Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.38071182A>C | CA346327707 | CYP1B1 | c.1172T>G (p.Phe391Cys) n.550T>G c.59T>G (p.Phe20Cys) n.567T>G | |
2 | g.38071182A>G | CA346327708 | CYP1B1 | c.1172T>C (p.Phe391Ser) n.550T>C c.59T>C (p.Phe20Ser) n.567T>C | gnomAD v4 |
2 | g.38071182A>T | CA346327709 | CYP1B1 | c.1172T>A (p.Phe391Tyr) n.550T>A c.59T>A (p.Phe20Tyr) n.567T>A | |
2 | g.38071183A>C | CA346327710 | CYP1B1 | c.1171T>G (p.Phe391Val) n.549T>G c.58T>G (p.Phe20Val) n.566T>G | |
2 | g.38071183A>G | CA346327711 | CYP1B1 | c.1171T>C (p.Phe391Leu) n.549T>C c.58T>C (p.Phe20Leu) n.566T>C | gnomAD v4 |
2 | g.38071183A>T | CA346327712 | CYP1B1 | c.1171T>A (p.Phe391Ile) n.549T>A c.58T>A (p.Phe20Ile) n.566T>A | |
2 | g.38071184G>A | CA425690746 | CYP1B1 | c.1170C>T (p.Arg390=) n.548C>T c.57C>T (p.Arg19=) n.565C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.38071184G>C | CA425690747 | CYP1B1 | c.1170C>G (p.Arg390=) n.548C>G c.57C>G (p.Arg19=) n.565C>G | |
2 | g.38071184G= | CA1245626164 | CYP1B1 | c.1170C= (p.Arg390=) n.548C= c.57C= (p.Arg19=) n.565C= | |
2 | g.38071184G>T | CA425690748 | CYP1B1 | c.1170C>A (p.Arg390=) n.548C>A c.57C>A (p.Arg19=) n.565C>A | |
2 | g.38071185C>A | CA346327713 | CYP1B1 | c.1169G>T (p.Arg390Leu) n.547G>T c.56G>T (p.Arg19Leu) n.564G>T | |
2 | g.38071185C= | CA1245626165 | CYP1B1 | c.1169G= (p.Arg390=) n.547G= c.56G= (p.Arg19=) n.564G= | |
2 | g.38071185C>G | CA346327714 | CYP1B1 | c.1169G>C (p.Arg390Pro) n.547G>C c.56G>C (p.Arg19Pro) n.564G>C | |
2 | g.38071185C>T | CA1619846 | CYP1B1 | c.1169G>A (p.Arg390His) n.547G>A c.56G>A (p.Arg19His) n.564G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.38071186G>A | CA1619847 | CYP1B1 | c.1168C>T (p.Arg390Cys) n.546C>T c.55C>T (p.Arg19Cys) n.563C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.38071186G>C | CA346327715 | CYP1B1 | c.1168C>G (p.Arg390Gly) n.546C>G c.55C>G (p.Arg19Gly) n.563C>G | gnomAD v4 COSMIC |
2 | g.38071186G= | CA1245626166 | CYP1B1 | c.1168C= (p.Arg390=) n.546C= c.55C= (p.Arg19=) n.563C= | |
2 | g.38071186G>T | CA1619848 | CYP1B1 | c.1168C>A (p.Arg390Ser) n.546C>A c.55C>A (p.Arg19Ser) n.563C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.38071187C>A | CA346327716 | CYP1B1 | c.1167G>T (p.Met389Ile) n.545G>T c.54G>T (p.Met18Ile) n.562G>T | |
2 | g.38071187C= | CA1245626167 | CYP1B1 | c.1167G= (p.Met389=) n.545G= c.54G= (p.Met18=) n.562G= | |
2 | g.38071187C>G | CA346327717 | CYP1B1 | c.1167G>C (p.Met389Ile) n.545G>C c.54G>C (p.Met18Ile) n.562G>C | |
2 | g.38071187C>T | CA45506579 | CYP1B1 | c.1167G>A (p.Met389Ile) n.545G>A c.54G>A (p.Met18Ile) n.562G>A | dbSNP gnomAD v2 gnomAD v4 |
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 |