Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.229431510_229431534del | CA645538675 | ACTA1 | c.1021_1045del (p.Ala341AsnfsTer?) c.964_988del (p.Ala322AsnfsTer?) c.730_754del (p.Ala244AsnfsTer?) c.1099_1123del (p.Ala367AsnfsTer?) | COSMIC |
1 | g.229431531C>A | CA345144227 | ACTA1 | c.1024G>T (p.Gly342Cys) c.967G>T (p.Gly323Cys) c.733G>T (p.Gly245Cys) c.1102G>T (p.Gly368Cys) | |
1 | g.229431531C>G | CA345144229 | ACTA1 | c.1024G>C (p.Gly342Arg) c.967G>C (p.Gly323Arg) c.733G>C (p.Gly245Arg) c.1102G>C (p.Gly368Arg) | |
1 | g.229431531C>T | CA345144231 | ACTA1 | c.1024G>A (p.Gly342Ser) c.967G>A (p.Gly323Ser) c.733G>A (p.Gly245Ser) c.1102G>A (p.Gly368Ser) | COSMIC |
1 | g.229431532G>A | CA1442706 | ACTA1 | c.1023C>T (p.Ala341=) c.966C>T (p.Ala322=) c.732C>T (p.Ala244=) c.1101C>T (p.Ala367=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.229431532G>C | CA423754809 | ACTA1 | c.1023C>G (p.Ala341=) c.966C>G (p.Ala322=) c.732C>G (p.Ala244=) c.1101C>G (p.Ala367=) | |
1 | g.229431532G= | CA1226125371 | ACTA1 | c.1023C= (p.Ala341=) c.966C= (p.Ala322=) c.732C= (p.Ala244=) c.1101C= (p.Ala367=) | |
1 | g.229431532G>T | CA423754808 | ACTA1 | c.1023C>A (p.Ala341=) c.966C>A (p.Ala322=) c.732C>A (p.Ala244=) c.1101C>A (p.Ala367=) | |
1 | g.229431533G>A | CA345144235 | ACTA1 | c.1022C>T (p.Ala341Val) c.965C>T (p.Ala322Val) c.731C>T (p.Ala244Val) c.1100C>T (p.Ala367Val) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.229431533G>C | CA345144238 | ACTA1 | c.1022C>G (p.Ala341Gly) c.965C>G (p.Ala322Gly) c.731C>G (p.Ala244Gly) c.1100C>G (p.Ala367Gly) | |
1 | g.229431533G= | CA1226125372 | ACTA1 | c.1022C= (p.Ala341=) c.965C= (p.Ala322=) c.731C= (p.Ala244=) c.1100C= (p.Ala367=) | |
1 | g.229431533G>T | CA345144241 | ACTA1 | c.1022C>A (p.Ala341Asp) c.965C>A (p.Ala322Asp) c.731C>A (p.Ala244Asp) c.1100C>A (p.Ala367Asp) | |
1 | g.229431534C>A | CA345144244 | ACTA1 | c.1021G>T (p.Ala341Ser) c.964G>T (p.Ala322Ser) c.730G>T (p.Ala244Ser) c.1099G>T (p.Ala367Ser) | COSMIC |
1 | g.229431534C= | CA1226125373 | ACTA1 | c.1021G= (p.Ala341=) c.964G= (p.Ala322=) c.730G= (p.Ala244=) c.1099G= (p.Ala367=) | |
1 | g.229431534C>G | CA345144245 | ACTA1 | c.1021G>C (p.Ala341Pro) c.964G>C (p.Ala322Pro) c.730G>C (p.Ala244Pro) c.1099G>C (p.Ala367Pro) | |
1 | g.229431534C>T | CA345144246 | ACTA1 | c.1021G>A (p.Ala341Thr) c.964G>A (p.Ala322Thr) c.730G>A (p.Ala244Thr) c.1099G>A (p.Ala367Thr) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.229431535C>A | CA345144250 | ACTA1 | c.1020G>T (p.Glu340Asp) c.963G>T (p.Glu321Asp) c.729G>T (p.Glu243Asp) c.1098G>T (p.Glu366Asp) | |
1 | g.229431535C= | CA1226125374 | ACTA1 | c.1020G= (p.Glu340=) c.963G= (p.Glu321=) c.729G= (p.Glu243=) c.1098G= (p.Glu366=) | |
1 | g.229431535C>G | CA345144253 | ACTA1 | c.1020G>C (p.Glu340Asp) c.963G>C (p.Glu321Asp) c.729G>C (p.Glu243Asp) c.1098G>C (p.Glu366Asp) | |
1 | g.229431535C>T | CA423754814 | ACTA1 | c.1020G>A (p.Glu340=) c.963G>A (p.Glu321=) c.729G>A (p.Glu243=) c.1098G>A (p.Glu366=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431536T>A | CA345144256 | ACTA1 | c.1019A>T (p.Glu340Val) c.962A>T (p.Glu321Val) c.728A>T (p.Glu243Val) c.1097A>T (p.Glu366Val) | |
1 | g.229431536T>C | CA345144260 | ACTA1 | c.1019A>G (p.Glu340Gly) c.962A>G (p.Glu321Gly) c.728A>G (p.Glu243Gly) c.1097A>G (p.Glu366Gly) | |
1 | g.229431536T>G | CA345144258 | ACTA1 | c.1019A>C (p.Glu340Ala) c.962A>C (p.Glu321Ala) c.728A>C (p.Glu243Ala) c.1097A>C (p.Glu366Ala) | |
1 | g.229431537C>A | CA345144265 | ACTA1 | c.1018G>T (p.Glu340Ter) c.961G>T (p.Glu321Ter) c.727G>T (p.Glu243Ter) c.1096G>T (p.Glu366Ter) | |
1 | g.229431537C>G | CA345144268 | ACTA1 | c.1018G>C (p.Glu340Gln) c.961G>C (p.Glu321Gln) c.727G>C (p.Glu243Gln) c.1096G>C (p.Glu366Gln) | |
1 | g.229431537C>T | CA345144270 | ACTA1 | c.1018G>A (p.Glu340Lys) c.961G>A (p.Glu321Lys) c.727G>A (p.Glu243Lys) c.1096G>A (p.Glu366Lys) | |
1 | g.229431538G>A | CA1442708 | ACTA1 | c.1017C>T (p.Asp339=) c.960C>T (p.Asp320=) c.726C>T (p.Asp242=) c.1095C>T (p.Asp365=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.229431538G>C | CA1442707 | ACTA1 | c.1017C>G (p.Asp339Glu) c.960C>G (p.Asp320Glu) c.726C>G (p.Asp242Glu) c.1095C>G (p.Asp365Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.229431538G= | CA1143959170 | ACTA1 | c.1017C= (p.Asp339=) c.960C= (p.Asp320=) c.726C= (p.Asp242=) c.1095C= (p.Asp365=) | |
1 | g.229431538G>T | CA345144280 | ACTA1 | c.1017C>A (p.Asp339Glu) c.960C>A (p.Asp320Glu) c.726C>A (p.Asp242Glu) c.1095C>A (p.Asp365Glu) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.229431539T>A | CA345144283 | ACTA1 | c.1016A>T (p.Asp339Val) c.959A>T (p.Asp320Val) c.725A>T (p.Asp242Val) c.1094A>T (p.Asp365Val) | |
1 | g.229431539T>C | CA345144285 | ACTA1 | c.1016A>G (p.Asp339Gly) c.959A>G (p.Asp320Gly) c.725A>G (p.Asp242Gly) c.1094A>G (p.Asp365Gly) | |
1 | g.229431539T>G | CA345144287 | ACTA1 | c.1016A>C (p.Asp339Ala) c.959A>C (p.Asp320Ala) c.725A>C (p.Asp242Ala) c.1094A>C (p.Asp365Ala) | |
1 | g.229431540del | CA2698259255 | ACTA1 | c.1015del (p.Asp339ThrfsTer?) c.958del (p.Asp320ThrfsTer?) c.724del (p.Asp242ThrfsTer?) c.1093del (p.Asp365ThrfsTer?) | dbSNP |
1 | g.229431540C>A | CA345144291 | ACTA1 | c.1015G>T (p.Asp339Tyr) c.958G>T (p.Asp320Tyr) c.724G>T (p.Asp242Tyr) c.1093G>T (p.Asp365Tyr) | |
1 | g.229431540C>G | CA345144294 | ACTA1 | c.1015G>C (p.Asp339His) c.958G>C (p.Asp320His) c.724G>C (p.Asp242His) c.1093G>C (p.Asp365His) | |
1 | g.229431540C>T | CA345144297 | ACTA1 | c.1015G>A (p.Asp339Asn) c.958G>A (p.Asp320Asn) c.724G>A (p.Asp242Asn) c.1093G>A (p.Asp365Asn) | |
1 | g.229431540dup | CA2650926579 | ACTA1 | c.1015dup (p.Asp339GlyfsTer?) c.958dup (p.Asp320GlyfsTer?) c.724dup (p.Asp242GlyfsTer?) c.1093dup (p.Asp365GlyfsTer?) | gnomAD v4 |
1 | g.229431541del | CA915940544 | ACTA1 | c.1014del (p.Tyr338Ter) c.957del (p.Tyr319Ter) c.723del (p.Tyr241Ter) c.1092del (p.Tyr364Ter) | |
1 | g.229431541G>A | CA38814650 | ACTA1 | c.1014C>T (p.Tyr338=) c.957C>T (p.Tyr319=) c.723C>T (p.Tyr241=) c.1092C>T (p.Tyr364=) | dbSNP gnomAD v4 |
1 | g.229431541G>C | CA345144302 | ACTA1 | c.1014C>G (p.Tyr338Ter) c.957C>G (p.Tyr319Ter) c.723C>G (p.Tyr241Ter) c.1092C>G (p.Tyr364Ter) | dbSNP |
1 | g.229431541G= | CA1226125375 | ACTA1 | c.1014C= (p.Tyr338=) c.957C= (p.Tyr319=) c.723C= (p.Tyr241=) c.1092C= (p.Tyr364=) | |
1 | g.229431541G>T | CA345144306 | ACTA1 | c.1014C>A (p.Tyr338Ter) c.957C>A (p.Tyr319Ter) c.723C>A (p.Tyr241Ter) c.1092C>A (p.Tyr364Ter) | |
1 | g.229431542T>A | CA345144311 | ACTA1 | c.1013A>T (p.Tyr338Phe) c.956A>T (p.Tyr319Phe) c.722A>T (p.Tyr241Phe) c.1091A>T (p.Tyr364Phe) | |
1 | g.229431542T>C | CA345144314 | ACTA1 | c.1013A>G (p.Tyr338Cys) c.956A>G (p.Tyr319Cys) c.722A>G (p.Tyr241Cys) c.1091A>G (p.Tyr364Cys) | |
1 | g.229431542T>G | CA345144316 | ACTA1 | c.1013A>C (p.Tyr338Ser) c.956A>C (p.Tyr319Ser) c.722A>C (p.Tyr241Ser) c.1091A>C (p.Tyr364Ser) | |
1 | g.229431543A>C | CA345144320 | ACTA1 | c.1012T>G (p.Tyr338Asp) c.955T>G (p.Tyr319Asp) c.721T>G (p.Tyr241Asp) c.1090T>G (p.Tyr364Asp) | |
1 | g.229431543A>G | CA345144322 | ACTA1 | c.1012T>C (p.Tyr338His) c.955T>C (p.Tyr319His) c.721T>C (p.Tyr241His) c.1090T>C (p.Tyr364His) | |
1 | g.229431543A>T | CA345144330 | ACTA1 | c.1012T>A (p.Tyr338Asn) c.955T>A (p.Tyr319Asn) c.721T>A (p.Tyr241Asn) c.1090T>A (p.Tyr364Asn) | |
1 | g.229431544C>A | CA345144336 | ACTA1 | c.1011G>T (p.Glu337Asp) c.954G>T (p.Glu318Asp) c.720G>T (p.Glu240Asp) c.1089G>T (p.Glu363Asp) | |
1 | g.229431544C>G | CA345144338 | ACTA1 | c.1011G>C (p.Glu337Asp) c.954G>C (p.Glu318Asp) c.720G>C (p.Glu240Asp) c.1089G>C (p.Glu363Asp) | |
1 | g.229431544C>T | CA423754830 | ACTA1 | c.1011G>A (p.Glu337=) c.954G>A (p.Glu318=) c.720G>A (p.Glu240=) c.1089G>A (p.Glu363=) | |
1 | g.229431545T>A | CA345144342 | ACTA1 | c.1010A>T (p.Glu337Val) c.953A>T (p.Glu318Val) c.719A>T (p.Glu240Val) c.1088A>T (p.Glu363Val) | |
1 | g.229431545T>C | CA345144343 | ACTA1 | c.1010A>G (p.Glu337Gly) c.953A>G (p.Glu318Gly) c.719A>G (p.Glu240Gly) c.1088A>G (p.Glu363Gly) | gnomAD v4 |
1 | g.229431545T>G | CA345144345 | ACTA1 | c.1010A>C (p.Glu337Ala) c.953A>C (p.Glu318Ala) c.719A>C (p.Glu240Ala) c.1088A>C (p.Glu363Ala) | gnomAD v4 |
1 | g.229431546C>A | CA345144352 | ACTA1 | c.1009G>T (p.Glu337Ter) c.952G>T (p.Glu318Ter) c.718G>T (p.Glu240Ter) c.1087G>T (p.Glu363Ter) | |
1 | g.229431546C>G | CA345144353 | ACTA1 | c.1009G>C (p.Glu337Gln) c.952G>C (p.Glu318Gln) c.718G>C (p.Glu240Gln) c.1087G>C (p.Glu363Gln) | |
1 | g.229431546C>T | CA345144350 | ACTA1 | c.1009G>A (p.Glu337Lys) c.952G>A (p.Glu318Lys) c.718G>A (p.Glu240Lys) c.1087G>A (p.Glu363Lys) | |
1 | g.229431547C>A | CA345144356 | ACTA1 | c.1008G>T (p.Gln336His) c.951G>T (p.Gln317His) c.717G>T (p.Gln239His) c.1086G>T (p.Gln362His) | |
1 | g.229431547C>G | CA345144359 | ACTA1 | c.1008G>C (p.Gln336His) c.951G>C (p.Gln317His) c.717G>C (p.Gln239His) c.1086G>C (p.Gln362His) | |
1 | g.229431547C>T | CA423754835 | ACTA1 | c.1008G>A (p.Gln336=) c.951G>A (p.Gln317=) c.717G>A (p.Gln239=) c.1086G>A (p.Gln362=) | gnomAD v4 |
1 | g.229431548T>A | CA345144361 | ACTA1 | c.1007A>T (p.Gln336Leu) c.950A>T (p.Gln317Leu) c.716A>T (p.Gln239Leu) c.1085A>T (p.Gln362Leu) | |
1 | g.229431548T>C | CA345144362 | ACTA1 | c.1007A>G (p.Gln336Arg) c.950A>G (p.Gln317Arg) c.716A>G (p.Gln239Arg) c.1085A>G (p.Gln362Arg) | |
1 | g.229431548T>G | CA345144365 | ACTA1 | c.1007A>C (p.Gln336Pro) c.950A>C (p.Gln317Pro) c.716A>C (p.Gln239Pro) c.1085A>C (p.Gln362Pro) | |
1 | g.229431549G>A | CA345144370 | ACTA1 | c.1006C>T (p.Gln336Ter) c.949C>T (p.Gln317Ter) c.715C>T (p.Gln239Ter) c.1084C>T (p.Gln362Ter) | |
1 | g.229431549G>C | CA345144374 | ACTA1 | c.1006C>G (p.Gln336Glu) c.949C>G (p.Gln317Glu) c.715C>G (p.Gln239Glu) c.1084C>G (p.Gln362Glu) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.229431549G= | CA1226125376 | ACTA1 | c.1006C= (p.Gln336=) c.949C= (p.Gln317=) c.715C= (p.Gln239=) c.1084C= (p.Gln362=) | |
1 | g.229431549G>T | CA345144377 | ACTA1 | c.1006C>A (p.Gln336Lys) c.949C>A (p.Gln317Lys) c.715C>A (p.Gln239Lys) c.1084C>A (p.Gln362Lys) | |
1 | g.229431550C>A | CA345144380 | ACTA1 | c.1005G>T (p.Lys335Asn) c.948G>T (p.Lys316Asn) c.714G>T (p.Lys238Asn) c.1083G>T (p.Lys361Asn) | |
1 | g.229431550C= | CA1226125377 | ACTA1 | c.1005G= (p.Lys335=) c.948G= (p.Lys316=) c.714G= (p.Lys238=) c.1083G= (p.Lys361=) | |
1 | g.229431550C>G | CA345144384 | ACTA1 | c.1005G>C (p.Lys335Asn) c.948G>C (p.Lys316Asn) c.714G>C (p.Lys238Asn) c.1083G>C (p.Lys361Asn) | |
1 | g.229431550C>T | CA423754841 | ACTA1 | c.1005G>A (p.Lys335=) c.948G>A (p.Lys316=) c.714G>A (p.Lys238=) c.1083G>A (p.Lys361=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431551T>A | CA345144388 | ACTA1 | c.1004A>T (p.Lys335Met) c.947A>T (p.Lys316Met) c.713A>T (p.Lys238Met) c.1082A>T (p.Lys361Met) | |
1 | g.229431551T>C | CA1442709 | ACTA1 | c.1004A>G (p.Lys335Arg) c.947A>G (p.Lys316Arg) c.713A>G (p.Lys238Arg) c.1082A>G (p.Lys361Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431551T>G | CA345144392 | ACTA1 | c.1004A>C (p.Lys335Thr) c.947A>C (p.Lys316Thr) c.713A>C (p.Lys238Thr) c.1082A>C (p.Lys361Thr) | |
1 | g.229431551T= | CA1226125378 | ACTA1 | c.1004A= (p.Lys335=) c.947A= (p.Lys316=) c.713A= (p.Lys238=) c.1082A= (p.Lys361=) | |
1 | g.229431552T>A | CA345144404 | ACTA1 | c.1003A>T (p.Lys335Ter) c.946A>T (p.Lys316Ter) c.712A>T (p.Lys238Ter) c.1081A>T (p.Lys361Ter) | |
1 | g.229431552T>C | CA345144399 | ACTA1 | c.1003A>G (p.Lys335Glu) c.946A>G (p.Lys316Glu) c.712A>G (p.Lys238Glu) c.1081A>G (p.Lys361Glu) | |
1 | g.229431552T>G | CA345144398 | ACTA1 | c.1003A>C (p.Lys335Gln) c.946A>C (p.Lys316Gln) c.712A>C (p.Lys238Gln) c.1081A>C (p.Lys361Gln) | |
1 | g.229431553G>A | CA423754795 | ACTA1 | c.1002C>T (p.Thr334=) c.945C>T (p.Thr315=) c.711C>T (p.Thr237=) c.1080C>T (p.Thr360=) | |
1 | g.229431553G>C | CA423754796 | ACTA1 | c.1002C>G (p.Thr334=) c.945C>G (p.Thr315=) c.711C>G (p.Thr237=) c.1080C>G (p.Thr360=) | |
1 | g.229431553G>T | CA423754797 | ACTA1 | c.1002C>A (p.Thr334=) c.945C>A (p.Thr315=) c.711C>A (p.Thr237=) c.1080C>A (p.Thr360=) | |
1 | g.229431554G>A | CA345144407 | ACTA1 | c.1001C>T (p.Thr334Ile) c.944C>T (p.Thr315Ile) c.710C>T (p.Thr237Ile) c.1079C>T (p.Thr360Ile) | |
1 | g.229431554G>C | CA345144409 | ACTA1 | c.1001C>G (p.Thr334Ser) c.944C>G (p.Thr315Ser) c.710C>G (p.Thr237Ser) c.1079C>G (p.Thr360Ser) | |
1 | g.229431554G>T | CA345144412 | ACTA1 | c.1001C>A (p.Thr334Asn) c.944C>A (p.Thr315Asn) c.710C>A (p.Thr237Asn) c.1079C>A (p.Thr360Asn) | |
1 | g.229431555T>A | CA345144413 | ACTA1 | c.1000A>T (p.Thr334Ser) c.943A>T (p.Thr315Ser) c.709A>T (p.Thr237Ser) c.1078A>T (p.Thr360Ser) | dbSNP |
1 | g.229431555T>C | CA345144414 | ACTA1 | c.1000A>G (p.Thr334Ala) c.943A>G (p.Thr315Ala) c.709A>G (p.Thr237Ala) c.1078A>G (p.Thr360Ala) | |
1 | g.229431555T>G | CA345144415 | ACTA1 | c.1000A>C (p.Thr334Pro) c.943A>C (p.Thr315Pro) c.709A>C (p.Thr237Pro) c.1078A>C (p.Thr360Pro) | |
1 | g.229431555T= | CA1226125379 | ACTA1 | c.1000A= (p.Thr334=) c.943A= (p.Thr315=) c.709A= (p.Thr237=) c.1078A= (p.Thr360=) | |
1 | g.229431556G>A | CA423754798 | ACTA1 | c.999C>T (p.Ile333=) c.942C>T (p.Ile314=) c.708C>T (p.Ile236=) c.1077C>T (p.Ile359=) | |
1 | g.229431556G>C | CA345144417 | ACTA1 | c.999C>G (p.Ile333Met) c.942C>G (p.Ile314Met) c.708C>G (p.Ile236Met) c.1077C>G (p.Ile359Met) | |
1 | g.229431556G>T | CA423754800 | ACTA1 | c.999C>A (p.Ile333=) c.942C>A (p.Ile314=) c.708C>A (p.Ile236=) c.1077C>A (p.Ile359=) | |
1 | g.229431557A>C | CA345144421 | ACTA1 | c.998T>G (p.Ile333Ser) c.941T>G (p.Ile314Ser) c.707T>G (p.Ile236Ser) c.1076T>G (p.Ile359Ser) | |
1 | g.229431557A>G | CA345144423 | ACTA1 | c.998T>C (p.Ile333Thr) c.941T>C (p.Ile314Thr) c.707T>C (p.Ile236Thr) c.1076T>C (p.Ile359Thr) | |
1 | g.229431557A>T | CA345144426 | ACTA1 | c.998T>A (p.Ile333Asn) c.941T>A (p.Ile314Asn) c.707T>A (p.Ile236Asn) c.1076T>A (p.Ile359Asn) | |
1 | g.229431558T>A | CA345144427 | ACTA1 | c.997A>T (p.Ile333Phe) c.940A>T (p.Ile314Phe) c.706A>T (p.Ile236Phe) c.1075A>T (p.Ile359Phe) | |
1 | g.229431558T>C | CA345144440 | ACTA1 | c.997A>G (p.Ile333Val) c.940A>G (p.Ile314Val) c.706A>G (p.Ile236Val) c.1075A>G (p.Ile359Val) | ClinVar |
1 | g.229431558T>G | CA258138 | ACTA1 | c.997A>C (p.Ile333Leu) c.940A>C (p.Ile314Leu) c.706A>C (p.Ile236Leu) c.1075A>C (p.Ile359Leu) | ClinVar dbSNP |
1 | g.229431558T= | CA1141581370 | ACTA1 | c.997A= (p.Ile333=) c.940A= (p.Ile314=) c.706A= (p.Ile236=) c.1075A= (p.Ile359=) | |
1 | g.229431559C>A | CA269775 | ACTA1 | c.996G>T (p.Trp332Cys) c.939G>T (p.Trp313Cys) c.705G>T (p.Trp235Cys) c.1074G>T (p.Trp358Cys) | ClinVar dbSNP |
1 | g.229431559C= | CA1148225031 | ACTA1 | c.996G= (p.Trp332=) c.939G= (p.Trp313=) c.705G= (p.Trp235=) c.1074G= (p.Trp358=) | |
1 | g.229431559C>G | CA345144451 | ACTA1 | c.996G>C (p.Trp332Cys) c.939G>C (p.Trp313Cys) c.705G>C (p.Trp235Cys) c.1074G>C (p.Trp358Cys) | |
1 | g.229431559C>T | CA345144447 | ACTA1 | c.996G>A (p.Trp332Ter) c.939G>A (p.Trp313Ter) c.705G>A (p.Trp235Ter) c.1074G>A (p.Trp358Ter) | |
1 | g.229431560C>A | CA345144454 | ACTA1 | c.995G>T (p.Trp332Leu) c.938G>T (p.Trp313Leu) c.704G>T (p.Trp235Leu) c.1073G>T (p.Trp358Leu) | |
1 | g.229431560C>G | CA345144460 | ACTA1 | c.995G>C (p.Trp332Ser) c.938G>C (p.Trp313Ser) c.704G>C (p.Trp235Ser) c.1073G>C (p.Trp358Ser) | |
1 | g.229431560C>T | CA345144456 | ACTA1 | c.995G>A (p.Trp332Ter) c.938G>A (p.Trp313Ter) c.704G>A (p.Trp235Ter) c.1073G>A (p.Trp358Ter) | gnomAD v4 |
1 | g.229431561A>C | CA345144466 | ACTA1 | c.994T>G (p.Trp332Gly) c.937T>G (p.Trp313Gly) c.703T>G (p.Trp235Gly) c.1072T>G (p.Trp358Gly) | |
1 | g.229431561A>G | CA345144469 | ACTA1 | c.994T>C (p.Trp332Arg) c.937T>C (p.Trp313Arg) c.703T>C (p.Trp235Arg) c.1072T>C (p.Trp358Arg) | |
1 | g.229431561A>T | CA345144472 | ACTA1 | c.994T>A (p.Trp332Arg) c.937T>A (p.Trp313Arg) c.703T>A (p.Trp235Arg) c.1072T>A (p.Trp358Arg) | |
1 | g.229431562C>A | CA345144475 | ACTA1 | c.993G>T (p.Met331Ile) c.936G>T (p.Met312Ile) c.702G>T (p.Met234Ile) c.1071G>T (p.Met357Ile) | |
1 | g.229431562C= | CA1148239652 | ACTA1 | c.993G= (p.Met331=) c.936G= (p.Met312=) c.702G= (p.Met234=) c.1071G= (p.Met357=) | |
1 | g.229431562C>G | CA345144479 | ACTA1 | c.993G>C (p.Met331Ile) c.936G>C (p.Met312Ile) c.702G>C (p.Met234Ile) c.1071G>C (p.Met357Ile) | ClinVar dbSNP gnomAD v4 |
1 | g.229431562C>T | CA1442710 | ACTA1 | c.993G>A (p.Met331Ile) c.936G>A (p.Met312Ile) c.702G>A (p.Met234Ile) c.1071G>A (p.Met357Ile) | dbSNP ExAC gnomAD v2 |
1 | g.229431563A= | CA1147059542 | ACTA1 | c.992T= (p.Met331=) c.935T= (p.Met312=) c.701T= (p.Met234=) c.1070T= (p.Met357=) | |
1 | g.229431563A>C | CA345144484 | ACTA1 | c.992T>G (p.Met331Arg) c.935T>G (p.Met312Arg) c.701T>G (p.Met234Arg) c.1070T>G (p.Met357Arg) | |
1 | g.229431563A>G | CA1442711 | ACTA1 | c.992T>C (p.Met331Thr) c.935T>C (p.Met312Thr) c.701T>C (p.Met234Thr) c.1070T>C (p.Met357Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 |
1 | g.229431563A>T | CA345144492 | ACTA1 | c.992T>A (p.Met331Lys) c.935T>A (p.Met312Lys) c.701T>A (p.Met234Lys) c.1070T>A (p.Met357Lys) | |
1 | g.229431564T>A | CA345144496 | ACTA1 | c.991A>T (p.Met331Leu) c.934A>T (p.Met312Leu) c.700A>T (p.Met234Leu) c.1069A>T (p.Met357Leu) | |
1 | g.229431564T>C | CA345144500 | ACTA1 | c.991A>G (p.Met331Val) c.934A>G (p.Met312Val) c.700A>G (p.Met234Val) c.1069A>G (p.Met357Val) | ClinVar dbSNP |
1 | g.229431564T>G | CA345144502 | ACTA1 | c.991A>C (p.Met331Leu) c.934A>C (p.Met312Leu) c.700A>C (p.Met234Leu) c.1069A>C (p.Met357Leu) | |
1 | g.229431564T= | CA1226125380 | ACTA1 | c.991A= (p.Met331=) c.934A= (p.Met312=) c.700A= (p.Met234=) c.1069A= (p.Met357=) | |
1 | g.229431565C>A | CA345144509 | ACTA1 | c.991-1G>T (n.991-1G>T) c.933G>T (p.Gln311His) c.699G>T (p.Gln233His) c.1068G>T (p.Gln356His) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.229431565C= | CA1226125381 | ACTA1 | c.991-1G= (n.991-1G=) c.933G= (p.Gln311=) c.699G= (p.Gln233=) c.1068G= (p.Gln356=) | |
1 | g.229431565C>G | CA345144505 | ACTA1 | c.991-1G>C (n.991-1G>C) c.933G>C (p.Gln311His) c.699G>C (p.Gln233His) c.1068G>C (p.Gln356His) | |
1 | g.229431565C>T | CA423754805 | ACTA1 | c.991-1G>A (n.991-1G>A) c.933G>A (p.Gln311=) c.699G>A (p.Gln233=) c.1068G>A (p.Gln356=) | |
1 | g.229431566T>A | CA345144513 | ACTA1 | c.991-2A>T (n.991-2A>T) c.932A>T (p.Gln311Leu) c.698A>T (p.Gln233Leu) c.1067A>T (p.Gln356Leu) | |
1 | g.229431566T>C | CA345144516 | ACTA1 | c.991-2A>G (n.991-2A>G) c.932A>G (p.Gln311Arg) c.698A>G (p.Gln233Arg) c.1067A>G (p.Gln356Arg) | dbSNP |
1 | g.229431566T>G | CA345144518 | ACTA1 | c.991-2A>C (n.991-2A>C) c.932A>C (p.Gln311Pro) c.698A>C (p.Gln233Pro) c.1067A>C (p.Gln356Pro) | |
1 | g.229431566T= | CA1226125382 | ACTA1 | c.991-2A= (n.991-2A=) c.932A= (p.Gln311=) c.698A= (p.Gln233=) c.1067A= (p.Gln356=) | |
1 | g.229431567G>A | CA345144523 | ACTA1 | c.991-3C>T (n.991-3C>T) c.931C>T (p.Gln311Ter) c.697C>T (p.Gln233Ter) c.1066C>T (p.Gln356Ter) | |
1 | g.229431567G>C | CA345144526 | ACTA1 | c.991-3C>G (n.991-3C>G) c.931C>G (p.Gln311Glu) c.697C>G (p.Gln233Glu) c.1066C>G (p.Gln356Glu) | |
1 | g.229431567G>T | CA345144528 | ACTA1 | c.991-3C>A (n.991-3C>A) c.931C>A (p.Gln311Lys) c.697C>A (p.Gln233Lys) c.1066C>A (p.Gln356Lys) | |
1 | g.229431568C>A | CA345144531 | ACTA1 | c.991-4G>T (n.991-4G>T) c.930G>T (p.Gln310His) c.696G>T (p.Gln232His) c.1065G>T (p.Gln355His) | |
1 | g.229431568C= | CA1144093655 | ACTA1 | c.991-4G= (n.991-4G=) c.930G= (p.Gln310=) c.696G= (p.Gln232=) c.1065G= (p.Gln355=) | |
1 | g.229431568C>G | CA345144535 | ACTA1 | c.991-4G>C (n.991-4G>C) c.930G>C (p.Gln310His) c.696G>C (p.Gln232His) c.1065G>C (p.Gln355His) | |
1 | g.229431568C>T | CA1442712 | ACTA1 | c.991-4G>A (n.991-4G>A) c.930G>A (p.Gln310=) c.696G>A (p.Gln232=) c.1065G>A (p.Gln355=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431569T>A | CA345144540 | ACTA1 | c.991-5A>T (n.991-5A>T) c.929A>T (p.Gln310Leu) c.695A>T (p.Gln232Leu) c.1064A>T (p.Gln355Leu) | dbSNP gnomAD v2 |
1 | g.229431569T>C | CA345144542 | ACTA1 | c.991-5A>G (n.991-5A>G) c.929A>G (p.Gln310Arg) c.695A>G (p.Gln232Arg) c.1064A>G (p.Gln355Arg) | |
1 | g.229431569T>G | CA345144545 | ACTA1 | c.991-5A>C (n.991-5A>C) c.929A>C (p.Gln310Pro) c.695A>C (p.Gln232Pro) c.1064A>C (p.Gln355Pro) | |
1 | g.229431569T= | CA1226125383 | ACTA1 | c.991-5A= (n.991-5A=) c.929A= (p.Gln310=) c.695A= (p.Gln232=) c.1064A= (p.Gln355=) | |
1 | g.229431570G>A | CA345144548 | ACTA1 | c.991-6C>T (n.991-6C>T) c.928C>T (p.Gln310Ter) c.694C>T (p.Gln232Ter) c.1063C>T (p.Gln355Ter) | |
1 | g.229431570G>C | CA345144547 | ACTA1 | c.991-6C>G (n.991-6C>G) c.928C>G (p.Gln310Glu) c.694C>G (p.Gln232Glu) c.1063C>G (p.Gln355Glu) | |
1 | g.229431570G= | CA1226125384 | ACTA1 | c.991-6C= (n.991-6C=) c.928C= (p.Gln310=) c.694C= (p.Gln232=) c.1063C= (p.Gln355=) | |
1 | g.229431570G>T | CA345144546 | ACTA1 | c.991-6C>A (n.991-6C>A) c.928C>A (p.Gln310Lys) c.694C>A (p.Gln232Lys) c.1063C>A (p.Gln355Lys) | dbSNP gnomAD v2 |
1 | g.229431571G>A | CA423754810 | ACTA1 | c.991-7C>T (n.991-7C>T) c.927C>T (p.Phe309=) c.693C>T (p.Phe231=) c.1062C>T (p.Phe354=) | |
1 | g.229431571G>C | CA345144551 | ACTA1 | c.991-7C>G (n.991-7C>G) c.927C>G (p.Phe309Leu) c.693C>G (p.Phe231Leu) c.1062C>G (p.Phe354Leu) | |
1 | g.229431571G>T | CA345144549 | ACTA1 | c.991-7C>A (n.991-7C>A) c.927C>A (p.Phe309Leu) c.693C>A (p.Phe231Leu) c.1062C>A (p.Phe354Leu) | |
1 | g.229431572A>C | CA345144553 | ACTA1 | c.991-8T>G (n.991-8T>G) c.926T>G (p.Phe309Cys) c.692T>G (p.Phe231Cys) c.1061T>G (p.Phe354Cys) | |
1 | g.229431572A>G | CA345144556 | ACTA1 | c.991-8T>C (n.991-8T>C) c.926T>C (p.Phe309Ser) c.692T>C (p.Phe231Ser) c.1061T>C (p.Phe354Ser) | ClinVar |
1 | g.229431572A>T | CA345144560 | ACTA1 | c.991-8T>A (n.991-8T>A) c.926T>A (p.Phe309Tyr) c.692T>A (p.Phe231Tyr) c.1061T>A (p.Phe354Tyr) | |
1 | g.229431573A>C | CA345144564 | ACTA1 | c.991-9T>G (n.991-9T>G) c.925T>G (p.Phe309Val) c.691T>G (p.Phe231Val) c.1060T>G (p.Phe354Val) | |
1 | g.229431573A>G | CA345144566 | ACTA1 | c.991-9T>C (n.991-9T>C) c.925T>C (p.Phe309Leu) c.691T>C (p.Phe231Leu) c.1060T>C (p.Phe354Leu) | ClinVar dbSNP |
1 | g.229431573A>T | CA345144568 | ACTA1 | c.991-9T>A (n.991-9T>A) c.925T>A (p.Phe309Ile) c.691T>A (p.Phe231Ile) c.1060T>A (p.Phe354Ile) | |
1 | g.229431576_229431592del | CA2573132002 | ACTA1 | c.991-25_991-9del (n.991-25_991-9del) c.909_925del (p.Ala304ProfsTer?) c.675_691del (p.Ala226ProfsTer?) c.1044_1060del (p.Ala349ProfsTer?) | ClinVar dbSNP |
1 | g.229431574G>A | CA423754811 | ACTA1 | c.991-10C>T (n.991-10C>T) c.924C>T (p.Thr308=) c.690C>T (p.Thr230=) c.1059C>T (p.Thr353=) | |
1 | g.229431574G>C | CA423754812 | ACTA1 | c.991-10C>G (n.991-10C>G) c.924C>G (p.Thr308=) c.690C>G (p.Thr230=) c.1059C>G (p.Thr353=) | |
1 | g.229431574G>T | CA423754813 | ACTA1 | c.991-10C>A (n.991-10C>A) c.924C>A (p.Thr308=) c.690C>A (p.Thr230=) c.1059C>A (p.Thr353=) | |
1 | g.229431575G>A | CA345144571 | ACTA1 | c.991-11C>T (n.991-11C>T) c.923C>T (p.Thr308Ile) c.689C>T (p.Thr230Ile) c.1058C>T (p.Thr353Ile) | |
1 | g.229431575G>C | CA345144575 | ACTA1 | c.991-11C>G (n.991-11C>G) c.923C>G (p.Thr308Ser) c.689C>G (p.Thr230Ser) c.1058C>G (p.Thr353Ser) | |
1 | g.229431575G>T | CA345144577 | ACTA1 | c.991-11C>A (n.991-11C>A) c.923C>A (p.Thr308Asn) c.689C>A (p.Thr230Asn) c.1058C>A (p.Thr353Asn) | |
1 | g.229431576T>A | CA345144578 | ACTA1 | c.991-12A>T (n.991-12A>T) c.922A>T (p.Thr308Ser) c.688A>T (p.Thr230Ser) c.1057A>T (p.Thr353Ser) | |
1 | g.229431576T>C | CA345144580 | ACTA1 | c.991-12A>G (n.991-12A>G) c.922A>G (p.Thr308Ala) c.688A>G (p.Thr230Ala) c.1057A>G (p.Thr353Ala) | ClinVar dbSNP |
1 | g.229431576T>G | CA345144582 | ACTA1 | c.991-12A>C (n.991-12A>C) c.922A>C (p.Thr308Pro) c.688A>C (p.Thr230Pro) c.1057A>C (p.Thr353Pro) | |
1 | g.229431576T= | CA1226125385 | ACTA1 | c.991-12A= (n.991-12A=) c.922A= (p.Thr308=) c.688A= (p.Thr230=) c.1057A= (p.Thr353=) | |
1 | g.229431577G>A | CA423754815 | ACTA1 | c.991-13C>T (n.991-13C>T) c.921C>T (p.Ser307=) c.687C>T (p.Ser229=) c.1056C>T (p.Ser352=) | dbSNP gnomAD v4 |
1 | g.229431577G>C | CA423754817 | ACTA1 | c.991-13C>G (n.991-13C>G) c.921C>G (p.Ser307=) c.687C>G (p.Ser229=) c.1056C>G (p.Ser352=) | |
1 | g.229431577G= | CA1226125386 | ACTA1 | c.991-13C= (n.991-13C=) c.921C= (p.Ser307=) c.687C= (p.Ser229=) c.1056C= (p.Ser352=) | |
1 | g.229431577G>T | CA423754816 | ACTA1 | c.991-13C>A (n.991-13C>A) c.921C>A (p.Ser307=) c.687C>A (p.Ser229=) c.1056C>A (p.Ser352=) | |
1 | g.229431577_229431578insTTTTTTAAT | CA1013145097 | ACTA1 | c.991-14_991-13insATTAAAAAA (n.991-14_991-13insATTAAAAAA) c.920_921insATTAAAAAA (p.Ser307_Thr308insLeuLysAsn) c.686_687insATTAAAAAA (p.Ser229_Thr230insLeuLysAsn) c.1055_1056insATTAAAAAA (p.Ser352_Thr353insLeuLysAsn) | gnomAD v3 gnomAD v4 |
1 | g.229431578G>A | CA345144589 | ACTA1 | c.991-14C>T (n.991-14C>T) c.920C>T (p.Ser307Phe) c.686C>T (p.Ser229Phe) c.1055C>T (p.Ser352Phe) | ClinVar COSMIC |
1 | g.229431578G>C | CA345144585 | ACTA1 | c.991-14C>G (n.991-14C>G) c.920C>G (p.Ser307Cys) c.686C>G (p.Ser229Cys) c.1055C>G (p.Ser352Cys) | |
1 | g.229431578G>T | CA345144588 | ACTA1 | c.991-14C>A (n.991-14C>A) c.920C>A (p.Ser307Tyr) c.686C>A (p.Ser229Tyr) c.1055C>A (p.Ser352Tyr) | |
1 | g.229431579A= | CA1226125387 | ACTA1 | c.991-15T= (n.991-15T=) c.919T= (p.Ser307=) c.685T= (p.Ser229=) c.1054T= (p.Ser352=) | |
1 | g.229431579A>C | CA345144593 | ACTA1 | c.991-15T>G (n.991-15T>G) c.919T>G (p.Ser307Ala) c.685T>G (p.Ser229Ala) c.1054T>G (p.Ser352Ala) | |
1 | g.229431579A>G | CA345144596 | ACTA1 | c.991-15T>C (n.991-15T>C) c.919T>C (p.Ser307Pro) c.685T>C (p.Ser229Pro) c.1054T>C (p.Ser352Pro) | ClinVar dbSNP |
1 | g.229431579A>T | CA345144598 | ACTA1 | c.991-15T>A (n.991-15T>A) c.919T>A (p.Ser307Thr) c.685T>A (p.Ser229Thr) c.1054T>A (p.Ser352Thr) | |
1 | g.229431579_229431580insTA | CA1013145101 | ACTA1 | c.991-15_991-14insAT (n.991-15_991-14insAT) c.919_920insAT (p.Ser307TyrfsTer?) c.685_686insAT (p.Ser229TyrfsTer?) c.1054_1055insAT (p.Ser352TyrfsTer?) | gnomAD v3 gnomAD v4 |
1 | g.229431580C>A | CA423754820 | ACTA1 | c.991-16G>T (n.991-16G>T) c.918G>T (p.Leu306=) c.684G>T (p.Leu228=) c.1053G>T (p.Leu351=) | |
1 | g.229431580C= | CA1226125388 | ACTA1 | c.991-16G= (n.991-16G=) c.918G= (p.Leu306=) c.684G= (p.Leu228=) c.1053G= (p.Leu351=) | |
1 | g.229431580C>G | CA423754818 | ACTA1 | c.991-16G>C (n.991-16G>C) c.918G>C (p.Leu306=) c.684G>C (p.Leu228=) c.1053G>C (p.Leu351=) | dbSNP |
1 | g.229431580C>T | CA423754819 | ACTA1 | c.991-16G>A (n.991-16G>A) c.918G>A (p.Leu306=) c.684G>A (p.Leu228=) c.1053G>A (p.Leu351=) | |
1 | g.229431581A>C | CA345144601 | ACTA1 | c.991-17T>G (n.991-17T>G) c.917T>G (p.Leu306Arg) c.683T>G (p.Leu228Arg) c.1052T>G (p.Leu351Arg) | |
1 | g.229431581A>G | CA345144603 | ACTA1 | c.991-17T>C (n.991-17T>C) c.917T>C (p.Leu306Pro) c.683T>C (p.Leu228Pro) c.1052T>C (p.Leu351Pro) | gnomAD v3 gnomAD v4 |
1 | g.229431581A>T | CA345144607 | ACTA1 | c.991-17T>A (n.991-17T>A) c.917T>A (p.Leu306Gln) c.683T>A (p.Leu228Gln) c.1052T>A (p.Leu351Gln) | |
1 | g.229431582G>A | CA423754821 | ACTA1 | c.991-18C>T (n.991-18C>T) c.916C>T (p.Leu306=) c.682C>T (p.Leu228=) c.1051C>T (p.Leu351=) | dbSNP gnomAD v4 |
1 | g.229431582G>C | CA345144609 | ACTA1 | c.991-18C>G (n.991-18C>G) c.916C>G (p.Leu306Val) c.682C>G (p.Leu228Val) c.1051C>G (p.Leu351Val) | |
1 | g.229431582G= | CA1226125389 | ACTA1 | c.991-18C= (n.991-18C=) c.916C= (p.Leu306=) c.682C= (p.Leu228=) c.1051C= (p.Leu351=) | |
1 | g.229431582G>T | CA345144612 | ACTA1 | c.991-18C>A (n.991-18C>A) c.916C>A (p.Leu306Met) c.682C>A (p.Leu228Met) c.1051C>A (p.Leu351Met) | |
1 | g.229431583C>A | CA1442713 | ACTA1 | c.991-19G>T (n.991-19G>T) c.915G>T (p.Ser305=) c.681G>T (p.Ser227=) c.1050G>T (p.Ser350=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431583C= | CA1148416440 | ACTA1 | c.991-19G= (n.991-19G=) c.915G= (p.Ser305=) c.681G= (p.Ser227=) c.1050G= (p.Ser350=) | |
1 | g.229431583C>G | CA423754823 | ACTA1 | c.991-19G>C (n.991-19G>C) c.915G>C (p.Ser305=) c.681G>C (p.Ser227=) c.1050G>C (p.Ser350=) | dbSNP |
1 | g.229431583C>T | CA423754822 | ACTA1 | c.991-19G>A (n.991-19G>A) c.915G>A (p.Ser305=) c.681G>A (p.Ser227=) c.1050G>A (p.Ser350=) | |
1 | g.229431584G>A | CA345144616 | ACTA1 | c.991-20C>T (n.991-20C>T) c.914C>T (p.Ser305Leu) c.680C>T (p.Ser227Leu) c.1049C>T (p.Ser350Leu) | ClinVar dbSNP |
1 | g.229431584G>C | CA345144619 | ACTA1 | c.991-20C>G (n.991-20C>G) c.914C>G (p.Ser305Trp) c.680C>G (p.Ser227Trp) c.1049C>G (p.Ser350Trp) | ClinVar COSMIC |
1 | g.229431584G>T | CA345144622 | ACTA1 | c.991-20C>A (n.991-20C>A) c.914C>A (p.Ser305Ter) c.680C>A (p.Ser227Ter) c.1049C>A (p.Ser350Ter) | |
1 | g.229431585A>C | CA345144628 | ACTA1 | c.991-21T>G (n.991-21T>G) c.913T>G (p.Ser305Ala) c.679T>G (p.Ser227Ala) c.1048T>G (p.Ser350Ala) | |
1 | g.229431585A>G | CA345144631 | ACTA1 | c.991-21T>C (n.991-21T>C) c.913T>C (p.Ser305Pro) c.679T>C (p.Ser227Pro) c.1048T>C (p.Ser350Pro) | |
1 | g.229431585A>T | CA345144626 | ACTA1 | c.991-21T>A (n.991-21T>A) c.913T>A (p.Ser305Thr) c.679T>A (p.Ser227Thr) c.1048T>A (p.Ser350Thr) | |
1 | g.229431586G>A | CA423754824 | ACTA1 | c.991-22C>T (n.991-22C>T) c.912C>T (p.Ala304=) c.678C>T (p.Ala226=) c.1047C>T (p.Ala349=) | dbSNP |
1 | g.229431586G>C | CA423754825 | ACTA1 | c.991-22C>G (n.991-22C>G) c.912C>G (p.Ala304=) c.678C>G (p.Ala226=) c.1047C>G (p.Ala349=) | |
1 | g.229431586G= | CA1226125390 | ACTA1 | c.991-22C= (n.991-22C=) c.912C= (p.Ala304=) c.678C= (p.Ala226=) c.1047C= (p.Ala349=) | |
1 | g.229431586G>T | CA423754826 | ACTA1 | c.991-22C>A (n.991-22C>A) c.912C>A (p.Ala304=) c.678C>A (p.Ala226=) c.1047C>A (p.Ala349=) | dbSNP gnomAD v2 |
1 | g.229431586_229431587del | CA1013145112 | ACTA1 | c.991-23_991-22del (n.991-23_991-22del) c.911_912del (p.Ala304ValfsTer?) c.677_678del (p.Ala226ValfsTer?) c.1046_1047del (p.Ala349ValfsTer?) | gnomAD v3 gnomAD v4 |
1 | g.229431587G>A | CA345144633 | ACTA1 | c.991-23C>T (n.991-23C>T) c.911C>T (p.Ala304Val) c.677C>T (p.Ala226Val) c.1046C>T (p.Ala349Val) | ClinVar dbSNP |
1 | g.229431587G>C | CA345144639 | ACTA1 | c.991-23C>G (n.991-23C>G) c.911C>G (p.Ala304Gly) c.677C>G (p.Ala226Gly) c.1046C>G (p.Ala349Gly) | |
1 | g.229431587G= | CA1226125391 | ACTA1 | c.991-23C= (n.991-23C=) c.911C= (p.Ala304=) c.677C= (p.Ala226=) c.1046C= (p.Ala349=) | |
1 | g.229431587G>T | CA345144635 | ACTA1 | c.991-23C>A (n.991-23C>A) c.911C>A (p.Ala304Asp) c.677C>A (p.Ala226Asp) c.1046C>A (p.Ala349Asp) | |
1 | g.229431588C>A | CA345144642 | ACTA1 | c.991-24G>T (n.991-24G>T) c.910G>T (p.Ala304Ser) c.676G>T (p.Ala226Ser) c.1045G>T (p.Ala349Ser) | |
1 | g.229431588C= | CA1226125392 | ACTA1 | c.991-24G= (n.991-24G=) c.910G= (p.Ala304=) c.676G= (p.Ala226=) c.1045G= (p.Ala349=) | |
1 | g.229431588C>G | CA345144644 | ACTA1 | c.991-24G>C (n.991-24G>C) c.910G>C (p.Ala304Pro) c.676G>C (p.Ala226Pro) c.1045G>C (p.Ala349Pro) | |
1 | g.229431588C>T | CA345144647 | ACTA1 | c.991-24G>A (n.991-24G>A) c.910G>A (p.Ala304Thr) c.676G>A (p.Ala226Thr) c.1045G>A (p.Ala349Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431589C>A | CA423754827 | ACTA1 | c.991-25G>T (n.991-25G>T) c.909G>T (p.Leu303=) c.675G>T (p.Leu225=) c.1044G>T (p.Leu348=) | dbSNP |
1 | g.229431589C= | CA1226125393 | ACTA1 | c.991-25G= (n.991-25G=) c.909G= (p.Leu303=) c.675G= (p.Leu225=) c.1044G= (p.Leu348=) | |
1 | g.229431589C>G | CA423754828 | ACTA1 | c.991-25G>C (n.991-25G>C) c.909G>C (p.Leu303=) c.675G>C (p.Leu225=) c.1044G>C (p.Leu348=) | |
1 | g.229431589C>T | CA423754829 | ACTA1 | c.991-25G>A (n.991-25G>A) c.909G>A (p.Leu303=) c.675G>A (p.Leu225=) c.1044G>A (p.Leu348=) | |
1 | g.229431590A>C | CA345144650 | ACTA1 | c.991-26T>G (n.991-26T>G) c.908T>G (p.Leu303Arg) c.674T>G (p.Leu225Arg) c.1043T>G (p.Leu348Arg) | |
1 | g.229431590A>G | CA345144654 | ACTA1 | c.991-26T>C (n.991-26T>C) c.908T>C (p.Leu303Pro) c.674T>C (p.Leu225Pro) c.1043T>C (p.Leu348Pro) | |
1 | g.229431590A>T | CA345144656 | ACTA1 | c.991-26T>A (n.991-26T>A) c.908T>A (p.Leu303Gln) c.674T>A (p.Leu225Gln) c.1043T>A (p.Leu348Gln) | ClinVar dbSNP |
1 | g.229431591G>A | CA423754831 | ACTA1 | c.991-27C>T (n.991-27C>T) c.907C>T (p.Leu303=) c.673C>T (p.Leu225=) c.1042C>T (p.Leu348=) | dbSNP gnomAD v4 |
1 | g.229431591G>C | CA345144659 | ACTA1 | c.991-27C>G (n.991-27C>G) c.907C>G (p.Leu303Val) c.673C>G (p.Leu225Val) c.1042C>G (p.Leu348Val) | |
1 | g.229431591G= | CA1226125394 | ACTA1 | c.991-27C= (n.991-27C=) c.907C= (p.Leu303=) c.673C= (p.Leu225=) c.1042C= (p.Leu348=) | |
1 | g.229431591G>T | CA345144661 | ACTA1 | c.991-27C>A (n.991-27C>A) c.907C>A (p.Leu303Met) c.673C>A (p.Leu225Met) c.1042C>A (p.Leu348Met) | |
1 | g.229431591_229431598del | CA1013145118 | ACTA1 | c.991-34_991-27del (n.991-34_991-27del) c.900_907del (p.Ser301GlyfsTer?) c.666_673del (p.Ser223GlyfsTer?) c.1035_1042del (p.Ser346GlyfsTer?) | gnomAD v3 gnomAD v4 |
1 | g.229431592G>A | CA423754832 | ACTA1 | c.991-28C>T (n.991-28C>T) c.906C>T (p.Ile302=) c.672C>T (p.Ile224=) c.1041C>T (p.Ile347=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431592G>C | CA345144665 | ACTA1 | c.991-28C>G (n.991-28C>G) c.906C>G (p.Ile302Met) c.672C>G (p.Ile224Met) c.1041C>G (p.Ile347Met) | |
1 | g.229431592G= | CA1226125395 | ACTA1 | c.991-28C= (n.991-28C=) c.906C= (p.Ile302=) c.672C= (p.Ile224=) c.1041C= (p.Ile347=) | |
1 | g.229431592G>T | CA423754833 | ACTA1 | c.991-28C>A (n.991-28C>A) c.906C>A (p.Ile302=) c.672C>A (p.Ile224=) c.1041C>A (p.Ile347=) | |
1 | g.229431593A>C | CA345144669 | ACTA1 | c.991-29T>G (n.991-29T>G) c.905T>G (p.Ile302Ser) c.671T>G (p.Ile224Ser) c.1040T>G (p.Ile347Ser) | |
1 | g.229431593A>G | CA345144671 | ACTA1 | c.991-29T>C (n.991-29T>C) c.905T>C (p.Ile302Thr) c.671T>C (p.Ile224Thr) c.1040T>C (p.Ile347Thr) | |
1 | g.229431593A>T | CA345144674 | ACTA1 | c.991-29T>A (n.991-29T>A) c.905T>A (p.Ile302Asn) c.671T>A (p.Ile224Asn) c.1040T>A (p.Ile347Asn) | |
1 | g.229431594T>A | CA345144680 | ACTA1 | c.991-30A>T (n.991-30A>T) c.904A>T (p.Ile302Phe) c.670A>T (p.Ile224Phe) c.1039A>T (p.Ile347Phe) | |
1 | g.229431594T>C | CA345144684 | ACTA1 | c.991-30A>G (n.991-30A>G) c.904A>G (p.Ile302Val) c.670A>G (p.Ile224Val) c.1039A>G (p.Ile347Val) | |
1 | g.229431594T>G | CA345144683 | ACTA1 | c.991-30A>C (n.991-30A>C) c.904A>C (p.Ile302Leu) c.670A>C (p.Ile224Leu) c.1039A>C (p.Ile347Leu) | |
1 | g.229431595G>A | CA423754834 | ACTA1 | c.991-31C>T (n.991-31C>T) c.903C>T (p.Ser301=) c.669C>T (p.Ser223=) c.1038C>T (p.Ser346=) | gnomAD v4 |
1 | g.229431595G>C | CA423754837 | ACTA1 | c.991-31C>G (n.991-31C>G) c.903C>G (p.Ser301=) c.669C>G (p.Ser223=) c.1038C>G (p.Ser346=) | |
1 | g.229431595G>T | CA423754836 | ACTA1 | c.991-31C>A (n.991-31C>A) c.903C>A (p.Ser301=) c.669C>A (p.Ser223=) c.1038C>A (p.Ser346=) | |
1 | g.229431596G>A | CA345144689 | ACTA1 | c.991-32C>T (n.991-32C>T) c.902C>T (p.Ser301Phe) c.668C>T (p.Ser223Phe) c.1037C>T (p.Ser346Phe) | COSMIC |
1 | g.229431596G>C | CA345144691 | ACTA1 | c.991-32C>G (n.991-32C>G) c.902C>G (p.Ser301Cys) c.668C>G (p.Ser223Cys) c.1037C>G (p.Ser346Cys) | |
1 | g.229431596G>T | CA345144693 | ACTA1 | c.991-32C>A (n.991-32C>A) c.902C>A (p.Ser301Tyr) c.668C>A (p.Ser223Tyr) c.1037C>A (p.Ser346Tyr) | |
1 | g.229431597A>C | CA345144699 | ACTA1 | c.991-33T>G (n.991-33T>G) c.901T>G (p.Ser301Ala) c.667T>G (p.Ser223Ala) c.1036T>G (p.Ser346Ala) | |
1 | g.229431597A>G | CA345144702 | ACTA1 | c.991-33T>C (n.991-33T>C) c.901T>C (p.Ser301Pro) c.667T>C (p.Ser223Pro) c.1036T>C (p.Ser346Pro) | |
1 | g.229431597A>T | CA345144705 | ACTA1 | c.991-33T>A (n.991-33T>A) c.901T>A (p.Ser301Thr) c.667T>A (p.Ser223Thr) c.1036T>A (p.Ser346Thr) | |
1 | g.229431598G>A | CA423754838 | ACTA1 | c.991-34C>T (n.991-34C>T) c.900C>T (p.Gly300=) c.666C>T (p.Gly222=) c.1035C>T (p.Gly345=) | dbSNP |
1 | g.229431598G>C | CA423754840 | ACTA1 | c.991-34C>G (n.991-34C>G) c.900C>G (p.Gly300=) c.666C>G (p.Gly222=) c.1035C>G (p.Gly345=) | dbSNP gnomAD v2 |
1 | g.229431598G= | CA1226125396 | ACTA1 | c.991-34C= (n.991-34C=) c.900C= (p.Gly300=) c.666C= (p.Gly222=) c.1035C= (p.Gly345=) | |
1 | g.229431598G>T | CA423754839 | ACTA1 | c.991-34C>A (n.991-34C>A) c.900C>A (p.Gly300=) c.666C>A (p.Gly222=) c.1035C>A (p.Gly345=) | |
1 | g.229431599C>A | CA345144708 | ACTA1 | c.991-35G>T (n.991-35G>T) c.899G>T (p.Gly300Val) c.665G>T (p.Gly222Val) c.1034G>T (p.Gly345Val) | |
1 | g.229431599C>G | CA345144711 | ACTA1 | c.991-35G>C (n.991-35G>C) c.899G>C (p.Gly300Ala) c.665G>C (p.Gly222Ala) c.1034G>C (p.Gly345Ala) | |
1 | g.229431599C>T | CA345144714 | ACTA1 | c.991-35G>A (n.991-35G>A) c.899G>A (p.Gly300Asp) c.665G>A (p.Gly222Asp) c.1034G>A (p.Gly345Asp) | COSMIC |
1 | g.229431600C>A | CA345144722 | ACTA1 | c.991-36G>T (n.991-36G>T) c.898G>T (p.Gly300Cys) c.664G>T (p.Gly222Cys) c.1033G>T (p.Gly345Cys) | |
1 | g.229431600C>G | CA345144723 | ACTA1 | c.991-36G>C (n.991-36G>C) c.898G>C (p.Gly300Arg) c.664G>C (p.Gly222Arg) c.1033G>C (p.Gly345Arg) | |
1 | g.229431600C>T | CA345144718 | ACTA1 | c.991-36G>A (n.991-36G>A) c.898G>A (p.Gly300Ser) c.664G>A (p.Gly222Ser) c.1033G>A (p.Gly345Ser) | ClinVar gnomAD v4 |
1 | g.229431601G>A | CA423754843 | ACTA1 | c.991-37C>T (n.991-37C>T) c.897C>T (p.Gly299=) c.663C>T (p.Gly221=) c.1032C>T (p.Gly344=) | dbSNP COSMIC |
1 | g.229431601G>C | CA423754842 | ACTA1 | c.991-37C>G (n.991-37C>G) c.897C>G (p.Gly299=) c.663C>G (p.Gly221=) c.1032C>G (p.Gly344=) | |
1 | g.229431601G= | CA1226125397 | ACTA1 | c.991-37C= (n.991-37C=) c.897C= (p.Gly299=) c.663C= (p.Gly221=) c.1032C= (p.Gly344=) | |
1 | g.229431601G>T | CA1442714 | ACTA1 | c.991-37C>A (n.991-37C>A) c.897C>A (p.Gly299=) c.663C>A (p.Gly221=) c.1032C>A (p.Gly344=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.229431602C>A | CA345144727 | ACTA1 | c.991-38G>T (n.991-38G>T) c.896G>T (p.Gly299Val) c.662G>T (p.Gly221Val) c.1031G>T (p.Gly344Val) | |
1 | g.229431602C= | CA1226125398 | ACTA1 | c.991-38G= (n.991-38G=) c.896G= (p.Gly299=) c.662G= (p.Gly221=) c.1031G= (p.Gly344=) | |
1 | g.229431602C>G | CA345144729 | ACTA1 | c.991-38G>C (n.991-38G>C) c.896G>C (p.Gly299Ala) c.662G>C (p.Gly221Ala) c.1031G>C (p.Gly344Ala) | |
1 | g.229431602C>T | CA345144733 | ACTA1 | c.991-38G>A (n.991-38G>A) c.896G>A (p.Gly299Asp) c.662G>A (p.Gly221Asp) c.1031G>A (p.Gly344Asp) | ClinVar dbSNP |
1 | g.229431603del | CA1013145126 | ACTA1 | c.991-38del (n.991-38del) c.896del (p.Gly299AlafsTer?) c.662del (p.Gly221AlafsTer?) c.1031del (p.Gly344AlafsTer?) | gnomAD v3 gnomAD v4 |
1 | g.229431603C>A | CA345144736 | ACTA1 | c.991-39G>T (n.991-39G>T) c.895G>T (p.Gly299Cys) c.661G>T (p.Gly221Cys) c.1030G>T (p.Gly344Cys) | gnomAD v3 gnomAD v4 |
1 | g.229431603C>G | CA345144738 | ACTA1 | c.991-39G>C (n.991-39G>C) c.895G>C (p.Gly299Arg) c.661G>C (p.Gly221Arg) c.1030G>C (p.Gly344Arg) | ClinVar dbSNP |
1 | g.229431603C>T | CA345144742 | ACTA1 | c.991-39G>A (n.991-39G>A) c.895G>A (p.Gly299Ser) c.661G>A (p.Gly221Ser) c.1030G>A (p.Gly344Ser) | ClinVar |
1 | g.229431604G>A | CA423754845 | ACTA1 | c.991-40C>T (n.991-40C>T) c.894C>T (p.Ile298=) c.660C>T (p.Ile220=) c.1029C>T (p.Ile343=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.229431604G>C | CA345144745 | ACTA1 | c.991-40C>G (n.991-40C>G) c.894C>G (p.Ile298Met) c.660C>G (p.Ile220Met) c.1029C>G (p.Ile343Met) | ClinVar dbSNP |
1 | g.229431604G= | CA1226125399 | ACTA1 | c.991-40C= (n.991-40C=) c.894C= (p.Ile298=) c.660C= (p.Ile220=) c.1029C= (p.Ile343=) | |
1 | g.229431604G>T | CA423754844 | ACTA1 | c.991-40C>A (n.991-40C>A) c.894C>A (p.Ile298=) c.660C>A (p.Ile220=) c.1029C>A (p.Ile343=) | gnomAD v4 |
1 | g.229431605A>C | CA345144746 | ACTA1 | c.991-41T>G (n.991-41T>G) c.893T>G (p.Ile298Ser) c.659T>G (p.Ile220Ser) c.1028T>G (p.Ile343Ser) | |
1 | g.229431605A>G | CA345144753 | ACTA1 | c.991-41T>C (n.991-41T>C) c.893T>C (p.Ile298Thr) c.659T>C (p.Ile220Thr) c.1028T>C (p.Ile343Thr) | |
1 | g.229431605A>T | CA345144765 | ACTA1 | c.991-41T>A (n.991-41T>A) c.893T>A (p.Ile298Asn) c.659T>A (p.Ile220Asn) c.1028T>A (p.Ile343Asn) | |
1 | g.229431606T>A | CA345144769 | ACTA1 | c.991-42A>T (n.991-42A>T) c.892A>T (p.Ile298Phe) c.658A>T (p.Ile220Phe) c.1027A>T (p.Ile343Phe) | |
1 | g.229431606T>C | CA345144772 | ACTA1 | c.991-42A>G (n.991-42A>G) c.892A>G (p.Ile298Val) c.658A>G (p.Ile220Val) c.1027A>G (p.Ile343Val) | ClinVar |
1 | g.229431606T>G | CA345144775 | ACTA1 | c.991-42A>C (n.991-42A>C) c.892A>C (p.Ile298Leu) c.658A>C (p.Ile220Leu) c.1027A>C (p.Ile343Leu) | |
1 | g.229431607C>A | CA345144779 | ACTA1 | c.991-43G>T (n.991-43G>T) c.891G>T (p.Trp297Cys) c.657G>T (p.Trp219Cys) c.1026G>T (p.Trp342Cys) | |
1 | g.229431607C>G | CA345144784 | ACTA1 | c.991-43G>C (n.991-43G>C) c.891G>C (p.Trp297Cys) c.657G>C (p.Trp219Cys) c.1026G>C (p.Trp342Cys) | |
1 | g.229431607C>T | CA345144782 | ACTA1 | c.991-43G>A (n.991-43G>A) c.891G>A (p.Trp297Ter) c.657G>A (p.Trp219Ter) c.1026G>A (p.Trp342Ter) | |
1 | g.229431607_229431608insAACCACACCAAACACACCCAA | CA2748054878 | ACTA1 | c.991-44_991-43insTTGGGTGTGTTTGGTGTGGTT (n.991-44_991-43insTTGGGTGTGTTTGGTGTGGTT) c.890_891insTTGGGTGTGTTTGGTGTGGTT (p.Trp297delinsCysTrpValCysLeuValTrpLeu) c.656_657insTTGGGTGTGTTTGGTGTGGTT (p.Trp219delinsCysTrpValCysLeuValTrpLeu) c.1025_1026insTTGGGTGTGTTTGGTGTGGTT (p.Trp342delinsCysTrpValCysLeuValTrpLeu) | |
1 | g.229431608C>A | CA345144789 | ACTA1 | c.991-44G>T (n.991-44G>T) c.890G>T (p.Trp297Leu) c.656G>T (p.Trp219Leu) c.1025G>T (p.Trp342Leu) | |
1 | g.229431608C>G | CA345144791 | ACTA1 | c.991-44G>C (n.991-44G>C) c.890G>C (p.Trp297Ser) c.656G>C (p.Trp219Ser) c.1025G>C (p.Trp342Ser) | |
1 | g.229431608C>T | CA345144794 | ACTA1 | c.991-44G>A (n.991-44G>A) c.890G>A (p.Trp297Ter) c.656G>A (p.Trp219Ter) c.1025G>A (p.Trp342Ter) | gnomAD v3 gnomAD v4 |
1 | g.229431609A>C | CA345144797 | ACTA1 | c.991-45T>G (n.991-45T>G) c.889T>G (p.Trp297Gly) c.655T>G (p.Trp219Gly) c.1024T>G (p.Trp342Gly) | |
1 | g.229431609A>G | CA345144805 | ACTA1 | c.991-45T>C (n.991-45T>C) c.889T>C (p.Trp297Arg) c.655T>C (p.Trp219Arg) c.1024T>C (p.Trp342Arg) | gnomAD v4 |
1 | g.229431609A>T | CA345144807 | ACTA1 | c.991-45T>A (n.991-45T>A) c.889T>A (p.Trp297Arg) c.655T>A (p.Trp219Arg) c.1024T>A (p.Trp342Arg) | |
1 | g.229431610C>A | CA423754846 | ACTA1 | c.991-46G>T (n.991-46G>T) c.888G>T (p.Val296=) c.654G>T (p.Val218=) c.1023G>T (p.Val341=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.229431610C= | CA1226125400 | ACTA1 | c.991-46G= (n.991-46G=) c.888G= (p.Val296=) c.654G= (p.Val218=) c.1023G= (p.Val341=) | |
1 | g.229431610C>G | CA423754847 | ACTA1 | c.991-46G>C (n.991-46G>C) c.888G>C (p.Val296=) c.654G>C (p.Val218=) c.1023G>C (p.Val341=) | |
1 | g.229431610C>T | CA423754848 | ACTA1 | c.991-46G>A (n.991-46G>A) c.888G>A (p.Val296=) c.654G>A (p.Val218=) c.1023G>A (p.Val341=) | dbSNP gnomAD v4 |
1 | g.229431611A>C | CA345144808 | ACTA1 | c.991-47T>G (n.991-47T>G) c.887T>G (p.Val296Gly) c.653T>G (p.Val218Gly) c.1022T>G (p.Val341Gly) | |
1 | g.229431611A>G | CA345144809 | ACTA1 | c.991-47T>C (n.991-47T>C) c.887T>C (p.Val296Ala) c.653T>C (p.Val218Ala) c.1022T>C (p.Val341Ala) | |
1 | g.229431611A>T | CA345144810 | ACTA1 | c.991-47T>A (n.991-47T>A) c.887T>A (p.Val296Glu) c.653T>A (p.Val218Glu) c.1022T>A (p.Val341Glu) | |
1 | g.229431612C>A | CA345144812 | ACTA1 | c.991-48G>T (n.991-48G>T) c.886G>T (p.Val296Leu) c.652G>T (p.Val218Leu) c.1021G>T (p.Val341Leu) | |
1 | g.229431612C= | CA1226125401 | ACTA1 | c.991-48G= (n.991-48G=) c.886G= (p.Val296=) c.652G= (p.Val218=) c.1021G= (p.Val341=) | |
1 | g.229431612C>G | CA345144813 | ACTA1 | c.991-48G>C (n.991-48G>C) c.886G>C (p.Val296Leu) c.652G>C (p.Val218Leu) c.1021G>C (p.Val341Leu) | |
1 | g.229431612C>T | CA345144815 | ACTA1 | c.991-48G>A (n.991-48G>A) c.886G>A (p.Val296Met) c.652G>A (p.Val218Met) c.1021G>A (p.Val341Met) | dbSNP |
1 | g.229431613C>A | CA1442716 | ACTA1 | c.991-49G>T (n.991-49G>T) c.885G>T (p.Ser295=) c.651G>T (p.Ser217=) c.1020G>T (p.Ser340=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431613C= | CA1226125402 | ACTA1 | c.991-49G= (n.991-49G=) c.885G= (p.Ser295=) c.651G= (p.Ser217=) c.1020G= (p.Ser340=) | |
1 | g.229431613C>G | CA423754849 | ACTA1 | c.991-49G>C (n.991-49G>C) c.885G>C (p.Ser295=) c.651G>C (p.Ser217=) c.1020G>C (p.Ser340=) | dbSNP |
1 | g.229431613C>T | CA1442715 | ACTA1 | c.991-49G>A (n.991-49G>A) c.885G>A (p.Ser295=) c.651G>A (p.Ser217=) c.1020G>A (p.Ser340=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431614G>A | CA345144820 | ACTA1 | c.991-50C>T (n.991-50C>T) c.884C>T (p.Ser295Leu) c.650C>T (p.Ser217Leu) c.1019C>T (p.Ser340Leu) | |
1 | g.229431614G>C | CA345144824 | ACTA1 | c.991-50C>G (n.991-50C>G) c.884C>G (p.Ser295Trp) c.650C>G (p.Ser217Trp) c.1019C>G (p.Ser340Trp) | |
1 | g.229431614G>T | CA345144822 | ACTA1 | c.991-50C>A (n.991-50C>A) c.884C>A (p.Ser295Ter) c.650C>A (p.Ser217Ter) c.1019C>A (p.Ser340Ter) | |
1 | g.229431615A>C | CA345144826 | ACTA1 | c.991-51T>G (n.991-51T>G) c.883T>G (p.Ser295Ala) c.649T>G (p.Ser217Ala) c.1018T>G (p.Ser340Ala) | ClinVar |
1 | g.229431615A>G | CA345144839 | ACTA1 | c.991-51T>C (n.991-51T>C) c.883T>C (p.Ser295Pro) c.649T>C (p.Ser217Pro) c.1018T>C (p.Ser340Pro) | |
1 | g.229431615A>T | CA345144828 | ACTA1 | c.991-51T>A (n.991-51T>A) c.883T>A (p.Ser295Thr) c.649T>A (p.Ser217Thr) c.1018T>A (p.Ser340Thr) | |
1 | g.229431616G>A | CA1442717 | ACTA1 | c.991-52C>T (n.991-52C>T) c.882C>T (p.Tyr294=) c.648C>T (p.Tyr216=) c.1017C>T (p.Tyr339=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431616G>C | CA345144848 | ACTA1 | c.991-52C>G (n.991-52C>G) c.882C>G (p.Tyr294Ter) c.648C>G (p.Tyr216Ter) c.1017C>G (p.Tyr339Ter) | |
1 | g.229431616G= | CA1226125403 | ACTA1 | c.991-52C= (n.991-52C=) c.882C= (p.Tyr294=) c.648C= (p.Tyr216=) c.1017C= (p.Tyr339=) | |
1 | g.229431616G>T | CA345144847 | ACTA1 | c.991-52C>A (n.991-52C>A) c.882C>A (p.Tyr294Ter) c.648C>A (p.Tyr216Ter) c.1017C>A (p.Tyr339Ter) | |
1 | g.229431617T>A | CA345144849 | ACTA1 | c.991-53A>T (n.991-53A>T) c.881A>T (p.Tyr294Phe) c.647A>T (p.Tyr216Phe) c.1016A>T (p.Tyr339Phe) | |
1 | g.229431617T>C | CA345144851 | ACTA1 | c.991-53A>G (n.991-53A>G) c.881A>G (p.Tyr294Cys) c.647A>G (p.Tyr216Cys) c.1016A>G (p.Tyr339Cys) | |
1 | g.229431617T>G | CA345144850 | ACTA1 | c.991-53A>C (n.991-53A>C) c.881A>C (p.Tyr294Ser) c.647A>C (p.Tyr216Ser) c.1016A>C (p.Tyr339Ser) | |
1 | g.229431618A>C | CA345144853 | ACTA1 | c.991-54T>G (n.991-54T>G) c.880T>G (p.Tyr294Asp) c.646T>G (p.Tyr216Asp) c.1015T>G (p.Tyr339Asp) | |
1 | g.229431618A>G | CA345144854 | ACTA1 | c.991-54T>C (n.991-54T>C) c.880T>C (p.Tyr294His) c.646T>C (p.Tyr216His) c.1015T>C (p.Tyr339His) | |
1 | g.229431618A>T | CA345144858 | ACTA1 | c.991-54T>A (n.991-54T>A) c.880T>A (p.Tyr294Asn) c.646T>A (p.Tyr216Asn) c.1015T>A (p.Tyr339Asn) | ClinVar |
1 | g.229431619T>A | CA345144861 | ACTA1 | c.991-55A>T (n.991-55A>T) c.879A>T (p.Lys293Asn) c.645A>T (p.Lys215Asn) c.1014A>T (p.Lys338Asn) | |
1 | g.229431619T>C | CA423754850 | ACTA1 | c.991-55A>G (n.991-55A>G) c.879A>G (p.Lys293=) c.645A>G (p.Lys215=) c.1014A>G (p.Lys338=) | dbSNP |
1 | g.229431619T>G | CA345144865 | ACTA1 | c.991-55A>C (n.991-55A>C) c.879A>C (p.Lys293Asn) c.645A>C (p.Lys215Asn) c.1014A>C (p.Lys338Asn) | ClinVar dbSNP |
1 | g.229431619T= | CA1226125404 | ACTA1 | c.991-55A= (n.991-55A=) c.879A= (p.Lys293=) c.645A= (p.Lys215=) c.1014A= (p.Lys338=) | |
1 | g.229431620T>A | CA345144867 | ACTA1 | c.991-56A>T (n.991-56A>T) c.878A>T (p.Lys293Ile) c.644A>T (p.Lys215Ile) c.1013A>T (p.Lys338Ile) | |
1 | g.229431620T>C | CA345144870 | ACTA1 | c.991-56A>G (n.991-56A>G) c.878A>G (p.Lys293Arg) c.644A>G (p.Lys215Arg) c.1013A>G (p.Lys338Arg) | |
1 | g.229431620T>G | CA345144874 | ACTA1 | c.991-56A>C (n.991-56A>C) c.878A>C (p.Lys293Thr) c.644A>C (p.Lys215Thr) c.1013A>C (p.Lys338Thr) | |
1 | g.229431621T>A | CA345144878 | ACTA1 | c.991-57A>T (n.991-57A>T) c.877A>T (p.Lys293Ter) c.643A>T (p.Lys215Ter) c.1012A>T (p.Lys338Ter) | |
1 | g.229431621T>C | CA345144881 | ACTA1 | c.991-57A>G (n.991-57A>G) c.877A>G (p.Lys293Glu) c.643A>G (p.Lys215Glu) c.1012A>G (p.Lys338Glu) | |
1 | g.229431621T>G | CA345144883 | ACTA1 | c.991-57A>C (n.991-57A>C) c.877A>C (p.Lys293Gln) c.643A>C (p.Lys215Gln) c.1012A>C (p.Lys338Gln) | |
1 | g.229431622G>A | CA423754851 | ACTA1 | c.991-58C>T (n.991-58C>T) c.876C>T (p.Arg292=) c.642C>T (p.Arg214=) c.1011C>T (p.Arg337=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.229431622G>C | CA423754852 | ACTA1 | c.991-58C>G (n.991-58C>G) c.876C>G (p.Arg292=) c.642C>G (p.Arg214=) c.1011C>G (p.Arg337=) | |
1 | g.229431622G= | CA1226125405 | ACTA1 | c.991-58C= (n.991-58C=) c.876C= (p.Arg292=) c.642C= (p.Arg214=) c.1011C= (p.Arg337=) | |
1 | g.229431622G>T | CA423754853 | ACTA1 | c.991-58C>A (n.991-58C>A) c.876C>A (p.Arg292=) c.642C>A (p.Arg214=) c.1011C>A (p.Arg337=) | |
1 | g.229431623C>A | CA345144892 | ACTA1 | c.991-59G>T (n.991-59G>T) c.875G>T (p.Arg292Leu) c.641G>T (p.Arg214Leu) c.1010G>T (p.Arg337Leu) | |
1 | g.229431623C= | CA1143486378 | ACTA1 | c.991-59G= (n.991-59G=) c.875G= (p.Arg292=) c.641G= (p.Arg214=) c.1010G= (p.Arg337=) | |
1 | g.229431623C>G | CA345144889 | ACTA1 | c.991-59G>C (n.991-59G>C) c.875G>C (p.Arg292Pro) c.641G>C (p.Arg214Pro) c.1010G>C (p.Arg337Pro) | |
1 | g.229431623C>T | CA38814755 | ACTA1 | c.991-59G>A (n.991-59G>A) c.875G>A (p.Arg292His) c.641G>A (p.Arg214His) c.1010G>A (p.Arg337His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.229431624G>A | CA345144893 | ACTA1 | c.991-60C>T (n.991-60C>T) c.874C>T (p.Arg292Cys) c.640C>T (p.Arg214Cys) c.1009C>T (p.Arg337Cys) | |
1 | g.229431624G>C | CA345144894 | ACTA1 | c.991-60C>G (n.991-60C>G) c.874C>G (p.Arg292Gly) c.640C>G (p.Arg214Gly) c.1009C>G (p.Arg337Gly) | gnomAD v4 |
1 | g.229431624G= | CA1226125406 | ACTA1 | c.991-60C= (n.991-60C=) c.874C= (p.Arg292=) c.640C= (p.Arg214=) c.1009C= (p.Arg337=) | |
1 | g.229431624G>T | CA1442718 | ACTA1 | c.991-60C>A (n.991-60C>A) c.874C>A (p.Arg292Ser) c.640C>A (p.Arg214Ser) c.1009C>A (p.Arg337Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.229431625C>A | CA345144898 | ACTA1 | c.991-61G>T (n.991-61G>T) c.873G>T (p.Glu291Asp) c.639G>T (p.Glu213Asp) c.1008G>T (p.Glu336Asp) | |
1 | g.229431625C= | CA1226125407 | ACTA1 | c.991-61G= (n.991-61G=) c.873G= (p.Glu291=) c.639G= (p.Glu213=) c.1008G= (p.Glu336=) | |
1 | g.229431625C>G | CA345144901 | ACTA1 | c.991-61G>C (n.991-61G>C) c.873G>C (p.Glu291Asp) c.639G>C (p.Glu213Asp) c.1008G>C (p.Glu336Asp) | ClinVar |
1 | g.229431625C>T | CA423754857 | ACTA1 | c.991-61G>A (n.991-61G>A) c.873G>A (p.Glu291=) c.639G>A (p.Glu213=) c.1008G>A (p.Glu336=) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.229431626T>A | CA345144906 | ACTA1 | c.991-62A>T (n.991-62A>T) c.872A>T (p.Glu291Val) c.638A>T (p.Glu213Val) c.1007A>T (p.Glu336Val) | |
1 | g.229431626T>C | CA38814782 | ACTA1 | c.991-62A>G (n.991-62A>G) c.872A>G (p.Glu291Gly) c.638A>G (p.Glu213Gly) c.1007A>G (p.Glu336Gly) | dbSNP |
1 | g.229431626T>G | CA128033 | ACTA1 | c.991-62A>C (n.991-62A>C) c.872A>C (p.Glu291Ala) c.638A>C (p.Glu213Ala) c.1007A>C (p.Glu336Ala) | ClinVar dbSNP |
1 | g.229431626T= | CA1141581371 | ACTA1 | c.991-62A= (n.991-62A=) c.872A= (p.Glu291=) c.638A= (p.Glu213=) c.1007A= (p.Glu336=) | |
1 | g.229431627C>A | CA345144911 | ACTA1 | c.991-63G>T (n.991-63G>T) c.871G>T (p.Glu291Ter) c.637G>T (p.Glu213Ter) c.1006G>T (p.Glu336Ter) | |
1 | g.229431627C>G | CA345144912 | ACTA1 | c.991-63G>C (n.991-63G>C) c.871G>C (p.Glu291Gln) c.637G>C (p.Glu213Gln) c.1006G>C (p.Glu336Gln) | |
1 | g.229431627C>T | CA345144929 | ACTA1 | c.991-63G>A (n.991-63G>A) c.871G>A (p.Glu291Lys) c.637G>A (p.Glu213Lys) c.1006G>A (p.Glu336Lys) | COSMIC |
1 | g.229431628del | CA2739273919 | ACTA1 | c.991-63del (n.991-63del) c.871del (p.Glu291SerfsTer?) c.637del (p.Glu213SerfsTer?) c.1006del (p.Glu336SerfsTer?) | ClinVar |
1 | g.229431628C>A | CA423754858 | ACTA1 | c.991-64G>T (n.991-64G>T) c.870G>T (p.Pro290=) c.636G>T (p.Pro212=) c.1005G>T (p.Pro335=) | dbSNP |
1 | g.229431628C= | CA1226125408 | ACTA1 | c.991-64G= (n.991-64G=) c.870G= (p.Pro290=) c.636G= (p.Pro212=) c.1005G= (p.Pro335=) | |
1 | g.229431628C>G | CA423754859 | ACTA1 | c.991-64G>C (n.991-64G>C) c.870G>C (p.Pro290=) c.636G>C (p.Pro212=) c.1005G>C (p.Pro335=) | |
1 | g.229431628C>T | CA1442719 | ACTA1 | c.991-64G>A (n.991-64G>A) c.870G>A (p.Pro290=) c.636G>A (p.Pro212=) c.1005G>A (p.Pro335=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.229431629G>A | CA345144942 | ACTA1 | c.991-65C>T (n.991-65C>T) c.869C>T (p.Pro290Leu) c.635C>T (p.Pro212Leu) c.1004C>T (p.Pro335Leu) | ClinVar dbSNP |
1 | g.229431629G>C | CA345144937 | ACTA1 | c.991-65C>G (n.991-65C>G) c.869C>G (p.Pro290Arg) c.635C>G (p.Pro212Arg) c.1004C>G (p.Pro335Arg) | ClinVar dbSNP |
1 | g.229431629G= | CA1226125409 | ACTA1 | c.991-65C= (n.991-65C=) c.869C= (p.Pro290=) c.635C= (p.Pro212=) c.1004C= (p.Pro335=) | |
1 | g.229431629G>T | CA16042312 | ACTA1 | c.991-65C>A (n.991-65C>A) c.869C>A (p.Pro290Gln) c.635C>A (p.Pro212Gln) c.1004C>A (p.Pro335Gln) | ClinVar dbSNP |
1 | g.229431630G>A | CA345144947 | ACTA1 | c.991-66C>T (n.991-66C>T) c.868C>T (p.Pro290Ser) c.634C>T (p.Pro212Ser) c.1003C>T (p.Pro335Ser) | |
1 | g.229431630G>C | CA345144949 | ACTA1 | c.991-66C>G (n.991-66C>G) c.868C>G (p.Pro290Ala) c.634C>G (p.Pro212Ala) c.1003C>G (p.Pro335Ala) | ClinVar dbSNP |
1 | g.229431630G= | CA1226125410 | ACTA1 | c.991-66C= (n.991-66C=) c.868C= (p.Pro290=) c.634C= (p.Pro212=) c.1003C= (p.Pro335=) | |
1 | g.229431630G>T | CA345144958 | ACTA1 | c.991-66C>A (n.991-66C>A) c.868C>A (p.Pro290Thr) c.634C>A (p.Pro212Thr) c.1003C>A (p.Pro335Thr) | |
1 | g.229431631C>A | CA1442720 | ACTA1 | c.991-67G>T (n.991-67G>T) c.867G>T (p.Pro289=) c.633G>T (p.Pro211=) c.1002G>T (p.Pro334=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.229431631C= | CA1226125411 | ACTA1 | c.991-67G= (n.991-67G=) c.867G= (p.Pro289=) c.633G= (p.Pro211=) c.1002G= (p.Pro334=) | |
1 | g.229431631C>G | CA423754862 | ACTA1 | c.991-67G>C (n.991-67G>C) c.867G>C (p.Pro289=) c.633G>C (p.Pro211=) c.1002G>C (p.Pro334=) | |
1 | g.229431631C>T | CA423754864 | ACTA1 | c.991-67G>A (n.991-67G>A) c.867G>A (p.Pro289=) c.633G>A (p.Pro211=) c.1002G>A (p.Pro334=) | dbSNP |