| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 | |
| 17 | g.8075705T>A | CA397990060 | ALOX12B | c.1544A>T (p.Glu515Val) c.608A>T (p.Glu203Val) n.479+470A>T | |
| 17 | g.8075705T>C | CA397990063 | ALOX12B | c.1544A>G (p.Glu515Gly) c.608A>G (p.Glu203Gly) n.479+470A>G | |
| 17 | g.8075705T>G | CA397990061 | ALOX12B | c.1544A>C (p.Glu515Ala) c.608A>C (p.Glu203Ala) n.479+470A>C | |
| 17 | g.8075706C>A | CA397990065 | ALOX12B | c.1543G>T (p.Glu515Ter) c.607G>T (p.Glu203Ter) n.479+469G>T | |
| 17 | g.8075706C>G | CA397990067 | ALOX12B | c.1543G>C (p.Glu515Gln) c.607G>C (p.Glu203Gln) n.479+469G>C | |
| 17 | g.8075706C>T | CA397990069 | ALOX12B | c.1543G>A (p.Glu515Lys) c.607G>A (p.Glu203Lys) n.479+469G>A | |
| 17 | g.8075707C>A | CA497758200 | ALOX12B | c.1542G>T (p.Thr514=) c.606G>T (p.Thr202=) n.479+468G>T | |
| 17 | g.8075707C= | CA2246125786 | ALOX12B | c.1542G= (p.Thr514=) c.606G= (p.Thr202=) n.479+468G= | |
| 17 | g.8075707C>G | CA497758204 | ALOX12B | c.1542G>C (p.Thr514=) c.606G>C (p.Thr202=) n.479+468G>C | |
| 17 | g.8075707C>T | CA8367265 | ALOX12B | c.1542G>A (p.Thr514=) c.606G>A (p.Thr202=) n.479+468G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075708G>A | CA8367266 | ALOX12B | c.1541C>T (p.Thr514Met) c.605C>T (p.Thr202Met) n.479+467C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075708G>C | CA397990073 | ALOX12B | c.1541C>G (p.Thr514Arg) c.605C>G (p.Thr202Arg) n.479+467C>G | |
| 17 | g.8075708G= | CA2246125789 | ALOX12B | c.1541C= (p.Thr514=) c.605C= (p.Thr202=) n.479+467C= | |
| 17 | g.8075708G>T | CA397990074 | ALOX12B | c.1541C>A (p.Thr514Lys) c.605C>A (p.Thr202Lys) n.479+467C>A | |
| 17 | g.8075709T>A | CA397990076 | ALOX12B | c.1540A>T (p.Thr514Ser) c.604A>T (p.Thr202Ser) n.479+466A>T | |
| 17 | g.8075709T>C | CA397990078 | ALOX12B | c.1540A>G (p.Thr514Ala) c.604A>G (p.Thr202Ala) n.479+466A>G | gnomAD v4 |
| 17 | g.8075709T>G | CA397990080 | ALOX12B | c.1540A>C (p.Thr514Pro) c.604A>C (p.Thr202Pro) n.479+466A>C | |
| 17 | g.8075710C>A | CA497758213 | ALOX12B | c.1539G>T (p.Val513=) c.603G>T (p.Val201=) n.479+465G>T | |
| 17 | g.8075710C>G | CA497758214 | ALOX12B | c.1539G>C (p.Val513=) c.603G>C (p.Val201=) n.479+465G>C | |
| 17 | g.8075710C>T | CA497758217 | ALOX12B | c.1539G>A (p.Val513=) c.603G>A (p.Val201=) n.479+465G>A | |
| 17 | g.8075711A>C | CA397990084 | ALOX12B | c.1538T>G (p.Val513Gly) c.602T>G (p.Val201Gly) n.479+464T>G | gnomAD v4 |
| 17 | g.8075711A>G | CA397990087 | ALOX12B | c.1538T>C (p.Val513Ala) c.602T>C (p.Val201Ala) n.479+464T>C | |
| 17 | g.8075711A>T | CA397990082 | ALOX12B | c.1538T>A (p.Val513Glu) c.602T>A (p.Val201Glu) n.479+464T>A | |
| 17 | g.8075712C>A | CA397990088 | ALOX12B | c.1537G>T (p.Val513Leu) c.601G>T (p.Val201Leu) n.479+463G>T | |
| 17 | g.8075712C>G | CA397990089 | ALOX12B | c.1537G>C (p.Val513Leu) c.601G>C (p.Val201Leu) n.479+463G>C | |
| 17 | g.8075712C>T | CA397990091 | ALOX12B | c.1537G>A (p.Val513Met) c.601G>A (p.Val201Met) n.479+463G>A | |
| 17 | g.8075713A= | CA2246125793 | ALOX12B | c.1536T= (p.Tyr512=) c.600T= (p.Tyr200=) n.479+462T= | |
| 17 | g.8075713A>C | CA397990093 | ALOX12B | c.1536T>G (p.Tyr512Ter) c.600T>G (p.Tyr200Ter) n.479+462T>G | |
| 17 | g.8075713A>G | CA8367267 | ALOX12B | c.1536T>C (p.Tyr512=) c.600T>C (p.Tyr200=) n.479+462T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075713A>T | CA397990095 | ALOX12B | c.1536T>A (p.Tyr512Ter) c.600T>A (p.Tyr200Ter) n.479+462T>A | |
| 17 | g.8075714T>A | CA397990102 | ALOX12B | c.1535A>T (p.Tyr512Phe) c.599A>T (p.Tyr200Phe) n.479+461A>T | |
| 17 | g.8075714T>C | CA397990097 | ALOX12B | c.1535A>G (p.Tyr512Cys) c.599A>G (p.Tyr200Cys) n.479+461A>G | dbSNP gnomAD v4 |
| 17 | g.8075714T>G | CA397990100 | ALOX12B | c.1535A>C (p.Tyr512Ser) c.599A>C (p.Tyr200Ser) n.479+461A>C | |
| 17 | g.8075714T= | CA2246125797 | ALOX12B | c.1535A= (p.Tyr512=) c.599A= (p.Tyr200=) n.479+461A= | |
| 17 | g.8075715A>C | CA397990104 | ALOX12B | c.1534T>G (p.Tyr512Asp) c.598T>G (p.Tyr200Asp) n.479+460T>G | |
| 17 | g.8075715A>G | CA397990106 | ALOX12B | c.1534T>C (p.Tyr512His) c.598T>C (p.Tyr200His) n.479+460T>C | |
| 17 | g.8075715A>T | CA397990107 | ALOX12B | c.1534T>A (p.Tyr512Asn) c.598T>A (p.Tyr200Asn) n.479+460T>A | |
| 17 | g.8075716C>A | CA397990110 | ALOX12B | c.1533G>T (p.Lys511Asn) c.597G>T (p.Lys199Asn) n.479+459G>T | |
| 17 | g.8075716C= | CA2246125801 | ALOX12B | c.1533G= (p.Lys511=) c.597G= (p.Lys199=) n.479+459G= | |
| 17 | g.8075716C>G | CA397990111 | ALOX12B | c.1533G>C (p.Lys511Asn) c.597G>C (p.Lys199Asn) n.479+459G>C | |
| 17 | g.8075716C>T | CA497758239 | ALOX12B | c.1533G>A (p.Lys511=) c.597G>A (p.Lys199=) n.479+459G>A | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.8075717C>A | CA397990114 | ALOX12B | c.1533-1G>T (n.1533-1G>T) c.597-1G>T (n.597-1G>T) n.479+458G>T | ClinVar dbSNP |
| 17 | g.8075717C= | CA2246125808 | ALOX12B | c.1533-1G= (n.1533-1G=) c.597-1G= (n.597-1G=) n.479+458G= | |
| 17 | g.8075717C>G | CA397990117 | ALOX12B | c.1533-1G>C (n.1533-1G>C) c.597-1G>C (n.597-1G>C) n.479+458G>C | |
| 17 | g.8075717C>T | CA397990116 | ALOX12B | c.1533-1G>A (n.1533-1G>A) c.597-1G>A (n.597-1G>A) n.479+458G>A | |
| 17 | g.8075718T>A | CA397990120 | ALOX12B | c.1533-2A>T (n.1533-2A>T) c.597-2A>T (n.597-2A>T) n.479+457A>T | |
| 17 | g.8075718T>C | CA397990121 | ALOX12B | c.1533-2A>G (n.1533-2A>G) c.597-2A>G (n.597-2A>G) n.479+457A>G | |
| 17 | g.8075718T>G | CA397990123 | ALOX12B | c.1533-2A>C (n.1533-2A>C) c.597-2A>C (n.597-2A>C) n.479+457A>C | |
| 17 | g.8075721C= | CA2246125813 | ALOX12B | c.1533-5G= (n.1533-5G=) c.597-5G= (n.597-5G=) n.479+454G= | |
| 17 | g.8075721C>G | CA2576161013 | ALOX12B | c.1533-5G>C (n.1533-5G>C) c.597-5G>C (n.597-5G>C) n.479+454G>C | gnomAD v4 |
| 17 | g.8075721C>T | CA624727671 | ALOX12B | c.1533-5G>A (n.1533-5G>A) c.597-5G>A (n.597-5G>A) n.479+454G>A | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.8075722C= | CA2246125817 | ALOX12B | c.1533-6G= (n.1533-6G=) c.597-6G= (n.597-6G=) n.479+453G= | |
| 17 | g.8075722C>G | CA2246125816 | ALOX12B | c.1533-6G>C (n.1533-6G>C) c.597-6G>C (n.597-6G>C) n.479+453G>C | dbSNP |
| 17 | g.8075722_8075723delinsCA | CA2246125819 | ALOX12B | c.1533-7_1533-6delinsTG (n.1533-7_1533-6delinsTG) c.597-7_597-6delinsTG (n.597-7_597-6delinsTG) n.479+452_479+453delinsTG | |
| 17 | g.8075723del | CA775581061 | ALOX12B | c.1533-7del (n.1533-7del) c.597-7del (n.597-7del) n.479+452del | dbSNP |
| 17 | g.8075723A= | CA2246125822 | ALOX12B | c.1533-7T= (n.1533-7T=) c.597-7T= (n.597-7T=) n.479+452T= | |
| 17 | g.8075723A>G | CA624727672 | ALOX12B | c.1533-7T>C (n.1533-7T>C) c.597-7T>C (n.597-7T>C) n.479+452T>C | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.8075727del | CA2576161014 | ALOX12B | c.1533-8del (n.1533-8del) c.597-8del (n.597-8del) n.479+451del | gnomAD v4 |
| 17 | g.8075725G>A | CA8367268 | ALOX12B | c.1533-9C>T (n.1533-9C>T) c.597-9C>T (n.597-9C>T) n.479+450C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075725G>C | CA287543394 | ALOX12B | c.1533-9C>G (n.1533-9C>G) c.597-9C>G (n.597-9C>G) n.479+450C>G | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.8075725G= | CA2246125824 | ALOX12B | c.1533-9C= (n.1533-9C=) c.597-9C= (n.597-9C=) n.479+450C= | |
| 17 | g.8075726G>C | CA2635958105 | ALOX12B | c.1533-10C>G (n.1533-10C>G) c.597-10C>G (n.597-10C>G) n.479+449C>G | gnomAD v4 |
| 17 | g.8075727G>A | CA8367270 | ALOX12B | c.1533-11C>T (n.1533-11C>T) c.597-11C>T (n.597-11C>T) n.479+448C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.8075727G>C | CA8367269 | ALOX12B | c.1533-11C>G (n.1533-11C>G) c.597-11C>G (n.597-11C>G) n.479+448C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075727G= | CA2246125832 | ALOX12B | c.1533-11C= (n.1533-11C=) c.597-11C= (n.597-11C=) n.479+448C= | |
| 17 | g.8075727G>T | CA2635958119 | ALOX12B | c.1533-11C>A (n.1533-11C>A) c.597-11C>A (n.597-11C>A) n.479+448C>A | gnomAD v4 |
| 17 | g.8075729C>T | CA2635958124 | ALOX12B | c.1533-13G>A (n.1533-13G>A) c.597-13G>A (n.597-13G>A) n.479+446G>A | gnomAD v4 |
| 17 | g.8075730A= | CA2246125837 | ALOX12B | c.1533-14T= (n.1533-14T=) c.597-14T= (n.597-14T=) n.479+445T= | |
| 17 | g.8075730A>G | CA775581078 | ALOX12B | c.1533-14T>C (n.1533-14T>C) c.597-14T>C (n.597-14T>C) n.479+445T>C | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.8075730A>T | CA2576161015 | ALOX12B | c.1533-14T>A (n.1533-14T>A) c.597-14T>A (n.597-14T>A) n.479+445T>A | |
| 17 | g.8075731G>T | CA2635958147 | ALOX12B | c.1533-15C>A (n.1533-15C>A) c.597-15C>A (n.597-15C>A) n.479+444C>A | gnomAD v4 |
| 17 | g.8075732G>A | CA2246125844 | ALOX12B | c.1533-16C>T (n.1533-16C>T) c.597-16C>T (n.597-16C>T) n.479+443C>T | dbSNP |
| 17 | g.8075732G= | CA2246125841 | ALOX12B | c.1533-16C= (n.1533-16C=) c.597-16C= (n.597-16C=) n.479+443C= | |
| 17 | g.8075732G>T | CA656676396 | ALOX12B | c.1533-16C>A (n.1533-16C>A) c.597-16C>A (n.597-16C>A) n.479+443C>A | COSMIC |
| 17 | g.8075733G>A | CA8367272 | ALOX12B | c.1533-17C>T (n.1533-17C>T) c.597-17C>T (n.597-17C>T) n.479+442C>T | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 17 | g.8075733G= | CA2246125849 | ALOX12B | c.1533-17C= (n.1533-17C=) c.597-17C= (n.597-17C=) n.479+442C= | |
| 17 | g.8075733G>T | CA8367271 | ALOX12B | c.1533-17C>A (n.1533-17C>A) c.597-17C>A (n.597-17C>A) n.479+442C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.8075734C>A | CA2635958158 | ALOX12B | c.1533-18G>T (n.1533-18G>T) c.597-18G>T (n.597-18G>T) n.479+441G>T | gnomAD v4 |
| 17 | g.8075734C= | CA2246125853 | ALOX12B | c.1533-18G= (n.1533-18G=) c.597-18G= (n.597-18G=) n.479+441G= | |
| 17 | g.8075734C>T | CA8367273 | ALOX12B | c.1533-18G>A (n.1533-18G>A) c.597-18G>A (n.597-18G>A) n.479+441G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |