Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.38071188A= | CA1245626168 | CYP1B1 | c.1166T= (p.Met389=) n.544T= c.53T= (p.Met18=) n.561T= | |
2 | g.38071188A>C | CA346327718 | CYP1B1 | c.1166T>G (p.Met389Arg) n.544T>G c.53T>G (p.Met18Arg) n.561T>G | |
2 | g.38071188A>G | CA346327719 | CYP1B1 | c.1166T>C (p.Met389Thr) n.544T>C c.53T>C (p.Met18Thr) n.561T>C | |
2 | g.38071188A>T | CA346327720 | CYP1B1 | c.1166T>A (p.Met389Lys) n.544T>A c.53T>A (p.Met18Lys) n.561T>A | dbSNP gnomAD v3 gnomAD v4 |
2 | g.38071189T>A | CA346327721 | CYP1B1 | c.1165A>T (p.Met389Leu) n.543A>T c.52A>T (p.Met18Leu) n.560A>T | |
2 | g.38071189T>C | CA346327722 | CYP1B1 | c.1165A>G (p.Met389Val) n.543A>G c.52A>G (p.Met18Val) n.560A>G | gnomAD v4 |
2 | g.38071189T>G | CA346327723 | CYP1B1 | c.1165A>C (p.Met389Leu) n.543A>C c.52A>C (p.Met18Leu) n.560A>C | |
2 | g.38071190G>A | CA425690749 | CYP1B1 | c.1164C>T (p.Ala388=) n.542C>T c.51C>T (p.Ala17=) n.559C>T | |
2 | g.38071190G>C | CA425690750 | CYP1B1 | c.1164C>G (p.Ala388=) n.542C>G c.51C>G (p.Ala17=) n.559C>G | |
2 | g.38071190G>T | CA425690751 | CYP1B1 | c.1164C>A (p.Ala388=) n.542C>A c.51C>A (p.Ala17=) n.559C>A | |
2 | g.38071191G>A | CA346327724 | CYP1B1 | c.1163C>T (p.Ala388Val) n.541C>T c.50C>T (p.Ala17Val) n.558C>T | |
2 | g.38071191G>C | CA346327725 | CYP1B1 | c.1163C>G (p.Ala388Gly) n.541C>G c.50C>G (p.Ala17Gly) n.558C>G | |
2 | g.38071191G>T | CA346327726 | CYP1B1 | c.1163C>A (p.Ala388Asp) n.541C>A c.50C>A (p.Ala17Asp) n.558C>A | |
2 | g.38071192C>A | CA346327729 | CYP1B1 | c.1162G>T (p.Ala388Ser) n.540G>T c.49G>T (p.Ala17Ser) n.557G>T | |
2 | g.38071192C>G | CA346327728 | CYP1B1 | c.1162G>C (p.Ala388Pro) n.540G>C c.49G>C (p.Ala17Pro) n.557G>C | |
2 | g.38071192C>T | CA346327727 | CYP1B1 | c.1162G>A (p.Ala388Thr) n.540G>A c.49G>A (p.Ala17Thr) n.557G>A | |
2 | g.38071193T>A | CA346327730 | CYP1B1 | c.1161A>T (p.Glu387Asp) n.539A>T c.48A>T (p.Glu16Asp) n.556A>T | |
2 | g.38071193T>C | CA425690752 | CYP1B1 | c.1161A>G (p.Glu387=) n.539A>G c.48A>G (p.Glu16=) n.556A>G | |
2 | g.38071193T>G | CA346327731 | CYP1B1 | c.1161A>C (p.Glu387Asp) n.539A>C c.48A>C (p.Glu16Asp) n.556A>C | |
2 | g.38071194T>A | CA346327732 | CYP1B1 | c.1160A>T (p.Glu387Val) n.538A>T c.47A>T (p.Glu16Val) n.555A>T | |
2 | g.38071194T>C | CA346327733 | CYP1B1 | c.1160A>G (p.Glu387Gly) n.538A>G c.47A>G (p.Glu16Gly) n.555A>G | gnomAD v4 |
2 | g.38071194T>G | CA346327734 | CYP1B1 | c.1160A>C (p.Glu387Ala) n.538A>C c.47A>C (p.Glu16Ala) n.555A>C | |
2 | g.38071195C>A | CA346327735 | CYP1B1 | c.1159G>T (p.Glu387Ter) n.537G>T c.46G>T (p.Glu16Ter) n.554G>T | |
2 | g.38071195C= | CA1245626169 | CYP1B1 | c.1159G= (p.Glu387=) n.537G= c.46G= (p.Glu16=) n.554G= | |
2 | g.38071195C>G | CA45506580 | CYP1B1 | c.1159G>C (p.Glu387Gln) n.537G>C c.46G>C (p.Glu16Gln) n.554G>C | dbSNP |
2 | g.38071195C>T | CA254241 | CYP1B1 | c.1159G>A (p.Glu387Lys) n.537G>A c.46G>A (p.Glu16Lys) n.554G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.38071196A>C | CA346327736 | CYP1B1 | c.1158T>G (p.Tyr386Ter) n.536T>G c.45T>G (p.Tyr15Ter) n.553T>G | |
2 | g.38071196A>G | CA425690753 | CYP1B1 | c.1158T>C (p.Tyr386=) n.536T>C c.45T>C (p.Tyr15=) n.553T>C | |
2 | g.38071196A>T | CA346327737 | CYP1B1 | c.1158T>A (p.Tyr386Ter) n.536T>A c.45T>A (p.Tyr15Ter) n.553T>A | |
2 | g.38071197T>A | CA346327738 | CYP1B1 | c.1157A>T (p.Tyr386Phe) n.535A>T c.44A>T (p.Tyr15Phe) n.552A>T | |
2 | g.38071197T>C | CA346327739 | CYP1B1 | c.1157A>G (p.Tyr386Cys) n.535A>G c.44A>G (p.Tyr15Cys) n.552A>G | gnomAD v4 |
2 | g.38071197T>G | CA346327740 | CYP1B1 | c.1157A>C (p.Tyr386Ser) n.535A>C c.44A>C (p.Tyr15Ser) n.552A>C | |
2 | g.38071198A>C | CA346327742 | CYP1B1 | c.1156T>G (p.Tyr386Asp) n.534T>G c.43T>G (p.Tyr15Asp) n.551T>G | |
2 | g.38071198A>G | CA346327743 | CYP1B1 | c.1156T>C (p.Tyr386His) n.534T>C c.43T>C (p.Tyr15His) n.551T>C | |
2 | g.38071198A>T | CA346327741 | CYP1B1 | c.1156T>A (p.Tyr386Asn) n.534T>A c.43T>A (p.Tyr15Asn) n.551T>A | |
2 | g.38071199A>C | CA425690756 | CYP1B1 | c.1155T>G (p.Leu385=) n.533T>G c.42T>G (p.Leu14=) n.550T>G | |
2 | g.38071199A>G | CA425690754 | CYP1B1 | c.1155T>C (p.Leu385=) n.533T>C c.42T>C (p.Leu14=) n.550T>C | gnomAD v4 |
2 | g.38071199A>T | CA425690755 | CYP1B1 | c.1155T>A (p.Leu385=) n.533T>A c.42T>A (p.Leu14=) n.550T>A | |
2 | g.38071200A>C | CA346327746 | CYP1B1 | c.1154T>G (p.Leu385Arg) n.532T>G c.41T>G (p.Leu14Arg) n.549T>G | |
2 | g.38071200A>G | CA346327744 | CYP1B1 | c.1154T>C (p.Leu385Pro) n.532T>C c.41T>C (p.Leu14Pro) n.549T>C | |
2 | g.38071200A>T | CA346327745 | CYP1B1 | c.1154T>A (p.Leu385His) n.532T>A c.41T>A (p.Leu14His) n.549T>A | |
2 | g.38071201G>A | CA45506612 | CYP1B1 | c.1153C>T (p.Leu385Phe) n.531C>T c.40C>T (p.Leu14Phe) n.548C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.38071201G>C | CA346327747 | CYP1B1 | c.1153C>G (p.Leu385Val) n.531C>G c.40C>G (p.Leu14Val) n.548C>G | |
2 | g.38071201G= | CA1245626170 | CYP1B1 | c.1153C= (p.Leu385=) n.531C= c.40C= (p.Leu14=) n.548C= | |
2 | g.38071201G>T | CA346327748 | CYP1B1 | c.1153C>A (p.Leu385Ile) n.531C>A c.40C>A (p.Leu14Ile) n.548C>A | |
2 | g.38071202G>A | CA425690757 | CYP1B1 | c.1152C>T (p.Phe384=) n.530C>T c.39C>T (p.Phe13=) n.547C>T | |
2 | g.38071202G>C | CA346327749 | CYP1B1 | c.1152C>G (p.Phe384Leu) n.530C>G c.39C>G (p.Phe13Leu) n.547C>G | |
2 | g.38071202G>T | CA346327750 | CYP1B1 | c.1152C>A (p.Phe384Leu) n.530C>A c.39C>A (p.Phe13Leu) n.547C>A | |
2 | g.38071203A>C | CA346327751 | CYP1B1 | c.1151T>G (p.Phe384Cys) n.529T>G c.38T>G (p.Phe13Cys) n.546T>G | |
2 | g.38071203A>G | CA346327752 | CYP1B1 | c.1151T>C (p.Phe384Ser) n.529T>C c.38T>C (p.Phe13Ser) n.546T>C |