| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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= |