| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.8075604C>A | CA397988350 | ALOX12B | c.1645G>T (p.Glu549Ter) c.709G>T (p.Glu237Ter) n.479+571G>T | |
| 17 | g.8075604C>G | CA397988353 | ALOX12B | c.1645G>C (p.Glu549Gln) c.709G>C (p.Glu237Gln) n.479+571G>C | |
| 17 | g.8075604C>T | CA397988356 | ALOX12B | c.1645G>A (p.Glu549Lys) c.709G>A (p.Glu237Lys) n.479+571G>A | |
| 17 | g.8075605C>A | CA497757463 | ALOX12B | c.1644G>T (p.Arg548=) c.708G>T (p.Arg236=) n.479+570G>T | |
| 17 | g.8075605C>G | CA497757465 | ALOX12B | c.1644G>C (p.Arg548=) c.708G>C (p.Arg236=) n.479+570G>C | |
| 17 | g.8075605C>T | CA497757467 | ALOX12B | c.1644G>A (p.Arg548=) c.708G>A (p.Arg236=) n.479+570G>A | |
| 17 | g.8075606C>A | CA397988358 | ALOX12B | c.1643G>T (p.Arg548Leu) c.707G>T (p.Arg236Leu) n.479+569G>T | |
| 17 | g.8075606C= | CA2246125509 | ALOX12B | c.1643G= (p.Arg548=) c.707G= (p.Arg236=) n.479+569G= | |
| 17 | g.8075606C>G | CA397988361 | ALOX12B | c.1643G>C (p.Arg548Pro) c.707G>C (p.Arg236Pro) n.479+569G>C | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.8075606C>T | CA8367241 | ALOX12B | c.1643G>A (p.Arg548Gln) c.707G>A (p.Arg236Gln) n.479+569G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075607G>A | CA261171 | ALOX12B | c.1642C>T (p.Arg548Trp) c.706C>T (p.Arg236Trp) n.479+568C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.8075607G>C | CA397988368 | ALOX12B | c.1642C>G (p.Arg548Gly) c.706C>G (p.Arg236Gly) n.479+568C>G | |
| 17 | g.8075607G= | CA2246125520 | ALOX12B | c.1642C= (p.Arg548=) c.706C= (p.Arg236=) n.479+568C= | |
| 17 | g.8075607G>T | CA497757475 | ALOX12B | c.1642C>A (p.Arg548=) c.706C>A (p.Arg236=) n.479+568C>A | |
| 17 | g.8075608C>A | CA497757477 | ALOX12B | c.1641G>T (p.Gly547=) c.705G>T (p.Gly235=) n.479+567G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075608C= | CA2246125525 | ALOX12B | c.1641G= (p.Gly547=) c.705G= (p.Gly235=) n.479+567G= | |
| 17 | g.8075608C>G | CA497757479 | ALOX12B | c.1641G>C (p.Gly547=) c.705G>C (p.Gly235=) n.479+567G>C | |
| 17 | g.8075608C>T | CA8367242 | ALOX12B | c.1641G>A (p.Gly547=) c.705G>A (p.Gly235=) n.479+567G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075609C>A | CA397988377 | ALOX12B | c.1640G>T (p.Gly547Val) c.704G>T (p.Gly235Val) n.479+566G>T | gnomAD v4 |
| 17 | g.8075609C>G | CA397988373 | ALOX12B | c.1640G>C (p.Gly547Ala) c.704G>C (p.Gly235Ala) n.479+566G>C | |
| 17 | g.8075609C>T | CA397988375 | ALOX12B | c.1640G>A (p.Gly547Glu) c.704G>A (p.Gly235Glu) n.479+566G>A | gnomAD v4 |
| 17 | g.8075610C>A | CA397988382 | ALOX12B | c.1639G>T (p.Gly547Trp) c.703G>T (p.Gly235Trp) n.479+565G>T | |
| 17 | g.8075610C= | CA2246125533 | ALOX12B | c.1639G= (p.Gly547=) c.703G= (p.Gly235=) n.479+565G= | |
| 17 | g.8075610C>G | CA397988385 | ALOX12B | c.1639G>C (p.Gly547Arg) c.703G>C (p.Gly235Arg) n.479+565G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075610C>T | CA287540246 | ALOX12B | c.1639G>A (p.Gly547Arg) c.703G>A (p.Gly235Arg) n.479+565G>A | dbSNP gnomAD v4 |
| 17 | g.8075611C>A | CA497757492 | ALOX12B | c.1638G>T (p.Leu546=) c.702G>T (p.Leu234=) n.479+564G>T | |
| 17 | g.8075611C= | CA2246125538 | ALOX12B | c.1638G= (p.Leu546=) c.702G= (p.Leu234=) n.479+564G= | |
| 17 | g.8075611C>G | CA497757489 | ALOX12B | c.1638G>C (p.Leu546=) c.702G>C (p.Leu234=) n.479+564G>C | |
| 17 | g.8075611C>T | CA8367243 | ALOX12B | c.1638G>A (p.Leu546=) c.702G>A (p.Leu234=) n.479+564G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075612A>C | CA397989526 | ALOX12B | c.1637T>G (p.Leu546Arg) c.701T>G (p.Leu234Arg) n.479+563T>G | |
| 17 | g.8075612A>G | CA397989530 | ALOX12B | c.1637T>C (p.Leu546Pro) c.701T>C (p.Leu234Pro) n.479+563T>C | |
| 17 | g.8075612A>T | CA397989534 | ALOX12B | c.1637T>A (p.Leu546Gln) c.701T>A (p.Leu234Gln) n.479+563T>A | |
| 17 | g.8075613G>A | CA497757855 | ALOX12B | c.1636C>T (p.Leu546=) c.700C>T (p.Leu234=) n.479+562C>T | |
| 17 | g.8075613G>C | CA397989539 | ALOX12B | c.1636C>G (p.Leu546Val) c.700C>G (p.Leu234Val) n.479+562C>G | |
| 17 | g.8075613G>T | CA397989546 | ALOX12B | c.1636C>A (p.Leu546Met) c.700C>A (p.Leu234Met) n.479+562C>A | |
| 17 | g.8075614G>A | CA287543279 | ALOX12B | c.1635C>T (p.Leu545=) c.699C>T (p.Leu233=) n.479+561C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075614G>C | CA497757861 | ALOX12B | c.1635C>G (p.Leu545=) c.699C>G (p.Leu233=) n.479+561C>G | gnomAD v4 |
| 17 | g.8075614G= | CA2246125540 | ALOX12B | c.1635C= (p.Leu545=) c.699C= (p.Leu233=) n.479+561C= | |
| 17 | g.8075614G>T | CA497757863 | ALOX12B | c.1635C>A (p.Leu545=) c.699C>A (p.Leu233=) n.479+561C>A | |
| 17 | g.8075615A= | CA2246125545 | ALOX12B | c.1634T= (p.Leu545=) c.698T= (p.Leu233=) n.479+560T= | |
| 17 | g.8075615A>C | CA397989553 | ALOX12B | c.1634T>G (p.Leu545Arg) c.698T>G (p.Leu233Arg) n.479+560T>G | ClinVar dbSNP |
| 17 | g.8075615A>G | CA397989554 | ALOX12B | c.1634T>C (p.Leu545Pro) c.698T>C (p.Leu233Pro) n.479+560T>C | |
| 17 | g.8075615A>T | CA397989552 | ALOX12B | c.1634T>A (p.Leu545His) c.698T>A (p.Leu233His) n.479+560T>A | |
| 17 | g.8075616G>A | CA397989555 | ALOX12B | c.1633C>T (p.Leu545Phe) c.697C>T (p.Leu233Phe) n.479+559C>T | |
| 17 | g.8075616G>C | CA397989558 | ALOX12B | c.1633C>G (p.Leu545Val) c.697C>G (p.Leu233Val) n.479+559C>G | |
| 17 | g.8075616G>T | CA397989562 | ALOX12B | c.1633C>A (p.Leu545Ile) c.697C>A (p.Leu233Ile) n.479+559C>A | |
| 17 | g.8075617G>A | CA497757871 | ALOX12B | c.1632C>T (p.Cys544=) c.696C>T (p.Cys232=) n.479+558C>T | gnomAD v4 |
| 17 | g.8075617G>C | CA397989565 | ALOX12B | c.1632C>G (p.Cys544Trp) c.696C>G (p.Cys232Trp) n.479+558C>G | |
| 17 | g.8075617G>T | CA397989568 | ALOX12B | c.1632C>A (p.Cys544Ter) c.696C>A (p.Cys232Ter) n.479+558C>A | |
| 17 | g.8075618C>A | CA397989576 | ALOX12B | c.1631G>T (p.Cys544Phe) c.695G>T (p.Cys232Phe) n.479+557G>T | |
| 17 | g.8075618C>G | CA397989570 | ALOX12B | c.1631G>C (p.Cys544Ser) c.695G>C (p.Cys232Ser) n.479+557G>C | |
| 17 | g.8075618C>T | CA397989572 | ALOX12B | c.1631G>A (p.Cys544Tyr) c.695G>A (p.Cys232Tyr) n.479+557G>A | |
| 17 | g.8075619A= | CA2246125552 | ALOX12B | c.1630T= (p.Cys544=) c.694T= (p.Cys232=) n.479+556T= | |
| 17 | g.8075619A>C | CA397989582 | ALOX12B | c.1630T>G (p.Cys544Gly) c.694T>G (p.Cys232Gly) n.479+556T>G | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.8075619A>G | CA397989585 | ALOX12B | c.1630T>C (p.Cys544Arg) c.694T>C (p.Cys232Arg) n.479+556T>C | ClinVar dbSNP |
| 17 | g.8075619A>T | CA397989600 | ALOX12B | c.1630T>A (p.Cys544Ser) c.694T>A (p.Cys232Ser) n.479+556T>A | |
| 17 | g.8075620C>A | CA397989606 | ALOX12B | c.1629G>T (p.Glu543Asp) c.693G>T (p.Glu231Asp) n.479+555G>T | |
| 17 | g.8075620C>G | CA397989609 | ALOX12B | c.1629G>C (p.Glu543Asp) c.693G>C (p.Glu231Asp) n.479+555G>C | |
| 17 | g.8075620C>T | CA497757879 | ALOX12B | c.1629G>A (p.Glu543=) c.693G>A (p.Glu231=) n.479+555G>A | |
| 17 | g.8075621T>A | CA397989634 | ALOX12B | c.1628A>T (p.Glu543Val) c.692A>T (p.Glu231Val) n.479+554A>T | gnomAD v4 |
| 17 | g.8075621T>C | CA397989627 | ALOX12B | c.1628A>G (p.Glu543Gly) c.692A>G (p.Glu231Gly) n.479+554A>G | |
| 17 | g.8075621T>G | CA397989619 | ALOX12B | c.1628A>C (p.Glu543Ala) c.692A>C (p.Glu231Ala) n.479+554A>C | dbSNP |
| 17 | g.8075621T= | CA2246125558 | ALOX12B | c.1628A= (p.Glu543=) c.692A= (p.Glu231=) n.479+554A= | |
| 17 | g.8075622del | CA2635957781 | ALOX12B | c.1627del (p.Glu543SerfsTer21) c.691del (p.Glu231SerfsTer21) n.479+553del | gnomAD v4 |
| 17 | g.8075622C>A | CA397989637 | ALOX12B | c.1627G>T (p.Glu543Ter) c.691G>T (p.Glu231Ter) n.479+553G>T | |
| 17 | g.8075622C>G | CA397989643 | ALOX12B | c.1627G>C (p.Glu543Gln) c.691G>C (p.Glu231Gln) n.479+553G>C | |
| 17 | g.8075622C>T | CA397989639 | ALOX12B | c.1627G>A (p.Glu543Lys) c.691G>A (p.Glu231Lys) n.479+553G>A | |
| 17 | g.8075622_8075624delinsCTT | CA2246125564 | ALOX12B | c.1625_1627delinsAAG (p.Lys542=) c.689_691delinsAAG (p.Lys230=) n.479+551_479+553delinsAAG | |
| 17 | g.8075623T>A | CA397989646 | ALOX12B | c.1626A>T (p.Lys542Asn) c.690A>T (p.Lys230Asn) n.479+552A>T | |
| 17 | g.8075623T>C | CA497757887 | ALOX12B | c.1626A>G (p.Lys542=) c.690A>G (p.Lys230=) n.479+552A>G | |
| 17 | g.8075623T>G | CA397989649 | ALOX12B | c.1626A>C (p.Lys542Asn) c.690A>C (p.Lys230Asn) n.479+552A>C | |
| 17 | g.8075624_8075625del | CA8367244 | ALOX12B | c.1625_1626del (p.Lys542ArgfsTer13) c.689_690del (p.Lys230ArgfsTer13) n.479+551_479+552del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075624T>A | CA397989654 | ALOX12B | c.1625A>T (p.Lys542Ile) c.689A>T (p.Lys230Ile) n.479+551A>T | |
| 17 | g.8075624T>C | CA397989657 | ALOX12B | c.1625A>G (p.Lys542Arg) c.689A>G (p.Lys230Arg) n.479+551A>G | |
| 17 | g.8075624T>G | CA397989660 | ALOX12B | c.1625A>C (p.Lys542Thr) c.689A>C (p.Lys230Thr) n.479+551A>C | |
| 17 | g.8075625T>A | CA397989662 | ALOX12B | c.1624A>T (p.Lys542Ter) c.688A>T (p.Lys230Ter) n.479+550A>T | |
| 17 | g.8075625T>C | CA397989665 | ALOX12B | c.1624A>G (p.Lys542Glu) c.688A>G (p.Lys230Glu) n.479+550A>G | |
| 17 | g.8075625T>G | CA397989667 | ALOX12B | c.1624A>C (p.Lys542Gln) c.688A>C (p.Lys230Gln) n.479+550A>C | |
| 17 | g.8075626A>C | CA397989670 | ALOX12B | c.1623T>G (p.Phe541Leu) c.687T>G (p.Phe229Leu) n.479+549T>G | |
| 17 | g.8075626A>G | CA497757897 | ALOX12B | c.1623T>C (p.Phe541=) c.687T>C (p.Phe229=) n.479+549T>C | |
| 17 | g.8075626A>T | CA397989673 | ALOX12B | c.1623T>A (p.Phe541Leu) c.687T>A (p.Phe229Leu) n.479+549T>A | |
| 17 | g.8075627A>C | CA397989686 | ALOX12B | c.1622T>G (p.Phe541Cys) c.686T>G (p.Phe229Cys) n.479+548T>G | |
| 17 | g.8075627A>G | CA397989683 | ALOX12B | c.1622T>C (p.Phe541Ser) c.686T>C (p.Phe229Ser) n.479+548T>C | |
| 17 | g.8075627A>T | CA397989676 | ALOX12B | c.1622T>A (p.Phe541Tyr) c.686T>A (p.Phe229Tyr) n.479+548T>A | |
| 17 | g.8075628A>C | CA397989693 | ALOX12B | c.1621T>G (p.Phe541Val) c.685T>G (p.Phe229Val) n.479+547T>G | |
| 17 | g.8075628A>G | CA397989696 | ALOX12B | c.1621T>C (p.Phe541Leu) c.685T>C (p.Phe229Leu) n.479+547T>C | gnomAD v4 |
| 17 | g.8075628A>T | CA397989699 | ALOX12B | c.1621T>A (p.Phe541Ile) c.685T>A (p.Phe229Ile) n.479+547T>A | |
| 17 | g.8075629T>A | CA497757907 | ALOX12B | c.1620A>T (p.Ile540=) c.684A>T (p.Ile228=) n.479+546A>T | |
| 17 | g.8075629T>C | CA397989702 | ALOX12B | c.1620A>G (p.Ile540Met) c.684A>G (p.Ile228Met) n.479+546A>G | |
| 17 | g.8075629T>G | CA497757910 | ALOX12B | c.1620A>C (p.Ile540=) c.684A>C (p.Ile228=) n.479+546A>C | |
| 17 | g.8075630A= | CA2246125574 | ALOX12B | c.1619T= (p.Ile540=) c.683T= (p.Ile228=) n.479+545T= | |
| 17 | g.8075630A>C | CA397989706 | ALOX12B | c.1619T>G (p.Ile540Arg) c.683T>G (p.Ile228Arg) n.479+545T>G | |
| 17 | g.8075630A>G | CA397989709 | ALOX12B | c.1619T>C (p.Ile540Thr) c.683T>C (p.Ile228Thr) n.479+545T>C | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 17 | g.8075630A>T | CA397989712 | ALOX12B | c.1619T>A (p.Ile540Lys) c.683T>A (p.Ile228Lys) n.479+545T>A | |
| 17 | g.8075631T>A | CA397989715 | ALOX12B | c.1618A>T (p.Ile540Leu) c.682A>T (p.Ile228Leu) n.479+544A>T | |
| 17 | g.8075631T>C | CA397989718 | ALOX12B | c.1618A>G (p.Ile540Val) c.682A>G (p.Ile228Val) n.479+544A>G | gnomAD v4 |
| 17 | g.8075631T>G | CA397989720 | ALOX12B | c.1618A>C (p.Ile540Leu) c.682A>C (p.Ile228Leu) n.479+544A>C | |
| 17 | g.8075632T>A | CA397989729 | ALOX12B | c.1617A>T (p.Glu539Asp) c.681A>T (p.Glu227Asp) n.479+543A>T | gnomAD v4 |
| 17 | g.8075632T>C | CA497757919 | ALOX12B | c.1617A>G (p.Glu539=) c.681A>G (p.Glu227=) n.479+543A>G | |
| 17 | g.8075632T>G | CA397989731 | ALOX12B | c.1617A>C (p.Glu539Asp) c.681A>C (p.Glu227Asp) n.479+543A>C | |
| 17 | g.8075633T>A | CA397989738 | ALOX12B | c.1616A>T (p.Glu539Val) c.680A>T (p.Glu227Val) n.479+542A>T | |
| 17 | g.8075633T>C | CA397989735 | ALOX12B | c.1616A>G (p.Glu539Gly) c.680A>G (p.Glu227Gly) n.479+542A>G | COSMIC |
| 17 | g.8075633T>G | CA397989733 | ALOX12B | c.1616A>C (p.Glu539Ala) c.680A>C (p.Glu227Ala) n.479+542A>C | |
| 17 | g.8075634C>A | CA397989745 | ALOX12B | c.1615G>T (p.Glu539Ter) c.679G>T (p.Glu227Ter) n.479+541G>T | |
| 17 | g.8075634C= | CA2246125581 | ALOX12B | c.1615G= (p.Glu539=) c.679G= (p.Glu227=) n.479+541G= | |
| 17 | g.8075634C>G | CA287543292 | ALOX12B | c.1615G>C (p.Glu539Gln) c.679G>C (p.Glu227Gln) n.479+541G>C | dbSNP |
| 17 | g.8075634C>T | CA8367245 | ALOX12B | c.1615G>A (p.Glu539Lys) c.679G>A (p.Glu227Lys) n.479+541G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075635C>A | CA397989748 | ALOX12B | c.1614G>T (p.Gln538His) c.678G>T (p.Gln226His) n.479+540G>T | |
| 17 | g.8075635C= | CA2246125584 | ALOX12B | c.1614G= (p.Gln538=) c.678G= (p.Gln226=) n.479+540G= | |
| 17 | g.8075635C>G | CA397989751 | ALOX12B | c.1614G>C (p.Gln538His) c.678G>C (p.Gln226His) n.479+540G>C | |
| 17 | g.8075635C>T | CA497757930 | ALOX12B | c.1614G>A (p.Gln538=) c.678G>A (p.Gln226=) n.479+540G>A | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.8075636T>A | CA397989754 | ALOX12B | c.1613A>T (p.Gln538Leu) c.677A>T (p.Gln226Leu) n.479+539A>T | |
| 17 | g.8075636T>C | CA397989757 | ALOX12B | c.1613A>G (p.Gln538Arg) c.677A>G (p.Gln226Arg) n.479+539A>G | |
| 17 | g.8075636T>G | CA397989760 | ALOX12B | c.1613A>C (p.Gln538Pro) c.677A>C (p.Gln226Pro) n.479+539A>C | ClinVar dbSNP gnomAD v4 |
| 17 | g.8075636T= | CA2246125589 | ALOX12B | c.1613A= (p.Gln538=) c.677A= (p.Gln226=) n.479+539A= | |
| 17 | g.8075637G>A | CA397989763 | ALOX12B | c.1612C>T (p.Gln538Ter) c.676C>T (p.Gln226Ter) n.479+538C>T | COSMIC COSMIC |
| 17 | g.8075637G>C | CA397989768 | ALOX12B | c.1612C>G (p.Gln538Glu) c.676C>G (p.Gln226Glu) n.479+538C>G | |
| 17 | g.8075637G>T | CA397989765 | ALOX12B | c.1612C>A (p.Gln538Lys) c.676C>A (p.Gln226Lys) n.479+538C>A | |
| 17 | g.8075638C>A | CA497757939 | ALOX12B | c.1611G>T (p.Val537=) c.675G>T (p.Val225=) n.479+537G>T | |
| 17 | g.8075638C= | CA2246125595 | ALOX12B | c.1611G= (p.Val537=) c.675G= (p.Val225=) n.479+537G= | |
| 17 | g.8075638C>G | CA497757941 | ALOX12B | c.1611G>C (p.Val537=) c.675G>C (p.Val225=) n.479+537G>C | |
| 17 | g.8075638C>T | CA8367246 | ALOX12B | c.1611G>A (p.Val537=) c.675G>A (p.Val225=) n.479+537G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075639A>C | CA397989774 | ALOX12B | c.1610T>G (p.Val537Gly) c.674T>G (p.Val225Gly) n.479+536T>G | |
| 17 | g.8075639A>G | CA397989777 | ALOX12B | c.1610T>C (p.Val537Ala) c.674T>C (p.Val225Ala) n.479+536T>C | |
| 17 | g.8075639A>T | CA397989778 | ALOX12B | c.1610T>A (p.Val537Glu) c.674T>A (p.Val225Glu) n.479+536T>A | |
| 17 | g.8075640C>A | CA397989783 | ALOX12B | c.1609G>T (p.Val537Leu) c.673G>T (p.Val225Leu) n.479+535G>T | |
| 17 | g.8075640C= | CA2246125602 | ALOX12B | c.1609G= (p.Val537=) c.673G= (p.Val225=) n.479+535G= | |
| 17 | g.8075640C>G | CA397989787 | ALOX12B | c.1609G>C (p.Val537Leu) c.673G>C (p.Val225Leu) n.479+535G>C | |
| 17 | g.8075640C>T | CA287543316 | ALOX12B | c.1609G>A (p.Val537Met) c.673G>A (p.Val225Met) n.479+535G>A | ClinVar dbSNP gnomAD v4 |
| 17 | g.8075641C>A | CA397989789 | ALOX12B | c.1608G>T (p.Trp536Cys) c.672G>T (p.Trp224Cys) n.479+534G>T | |
| 17 | g.8075641C= | CA2246125606 | ALOX12B | c.1608G= (p.Trp536=) c.672G= (p.Trp224=) n.479+534G= | |
| 17 | g.8075641C>G | CA397989791 | ALOX12B | c.1608G>C (p.Trp536Cys) c.672G>C (p.Trp224Cys) n.479+534G>C | |
| 17 | g.8075641C>T | CA397989792 | ALOX12B | c.1608G>A (p.Trp536Ter) c.672G>A (p.Trp224Ter) n.479+534G>A | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.8075642C>A | CA397989795 | ALOX12B | c.1607G>T (p.Trp536Leu) c.671G>T (p.Trp224Leu) n.479+533G>T | |
| 17 | g.8075642C>G | CA397989796 | ALOX12B | c.1607G>C (p.Trp536Ser) c.671G>C (p.Trp224Ser) n.479+533G>C | |
| 17 | g.8075642C>T | CA397989798 | ALOX12B | c.1607G>A (p.Trp536Ter) c.671G>A (p.Trp224Ter) n.479+533G>A | |
| 17 | g.8075643A>C | CA397989800 | ALOX12B | c.1606T>G (p.Trp536Gly) c.670T>G (p.Trp224Gly) n.479+532T>G | |
| 17 | g.8075643A>G | CA397989802 | ALOX12B | c.1606T>C (p.Trp536Arg) c.670T>C (p.Trp224Arg) n.479+532T>C | gnomAD v4 |
| 17 | g.8075643A>T | CA397989804 | ALOX12B | c.1606T>A (p.Trp536Arg) c.670T>A (p.Trp224Arg) n.479+532T>A | |
| 17 | g.8075644A>C | CA497757958 | ALOX12B | c.1605T>G (p.Ser535=) c.669T>G (p.Ser223=) n.479+531T>G | |
| 17 | g.8075644A>G | CA497757961 | ALOX12B | c.1605T>C (p.Ser535=) c.669T>C (p.Ser223=) n.479+531T>C | dbSNP |
| 17 | g.8075644A>T | CA497757959 | ALOX12B | c.1605T>A (p.Ser535=) c.669T>A (p.Ser223=) n.479+531T>A | |
| 17 | g.8075645G>A | CA397989806 | ALOX12B | c.1604C>T (p.Ser535Phe) c.668C>T (p.Ser223Phe) n.479+530C>T | gnomAD v4 |
| 17 | g.8075645G>C | CA397989807 | ALOX12B | c.1604C>G (p.Ser535Cys) c.668C>G (p.Ser223Cys) n.479+530C>G | |
| 17 | g.8075645G>T | CA397989808 | ALOX12B | c.1604C>A (p.Ser535Tyr) c.668C>A (p.Ser223Tyr) n.479+530C>A | gnomAD v4 |
| 17 | g.8075646A>C | CA397989812 | ALOX12B | c.1603T>G (p.Ser535Ala) c.667T>G (p.Ser223Ala) n.479+529T>G | |
| 17 | g.8075646A>G | CA397989813 | ALOX12B | c.1603T>C (p.Ser535Pro) c.667T>C (p.Ser223Pro) n.479+529T>C | |
| 17 | g.8075646A>T | CA397989810 | ALOX12B | c.1603T>A (p.Ser535Thr) c.667T>A (p.Ser223Thr) n.479+529T>A | |
| 17 | g.8075647C>A | CA397989814 | ALOX12B | c.1602G>T (p.Gln534His) c.666G>T (p.Gln222His) n.479+528G>T | |
| 17 | g.8075647C>G | CA397989815 | ALOX12B | c.1602G>C (p.Gln534His) c.666G>C (p.Gln222His) n.479+528G>C | |
| 17 | g.8075647C>T | CA497757973 | ALOX12B | c.1602G>A (p.Gln534=) c.666G>A (p.Gln222=) n.479+528G>A | |
| 17 | g.8075648T>A | CA397989816 | ALOX12B | c.1601A>T (p.Gln534Leu) c.665A>T (p.Gln222Leu) n.479+527A>T | |
| 17 | g.8075648T>C | CA397989817 | ALOX12B | c.1601A>G (p.Gln534Arg) c.665A>G (p.Gln222Arg) n.479+527A>G | |
| 17 | g.8075648T>G | CA397989818 | ALOX12B | c.1601A>C (p.Gln534Pro) c.665A>C (p.Gln222Pro) n.479+527A>C | |
| 17 | g.8075649G>A | CA397989819 | ALOX12B | c.1600C>T (p.Gln534Ter) c.664C>T (p.Gln222Ter) n.479+526C>T | |
| 17 | g.8075649G>C | CA397989820 | ALOX12B | c.1600C>G (p.Gln534Glu) c.664C>G (p.Gln222Glu) n.479+526C>G | |
| 17 | g.8075649G>T | CA397989821 | ALOX12B | c.1600C>A (p.Gln534Lys) c.664C>A (p.Gln222Lys) n.479+526C>A | |
| 17 | g.8075650C>A | CA397989822 | ALOX12B | c.1599G>T (p.Leu533Phe) c.663G>T (p.Leu221Phe) n.479+525G>T | |
| 17 | g.8075650C= | CA2246125607 | ALOX12B | c.1599G= (p.Leu533=) c.663G= (p.Leu221=) n.479+525G= | |
| 17 | g.8075650C>G | CA397989823 | ALOX12B | c.1599G>C (p.Leu533Phe) c.663G>C (p.Leu221Phe) n.479+525G>C | |
| 17 | g.8075650C>T | CA8367247 | ALOX12B | c.1599G>A (p.Leu533=) c.663G>A (p.Leu221=) n.479+525G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075651A>C | CA397989824 | ALOX12B | c.1598T>G (p.Leu533Trp) c.662T>G (p.Leu221Trp) n.479+524T>G | |
| 17 | g.8075651A>G | CA397989825 | ALOX12B | c.1598T>C (p.Leu533Ser) c.662T>C (p.Leu221Ser) n.479+524T>C | |
| 17 | g.8075651A>T | CA397989826 | ALOX12B | c.1598T>A (p.Leu533Ter) c.662T>A (p.Leu221Ter) n.479+524T>A | |
| 17 | g.8075652A>C | CA397989828 | ALOX12B | c.1597T>G (p.Leu533Val) c.661T>G (p.Leu221Val) n.479+523T>G | |
| 17 | g.8075652A>G | CA497757988 | ALOX12B | c.1597T>C (p.Leu533=) c.661T>C (p.Leu221=) n.479+523T>C | |
| 17 | g.8075652A>T | CA397989827 | ALOX12B | c.1597T>A (p.Leu533Met) c.661T>A (p.Leu221Met) n.479+523T>A | |
| 17 | g.8075653T>A | CA397989829 | ALOX12B | c.1596A>T (p.Glu532Asp) c.660A>T (p.Glu220Asp) n.479+522A>T | |
| 17 | g.8075653T>C | CA497757991 | ALOX12B | c.1596A>G (p.Glu532=) c.660A>G (p.Glu220=) n.479+522A>G | gnomAD v4 |
| 17 | g.8075653T>G | CA397989830 | ALOX12B | c.1596A>C (p.Glu532Asp) c.660A>C (p.Glu220Asp) n.479+522A>C | |
| 17 | g.8075654T>A | CA397989831 | ALOX12B | c.1595A>T (p.Glu532Val) c.659A>T (p.Glu220Val) n.479+521A>T | |
| 17 | g.8075654T>C | CA397989832 | ALOX12B | c.1595A>G (p.Glu532Gly) c.659A>G (p.Glu220Gly) n.479+521A>G | |
| 17 | g.8075654T>G | CA397989833 | ALOX12B | c.1595A>C (p.Glu532Ala) c.659A>C (p.Glu220Ala) n.479+521A>C | |
| 17 | g.8075655C>A | CA397989835 | ALOX12B | c.1594G>T (p.Glu532Ter) c.658G>T (p.Glu220Ter) n.479+520G>T | |
| 17 | g.8075655C= | CA2246125613 | ALOX12B | c.1594G= (p.Glu532=) c.658G= (p.Glu220=) n.479+520G= | |
| 17 | g.8075655C>G | CA397989837 | ALOX12B | c.1594G>C (p.Glu532Gln) c.658G>C (p.Glu220Gln) n.479+520G>C | |
| 17 | g.8075655C>T | CA8367248 | ALOX12B | c.1594G>A (p.Glu532Lys) c.658G>A (p.Glu220Lys) n.479+520G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075656C>A | CA497758001 | ALOX12B | c.1593G>T (p.Pro531=) c.657G>T (p.Pro219=) n.479+519G>T | |
| 17 | g.8075656C= | CA2246125621 | ALOX12B | c.1593G= (p.Pro531=) c.657G= (p.Pro219=) n.479+519G= | |
| 17 | g.8075656C>G | CA8367250 | ALOX12B | c.1593G>C (p.Pro531=) c.657G>C (p.Pro219=) n.479+519G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075656C>T | CA8367249 | ALOX12B | c.1593G>A (p.Pro531=) c.657G>A (p.Pro219=) n.479+519G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075657G>A | CA8367251 | ALOX12B | c.1592C>T (p.Pro531Leu) c.656C>T (p.Pro219Leu) n.479+518C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075657G>C | CA397989842 | ALOX12B | c.1592C>G (p.Pro531Arg) c.656C>G (p.Pro219Arg) n.479+518C>G | |
| 17 | g.8075657G= | CA2246125632 | ALOX12B | c.1592C= (p.Pro531=) c.656C= (p.Pro219=) n.479+518C= | |
| 17 | g.8075657G>T | CA397989844 | ALOX12B | c.1592C>A (p.Pro531Gln) c.656C>A (p.Pro219Gln) n.479+518C>A | |
| 17 | g.8075658G>A | CA397989846 | ALOX12B | c.1591C>T (p.Pro531Ser) c.655C>T (p.Pro219Ser) n.479+517C>T | dbSNP gnomAD v4 COSMIC COSMIC |
| 17 | g.8075658G>C | CA397989849 | ALOX12B | c.1591C>G (p.Pro531Ala) c.655C>G (p.Pro219Ala) n.479+517C>G | |
| 17 | g.8075658G= | CA2246125640 | ALOX12B | c.1591C= (p.Pro531=) c.655C= (p.Pro219=) n.479+517C= | |
| 17 | g.8075658G>T | CA397989848 | ALOX12B | c.1591C>A (p.Pro531Thr) c.655C>A (p.Pro219Thr) n.479+517C>A | |
| 17 | g.8075659A= | CA2246125643 | ALOX12B | c.1590T= (p.Asp530=) c.654T= (p.Asp218=) n.479+516T= | |
| 17 | g.8075659A>C | CA397989850 | ALOX12B | c.1590T>G (p.Asp530Glu) c.654T>G (p.Asp218Glu) n.479+516T>G | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.8075659A>G | CA8367252 | ALOX12B | c.1590T>C (p.Asp530=) c.654T>C (p.Asp218=) n.479+516T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075659A>T | CA397989855 | ALOX12B | c.1590T>A (p.Asp530Glu) c.654T>A (p.Asp218Glu) n.479+516T>A | |
| 17 | g.8075660T>A | CA397989857 | ALOX12B | c.1589A>T (p.Asp530Val) c.653A>T (p.Asp218Val) n.479+515A>T | gnomAD v4 |
| 17 | g.8075660T>C | CA397989859 | ALOX12B | c.1589A>G (p.Asp530Gly) c.653A>G (p.Asp218Gly) n.479+515A>G | |
| 17 | g.8075660T>G | CA397989861 | ALOX12B | c.1589A>C (p.Asp530Ala) c.653A>C (p.Asp218Ala) n.479+515A>C | |
| 17 | g.8075661C>A | CA397989862 | ALOX12B | c.1588G>T (p.Asp530Tyr) c.652G>T (p.Asp218Tyr) n.479+514G>T | |
| 17 | g.8075661C>G | CA397989864 | ALOX12B | c.1588G>C (p.Asp530His) c.652G>C (p.Asp218His) n.479+514G>C | |
| 17 | g.8075661C>T | CA397989866 | ALOX12B | c.1588G>A (p.Asp530Asn) c.652G>A (p.Asp218Asn) n.479+514G>A | |
| 17 | g.8075662A>C | CA497758022 | ALOX12B | c.1587T>G (p.Gly529=) c.651T>G (p.Gly217=) n.479+513T>G | gnomAD v3 gnomAD v4 |
| 17 | g.8075662A>G | CA497758023 | ALOX12B | c.1587T>C (p.Gly529=) c.651T>C (p.Gly217=) n.479+513T>C | |
| 17 | g.8075662A>T | CA497758025 | ALOX12B | c.1587T>A (p.Gly529=) c.651T>A (p.Gly217=) n.479+513T>A | |
| 17 | g.8075663C>A | CA397989868 | ALOX12B | c.1586G>T (p.Gly529Val) c.650G>T (p.Gly217Val) n.479+512G>T | gnomAD v4 |
| 17 | g.8075663C= | CA2246125648 | ALOX12B | c.1586G= (p.Gly529=) c.650G= (p.Gly217=) n.479+512G= | |
| 17 | g.8075663C>G | CA397989870 | ALOX12B | c.1586G>C (p.Gly529Ala) c.650G>C (p.Gly217Ala) n.479+512G>C | |
| 17 | g.8075663C>T | CA8367253 | ALOX12B | c.1586G>A (p.Gly529Asp) c.650G>A (p.Gly217Asp) n.479+512G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075664C>A | CA8367254 | ALOX12B | c.1585G>T (p.Gly529Cys) c.649G>T (p.Gly217Cys) n.479+511G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075664C= | CA2246125651 | ALOX12B | c.1585G= (p.Gly529=) c.649G= (p.Gly217=) n.479+511G= | |
| 17 | g.8075664C>G | CA397989873 | ALOX12B | c.1585G>C (p.Gly529Arg) c.649G>C (p.Gly217Arg) n.479+511G>C | dbSNP |
| 17 | g.8075664C>T | CA397989875 | ALOX12B | c.1585G>A (p.Gly529Ser) c.649G>A (p.Gly217Ser) n.479+511G>A | gnomAD v4 |
| 17 | g.8075665C>A | CA397989878 | ALOX12B | c.1584G>T (p.Glu528Asp) c.648G>T (p.Glu216Asp) n.479+510G>T | |
| 17 | g.8075665C>G | CA397989880 | ALOX12B | c.1584G>C (p.Glu528Asp) c.648G>C (p.Glu216Asp) n.479+510G>C | |
| 17 | g.8075665C>T | CA497758036 | ALOX12B | c.1584G>A (p.Glu528=) c.648G>A (p.Glu216=) n.479+510G>A | |
| 17 | g.8075666T>A | CA397989882 | ALOX12B | c.1583A>T (p.Glu528Val) c.647A>T (p.Glu216Val) n.479+509A>T | |
| 17 | g.8075666T>C | CA397989884 | ALOX12B | c.1583A>G (p.Glu528Gly) c.647A>G (p.Glu216Gly) n.479+509A>G | |
| 17 | g.8075666T>G | CA397989886 | ALOX12B | c.1583A>C (p.Glu528Ala) c.647A>C (p.Glu216Ala) n.479+509A>C | |
| 17 | g.8075667C>A | CA397989888 | ALOX12B | c.1582G>T (p.Glu528Ter) c.646G>T (p.Glu216Ter) n.479+508G>T | |
| 17 | g.8075667C>G | CA397989890 | ALOX12B | c.1582G>C (p.Glu528Gln) c.646G>C (p.Glu216Gln) n.479+508G>C | |
| 17 | g.8075667C>T | CA397989892 | ALOX12B | c.1582G>A (p.Glu528Lys) c.646G>A (p.Glu216Lys) n.479+508G>A | COSMIC COSMIC |
| 17 | g.8075668C>A | CA497758045 | ALOX12B | c.1581G>T (p.Val527=) c.645G>T (p.Val215=) n.479+507G>T | |
| 17 | g.8075668C>G | CA497758047 | ALOX12B | c.1581G>C (p.Val527=) c.645G>C (p.Val215=) n.479+507G>C | |
| 17 | g.8075668C>T | CA497758049 | ALOX12B | c.1581G>A (p.Val527=) c.645G>A (p.Val215=) n.479+507G>A | gnomAD v4 |
| 17 | g.8075669A>C | CA397989895 | ALOX12B | c.1580T>G (p.Val527Gly) c.644T>G (p.Val215Gly) n.479+506T>G | |
| 17 | g.8075669A>G | CA397989897 | ALOX12B | c.1580T>C (p.Val527Ala) c.644T>C (p.Val215Ala) n.479+506T>C | |
| 17 | g.8075669A>T | CA397989898 | ALOX12B | c.1580T>A (p.Val527Glu) c.644T>A (p.Val215Glu) n.479+506T>A | |
| 17 | g.8075670C>A | CA397989901 | ALOX12B | c.1579G>T (p.Val527Leu) c.643G>T (p.Val215Leu) n.479+505G>T | |
| 17 | g.8075670C= | CA2246125654 | ALOX12B | c.1579G= (p.Val527=) c.643G= (p.Val215=) n.479+505G= | |
| 17 | g.8075670C>G | CA397989904 | ALOX12B | c.1579G>C (p.Val527Leu) c.643G>C (p.Val215Leu) n.479+505G>C | gnomAD v4 |
| 17 | g.8075670C>T | CA277196 | ALOX12B | c.1579G>A (p.Val527Met) c.643G>A (p.Val215Met) n.479+505G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075671G>A | CA8367255 | ALOX12B | c.1578C>T (p.Ala526=) c.642C>T (p.Ala214=) n.479+504C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075671G>C | CA497758057 | ALOX12B | c.1578C>G (p.Ala526=) c.642C>G (p.Ala214=) n.479+504C>G | gnomAD v4 |
| 17 | g.8075671G= | CA2246125659 | ALOX12B | c.1578C= (p.Ala526=) c.642C= (p.Ala214=) n.479+504C= | |
| 17 | g.8075671G>T | CA497758058 | ALOX12B | c.1578C>A (p.Ala526=) c.642C>A (p.Ala214=) n.479+504C>A | |
| 17 | g.8075672G>A | CA397989909 | ALOX12B | c.1577C>T (p.Ala526Val) c.641C>T (p.Ala214Val) n.479+503C>T | dbSNP gnomAD v4 |
| 17 | g.8075672G>C | CA397989907 | ALOX12B | c.1577C>G (p.Ala526Gly) c.641C>G (p.Ala214Gly) n.479+503C>G | |
| 17 | g.8075672G= | CA2246125664 | ALOX12B | c.1577C= (p.Ala526=) c.641C= (p.Ala214=) n.479+503C= | |
| 17 | g.8075672G>T | CA397989911 | ALOX12B | c.1577C>A (p.Ala526Asp) c.641C>A (p.Ala214Asp) n.479+503C>A | ClinVar dbSNP gnomAD v4 |
| 17 | g.8075673C>A | CA397989914 | ALOX12B | c.1576G>T (p.Ala526Ser) c.640G>T (p.Ala214Ser) n.479+502G>T | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.8075673C= | CA2246125670 | ALOX12B | c.1576G= (p.Ala526=) c.640G= (p.Ala214=) n.479+502G= | |
| 17 | g.8075673C>G | CA397989917 | ALOX12B | c.1576G>C (p.Ala526Pro) c.640G>C (p.Ala214Pro) n.479+502G>C | |
| 17 | g.8075673C>T | CA8367256 | ALOX12B | c.1576G>A (p.Ala526Thr) c.640G>A (p.Ala214Thr) n.479+502G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075674T>A | CA497758073 | ALOX12B | c.1575A>T (p.Ala525=) c.639A>T (p.Ala213=) n.479+501A>T | |
| 17 | g.8075674T>C | CA497758070 | ALOX12B | c.1575A>G (p.Ala525=) c.639A>G (p.Ala213=) n.479+501A>G | gnomAD v4 |
| 17 | g.8075674T>G | CA497758072 | ALOX12B | c.1575A>C (p.Ala525=) c.639A>C (p.Ala213=) n.479+501A>C | |
| 17 | g.8075675G>A | CA397989918 | ALOX12B | c.1574C>T (p.Ala525Val) c.638C>T (p.Ala213Val) n.479+500C>T | |
| 17 | g.8075675G>C | CA397989922 | ALOX12B | c.1574C>G (p.Ala525Gly) c.638C>G (p.Ala213Gly) n.479+500C>G | |
| 17 | g.8075675G>T | CA397989920 | ALOX12B | c.1574C>A (p.Ala525Glu) c.638C>A (p.Ala213Glu) n.479+500C>A | |
| 17 | g.8075676C>A | CA397989924 | ALOX12B | c.1573G>T (p.Ala525Ser) c.637G>T (p.Ala213Ser) n.479+499G>T | |
| 17 | g.8075676C= | CA2246125674 | ALOX12B | c.1573G= (p.Ala525=) c.637G= (p.Ala213=) n.479+499G= | |
| 17 | g.8075676C>G | CA397989926 | ALOX12B | c.1573G>C (p.Ala525Pro) c.637G>C (p.Ala213Pro) n.479+499G>C | gnomAD v4 |
| 17 | g.8075676C>T | CA8367257 | ALOX12B | c.1573G>A (p.Ala525Thr) c.637G>A (p.Ala213Thr) n.479+499G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.8075677G>A | CA8367258 | ALOX12B | c.1572C>T (p.Asp524=) c.636C>T (p.Asp212=) n.479+498C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075677G>C | CA397989929 | ALOX12B | c.1572C>G (p.Asp524Glu) c.636C>G (p.Asp212Glu) n.479+498C>G | |
| 17 | g.8075677G= | CA2246125677 | ALOX12B | c.1572C= (p.Asp524=) c.636C= (p.Asp212=) n.479+498C= | |
| 17 | g.8075677G>T | CA397989930 | ALOX12B | c.1572C>A (p.Asp524Glu) c.636C>A (p.Asp212Glu) n.479+498C>A | |
| 17 | g.8075678T>A | CA397989935 | ALOX12B | c.1571A>T (p.Asp524Val) c.635A>T (p.Asp212Val) n.479+497A>T | |
| 17 | g.8075678T>C | CA397989933 | ALOX12B | c.1571A>G (p.Asp524Gly) c.635A>G (p.Asp212Gly) n.479+497A>G | |
| 17 | g.8075678T>G | CA397989931 | ALOX12B | c.1571A>C (p.Asp524Ala) c.635A>C (p.Asp212Ala) n.479+497A>C | |
| 17 | g.8075678T= | CA2246125680 | ALOX12B | c.1571A= (p.Asp524=) c.635A= (p.Asp212=) n.479+497A= | |
| 17 | g.8075679C>A | CA397989939 | ALOX12B | c.1570G>T (p.Asp524Tyr) c.634G>T (p.Asp212Tyr) n.479+496G>T | |
| 17 | g.8075679C= | CA2246125689 | ALOX12B | c.1570G= (p.Asp524=) c.634G= (p.Asp212=) n.479+496G= | |
| 17 | g.8075679C>G | CA397989941 | ALOX12B | c.1570G>C (p.Asp524His) c.634G>C (p.Asp212His) n.479+496G>C | |
| 17 | g.8075679C>T | CA10640919 | ALOX12B | c.1570G>A (p.Asp524Asn) c.634G>A (p.Asp212Asn) n.479+496G>A | ClinVar dbSNP |
| 17 | g.8075679dup | CA8367259 | ALOX12B | c.1570dup (p.Asp524GlyfsTer7) c.634dup (p.Asp212GlyfsTer7) n.479+496dup | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075680A= | CA2246125699 | ALOX12B | c.1569T= (p.Ser523=) c.633T= (p.Ser211=) n.479+495T= | |
| 17 | g.8075680A>C | CA397989944 | ALOX12B | c.1569T>G (p.Ser523Arg) c.633T>G (p.Ser211Arg) n.479+495T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075680A>G | CA497758094 | ALOX12B | c.1569T>C (p.Ser523=) c.633T>C (p.Ser211=) n.479+495T>C | gnomAD v4 |
| 17 | g.8075680A>T | CA397989946 | ALOX12B | c.1569T>A (p.Ser523Arg) c.633T>A (p.Ser211Arg) n.479+495T>A | |
| 17 | g.8075681C>A | CA397989947 | ALOX12B | c.1568G>T (p.Ser523Ile) c.632G>T (p.Ser211Ile) n.479+494G>T | |
| 17 | g.8075681C= | CA2246125707 | ALOX12B | c.1568G= (p.Ser523=) c.632G= (p.Ser211=) n.479+494G= | |
| 17 | g.8075681C>G | CA397989952 | ALOX12B | c.1568G>C (p.Ser523Thr) c.632G>C (p.Ser211Thr) n.479+494G>C | |
| 17 | g.8075681C>T | CA397989949 | ALOX12B | c.1568G>A (p.Ser523Asn) c.632G>A (p.Ser211Asn) n.479+494G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075682T>A | CA397989954 | ALOX12B | c.1567A>T (p.Ser523Cys) c.631A>T (p.Ser211Cys) n.479+493A>T | |
| 17 | g.8075682T>C | CA397989956 | ALOX12B | c.1567A>G (p.Ser523Gly) c.631A>G (p.Ser211Gly) n.479+493A>G | |
| 17 | g.8075682T>G | CA397989958 | ALOX12B | c.1567A>C (p.Ser523Arg) c.631A>C (p.Ser211Arg) n.479+493A>C | |
| 17 | g.8075683C>A | CA497758105 | ALOX12B | c.1566G>T (p.Pro522=) c.630G>T (p.Pro210=) n.479+492G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 17 | g.8075683C= | CA2246125714 | ALOX12B | c.1566G= (p.Pro522=) c.630G= (p.Pro210=) n.479+492G= | |
| 17 | g.8075683C>G | CA497758106 | ALOX12B | c.1566G>C (p.Pro522=) c.630G>C (p.Pro210=) n.479+492G>C | |
| 17 | g.8075683C>T | CA287543354 | ALOX12B | c.1566G>A (p.Pro522=) c.630G>A (p.Pro210=) n.479+492G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075684G>A | CA8367260 | ALOX12B | c.1565C>T (p.Pro522Leu) c.629C>T (p.Pro210Leu) n.479+491C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 17 | g.8075684G>C | CA397989961 | ALOX12B | c.1565C>G (p.Pro522Arg) c.629C>G (p.Pro210Arg) n.479+491C>G | |
| 17 | g.8075684G= | CA2246125723 | ALOX12B | c.1565C= (p.Pro522=) c.629C= (p.Pro210=) n.479+491C= | |
| 17 | g.8075684G>T | CA397989962 | ALOX12B | c.1565C>A (p.Pro522Gln) c.629C>A (p.Pro210Gln) n.479+491C>A | |
| 17 | g.8075685G>A | CA397989965 | ALOX12B | c.1564C>T (p.Pro522Ser) c.628C>T (p.Pro210Ser) n.479+490C>T | |
| 17 | g.8075685G>C | CA397989967 | ALOX12B | c.1564C>G (p.Pro522Ala) c.628C>G (p.Pro210Ala) n.479+490C>G | |
| 17 | g.8075685G>T | CA397989968 | ALOX12B | c.1564C>A (p.Pro522Thr) c.628C>A (p.Pro210Thr) n.479+490C>A | |
| 17 | g.8075686G>A | CA497758115 | ALOX12B | c.1563C>T (p.Tyr521=) c.627C>T (p.Tyr209=) n.479+489C>T | |
| 17 | g.8075686G>C | CA397989970 | ALOX12B | c.1563C>G (p.Tyr521Ter) c.627C>G (p.Tyr209Ter) n.479+489C>G | |
| 17 | g.8075686G>T | CA397989972 | ALOX12B | c.1563C>A (p.Tyr521Ter) c.627C>A (p.Tyr209Ter) n.479+489C>A | |
| 17 | g.8075687T>A | CA397989973 | ALOX12B | c.1562A>T (p.Tyr521Phe) c.626A>T (p.Tyr209Phe) n.479+488A>T | |
| 17 | g.8075687T>C | CA261173 | ALOX12B | c.1562A>G (p.Tyr521Cys) c.626A>G (p.Tyr209Cys) n.479+488A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.8075687T>G | CA397989975 | ALOX12B | c.1562A>C (p.Tyr521Ser) c.626A>C (p.Tyr209Ser) n.479+488A>C | |
| 17 | g.8075687T= | CA2246125736 | ALOX12B | c.1562A= (p.Tyr521=) c.626A= (p.Tyr209=) n.479+488A= | |
| 17 | g.8075688A>C | CA397989978 | ALOX12B | c.1561T>G (p.Tyr521Asp) c.625T>G (p.Tyr209Asp) n.479+487T>G | |
| 17 | g.8075688A>G | CA397989980 | ALOX12B | c.1561T>C (p.Tyr521His) c.625T>C (p.Tyr209His) n.479+487T>C | |
| 17 | g.8075688A>T | CA397989982 | ALOX12B | c.1561T>A (p.Tyr521Asn) c.625T>A (p.Tyr209Asn) n.479+487T>A | |
| 17 | g.8075689A>C | CA397989984 | ALOX12B | c.1560T>G (p.Tyr520Ter) c.624T>G (p.Tyr208Ter) n.479+486T>G | |
| 17 | g.8075689A>G | CA497758126 | ALOX12B | c.1560T>C (p.Tyr520=) c.624T>C (p.Tyr208=) n.479+486T>C | |
| 17 | g.8075689A>T | CA397989986 | ALOX12B | c.1560T>A (p.Tyr520Ter) c.624T>A (p.Tyr208Ter) n.479+486T>A | |
| 17 | g.8075690T>A | CA397989989 | ALOX12B | c.1559A>T (p.Tyr520Phe) c.623A>T (p.Tyr208Phe) n.479+485A>T | |
| 17 | g.8075690T>C | CA397989990 | ALOX12B | c.1559A>G (p.Tyr520Cys) c.623A>G (p.Tyr208Cys) n.479+485A>G | |
| 17 | g.8075690T>G | CA397989991 | ALOX12B | c.1559A>C (p.Tyr520Ser) c.623A>C (p.Tyr208Ser) n.479+485A>C | |
| 17 | g.8075691A= | CA2246125744 | ALOX12B | c.1558T= (p.Tyr520=) c.622T= (p.Tyr208=) n.479+484T= | |
| 17 | g.8075691A>C | CA397989994 | ALOX12B | c.1558T>G (p.Tyr520Asp) c.622T>G (p.Tyr208Asp) n.479+484T>G | |
| 17 | g.8075691A>G | CA397989996 | ALOX12B | c.1558T>C (p.Tyr520His) c.622T>C (p.Tyr208His) n.479+484T>C | dbSNP gnomAD v2 |
| 17 | g.8075691A>T | CA397989998 | ALOX12B | c.1558T>A (p.Tyr520Asn) c.622T>A (p.Tyr208Asn) n.479+484T>A | |
| 17 | g.8075692A= | CA2246125745 | ALOX12B | c.1557T= (p.Tyr519=) c.621T= (p.Tyr207=) n.479+483T= | |
| 17 | g.8075692A>C | CA397989999 | ALOX12B | c.1557T>G (p.Tyr519Ter) c.621T>G (p.Tyr207Ter) n.479+483T>G | |
| 17 | g.8075692A>G | CA497758136 | ALOX12B | c.1557T>C (p.Tyr519=) c.621T>C (p.Tyr207=) n.479+483T>C | dbSNP |
| 17 | g.8075692A>T | CA397990001 | ALOX12B | c.1557T>A (p.Tyr519Ter) c.621T>A (p.Tyr207Ter) n.479+483T>A | |
| 17 | g.8075693T>A | CA397990004 | ALOX12B | c.1556A>T (p.Tyr519Phe) c.620A>T (p.Tyr207Phe) n.479+482A>T | |
| 17 | g.8075693T>C | CA8367261 | ALOX12B | c.1556A>G (p.Tyr519Cys) c.620A>G (p.Tyr207Cys) n.479+482A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075693T>G | CA397990005 | ALOX12B | c.1556A>C (p.Tyr519Ser) c.620A>C (p.Tyr207Ser) n.479+482A>C | |
| 17 | g.8075693T= | CA2246125747 | ALOX12B | c.1556A= (p.Tyr519=) c.620A= (p.Tyr207=) n.479+482A= | |
| 17 | g.8075694A>C | CA397990009 | ALOX12B | c.1555T>G (p.Tyr519Asp) c.619T>G (p.Tyr207Asp) n.479+481T>G | |
| 17 | g.8075694A>G | CA397990010 | ALOX12B | c.1555T>C (p.Tyr519His) c.619T>C (p.Tyr207His) n.479+481T>C | |
| 17 | g.8075694A>T | CA397990012 | ALOX12B | c.1555T>A (p.Tyr519Asn) c.619T>A (p.Tyr207Asn) n.479+481T>A | |
| 17 | g.8075695G>A | CA8367262 | ALOX12B | c.1554C>T (p.Thr518=) c.618C>T (p.Thr206=) n.479+480C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.8075695G>C | CA497758145 | ALOX12B | c.1554C>G (p.Thr518=) c.618C>G (p.Thr206=) n.479+480C>G | |
| 17 | g.8075695G= | CA2246125753 | ALOX12B | c.1554C= (p.Thr518=) c.618C= (p.Thr206=) n.479+480C= | |
| 17 | g.8075695G>T | CA497758147 | ALOX12B | c.1554C>A (p.Thr518=) c.618C>A (p.Thr206=) n.479+480C>A | |
| 17 | g.8075696G>A | CA8367263 | ALOX12B | c.1553C>T (p.Thr518Ile) c.617C>T (p.Thr206Ile) n.479+479C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075696G>C | CA397990017 | ALOX12B | c.1553C>G (p.Thr518Ser) c.617C>G (p.Thr206Ser) n.479+479C>G | |
| 17 | g.8075696G= | CA2246125757 | ALOX12B | c.1553C= (p.Thr518=) c.617C= (p.Thr206=) n.479+479C= | |
| 17 | g.8075696G>T | CA397990021 | ALOX12B | c.1553C>A (p.Thr518Asn) c.617C>A (p.Thr206Asn) n.479+479C>A | |
| 17 | g.8075697T>A | CA397990025 | ALOX12B | c.1552A>T (p.Thr518Ser) c.616A>T (p.Thr206Ser) n.479+478A>T | |
| 17 | g.8075697T>C | CA397990027 | ALOX12B | c.1552A>G (p.Thr518Ala) c.616A>G (p.Thr206Ala) n.479+478A>G | |
| 17 | g.8075697T>G | CA397990029 | ALOX12B | c.1552A>C (p.Thr518Pro) c.616A>C (p.Thr206Pro) n.479+478A>C | |
| 17 | g.8075698G>A | CA497758156 | ALOX12B | c.1551C>T (p.Ile517=) c.615C>T (p.Ile205=) n.479+477C>T | dbSNP |
| 17 | g.8075698G>C | CA397990030 | ALOX12B | c.1551C>G (p.Ile517Met) c.615C>G (p.Ile205Met) n.479+477C>G | |
| 17 | g.8075698G= | CA2246125759 | ALOX12B | c.1551C= (p.Ile517=) c.615C= (p.Ile205=) n.479+477C= | |
| 17 | g.8075698G>T | CA497758158 | ALOX12B | c.1551C>A (p.Ile517=) c.615C>A (p.Ile205=) n.479+477C>A | |
| 17 | g.8075699A>C | CA397990034 | ALOX12B | c.1550T>G (p.Ile517Ser) c.614T>G (p.Ile205Ser) n.479+476T>G | |
| 17 | g.8075699A>G | CA397990032 | ALOX12B | c.1550T>C (p.Ile517Thr) c.614T>C (p.Ile205Thr) n.479+476T>C | |
| 17 | g.8075699A>T | CA397990035 | ALOX12B | c.1550T>A (p.Ile517Asn) c.614T>A (p.Ile205Asn) n.479+476T>A | |
| 17 | g.8075700T>A | CA397990038 | ALOX12B | c.1549A>T (p.Ile517Phe) c.613A>T (p.Ile205Phe) n.479+475A>T | dbSNP gnomAD v4 |
| 17 | g.8075700T>C | CA397990040 | ALOX12B | c.1549A>G (p.Ile517Val) c.613A>G (p.Ile205Val) n.479+475A>G | gnomAD v4 |
| 17 | g.8075700T>G | CA397990041 | ALOX12B | c.1549A>C (p.Ile517Leu) c.613A>C (p.Ile205Leu) n.479+475A>C | gnomAD v4 |
| 17 | g.8075700T= | CA2246125767 | ALOX12B | c.1549A= (p.Ile517=) c.613A= (p.Ile205=) n.479+475A= | |
| 17 | g.8075701G>A | CA497758169 | ALOX12B | c.1548C>T (p.Ile516=) c.612C>T (p.Ile204=) n.479+474C>T | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 17 | g.8075701G>C | CA397990044 | ALOX12B | c.1548C>G (p.Ile516Met) c.612C>G (p.Ile204Met) n.479+474C>G | |
| 17 | g.8075701G= | CA2246125772 | ALOX12B | c.1548C= (p.Ile516=) c.612C= (p.Ile204=) n.479+474C= | |
| 17 | g.8075701G>T | CA8367264 | ALOX12B | c.1548C>A (p.Ile516=) c.612C>A (p.Ile204=) n.479+474C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075702A= | CA2246125777 | ALOX12B | c.1547T= (p.Ile516=) c.611T= (p.Ile204=) n.479+473T= | |
| 17 | g.8075702A>C | CA397990046 | ALOX12B | c.1547T>G (p.Ile516Ser) c.611T>G (p.Ile204Ser) n.479+473T>G | |
| 17 | g.8075702A>G | CA287543389 | ALOX12B | c.1547T>C (p.Ile516Thr) c.611T>C (p.Ile204Thr) n.479+473T>C | dbSNP |
| 17 | g.8075702A>T | CA397990049 | ALOX12B | c.1547T>A (p.Ile516Asn) c.611T>A (p.Ile204Asn) n.479+473T>A | |
| 17 | g.8075703T>A | CA397990051 | ALOX12B | c.1546A>T (p.Ile516Phe) c.610A>T (p.Ile204Phe) n.479+472A>T | |
| 17 | g.8075703T>C | CA397990052 | ALOX12B | c.1546A>G (p.Ile516Val) c.610A>G (p.Ile204Val) n.479+472A>G | |
| 17 | g.8075703T>G | CA397990054 | ALOX12B | c.1546A>C (p.Ile516Leu) c.610A>C (p.Ile204Leu) n.479+472A>C | |
| 17 | g.8075704C>A | CA397990056 | ALOX12B | c.1545G>T (p.Glu515Asp) c.609G>T (p.Glu203Asp) n.479+471G>T | |
| 17 | g.8075704C>G | CA397990058 | ALOX12B | c.1545G>C (p.Glu515Asp) c.609G>C (p.Glu203Asp) n.479+471G>C | |
| 17 | g.8075704C>T | CA497758181 | ALOX12B | c.1545G>A (p.Glu515=) c.609G>A (p.Glu203=) n.479+471G>A |