397990450 | ALOX12B | c.1472A>G (p.Gln491Arg) c.536A>G (p.Gln179Arg) n.419A>G n.856A>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.8076235T>G | CA397990452 | ALOX12B | c.1472A>C (p.Gln491Pro) c.536A>C (p.Gln179Pro) n.419A>C n.856A>C | |
17 | g.8076235T= | CA2246126393 | ALOX12B | c.1472A= (p.Gln491=) c.536A= (p.Gln179=) n.419A= n.856A= | |
17 | g.8076236G>A | CA397990454 | ALOX12B | c.1471C>T (p.Gln491Ter) c.535C>T (p.Gln179Ter) n.418C>T n.855C>T | |
17 | g.8076236G>C | CA397990456 | ALOX12B | c.1471C>G (p.Gln491Glu) c.535C>G (p.Gln179Glu) n.418C>G n.855C>G | |
17 | g.8076236G>T | CA397990458 | ALOX12B | c.1471C>A (p.Gln491Lys) c.535C>A (p.Gln179Lys) n.418C>A n.855C>A | |
17 | g.8076237G>A | CA287543800 | ALOX12B | c.1470C>T (p.Val490=) c.534C>T (p.Val178=) n.417C>T n.854C>T | dbSNP gnomAD v4 |
17 | g.8076237G>C | CA497759075 | ALOX12B | c.1470C>G (p.Val490=) c.534C>G (p.Val178=) n.417C>G n.854C>G | |
17 | g.8076237G= | CA2246126394 | ALOX12B | c.1470C= (p.Val490=) c.534C= (p.Val178=) n.417C= n.854C= | |
17 | g.8076237G>T | CA497759078 | ALOX12B | c.1470C>A (p.Val490=) c.534C>A (p.Val178=) n.417C>A n.854C>A | |
17 | g.8076238A>C | CA397990461 | ALOX12B | c.1469T>G (p.Val490Gly) c.533T>G (p.Val178Gly) n.416T>G n.853T>G | |
17 | g.8076238A>G | CA397990463 | ALOX12B | c.1469T>C (p.Val490Ala) c.533T>C (p.Val178Ala) n.416T>C n.853T>C | |
17 | g.8076238A>T | CA397990465 | ALOX12B | c.1469T>A (p.Val490Asp) c.533T>A (p.Val178Asp) n.416T>A n.853T>A | |
17 | g.8076238_8076239delinsAC | CA2246126395 | ALOX12B | c.1468_1469delinsGT (p.Val490=) c.532_533delinsGT (p.Val178=) n.415_416delinsGT n.852_853delinsGT | |
17 | g.8076239C>A | CA397990471 | ALOX12B | c.1468G>T (p.Val490Phe) c.532G>T (p.Val178Phe) n.415G>T n.852G>T | |
17 | g.8076239C>G | CA397990469 | ALOX12B | c.1468G>C (p.Val490Leu) c.532G>C (p.Val178Leu) n.415G>C n.852G>C | |
17 | g.8076239C>T | CA397990467 | ALOX12B | c.1468G>A (p.Val490Ile) c.532G>A (p.Val178Ile) n.415G>A n.852G>A | |
17 | g.8076242del | CA2246126396 | ALOX12B | c.1468del (p.Val490SerfsTer24) c.532del (p.Val178SerfsTer24) n.415del n.852del | dbSNP |
17 | g.8076240C>A | CA497759092 | ALOX12B | c.1467G>T (p.Gly489=) c.531G>T (p.Gly177=) n.414G>T n.851G>T | |
17 | g.8076240C= | CA2246126397 | ALOX12B | c.1467G= (p.Gly489=) c.531G= (p.Gly177=) n.414G= n.851G= | |
17 | g.8076240C>G | CA497759093 | ALOX12B | c.1467G>C (p.Gly489=) c.531G>C (p.Gly177=) n.414G>C n.851G>C | |
17 | g.8076240C>T | CA497759091 | ALOX12B | c.1467G>A (p.Gly489=) c.531G>A (p.Gly177=) n.414G>A n.851G>A | dbSNP gnomAD v4 |
17 | g.8076241C>A | CA397990473 | ALOX12B | c.1466G>T (p.Gly489Val) c.530G>T (p.Gly177Val) n.413G>T n.850G>T | |
17 | g.8076241C= | CA2246126398 | ALOX12B | c.1466G= (p.Gly489=) c.530G= (p.Gly177=) n.413G= n.850G= | |
17 | g.8076241C>G | CA397990475 | ALOX12B | c.1466G>C (p.Gly489Ala) c.530G>C (p.Gly177Ala) n.413G>C n.850G>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.8076241C>T | CA397990476 | ALOX12B | c.1466G>A (p.Gly489Glu) c.530G>A (p.Gly177Glu) n.413G>A n.850G>A | COSMIC COSMIC |
17 | g.8076242C>A | CA397990478 | ALOX12B | c.1465G>T (p.Gly489Trp) c.529G>T (p.Gly177Trp) n.412G>T n.849G>T | |
17 | g.8076242C>G | CA397990480 | ALOX12B | c.1465G>C (p.Gly489Arg) c.529G>C (p.Gly177Arg) n.412G>C n.849G>C | |
17 | g.8076242C>T | CA397990482 | ALOX12B | c.1465G>A (p.Gly489Arg) c.529G>A (p.Gly177Arg) n.412G>A n.849G>A | |
17 | g.8076243A= | CA2246126399 | ALOX12B | c.1464T= (p.Arg488=) c.528T= (p.Arg176=) n.411T= n.848T= | |
17 | g.8076243A>C | CA497759099 | ALOX12B | c.1464T>G (p.Arg488=) c.528T>G (p.Arg176=) n.411T>G n.848T>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.8076243A>G | CA497759101 | ALOX12B | c.1464T>C (p.Arg488=) c.528T>C (p.Arg176=) n.411T>C n.848T>C | |
17 | g.8076243A>T | CA497759103 | ALOX12B | c.1464T>A (p.Arg488=) c.528T>A (p.Arg176=) n.411T>A n.848T>A | |
17 | g.8076244C>A | CA397990488 | ALOX12B | c.1463G>T (p.Arg488Leu) c.527G>T (p.Arg176Leu) n.410G>T n.847G>T | |
17 | g.8076244C= | CA2246126400 | ALOX12B | c.1463G= (p.Arg488=) c.527G= (p.Arg176=) n.410G= n.847G= | |
17 | g.8076244C>G | CA397990485 | ALOX12B | c.1463G>C (p.Arg488Pro) c.527G>C (p.Arg176Pro) n.410G>C n.847G>C | ClinVar |
17 | g.8076244C>T | CA8367295 | ALOX12B | c.1463G>A (p.Arg488His) c.527G>A (p.Arg176His) n.410G>A n.847G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076245G>A | CA397990490 | ALOX12B | c.1462C>T (p.Arg488Cys) c.526C>T (p.Arg176Cys) n.409C>T n.846C>T | ClinVar dbSNP gnomAD v4 |
17 | g.8076245G>C | CA397990492 | ALOX12B | c.1462C>G (p.Arg488Gly) c.526C>G (p.Arg176Gly) n.409C>G n.846C>G | gnomAD v4 |
17 | g.8076245G= | CA2246126401 | ALOX12B | c.1462C= (p.Arg488=) c.526C= (p.Arg176=) n.409C= n.846C= | |
17 | g.8076245G>T | CA397990493 | ALOX12B | c.1462C>A (p.Arg488Ser) c.526C>A (p.Arg176Ser) n.409C>A n.846C>A | |
17 | g.8076246C>A | CA397990495 | ALOX12B | c.1461G>T (p.Glu487Asp) c.525G>T (p.Glu175Asp) n.408G>T n.845G>T | gnomAD v4 |
17 | g.8076246C= | CA2246126402 | ALOX12B | c.1461G= (p.Glu487=) c.525G= (p.Glu175=) n.408G= n.845G= | |
17 | g.8076246C>G | CA8367296 | ALOX12B | c.1461G>C (p.Glu487Asp) c.525G>C (p.Glu175Asp) n.408G>C n.845G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076246C>T | CA8367297 | ALOX12B | c.1461G>A (p.Glu487=) c.525G>A (p.Glu175=) n.408G>A n.845G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076247T>A | CA397990498 | ALOX12B | c.1460A>T (p.Glu487Val) c.524A>T (p.Glu175Val) n.407A>T n.844A>T | |
17 | g.8076247T>C | CA397990502 | ALOX12B | c.1460A>G (p.Glu487Gly) c.524A>G (p.Glu175Gly) n.407A>G n.844A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.8076247T>G | CA397990500 | ALOX12B | c.1460A>C (p.Glu487Ala) c.524A>C (p.Glu175Ala) n.407A>C n.844A>C | |
17 | g.8076247T= | CA2246126403 | ALOX12B | c.1460A= (p.Glu487=) c.524A= (p.Glu175=) n.407A= n.844A= | |
17 | g.8076248C>A | CA397990504 | ALOX12B | c.1459G>T (p.Glu487Ter) c.523G>T (p.Glu175Ter) n.406G>T n.843G>T | |
17 | g.8076248C>G | CA397990506 | ALOX12B | c.1459G>C (p.Glu487Gln) c.523G>C (p.Glu175Gln) n.406G>C n.843G>C | |
17 | g.8076248C>T | CA397990508 | ALOX12B | c.1459G>A (p.Glu487Lys) c.523G>A (p.Glu175Lys) n.406G>A n.843G>A | |
17 | g.8076248_8076249insAAACACACCCAA | CA2808396188 | ALOX12B | c.1458_1459insTTGGGTGTGTTT (p.Val486_Glu487insLeuGlyValPhe) c.522_523insTTGGGTGTGTTT (p.Val174_Glu175insLeuGlyValPhe) n.405_406insTTGGGTGTGTTT n.842_843insTTGGGTGTGTTT | |
17 | g.8076248_8076249insAACCAAACACACCCAA | CA2808396189 | ALOX12B | c.1458_1459insTTGGGTGTGTTTGGTT (p.Glu487LeufsTer6) c.522_523insTTGGGTGTGTTTGGTT (p.Glu175LeufsTer6) n.405_406insTTGGGTGTGTTTGGTT n.842_843insTTGGGTGTGTTTGGTT | |
17 | g.8076249C>A | CA497759121 | ALOX12B | c.1458G>T (p.Val486=) c.522G>T (p.Val174=) n.405G>T n.842G>T | |
17 | g.8076249C>G | CA497759122 | ALOX12B | c.1458G>C (p.Val486=) c.522G>C (p.Val174=) n.405G>C n.842G>C | |
17 | g.8076249C>T | CA497759125 | ALOX12B | c.1458G>A (p.Val486=) c.522G>A (p.Val174=) n.405G>A n.842G>A | |
17 | g.8076250A>C | CA397990510 | ALOX12B | c.1457T>G (p.Val486Gly) c.521T>G (p.Val174Gly) n.404T>G n.841T>G | |
17 | g.8076250A>G | CA397990512 | ALOX12B | c.1457T>C (p.Val486Ala) c.521T>C (p.Val174Ala) n.404T>C n.841T>C | |
17 | g.8076250A>T | CA397990513 | ALOX12B | c.1457T>A (p.Val486Glu) c.521T>A (p.Val174Glu) n.404T>A n.841T>A | |
17 | g.8076251C>A | CA397990515 | ALOX12B | c.1456G>T (p.Val486Leu) c.520G>T (p.Val174Leu) n.403G>T n.840G>T | |
17 | g.8076251C>G | CA397990516 | ALOX12B | c.1456G>C (p.Val486Leu) c.520G>C (p.Val174Leu) n.403G>C n.840G>C | |
17 | g.8076251C>T | CA397990518 | ALOX12B | c.1456G>A (p.Val486Met) c.520G>A (p.Val174Met) n.403G>A n.840G>A | |
17 | g.8076251_8076253delinsCAA | CA2246126404 | ALOX12B | c.1454_1456delinsTTG (p.Phe485=) c.518_520delinsTTG (p.Phe173=) n.401_403delinsTTG n.838_840delinsTTG | |
17 | g.8076252A>C | CA397990520 | ALOX12B | c.1455T>G (p.Phe485Leu) c.519T>G (p.Phe173Leu) n.402T>G n.839T>G | |
17 | g.8076252A>G | CA497759137 | ALOX12B | c.1455T>C (p.Phe485=) c.519T>C (p.Phe173=) n.402T>C n.839T>C | |
17 | g.8076252A>T | CA397990522 | ALOX12B | c.1455T>A (p.Phe485Leu) c.519T>A (p.Phe173Leu) n.402T>A n.839T>A | |
17 | g.8076253_8076254del | CA2246126405 | ALOX12B | c.1454_1455del (p.Phe485CysfsTer16) c.518_519del (p.Phe173CysfsTer16) n.401_402del n.838_839del | dbSNP |
17 | g.8076253A>C | CA397990525 | ALOX12B | c.1454T>G (p.Phe485Cys) c.518T>G (p.Phe173Cys) n.401T>G n.838T>G | |
17 | g.8076253A>G | CA397990528 | ALOX12B | c.1454T>C (p.Phe485Ser) c.518T>C (p.Phe173Ser) n.401T>C n.838T>C | |
17 | g.8076253A>T | CA397990526 | ALOX12B | c.1454T>A (p.Phe485Tyr) c.518T>A (p.Phe173Tyr) n.401T>A n.838T>A | |
17 | g.8076254A>C | CA397990530 | ALOX12B | c.1453T>G (p.Phe485Val) c.517T>G (p.Phe173Val) n.400T>G n.837T>G | |
17 | g.8076254A>G | CA397990531 | ALOX12B | c.1453T>C (p.Phe485Leu) c.517T>C (p.Phe173Leu) n.400T>C n.837T>C | |
17 | g.8076254A>T | CA397990532 | ALOX12B | c.1453T>A (p.Phe485Ile) c.517T>A (p.Phe173Ile) n.400T>A n.837T>A | |
17 | g.8076255G>A | CA497759148 | ALOX12B | c.1452C>T (p.Asp484=) c.516C>T (p.Asp172=) n.399C>T n.836C>T | |
17 | g.8076255G>C | CA397990534 | ALOX12B | c.1452C>G (p.Asp484Glu) c.516C>G (p.Asp172Glu) n.399C>G n.836C>G | |
17 | g.8076255G>T | CA397990535 | ALOX12B | c.1452C>A (p.Asp484Glu) c.516C>A (p.Asp172Glu) n.399C>A n.836C>A | |
17 | g.8076256T>A | CA397990538 | ALOX12B | c.1451A>T (p.Asp484Val) c.515A>T (p.Asp172Val) n.398A>T n.835A>T | |
17 | g.8076256T>C | CA8367298 | ALOX12B | c.1451A>G (p.Asp484Gly) c.515A>G (p.Asp172Gly) n.398A>G n.835A>G | dbSNP ExAC gnomAD v2 |
17 | g.8076256T>G | CA397990541 | ALOX12B | c.1451A>C (p.Asp484Ala) c.515A>C (p.Asp172Ala) n.398A>C n.835A>C | |
17 | g.8076256T= | CA2246126406 | ALOX12B | c.1451A= (p.Asp484=) c.515A= (p.Asp172=) n.398A= n.835A= | |
17 | g.8076257C>A | CA397990543 | ALOX12B | c.1450G>T (p.Asp484Tyr) c.514G>T (p.Asp172Tyr) n.397G>T n.834G>T | |
17 | g.8076257C>G | CA397990545 | ALOX12B | c.1450G>C (p.Asp484His) c.514G>C (p.Asp172His) n.397G>C n.834G>C | |
17 | g.8076257C>T | CA397990547 | ALOX12B | c.1450G>A (p.Asp484Asn) c.514G>A (p.Asp172Asn) n.397G>A n.834G>A | |
17 | g.8076258A>C | CA397990549 | ALOX12B | c.1449T>G (p.Asn483Lys) c.513T>G (p.Asn171Lys) n.396T>G n.833T>G | |
17 | g.8076258A>G | CA497759160 | ALOX12B | c.1449T>C (p.Asn483=) c.513T>C (p.Asn171=) n.396T>C n.833T>C | |
17 | g.8076258A>T | CA397990551 | ALOX12B | c.1449T>A (p.Asn483Lys) c.513T>A (p.Asn171Lys) n.396T>A n.833T>A | gnomAD v4 |
17 | g.8076259T>A | CA397990553 | ALOX12B | c.1448A>T (p.Asn483Ile) c.512A>T (p.Asn171Ile) n.395A>T n.832A>T | gnomAD v4 |
17 | g.8076259T>C | CA8367299 | ALOX12B | c.1448A>G (p.Asn483Ser) c.512A>G (p.Asn171Ser) n.395A>G n.832A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076259T>G | CA397990555 | ALOX12B | c.1448A>C (p.Asn483Thr) c.512A>C (p.Asn171Thr) n.395A>C n.832A>C | |
17 | g.8076259T= | CA2246126407 | ALOX12B | c.1448A= (p.Asn483=) c.512A= (p.Asn171=) n.395A= n.832A= | |
17 | g.8076260T>A | CA397990557 | ALOX12B | c.1447A>T (p.Asn483Tyr) c.511A>T (p.Asn171Tyr) n.394A>T n.831A>T | |
17 | g.8076260T>C | CA397990559 | ALOX12B | c.1447A>G (p.Asn483Asp) c.511A>G (p.Asn171Asp) n.394A>G n.831A>G | |
17 | g.8076260T>G | CA397990561 | ALOX12B | c.1447A>C (p.Asn483His) c.511A>C (p.Asn171His) n.394A>C n.831A>C | |
17 | g.8076261G>A | CA8367300 | ALOX12B | c.1446C>T (p.Pro482=) c.510C>T (p.Pro170=) n.393C>T n.830C>T | dbSNP ExAC gnomAD v2 |
17 | g.8076261G>C | CA497759172 | ALOX12B | c.1446C>G (p.Pro482=) c.510C>G (p.Pro170=) n.393C>G n.830C>G | |
17 | g.8076261G= | CA2246126408 | ALOX12B | c.1446C= (p.Pro482=) c.510C= (p.Pro170=) n.393C= n.830C= | |
17 | g.8076261G>T | CA497759174 | ALOX12B | c.1446C>A (p.Pro482=) c.510C>A (p.Pro170=) n.393C>A n.830C>A | |
17 | g.8076264dup | CA645584315 | ALOX12B | c.1446dup (p.Asn483GlnfsTer2) c.510dup (p.Asn171GlnfsTer2) n.393dup n.830dup | COSMIC COSMIC |
17 | g.8076261_8076262insC | CA497759179 | ALOX12B | c.1445_1446insG (p.Asn483GlnfsTer2) c.509_510insG (p.Asn171GlnfsTer2) n.392_393insG n.829_830insG | |
17 | g.8076262G>A | CA397990564 | ALOX12B | c.1445C>T (p.Pro482Leu) c.509C>T (p.Pro170Leu) n.392C>T n.829C>T | |
17 | g.8076262G>C | CA397990567 | ALOX12B | c.1445C>G (p.Pro482Arg) c.509C>G (p.Pro170Arg) n.392C>G n.829C>G | gnomAD v4 |
17 | g.8076262G>T | CA397990568 | ALOX12B | c.1445C>A (p.Pro482His) c.509C>A (p.Pro170His) n.392C>A n.829C>A | |
17 | g.8076263G>A | CA397990570 | ALOX12B | c.1444C>T (p.Pro482Ser) c.508C>T (p.Pro170Ser) n.391C>T n.828C>T | gnomAD v4 |
17 | g.8076263G>C | CA397990572 | ALOX12B | c.1444C>G (p.Pro482Ala) c.508C>G (p.Pro170Ala) n.391C>G n.828C>G | gnomAD v4 |
17 | g.8076263G>T | CA397990573 | ALOX12B | c.1444C>A (p.Pro482Thr) c.508C>A (p.Pro170Thr) n.391C>A n.828C>A | |
17 | g.8076264G>A | CA497759187 | ALOX12B | c.1443C>T (p.Leu481=) c.507C>T (p.Leu169=) n.390C>T n.827C>T | |
17 | g.8076264G>C | CA497759189 | ALOX12B | c.1443C>G (p.Leu481=) c.507C>G (p.Leu169=) n.390C>G n.827C>G | |
17 | g.8076264G>T | CA497759191 | ALOX12B | c.1443C>A (p.Leu481=) c.507C>A (p.Leu169=) n.390C>A n.827C>A | |
17 | g.8076265A>C | CA397990579 | ALOX12B | c.1442T>G (p.Leu481Arg) c.506T>G (p.Leu169Arg) n.389T>G n.826T>G | |
17 | g.8076265A>G | CA397990578 | ALOX12B | c.1442T>C (p.Leu481Pro) c.506T>C (p.Leu169Pro) n.389T>C n.826T>C | |
17 | g.8076265A>T | CA397990576 | ALOX12B | c.1442T>A (p.Leu481His) c.506T>A (p.Leu169His) n.389T>A n.826T>A | |
17 | g.8076266G>A | CA397990582 | ALOX12B | c.1441C>T (p.Leu481Phe) c.505C>T (p.Leu169Phe) n.388C>T n.825C>T | |
17 | g.8076266G>C | CA397990584 | ALOX12B | c.1441C>G (p.Leu481Val) c.505C>G (p.Leu169Val) n.388C>G n.825C>G | |
17 | g.8076266G>T | CA397990585 | ALOX12B | c.1441C>A (p.Leu481Ile) c.505C>A (p.Leu169Ile) n.388C>A n.825C>A | gnomAD v4 |
17 | g.8076267G>A | CA8367301 | ALOX12B | c.1440C>T (p.Tyr480=) c.504C>T (p.Tyr168=) n.387C>T n.824C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076267G>C | CA397990587 | ALOX12B | c.1440C>G (p.Tyr480Ter) c.504C>G (p.Tyr168Ter) n.387C>G n.824C>G | gnomAD v4 |
17 | g.8076267G= | CA2246126409 | ALOX12B | c.1440C= (p.Tyr480=) c.504C= (p.Tyr168=) n.387C= n.824C= | |
17 | g.8076267G>T | CA397990589 | ALOX12B | c.1440C>A (p.Tyr480Ter) c.504C>A (p.Tyr168Ter) n.387C>A n.824C>A | |
17 | g.8076268T>A | CA397990591 | ALOX12B | c.1439A>T (p.Tyr480Phe) c.503A>T (p.Tyr168Phe) n.386A>T n.823A>T | |
17 | g.8076268T>C | CA397990593 | ALOX12B | c.1439A>G (p.Tyr480Cys) c.503A>G (p.Tyr168Cys) n.386A>G n.823A>G | COSMIC COSMIC |
17 | g.8076268T>G | CA397990595 | ALOX12B | c.1439A>C (p.Tyr480Ser) c.503A>C (p.Tyr168Ser) n.386A>C n.823A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076268T= | CA2246126410 | ALOX12B | c.1439A= (p.Tyr480=) c.503A= (p.Tyr168=) n.386A= n.823A= | |
17 | g.8076269A>C | CA397990597 | ALOX12B | c.1438T>G (p.Tyr480Asp) c.502T>G (p.Tyr168Asp) n.385T>G n.822T>G | |
17 | g.8076269A>G | CA397990598 | ALOX12B | c.1438T>C (p.Tyr480His) c.502T>C (p.Tyr168His) n.385T>C n.822T>C | |
17 | g.8076269A>T | CA397990600 | ALOX12B | c.1438T>A (p.Tyr480Asn) c.502T>A (p.Tyr168Asn) n.385T>A n.822T>A | |
17 | g.8076271_8076272del | CA645584316 | ALOX12B | c.1437_1438del (p.Tyr480ProfsTer4) c.501_502del (p.Tyr168ProfsTer4) n.384_385del n.821_822del | COSMIC COSMIC |
17 | g.8076270G>A | CA497759214 | ALOX12B | c.1437C>T (p.Leu479=) c.501C>T (p.Leu167=) n.384C>T n.821C>T | |
17 | g.8076270G>C | CA8367302 | ALOX12B | c.1437C>G (p.Leu479=) c.501C>G (p.Leu167=) n.384C>G n.821C>G | dbSNP ExAC gnomAD v4 |
17 | g.8076270G= | CA2246126411 | ALOX12B | c.1437C= (p.Leu479=) c.501C= (p.Leu167=) n.384C= n.821C= | |
17 | g.8076270G>T | CA497759217 | ALOX12B | c.1437C>A (p.Leu479=) c.501C>A (p.Leu167=) n.384C>A n.821C>A | |
17 | g.8076271A>C | CA397990607 | ALOX12B | c.1436T>G (p.Leu479Arg) c.500T>G (p.Leu167Arg) n.383T>G n.820T>G | |
17 | g.8076271A>G | CA397990603 | ALOX12B | c.1436T>C (p.Leu479Pro) c.500T>C (p.Leu167Pro) n.383T>C n.820T>C | gnomAD v4 |
17 | g.8076271A>T | CA397990605 | ALOX12B | c.1436T>A (p.Leu479His) c.500T>A (p.Leu167His) n.383T>A n.820T>A | |
17 | g.8076272G>A | CA8367303 | ALOX12B | c.1435C>T (p.Leu479Phe) c.499C>T (p.Leu167Phe) n.382C>T n.819C>T | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
17 | g.8076272G>C | CA397990625 | ALOX12B | c.1435C>G (p.Leu479Val) c.499C>G (p.Leu167Val) n.382C>G n.819C>G | dbSNP |
17 | g.8076272G= | CA2246126412 | ALOX12B | c.1435C= (p.Leu479=) c.499C= (p.Leu167=) n.382C= n.819C= | |
17 | g.8076272G>T | CA397990626 | ALOX12B | c.1435C>A (p.Leu479Ile) c.499C>A (p.Leu167Ile) n.382C>A n.819C>A | |
17 | g.8076273G>A | CA8367304 | ALOX12B | c.1434C>T (p.Ser478=) c.498C>T (p.Ser166=) n.381C>T n.818C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.8076273G>C | CA397990628 | ALOX12B | c.1434C>G (p.Ser478Arg) c.498C>G (p.Ser166Arg) n.381C>G n.818C>G | |
17 | g.8076273G= | CA2246126413 | ALOX12B | c.1434C= (p.Ser478=) c.498C= (p.Ser166=) n.381C= n.818C= | |
17 | g.8076273G>T | CA397990630 | ALOX12B | c.1434C>A (p.Ser478Arg) c.498C>A (p.Ser166Arg) n.381C>A n.818C>A | |
17 | g.8076274C>A | CA397990632 | ALOX12B | c.1433G>T (p.Ser478Ile) c.497G>T (p.Ser166Ile) n.380G>T n.817G>T | |
17 | g.8076274C= | CA2246126414 | ALOX12B | c.1433G= (p.Ser478=) c.497G= (p.Ser166=) n.380G= n.817G= | |
17 | g.8076274C>G | CA397990633 | ALOX12B | c.1433G>C (p.Ser478Thr) c.497G>C (p.Ser166Thr) n.380G>C n.817G>C | |
17 | g.8076274C>T | CA397990635 | ALOX12B | c.1433G>A (p.Ser478Asn) c.497G>A (p.Ser166Asn) n.380G>A n.817G>A | dbSNP gnomAD v2 COSMIC COSMIC |
17 | g.8076275T>A | CA397990638 | ALOX12B | c.1432A>T (p.Ser478Cys) c.496A>T (p.Ser166Cys) n.379A>T n.816A>T | |
17 | g.8076275T>C | CA397990639 | ALOX12B | c.1432A>G (p.Ser478Gly) c.496A>G (p.Ser166Gly) n.379A>G n.816A>G | |
17 | g.8076275T>G | CA397990642 | ALOX12B | c.1432A>C (p.Ser478Arg) c.496A>C (p.Ser166Arg) n.379A>C n.816A>C | |
17 | g.8076275_8076276delinsTG | CA2246126415 | ALOX12B | c.1431_1432delinsCA (p.Asp477=) c.495_496delinsCA (p.Asp165=) n.378_379delinsCA n.815_816delinsCA | |
17 | g.8076276del | CA8367305 | ALOX12B | c.1431del (p.Asp477GlufsTer?) c.495del (p.Asp165GlufsTer?) n.378del n.815del | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.8076276G>A | CA8367306 | ALOX12B | c.1431C>T (p.Asp477=) c.495C>T (p.Asp165=) n.378C>T n.815C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076276G>C | CA397990650 | ALOX12B | c.1431C>G (p.Asp477Glu) c.495C>G (p.Asp165Glu) n.378C>G n.815C>G | |
17 | g.8076276G= | CA2246126416 | ALOX12B | c.1431C= (p.Asp477=) c.495C= (p.Asp165=) n.378C= n.815C= | |
17 | g.8076276G>T | CA397990647 | ALOX12B | c.1431C>A (p.Asp477Glu) c.495C>A (p.Asp165Glu) n.378C>A n.815C>A | |
17 | g.8076277T>A | CA397990661 | ALOX12B | c.1430A>T (p.Asp477Val) c.494A>T (p.Asp165Val) n.377A>T n.814A>T | |
17 | g.8076277T>C | CA397990655 | ALOX12B | c.1430A>G (p.Asp477Gly) c.494A>G (p.Asp165Gly) n.377A>G n.814A>G | |
17 | g.8076277T>G | CA287543895 | ALOX12B | c.1430A>C (p.Asp477Ala) c.494A>C (p.Asp165Ala) n.377A>C n.814A>C | dbSNP |
17 | g.8076277T= | CA2246126417 | ALOX12B | c.1430A= (p.Asp477=) c.494A= (p.Asp165=) n.377A= n.814A= | |
17 | g.8076278C>A | CA397990663 | ALOX12B | c.1429G>T (p.Asp477Tyr) c.493G>T (p.Asp165Tyr) n.376G>T n.813G>T | |
17 | g.8076278C>G | CA397990666 | ALOX12B | c.1429G>C (p.Asp477His) c.493G>C (p.Asp165His) n.376G>C n.813G>C | |
17 | g.8076278C>T | CA397990668 | ALOX12B | c.1429G>A (p.Asp477Asn) c.493G>A (p.Asp165Asn) n.376G>A n.813G>A | |
17 | g.8076279A= | CA2246126418 | ALOX12B | c.1428T= (p.Tyr476=) c.492T= (p.Tyr164=) n.375T= n.812T= | |
17 | g.8076279A>C | CA397990670 | ALOX12B | c.1428T>G (p.Tyr476Ter) c.492T>G (p.Tyr164Ter) n.375T>G n.812T>G | |
17 | g.8076279A>G | CA497759249 | ALOX12B | c.1428T>C (p.Tyr476=) c.492T>C (p.Tyr164=) n.375T>C n.812T>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.8076279A>T | CA397990672 | ALOX12B | c.1428T>A (p.Tyr476Ter) c.492T>A (p.Tyr164Ter) n.375T>A n.812T>A | |
17 | g.8076280T>A | CA397990675 | ALOX12B | c.1427A>T (p.Tyr476Phe) c.491A>T (p.Tyr164Phe) n.374A>T n.811A>T | |
17 | g.8076280T>C | CA397990676 | ALOX12B | c.1427A>G (p.Tyr476Cys) c.491A>G (p.Tyr164Cys) n.374A>G n.811A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.8076280T>G | CA397990678 | ALOX12B | c.1427A>C (p.Tyr476Ser) c.491A>C (p.Tyr164Ser) n.374A>C n.811A>C | COSMIC COSMIC |
17 | g.8076280T= | CA2246126419 | ALOX12B | c.1427A= (p.Tyr476=) c.491A= (p.Tyr164=) n.374A= n.811A= | |
17 | g.8076281A>C | CA397990681 | ALOX12B | c.1426T>G (p.Tyr476Asp) c.490T>G (p.Tyr164Asp) n.373T>G n.810T>G | |
17 | g.8076281A>G | CA397990682 | ALOX12B | c.1426T>C (p.Tyr476His) c.490T>C (p.Tyr164His) n.373T>C n.810T>C | |
17 | g.8076281A>T | CA397990683 | ALOX12B | c.1426T>A (p.Tyr476Asn) c.490T>A (p.Tyr164Asn) n.373T>A n.810T>A | |
17 | g.8076282G>A | CA497759264 | ALOX12B | c.1425C>T (p.Thr475=) c.489C>T (p.Thr163=) n.372C>T n.809C>T | |
17 | g.8076282G>C | CA497759266 | ALOX12B | c.1425C>G (p.Thr475=) c.489C>G (p.Thr163=) n.372C>G n.809C>G | |
17 | g.8076282G>T | CA497759267 | ALOX12B | c.1425C>A (p.Thr475=) c.489C>A (p.Thr163=) n.372C>A n.809C>A | |
17 | g.8076283G>A | CA397990689 | ALOX12B | c.1424C>T (p.Thr475Ile) c.488C>T (p.Thr163Ile) n.371C>T n.808C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076283G>C | CA397990686 | ALOX12B | c.1424C>G (p.Thr475Ser) c.488C>G (p.Thr163Ser) n.371C>G n.808C>G | |
17 | g.8076283G= | CA2246126421 | ALOX12B | c.1424C= (p.Thr475=) c.488C= (p.Thr163=) n.371C= n.808C= | |
17 | g.8076283G>T | CA397990688 | ALOX12B | c.1424C>A (p.Thr475Asn) c.488C>A (p.Thr163Asn) n.371C>A n.808C>A | dbSNP gnomAD v4 |
17 | g.8076284T>A | CA397990690 | ALOX12B | c.1423A>T (p.Thr475Ser) c.487A>T (p.Thr163Ser) n.370A>T n.807A>T | |
17 | g.8076284T>C | CA397990691 | ALOX12B | c.1423A>G (p.Thr475Ala) c.487A>G (p.Thr163Ala) n.370A>G n.807A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076284T>G | CA397990692 | ALOX12B | c.1423A>C (p.Thr475Pro) c.487A>C (p.Thr163Pro) n.370A>C n.807A>C | dbSNP gnomAD v4 |
17 | g.8076284T= | CA2246126423 | ALOX12B | c.1423A= (p.Thr475=) c.487A= (p.Thr163=) n.370A= n.807A= | |
17 | g.8076285G>A | CA497759273 | ALOX12B | c.1422C>T (p.Leu474=) c.486C>T (p.Leu162=) n.369C>T n.806C>T | |
17 | g.8076285G>C | CA497759275 | ALOX12B | c.1422C>G (p.Leu474=) c.486C>G (p.Leu162=) n.369C>G n.806C>G | |
17 | g.8076285G= | CA2246126425 | ALOX12B | c.1422C= (p.Leu474=) c.486C= (p.Leu162=) n.369C= n.806C= | |
17 | g.8076285G>T | CA8367307 | ALOX12B | c.1422C>A (p.Leu474=) c.486C>A (p.Leu162=) n.369C>A n.806C>A | dbSNP ExAC gnomAD v2 |
17 | g.8076286A>C | CA397990693 | ALOX12B | c.1421T>G (p.Leu474Arg) c.485T>G (p.Leu162Arg) n.368T>G n.805T>G | |
17 | g.8076286A>G | CA397990695 | ALOX12B | c.1421T>C (p.Leu474Pro) c.485T>C (p.Leu162Pro) n.368T>C n.805T>C | |
17 | g.8076286A>T | CA397990696 | ALOX12B | c.1421T>A (p.Leu474His) c.485T>A (p.Leu162His) n.368T>A n.805T>A | |
17 | g.8076287G>A | CA397990697 | ALOX12B | c.1420C>T (p.Leu474Phe) c.484C>T (p.Leu162Phe) n.367C>T n.804C>T | gnomAD v4 |
17 | g.8076287G>C | CA397990699 | ALOX12B | c.1420C>G (p.Leu474Val) c.484C>G (p.Leu162Val) n.367C>G n.804C>G | |
17 | g.8076287G>T | CA397990700 | ALOX12B | c.1420C>A (p.Leu474Ile) c.484C>A (p.Leu162Ile) n.367C>A n.804C>A | COSMIC COSMIC |
17 | g.8076288C>A | CA397990701 | ALOX12B | c.1419G>T (p.Glu473Asp) c.483G>T (p.Glu161Asp) n.366G>T n.803G>T | |
17 | g.8076288C>G | CA397990702 | ALOX12B | c.1419G>C (p.Glu473Asp) c.483G>C (p.Glu161Asp) n.366G>C n.803G>C | |
17 | g.8076288C>T | CA497759287 | ALOX12B | c.1419G>A (p.Glu473=) c.483G>A (p.Glu161=) n.366G>A n.803G>A | |
17 | g.8076289T>A | CA397990704 | ALOX12B | c.1418A>T (p.Glu473Val) c.482A>T (p.Glu161Val) n.365A>T n.802A>T | |
17 | g.8076289T>C | CA397990705 | ALOX12B | c.1418A>G (p.Glu473Gly) c.482A>G (p.Glu161Gly) n.365A>G n.802A>G | gnomAD v4 |
17 | g.8076289T>G | CA397990703 | ALOX12B | c.1418A>C (p.Glu473Ala) c.482A>C (p.Glu161Ala) n.365A>C n.802A>C | |
17 | g.8076290C>A | CA397990706 | ALOX12B | c.1417G>T (p.Glu473Ter) c.481G>T (p.Glu161Ter) n.364G>T n.801G>T | |
17 | g.8076290C>G | CA397990708 | ALOX12B | c.1417G>C (p.Glu473Gln) c.481G>C (p.Glu161Gln) n.364G>C n.801G>C | gnomAD v4 |
17 | g.8076290C>T | CA397990707 | ALOX12B | c.1417G>A (p.Glu473Lys) c.481G>A (p.Glu161Lys) n.364G>A n.801G>A | |
17 | g.8076291C>A | CA497759296 | ALOX12B | c.1416G>T (p.Ser472=) c.480G>T (p.Ser160=) n.363G>T n.800G>T | |
17 | g.8076291C= | CA2246126427 | ALOX12B | c.1416G= (p.Ser472=) c.480G= (p.Ser160=) n.363G= n.800G= | |
17 | g.8076291C>G | CA497759295 | ALOX12B | c.1416G>C (p.Ser472=) c.480G>C (p.Ser160=) n.363G>C n.800G>C | gnomAD v4 |
17 | g.8076291C>T | CA8367308 | ALOX12B | c.1416G>A (p.Ser472=) c.480G>A (p.Ser160=) n.363G>A n.800G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
17 | g.8076292G>A | CA8367309 | ALOX12B | c.1415C>T (p.Ser472Leu) c.479C>T (p.Ser160Leu) n.362C>T n.799C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
17 | g.8076292G>C | CA397990712 | ALOX12B | c.1415C>G (p.Ser472Trp) c.479C>G (p.Ser160Trp) n.362C>G n.799C>G | |
17 | g.8076292G= | CA2246126429 | ALOX12B | c.1415C= (p.Ser472=) c.479C= (p.Ser160=) n.362C= n.799C= | |
17 | g.8076292G>T | CA397990715 | ALOX12B | c.1415C>A (p.Ser472Ter) c.479C>A (p.Ser160Ter) n.362C>A n.799C>A | |
17 | g.8076293A>C | CA397990716 | ALOX12B | c.1414T>G (p.Ser472Ala) c.478T>G (p.Ser160Ala) n.361T>G n.798T>G | |
17 | g.8076293A>G | CA397990718 | ALOX12B | c.1414T>C (p.Ser472Pro) c.478T>C (p.Ser160Pro) n.361T>C n.798T>C | |
17 | g.8076293A>T | CA397990720 | ALOX12B | c.1414T>A (p.Ser472Thr) c.478T>A (p.Ser160Thr) n.361T>A n.798T>A | |
17 | g.8076294C>A | CA497759305 | ALOX12B | c.1413G>T (p.Leu471=) c.477G>T (p.Leu159=) n.360G>T n.797G>T | |
17 | g.8076294C= | CA2246126431 | ALOX12B | c.1413G= (p.Leu471=) c.477G= (p.Leu159=) n.360G= n.797G= | |
17 | g.8076294C>G | CA497759308 | ALOX12B | c.1413G>C (p.Leu471=) c.477G>C (p.Leu159=) n.360G>C n.797G>C | |
17 | g.8076294C>T | CA10647102 | ALOX12B | c.1413G>A (p.Leu471=) c.477G>A (p.Leu159=) n.360G>A n.797G>A | ClinVar dbSNP |
17 | g.8076295A>C | CA397990726 | ALOX12B | c.1412T>G (p.Leu471Arg) c.476T>G (p.Leu159Arg) n.359T>G n.796T>G n.668T>G | |
17 | g.8076295A>G | CA397990728 | ALOX12B | c.1412T>C (p.Leu471Pro) c.476T>C (p.Leu159Pro) n.359T>C n.796T>C n.668T>C | ClinVar dbSNP |
17 | g.8076295A>T | CA397990731 | ALOX12B | c.1412T>A (p.Leu471Gln) c.476T>A (p.Leu159Gln) n.359T>A n.796T>A n.668T>A | |
17 | g.8076296G>A | CA497759313 | ALOX12B | c.1411C>T (p.Leu471=) c.475C>T (p.Leu159=) n.358C>T n.795C>T n.667C>T | |
17 | g.8076296G>C | CA397990736 | ALOX12B | c.1411C>G (p.Leu471Val) c.475C>G (p.Leu159Val) n.358C>G n.795C>G n.667C>G | |
17 | g.8076296G>T | CA397990734 | ALOX12B | c.1411C>A (p.Leu471Met) c.475C>A (p.Leu159Met) n.358C>A n.795C>A n.667C>A | |
17 | g.8076297A>C | CA497759317 | ALOX12B | c.1410T>G (p.Ala470=) c.474T>G (p.Ala158=) n.357T>G n.794T>G n.666T>G | |
17 | g.8076297A>G | CA497759319 | ALOX12B | c.1410T>C (p.Ala470=) c.474T>C (p.Ala158=) n.357T>C n.794T>C n.666T>C | |
17 | g.8076297A>T | CA497759321 | ALOX12B | c.1410T>A (p.Ala470=) c.474T>A (p.Ala158=) n.357T>A n.794T>A n.666T>A | |
17 | g.8076298G>A | CA397990739 | ALOX12B | c.1409C>T (p.Ala470Val) c.473C>T (p.Ala158Val) n.356C>T n.793C>T n.665C>T | |
17 | g.8076298G>C | CA397990741 | ALOX12B | c.1409C>G (p.Ala470Gly) c.473C>G (p.Ala158Gly) n.356C>G n.793C>G n.665C>G | |
17 | g.8076298G>T | CA397990745 | ALOX12B | c.1409C>A (p.Ala470Asp) c.473C>A (p.Ala158Asp) n.356C>A n.793C>A n.665C>A | |
17 | g.8076299C>A | CA397990749 | ALOX12B | c.1408G>T (p.Ala470Ser) c.472G>T (p.Ala158Ser) n.355G>T n.792G>T n.664G>T | ClinVar dbSNP |
17 | g.8076299C= | CA2246126434 | ALOX12B | c.1408G= (p.Ala470=) c.472G= (p.Ala158=) n.355G= n.792G= n.664G= | |
17 | g.8076299C>G | CA397990751 | ALOX12B | c.1408G>C (p.Ala470Pro) c.472G>C (p.Ala158Pro) n.355G>C n.792G>C n.664G>C | |
17 | g.8076299C>T | CA397990753 | ALOX12B | c.1408G>A (p.Ala470Thr) c.472G>A (p.Ala158Thr) n.355G>A n.792G>A n.664G>A | |
17 | g.8076300C>A | CA497759331 | ALOX12B | c.1407G>T (p.Arg469=) c.471G>T (p.Arg157=) n.354G>T n.791G>T n.663G>T | |
17 | g.8076300C>G | CA497759333 | ALOX12B | c.1407G>C (p.Arg469=) c.471G>C (p.Arg157=) n.354G>C n.791G>C n.663G>C | |
17 | g.8076300C>T | CA497759335 | ALOX12B | c.1407G>A (p.Arg469=) c.471G>A (p.Arg157=) n.354G>A n.791G>A n.663G>A | |
17 | g.8076300_8076303dup | CA624868411 | ALOX12B | c.1404_1407dup (p.Ala470ThrfsTer9) c.468_471dup (p.Ala158ThrfsTer9) n.351_354dup n.788_791dup n.660_663dup | dbSNP gnomAD v2 gnomAD v4 |
17 | g.8076301C>A | CA397990757 | ALOX12B | c.1406G>T (p.Arg469Leu) c.470G>T (p.Arg157Leu) n.353G>T n.790G>T n.662G>T | |
17 | g.8076301C= | CA2246126436 | ALOX12B | c.1406G= (p.Arg469=) c.470G= (p.Arg157=) n.353G= n.790G= n.662G= | |
17 | g.8076301C>G | CA397990759 | ALOX12B | c.1406G>C (p.Arg469Pro) c.470G>C (p.Arg157Pro) n.353G>C n.790G>C n.662G>C | |
17 | g.8076301C>T | CA8367310 | ALOX12B | c.1406G>A (p.Arg469Gln) c.470G>A (p.Arg157Gln) n.353G>A n.790G>A n.662G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076302G>A | CA8367311 | ALOX12B | c.1405C>T (p.Arg469Trp) c.469C>T (p.Arg157Trp) n.352C>T n.789C>T n.661C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
17 | g.8076302G>C | CA397990767 | ALOX12B | c.1405C>G (p.Arg469Gly) c.469C>G (p.Arg157Gly) n.352C>G n.789C>G n.661C>G | |
17 | g.8076302G= | CA2246126439 | ALOX12B | c.1405C= (p.Arg469=) c.469C= (p.Arg157=) n.352C= n.789C= n.661C= | |
17 | g.8076302G>T | CA497759342 | ALOX12B | c.1405C>A (p.Arg469=) c.469C>A (p.Arg157=) n.352C>A n.789C>A n.661C>A | |
17 | g.8076303T>A | CA497759347 | ALOX12B | c.1404A>T (p.Val468=) c.468A>T (p.Val156=) n.351A>T n.788A>T n.660A>T | |
17 | g.8076303T>C | CA497759349 | ALOX12B | c.1404A>G (p.Val468=) c.468A>G (p.Val156=) n.351A>G n.788A>G n.660A>G | |
17 | g.8076303T>G | CA497759345 | ALOX12B | c.1404A>C (p.Val468=) c.468A>C (p.Val156=) n.351A>C n.788A>C n.660A>C | |
17 | g.8076304A>C | CA397990773 | ALOX12B | c.1403T>G (p.Val468Gly) c.467T>G (p.Val156Gly) n.350T>G n.787T>G n.659T>G | |
17 | g.8076304A>G | CA397990776 | ALOX12B | c.1403T>C (p.Val468Ala) c.467T>C (p.Val156Ala) n.350T>C n.787T>C n.659T>C | |
17 | g.8076304A>T | CA397990771 | ALOX12B | c.1403T>A (p.Val468Glu) c.467T>A (p.Val156Glu) n.350T>A n.787T>A n.659T>A | |
17 | g.8076305C>A | CA397990781 | ALOX12B | c.1402G>T (p.Val468Leu) c.466G>T (p.Val156Leu) n.349G>T n.786G>T n.658G>T | dbSNP gnomAD v4 |
17 | g.8076305C= | CA2246126442 | ALOX12B | c.1402G= (p.Val468=) c.466G= (p.Val156=) n.349G= n.786G= n.658G= | |
17 | g.8076305C>G | CA397990783 | ALOX12B | c.1402G>C (p.Val468Leu) c.466G>C (p.Val156Leu) n.349G>C n.786G>C n.658G>C | |
17 | g.8076305C>T | CA397990786 | ALOX12B | c.1402G>A (p.Val468Ile) c.466G>A (p.Val156Ile) n.349G>A n.786G>A n.658G>A | |
17 | g.8076306C>A | CA397990788 | ALOX12B | c.1401G>T (p.Met467Ile) c.465G>T (p.Met155Ile) n.348G>T n.785G>T n.657G>T | |
17 | g.8076306C= | CA2246126444 | ALOX12B | c.1401G= (p.Met467=) c.465G= (p.Met155=) n.348G= n.785G= n.657G= | |
17 | g.8076306C>G | CA397990791 | ALOX12B | c.1401G>C (p.Met467Ile) c.465G>C (p.Met155Ile) n.348G>C n.785G>C n.657G>C | |
17 | g.8076306C>T | CA397990792 | ALOX12B | c.1401G>A (p.Met467Ile) c.465G>A (p.Met155Ile) n.348G>A n.785G>A n.657G>A | dbSNP gnomAD v4 |
17 | g.8076307A>C | CA397990794 | ALOX12B | c.1400T>G (p.Met467Arg) c.464T>G (p.Met155Arg) n.347T>G n.784T>G n.656T>G | |
17 | g.8076307A>G | CA397990797 | ALOX12B | c.1400T>C (p.Met467Thr) c.464T>C (p.Met155Thr) n.347T>C n.784T>C n.656T>C | |
17 | g.8076307A>T | CA397990799 | ALOX12B | c.1400T>A (p.Met467Lys) c.464T>A (p.Met155Lys) n.347T>A n.784T>A n.656T>A | |
17 | g.8076308T>A | CA397990806 | ALOX12B | c.1399A>T (p.Met467Leu) c.463A>T (p.Met155Leu) n.346A>T n.783A>T n.655A>T | dbSNP gnomAD v3 gnomAD v4 |
17 | g.8076308T>C | CA397990807 | ALOX12B | c.1399A>G (p.Met467Val) c.463A>G (p.Met155Val) n.346A>G n.783A>G n.655A>G | |
17 | g.8076308T>G | CA397990809 | ALOX12B | c.1399A>C (p.Met467Leu) c.463A>C (p.Met155Leu) n.346A>C n.783A>C n.655A>C | |
17 | g.8076308T= | CA2246126446 | ALOX12B | c.1399A= (p.Met467=) c.463A= (p.Met155=) n.346A= n.783A= n.655A= | |
17 | g.8076309C>A | CA497759366 | ALOX12B | c.1398G>T (p.Val466=) c.462G>T (p.Val154=) n.345G>T n.782G>T n.654G>T | |
17 | g.8076309C>G | CA497759367 | ALOX12B | c.1398G>C (p.Val466=) c.462G>C (p.Val154=) n.345G>C n.782G>C n.654G>C | |
17 | g.8076309C>T | CA497759369 | ALOX12B | c.1398G>A (p.Val466=) c.462G>A (p.Val154=) n.345G>A n.782G>A n.654G>A | |
17 | g.8076310A>C | CA397990814 | ALOX12B | c.1397T>G (p.Val466Gly) c.461T>G (p.Val154Gly) n.344T>G n.781T>G n.653T>G | |
17 | g.8076310A>G | CA397990817 | ALOX12B | c.1397T>C (p.Val466Ala) c.461T>C (p.Val154Ala) n.344T>C n.781T>C n.653T>C | |
17 | g.8076310A>T | CA397990812 | ALOX12B | c.1397T>A (p.Val466Glu) c.461T>A (p.Val154Glu) n.344T>A n.781T>A n.653T>A | |
17 | g.8076311C>A | CA397990820 | ALOX12B | c.1396G>T (p.Val466Leu) c.460G>T (p.Val154Leu) n.343G>T n.780G>T n.652G>T | |
17 | g.8076311C>G | CA397990821 | ALOX12B | c.1396G>C (p.Val466Leu) c.460G>C (p.Val154Leu) n.343G>C n.780G>C n.652G>C | |
17 | g.8076311C>T | CA397990823 | ALOX12B | c.1396G>A (p.Val466Met) c.460G>A (p.Val154Met) n.343G>A n.780G>A n.652G>A | |
17 | g.8076314dup | CA2843243273 | ALOX12B | c.1396dup (p.Val466GlyfsTer12) c.460dup (p.Val154GlyfsTer12) n.343dup n.780dup n.652dup | |
17 | g.8076312C>A | CA497759378 | ALOX12B | c.1395G>T (p.Gly465=) c.459G>T (p.Gly153=) n.342G>T n.779G>T n.651G>T | gnomAD v4 |
17 | g.8076312C= | CA2246126448 | ALOX12B | c.1395G= (p.Gly465=) c.459G= (p.Gly153=) n.342G= n.779G= n.651G= | |
17 | g.8076312C>G | CA497759381 | ALOX12B | c.1395G>C (p.Gly465=) c.459G>C (p.Gly153=) n.342G>C n.779G>C n.651G>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.8076312C>T | CA8367312 | ALOX12B | c.1395G>A (p.Gly465=) c.459G>A (p.Gly153=) n.342G>A n.779G>A n.651G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076313C>A | CA8367313 | ALOX12B | c.1394G>T (p.Gly465Val) c.458G>T (p.Gly153Val) n.341G>T n.778G>T n.650G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.8076313C= | CA2246126450 | ALOX12B | c.1394G= (p.Gly465=) c.458G= (p.Gly153=) n.341G= n.778G= n.650G= | |
17 | g.8076313C>G | CA397990830 | ALOX12B | c.1394G>C (p.Gly465Ala) c.458G>C (p.Gly153Ala) n.341G>C n.778G>C n.650G>C | |
17 | g.8076313C>T | CA397990827 | ALOX12B | c.1394G>A (p.Gly465Glu) c.458G>A (p.Gly153Glu) n.341G>A n.778G>A n.650G>A | COSMIC COSMIC |
17 | g.8076314C>A | CA397990842 | ALOX12B | c.1393G>T (p.Gly465Trp) c.457G>T (p.Gly153Trp) n.340G>T n.777G>T n.649G>T | |
17 | g.8076314C= | CA2246126453 | ALOX12B | c.1393G= (p.Gly465=) c.457G= (p.Gly153=) n.340G= n.777G= n.649G= | |
17 | g.8076314C>G | CA397990846 | ALOX12B | c.1393G>C (p.Gly465Arg) c.457G>C (p.Gly153Arg) n.340G>C n.777G>C n.649G>C | |
17 | g.8076314C>T | CA397990861 | ALOX12B | c.1393G>A (p.Gly465Arg) c.457G>A (p.Gly153Arg) n.340G>A n.777G>A n.649G>A | dbSNP gnomAD v4 |
17 | g.8076315A= | CA2246126454 | ALOX12B | c.1392T= (p.Ala464=) c.456T= (p.Ala152=) n.339T= n.776T= n.648T= | |
17 | g.8076315A>C | CA497759392 | ALOX12B | c.1392T>G (p.Ala464=) c.456T>G (p.Ala152=) n.339T>G n.776T>G n.648T>G | |
17 | g.8076315A>G | CA8367314 | ALOX12B | c.1392T>C (p.Ala464=) c.456T>C (p.Ala152=) n.339T>C n.776T>C n.648T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.8076315A>T | CA497759395 | ALOX12B | c.1392T>A (p.Ala464=) c.456T>A (p.Ala152=) n.339T>A n.776T>A n.648T>A | |
17 | g.8076316G>A | CA397990865 | ALOX12B | c.1391C>T (p.Ala464Val) c.455C>T (p.Ala152Val) n.338C>T n.775C>T n.647C>T | gnomAD v4 |
17 | g.8076316G>C | CA397990867 | ALOX12B | c.1391C>G (p.Ala464Gly) c.455C>G (p.Ala152Gly) n.338C>G n.775C>G n.647C>G | |
17 | g.8076316G>T | CA397990869 | ALOX12B | c.1391C>A (p.Ala464Asp) c.455C>A (p.Ala152Asp) n.338C>A n.775C>A n.647C>A | |
17 | g.8076317C>A | CA397990878 | ALOX12B | c.1390G>T (p.Ala464Ser) c.454G>T (p.Ala152Ser) n.337G>T n.774G>T n.646G>T | |
17 | g.8076317C>G | CA397990880 | ALOX12B | c.1390G>C (p.Ala464Pro) c.454G>C (p.Ala152Pro) n.337G>C n.774G>C n.646G>C | |
17 | g.8076317C>T | CA397990872 | ALOX12B | c.1390G>A (p.Ala464Thr) c.454G>A (p.Ala152Thr) n.337G>A n.774G>A n.646G>A | |
17 | g.8076317_8076318del | CA2635958976 | ALOX12B | c.1389_1390del (p.Ala464TrpfsTer13) c.453_454del (p.Ala152TrpfsTer13) n.336_337del n.773_774del n.645_646del | gnomAD v4 |
17 | g.8076317_8076318delinsCA | CA2246126456 | ALOX12B | c.1389_1390delinsTG (p.Phe463=) c.453_454delinsTG (p.Phe151=) n.336_337delinsTG n.773_774delinsTG n.645_646delinsTG | |
17 | g.8076318A>C | CA397990884 | ALOX12B | c.1389T>G (p.Phe463Leu) c.453T>G (p.Phe151Leu) n.336T>G n.773T>G n.645T>G | |
17 | g.8076318A>G | CA497759404 | ALOX12B | c.1389T>C (p.Phe463=) c.453T>C (p.Phe151=) n.336T>C n.773T>C n.645T>C | |
17 | g.8076318A>T | CA397990882 | ALOX12B | c.1389T>A (p.Phe463Leu) c.453T>A (p.Phe151Leu) n.336T>A n.773T>A n.645T>A | |
17 | g.8076320del | CA253764 | ALOX12B | c.1389del (p.Phe463LeufsTer4) c.453del (p.Phe151LeufsTer4) n.336del n.773del n.645del | ClinVar dbSNP |
17 | g.8076319A>C | CA397990900 | ALOX12B | c.1388T>G (p.Phe463Cys) c.452T>G (p.Phe151Cys) n.335T>G n.772T>G n.644T>G | |
17 | g.8076319A>G | CA397990901 | ALOX12B | c.1388T>C (p.Phe463Ser) c.452T>C (p.Phe151Ser) n.335T>C n.772T>C n.644T>C | |
17 | g.8076319A>T | CA397990897 | ALOX12B | c.1388T>A (p.Phe463Tyr) c.452T>A (p.Phe151Tyr) n.335T>A n.772T>A n.644T>A | |
17 | g.8076320A>C | CA397990905 | ALOX12B | c.1387T>G (p.Phe463Val) c.451T>G (p.Phe151Val) n.334T>G n.771T>G n.643T>G | |
17 | g.8076320A>G | CA397990907 | ALOX12B | c.1387T>C (p.Phe463Leu) c.451T>C (p.Phe151Leu) n.334T>C n.771T>C n.643T>C | |
17 | g.8076320A>T | CA397990910 | ALOX12B | c.1387T>A (p.Phe463Ile) c.451T>A (p.Phe151Ile) n.334T>A n.771T>A n.643T>A | |
17 | g.8076321G>A | CA497759413 | ALOX12B | c.1386C>T (p.Gly462=) c.450C>T (p.Gly150=) n.333C>T n.770C>T n.642C>T | gnomAD v4 |
17 | g.8076321G>C | CA497759415 | ALOX12B | c.1386C>G (p.Gly462=) c.450C>G (p.Gly150=) n.333C>G n.770C>G n.642C>G | |
17 | g.8076321G>T | CA497759417 | ALOX12B | c.1386C>A (p.Gly462=) c.450C>A (p.Gly150=) n.333C>A n.770C>A n.642C>A | |
17 | g.8076322C>A | CA397990914 | ALOX12B | c.1385G>T (p.Gly462Val) c.449G>T (p.Gly150Val) n.332G>T n.769G>T n.641G>T | dbSNP gnomAD v2 gnomAD v4 |
17 | g.8076322C= | CA2246126460 | ALOX12B | c.1385G= (p.Gly462=) c.449G= (p.Gly150=) n.332G= n.769G= n.641G= | |
17 | g.8076322C>G | CA397990916 | ALOX12B | c.1385G>C (p.Gly462Ala) c.449G>C (p.Gly150Ala) n.332G>C n.769G>C n.641G>C | gnomAD v4 |
17 | g.8076322C>T | CA8367315 | ALOX12B | c.1385G>A (p.Gly462Asp) c.449G>A (p.Gly150Asp) n.332G>A n.769G>A n.641G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.8076323C>A | CA397990933 | ALOX12B | c.1384G>T (p.Gly462Cys) c.448G>T (p.Gly150Cys) n.331G>T n.768G>T n.640G>T | |
17 | g.8076323C>G | CA397990935 | ALOX12B | c.1384G>C (p.Gly462Arg) c.448G>C (p.Gly150Arg) n.331G>C n.768G>C n.640G>C | |
17 | g.8076323C>T | CA397990937 | ALOX12B | c.1384G>A (p.Gly462Ser) c.448G>A (p.Gly150Ser) n.331G>A n.768G>A n.640G>A | |
17 | g.8076324T>A | CA397990941 | ALOX12B | c.1383A>T (p.Glu461Asp) c.447A>T (p.Glu149Asp) n.330A>T n.767A>T n.639A>T | |
17 | g.8076324T>C | CA497759427 | ALOX12B | c.1383A>G (p.Glu461=) c.447A>G (p.Glu149=) n.330A>G n.767A>G n.639A>G | gnomAD v4 |
17 | g.8076324T>G | CA397990942 | ALOX12B | c.1383A>C (p.Glu461Asp) c.447A>C (p.Glu149Asp) n.330A>C n.767A>C n.639A>C | |
17 | g.8076325T>A | CA397990944 | ALOX12B | c.1382A>T (p.Glu461Val) c.446A>T (p.Glu149Val) n.329A>T n.766A>T n.638A>T | |
17 | g.8076325T>C | CA397990948 | ALOX12B | c.1382A>G (p.Glu461Gly) c.446A>G (p.Glu149Gly) n.329A>G n.766A>G n.638A>G | |
17 | g.8076325T>G | CA397990946 | ALOX12B | c.1382A>C (p.Glu461Ala) c.446A>C (p.Glu149Ala) n.329A>C n.766A>C n.638A>C | |
17 | g.8076326C>A | CA397990951 | ALOX12B | c.1381G>T (p.Glu461Ter) c.445G>T (p.Glu149Ter) n.328G>T n.765G>T n.637G>T | |
17 | g.8076326C>G | CA397990954 | ALOX12B | c.1381G>C (p.Glu461Gln) c.445G>C (p.Glu149Gln) n.328G>C n.765G>C n.637G>C | |
17 | g.8076326C>T | CA397990957 | ALOX12B | c.1381G>A (p.Glu461Lys) c.445G>A (p.Glu149Lys) n.328G>A n.765G>A n.637G>A | COSMIC COSMIC |
17 | g.8076327C>A | CA497759435 | ALOX12B | c.1380G>T (p.Val460=) c.444G>T (p.Val148=) n.327G>T n.764G>T n.636G>T | |
17 | g.8076327C>G | CA497759437 | ALOX12B | c.1380G>C (p.Val460=) c.444G>C (p.Val148=) n.327G>C n.764G>C n.636G>C | |
17 | g.8076327C>T | CA497759439 | ALOX12B | c.1380G>A (p.Val460=) c.444G>A (p.Val148=) n.327G>A n.764G>A n.636G>A | COSMIC COSMIC |
17 | g.8076328A>C | CA397990960 | ALOX12B | c.1379T>G (p.Val460Gly) c.443T>G (p.Val148Gly) n.326T>G n.763T>G n.635T>G | |
17 | g.8076328A>G | CA397990963 | ALOX12B | c.1379T>C (p.Val460Ala) c.443T>C (p.Val148Ala) n.326T>C n.763T>C n.635T>C | |
17 | g.8076328A>T | CA397990966 | ALOX12B | c.1379T>A (p.Val460Glu) c.443T>A (p.Val148Glu) n.326T>A n.763T>A n.635T>A |