| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.102832626G>A | CA377938890 | CYP17A1,WBP1L | c.1024C>T (p.Pro342Ser) c.721C>T (p.Pro241Ser) c.568C>T (p.Pro190Ser) c.937C>T (p.Pro313Ser) n.786C>T c.*1657G>A (n.*1657G>A) | |
| 10 | g.102832626G>C | CA377938889 | CYP17A1,WBP1L | c.1024C>G (p.Pro342Ala) c.721C>G (p.Pro241Ala) c.568C>G (p.Pro190Ala) c.937C>G (p.Pro313Ala) n.786C>G c.*1657G>C (n.*1657G>C) | |
| 10 | g.102832626G= | CA1932870709 | CYP17A1,WBP1L | c.1024C= (p.Pro342=) c.721C= (p.Pro241=) c.568C= (p.Pro190=) c.937C= (p.Pro313=) n.786C= c.*1657G= (n.*1657G=) | |
| 10 | g.102832626G>T | CA115182 | CYP17A1,WBP1L | c.1024C>A (p.Pro342Thr) c.721C>A (p.Pro241Thr) c.568C>A (p.Pro190Thr) c.937C>A (p.Pro313Thr) n.786C>A c.*1657G>T (n.*1657G>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.102832627T>A | CA471288699 | CYP17A1,WBP1L | c.1023A>T (p.Thr341=) c.720A>T (p.Thr240=) c.567A>T (p.Thr189=) c.936A>T (p.Thr312=) n.785A>T c.*1658T>A (n.*1658T>A) | |
| 10 | g.102832627T>C | CA471288700 | CYP17A1,WBP1L | c.1023A>G (p.Thr341=) c.720A>G (p.Thr240=) c.567A>G (p.Thr189=) c.936A>G (p.Thr312=) n.785A>G c.*1658T>C (n.*1658T>C) | |
| 10 | g.102832627T>G | CA471288701 | CYP17A1,WBP1L | c.1023A>C (p.Thr341=) c.720A>C (p.Thr240=) c.567A>C (p.Thr189=) c.936A>C (p.Thr312=) n.785A>C c.*1658T>G (n.*1658T>G) | |
| 10 | g.102832628G>A | CA377938891 | CYP17A1,WBP1L | c.1022C>T (p.Thr341Ile) c.719C>T (p.Thr240Ile) c.566C>T (p.Thr189Ile) c.935C>T (p.Thr312Ile) n.784C>T c.*1659G>A (n.*1659G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102832628G>C | CA377938892 | CYP17A1,WBP1L | c.1022C>G (p.Thr341Arg) c.719C>G (p.Thr240Arg) c.566C>G (p.Thr189Arg) c.935C>G (p.Thr312Arg) n.784C>G c.*1659G>C (n.*1659G>C) | |
| 10 | g.102832628G= | CA1932870714 | CYP17A1,WBP1L | c.1022C= (p.Thr341=) c.719C= (p.Thr240=) c.566C= (p.Thr189=) c.935C= (p.Thr312=) n.784C= c.*1659G= (n.*1659G=) | |
| 10 | g.102832628G>T | CA377938893 | CYP17A1,WBP1L | c.1022C>A (p.Thr341Lys) c.719C>A (p.Thr240Lys) c.566C>A (p.Thr189Lys) c.935C>A (p.Thr312Lys) n.784C>A c.*1659G>T (n.*1659G>T) | gnomAD v4 |
| 10 | g.102832629T>A | CA377938894 | CYP17A1,WBP1L | c.1021A>T (p.Thr341Ser) c.718A>T (p.Thr240Ser) c.565A>T (p.Thr189Ser) c.934A>T (p.Thr312Ser) n.783A>T c.*1660T>A (n.*1660T>A) | |
| 10 | g.102832629T>C | CA377938895 | CYP17A1,WBP1L | c.1021A>G (p.Thr341Ala) c.718A>G (p.Thr240Ala) c.565A>G (p.Thr189Ala) c.934A>G (p.Thr312Ala) n.783A>G c.*1660T>C (n.*1660T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.102832629T>G | CA377938896 | CYP17A1,WBP1L | c.1021A>C (p.Thr341Pro) c.718A>C (p.Thr240Pro) c.565A>C (p.Thr189Pro) c.934A>C (p.Thr312Pro) n.783A>C c.*1660T>G (n.*1660T>G) | |
| 10 | g.102832629T= | CA1932870719 | CYP17A1,WBP1L | c.1021A= (p.Thr341=) c.718A= (p.Thr240=) c.565A= (p.Thr189=) c.934A= (p.Thr312=) n.783A= c.*1660T= (n.*1660T=) | |
| 10 | g.102832630G>A | CA471288708 | CYP17A1,WBP1L | c.1020C>T (p.Arg340=) c.717C>T (p.Arg239=) c.564C>T (p.Arg188=) c.933C>T (p.Arg311=) n.782C>T c.*1661G>A (n.*1661G>A) | |
| 10 | g.102832630G>C | CA471288712 | CYP17A1,WBP1L | c.1020C>G (p.Arg340=) c.717C>G (p.Arg239=) c.564C>G (p.Arg188=) c.933C>G (p.Arg311=) n.782C>G c.*1661G>C (n.*1661G>C) | |
| 10 | g.102832630G>T | CA471288710 | CYP17A1,WBP1L | c.1020C>A (p.Arg340=) c.717C>A (p.Arg239=) c.564C>A (p.Arg188=) c.933C>A (p.Arg311=) n.782C>A c.*1661G>T (n.*1661G>T) | gnomAD v4 |
| 10 | g.102832631C>A | CA377938897 | CYP17A1,WBP1L | c.1019G>T (p.Arg340Leu) c.716G>T (p.Arg239Leu) c.563G>T (p.Arg188Leu) c.932G>T (p.Arg311Leu) n.781G>T c.*1662C>A (n.*1662C>A) | |
| 10 | g.102832631C= | CA1932870727 | CYP17A1,WBP1L | c.1019G= (p.Arg340=) c.716G= (p.Arg239=) c.563G= (p.Arg188=) c.932G= (p.Arg311=) n.781G= c.*1662C= (n.*1662C=) | |
| 10 | g.102832631C>G | CA377938898 | CYP17A1,WBP1L | c.1019G>C (p.Arg340Pro) c.716G>C (p.Arg239Pro) c.563G>C (p.Arg188Pro) c.932G>C (p.Arg311Pro) n.781G>C c.*1662C>G (n.*1662C>G) | |
| 10 | g.102832631C>T | CA5669414 | CYP17A1,WBP1L | c.1019G>A (p.Arg340His) c.716G>A (p.Arg239His) c.563G>A (p.Arg188His) c.932G>A (p.Arg311His) n.781G>A c.*1662C>T (n.*1662C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.102832632G>A | CA377938899 | CYP17A1,WBP1L | c.1018C>T (p.Arg340Cys) c.715C>T (p.Arg239Cys) c.562C>T (p.Arg188Cys) c.931C>T (p.Arg311Cys) n.780C>T c.*1663G>A (n.*1663G>A) | dbSNP gnomAD v4 |
| 10 | g.102832632G>C | CA377938900 | CYP17A1,WBP1L | c.1018C>G (p.Arg340Gly) c.715C>G (p.Arg239Gly) c.562C>G (p.Arg188Gly) c.931C>G (p.Arg311Gly) n.780C>G c.*1663G>C (n.*1663G>C) | |
| 10 | g.102832632G= | CA1932870738 | CYP17A1,WBP1L | c.1018C= (p.Arg340=) c.715C= (p.Arg239=) c.562C= (p.Arg188=) c.931C= (p.Arg311=) n.780C= c.*1663G= (n.*1663G=) | |
| 10 | g.102832632G>T | CA377938901 | CYP17A1,WBP1L | c.1018C>A (p.Arg340Ser) c.715C>A (p.Arg239Ser) c.562C>A (p.Arg188Ser) c.931C>A (p.Arg311Ser) n.780C>A c.*1663G>T (n.*1663G>T) | gnomAD v4 |
| 10 | g.102832632_102832635delinsGGCT | CA1932870741 | CYP17A1,WBP1L | c.1015_1018delinsAGCC (p.Ser339=) c.712_715delinsAGCC (p.Ser238=) c.559_562delinsAGCC (p.Ser187=) c.928_931delinsAGCC (p.Ser310=) n.777_780delinsAGCC c.*1663_*1666delinsGGCT (n.*1663_*1666delinsGGCT) | |
| 10 | g.102832633G>A | CA471288719 | CYP17A1,WBP1L | c.1017C>T (p.Ser339=) c.714C>T (p.Ser238=) c.561C>T (p.Ser187=) c.930C>T (p.Ser310=) n.779C>T c.*1664G>A (n.*1664G>A) | gnomAD v4 |
| 10 | g.102832633G>C | CA377938902 | CYP17A1,WBP1L | c.1017C>G (p.Ser339Arg) c.714C>G (p.Ser238Arg) c.561C>G (p.Ser187Arg) c.930C>G (p.Ser310Arg) n.779C>G c.*1664G>C (n.*1664G>C) | dbSNP |
| 10 | g.102832633G= | CA1932870767 | CYP17A1,WBP1L | c.1017C= (p.Ser339=) c.714C= (p.Ser238=) c.561C= (p.Ser187=) c.930C= (p.Ser310=) n.779C= c.*1664G= (n.*1664G=) | |
| 10 | g.102832633G>T | CA377938903 | CYP17A1,WBP1L | c.1017C>A (p.Ser339Arg) c.714C>A (p.Ser238Arg) c.561C>A (p.Ser187Arg) c.930C>A (p.Ser310Arg) n.779C>A c.*1664G>T (n.*1664G>T) | gnomAD v4 |
| 10 | g.102832634_102832636del | CA595636697 | CYP17A1,WBP1L | c.1015_1017del (p.Ser339del) c.712_714del (p.Ser238del) c.559_561del (p.Ser187del) c.928_930del (p.Ser310del) n.777_779del c.*1665_*1667del (n.*1665_*1667del) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.102832634C>A | CA377938904 | CYP17A1,WBP1L | c.1016G>T (p.Ser339Ile) c.713G>T (p.Ser238Ile) c.560G>T (p.Ser187Ile) c.929G>T (p.Ser310Ile) n.778G>T c.*1665C>A (n.*1665C>A) | |
| 10 | g.102832634C>G | CA377938905 | CYP17A1,WBP1L | c.1016G>C (p.Ser339Thr) c.713G>C (p.Ser238Thr) c.560G>C (p.Ser187Thr) c.929G>C (p.Ser310Thr) n.778G>C c.*1665C>G (n.*1665C>G) | COSMIC |
| 10 | g.102832634C>T | CA377938906 | CYP17A1,WBP1L | c.1016G>A (p.Ser339Asn) c.713G>A (p.Ser238Asn) c.560G>A (p.Ser187Asn) c.929G>A (p.Ser310Asn) n.778G>A c.*1665C>T (n.*1665C>T) | |
| 10 | g.102832635T>A | CA377938907 | CYP17A1,WBP1L | c.1015A>T (p.Ser339Cys) c.712A>T (p.Ser238Cys) c.559A>T (p.Ser187Cys) c.928A>T (p.Ser310Cys) n.777A>T c.*1666T>A (n.*1666T>A) | |
| 10 | g.102832635T>C | CA377938908 | CYP17A1,WBP1L | c.1015A>G (p.Ser339Gly) c.712A>G (p.Ser238Gly) c.559A>G (p.Ser187Gly) c.928A>G (p.Ser310Gly) n.777A>G c.*1666T>C (n.*1666T>C) | gnomAD v4 |
| 10 | g.102832635T>G | CA377938909 | CYP17A1,WBP1L | c.1015A>C (p.Ser339Arg) c.712A>C (p.Ser238Arg) c.559A>C (p.Ser187Arg) c.928A>C (p.Ser310Arg) n.777A>C c.*1666T>G (n.*1666T>G) | |
| 10 | g.102832636G>A | CA5669415 | CYP17A1,WBP1L | c.1014C>T (p.Phe338=) c.711C>T (p.Phe237=) c.558C>T (p.Phe186=) c.927C>T (p.Phe309=) n.776C>T c.*1667G>A (n.*1667G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.102832636G>C | CA377938910 | CYP17A1,WBP1L | c.1014C>G (p.Phe338Leu) c.711C>G (p.Phe237Leu) c.558C>G (p.Phe186Leu) c.927C>G (p.Phe309Leu) n.776C>G c.*1667G>C (n.*1667G>C) | |
| 10 | g.102832636G= | CA1932870772 | CYP17A1,WBP1L | c.1014C= (p.Phe338=) c.711C= (p.Phe237=) c.558C= (p.Phe186=) c.927C= (p.Phe309=) n.776C= c.*1667G= (n.*1667G=) | |
| 10 | g.102832636G>T | CA377938911 | CYP17A1,WBP1L | c.1014C>A (p.Phe338Leu) c.711C>A (p.Phe237Leu) c.558C>A (p.Phe186Leu) c.927C>A (p.Phe309Leu) n.776C>A c.*1667G>T (n.*1667G>T) | gnomAD v4 |
| 10 | g.102832637A= | CA1932870775 | CYP17A1,WBP1L | c.1013T= (p.Phe338=) c.710T= (p.Phe237=) c.557T= (p.Phe186=) c.926T= (p.Phe309=) n.775T= c.*1668A= (n.*1668A=) | |
| 10 | g.102832637A>C | CA377938912 | CYP17A1,WBP1L | c.1013T>G (p.Phe338Cys) c.710T>G (p.Phe237Cys) c.557T>G (p.Phe186Cys) c.926T>G (p.Phe309Cys) n.775T>G c.*1668A>C (n.*1668A>C) | |
| 10 | g.102832637A>G | CA377938913 | CYP17A1,WBP1L | c.1013T>C (p.Phe338Ser) c.710T>C (p.Phe237Ser) c.557T>C (p.Phe186Ser) c.926T>C (p.Phe309Ser) n.775T>C c.*1668A>G (n.*1668A>G) | dbSNP gnomAD v4 |
| 10 | g.102832637A>T | CA377938914 | CYP17A1,WBP1L | c.1013T>A (p.Phe338Tyr) c.710T>A (p.Phe237Tyr) c.557T>A (p.Phe186Tyr) c.926T>A (p.Phe309Tyr) n.775T>A c.*1668A>T (n.*1668A>T) | |
| 10 | g.102832638A>C | CA377938915 | CYP17A1,WBP1L | c.1012T>G (p.Phe338Val) c.709T>G (p.Phe237Val) c.556T>G (p.Phe186Val) c.925T>G (p.Phe309Val) n.774T>G c.*1669A>C (n.*1669A>C) | |
| 10 | g.102832638A>G | CA377938916 | CYP17A1,WBP1L | c.1012T>C (p.Phe338Leu) c.709T>C (p.Phe237Leu) c.556T>C (p.Phe186Leu) c.925T>C (p.Phe309Leu) n.774T>C c.*1669A>G (n.*1669A>G) | gnomAD v4 |
| 10 | g.102832638A>T | CA377938917 | CYP17A1,WBP1L | c.1012T>A (p.Phe338Ile) c.709T>A (p.Phe237Ile) c.556T>A (p.Phe186Ile) c.925T>A (p.Phe309Ile) n.774T>A c.*1669A>T (n.*1669A>T) | |
| 10 | g.102832639A>C | CA471288733 | CYP17A1,WBP1L | c.1011T>G (p.Gly337=) c.708T>G (p.Gly236=) c.555T>G (p.Gly185=) c.924T>G (p.Gly308=) n.773T>G c.*1670A>C (n.*1670A>C) |