Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.122262174G>A | CA354152673 | CASR | c.1139G>A (p.Ser380Asn) c.656G>A (p.Ser219Asn) c.551G>A (p.Ser184Asn) | |
3 | g.122262174G>C | CA354152674 | CASR | c.1139G>C (p.Ser380Thr) c.656G>C (p.Ser219Thr) c.551G>C (p.Ser184Thr) | |
3 | g.122262174G>T | CA354152675 | CASR | c.1139G>T (p.Ser380Ile) c.656G>T (p.Ser219Ile) c.551G>T (p.Ser184Ile) | |
3 | g.122262175T>A | CA82738904 | CASR | c.1140T>A (p.Ser380Arg) c.657T>A (p.Ser219Arg) c.552T>A (p.Ser184Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262175T>C | CA435424534 | CASR | c.1140T>C (p.Ser380=) c.657T>C (p.Ser219=) c.552T>C (p.Ser184=) | ClinVar |
3 | g.122262175T>G | CA354152676 | CASR | c.1140T>G (p.Ser380Arg) c.657T>G (p.Ser219Arg) c.552T>G (p.Ser184Arg) | |
3 | g.122262175T= | CA1397873502 | CASR | c.1140T= (p.Ser380=) c.657T= (p.Ser219=) c.552T= (p.Ser184=) | |
3 | g.122262176G>A | CA354152679 | CASR | c.1141G>A (p.Gly381Ser) c.658G>A (p.Gly220Ser) c.553G>A (p.Gly185Ser) | |
3 | g.122262176G>C | CA354152677 | CASR | c.1141G>C (p.Gly381Arg) c.658G>C (p.Gly220Arg) c.553G>C (p.Gly185Arg) | |
3 | g.122262176G>T | CA354152678 | CASR | c.1141G>T (p.Gly381Cys) c.658G>T (p.Gly220Cys) c.553G>T (p.Gly185Cys) | |
3 | g.122262177G>A | CA354152680 | CASR | c.1142G>A (p.Gly381Asp) c.659G>A (p.Gly220Asp) c.554G>A (p.Gly185Asp) | |
3 | g.122262177G>C | CA354152681 | CASR | c.1142G>C (p.Gly381Ala) c.659G>C (p.Gly220Ala) c.554G>C (p.Gly185Ala) | dbSNP |
3 | g.122262177G>T | CA354152682 | CASR | c.1142G>T (p.Gly381Val) c.659G>T (p.Gly220Val) c.554G>T (p.Gly185Val) | COSMIC |
3 | g.122262178C>A | CA435424538 | CASR | c.1143C>A (p.Gly381=) c.660C>A (p.Gly220=) c.555C>A (p.Gly185=) | ClinVar dbSNP |
3 | g.122262178C= | CA1397873512 | CASR | c.1143C= (p.Gly381=) c.660C= (p.Gly220=) c.555C= (p.Gly185=) | |
3 | g.122262178C>G | CA435424539 | CASR | c.1143C>G (p.Gly381=) c.660C>G (p.Gly220=) c.555C>G (p.Gly185=) | |
3 | g.122262178C>T | CA2569601 | CASR | c.1143C>T (p.Gly381=) c.660C>T (p.Gly220=) c.555C>T (p.Gly185=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.122262179G>A | CA2569602 | CASR | c.1144G>A (p.Asp382Asn) c.661G>A (p.Asp221Asn) c.556G>A (p.Asp186Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.122262179G>C | CA354152683 | CASR | c.1144G>C (p.Asp382His) c.661G>C (p.Asp221His) c.556G>C (p.Asp186His) | gnomAD v4 |
3 | g.122262179G= | CA1397873515 | CASR | c.1144G= (p.Asp382=) c.661G= (p.Asp221=) c.556G= (p.Asp186=) | |
3 | g.122262179G>T | CA354152684 | CASR | c.1144G>T (p.Asp382Tyr) c.661G>T (p.Asp221Tyr) c.556G>T (p.Asp186Tyr) | ClinVar gnomAD v4 |
3 | g.122262180A= | CA1397873519 | CASR | c.1145A= (p.Asp382=) c.662A= (p.Asp221=) c.557A= (p.Asp186=) | |
3 | g.122262180A>C | CA354152685 | CASR | c.1145A>C (p.Asp382Ala) c.662A>C (p.Asp221Ala) c.557A>C (p.Asp186Ala) | |
3 | g.122262180A>G | CA354152686 | CASR | c.1145A>G (p.Asp382Gly) c.662A>G (p.Asp221Gly) c.557A>G (p.Asp186Gly) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.122262180A>T | CA354152687 | CASR | c.1145A>T (p.Asp382Val) c.662A>T (p.Asp221Val) c.557A>T (p.Asp186Val) | |
3 | g.122262181C>A | CA354152688 | CASR | c.1146C>A (p.Asp382Glu) c.663C>A (p.Asp221Glu) c.558C>A (p.Asp186Glu) | |
3 | g.122262181C= | CA1397873522 | CASR | c.1146C= (p.Asp382=) c.663C= (p.Asp221=) c.558C= (p.Asp186=) | |
3 | g.122262181C>G | CA354152689 | CASR | c.1146C>G (p.Asp382Glu) c.663C>G (p.Asp221Glu) c.558C>G (p.Asp186Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262181C>T | CA435424545 | CASR | c.1146C>T (p.Asp382=) c.663C>T (p.Asp221=) c.558C>T (p.Asp186=) | |
3 | g.122262182A= | CA1397873525 | CASR | c.1147A= (p.Arg383=) c.664A= (p.Arg222=) c.559A= (p.Arg187=) | |
3 | g.122262182A>C | CA435424546 | CASR | c.1147A>C (p.Arg383=) c.664A>C (p.Arg222=) c.559A>C (p.Arg187=) | |
3 | g.122262182A>G | CA354152690 | CASR | c.1147A>G (p.Arg383Gly) c.664A>G (p.Arg222Gly) c.559A>G (p.Arg187Gly) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.122262182A>T | CA354152691 | CASR | c.1147A>T (p.Arg383Trp) c.664A>T (p.Arg222Trp) c.559A>T (p.Arg187Trp) | |
3 | g.122262183G>A | CA354152692 | CASR | c.1148G>A (p.Arg383Lys) c.665G>A (p.Arg222Lys) c.560G>A (p.Arg187Lys) | |
3 | g.122262183G>C | CA354152694 | CASR | c.1148G>C (p.Arg383Thr) c.665G>C (p.Arg222Thr) c.560G>C (p.Arg187Thr) | |
3 | g.122262183G>T | CA354152693 | CASR | c.1148G>T (p.Arg383Met) c.665G>T (p.Arg222Met) c.560G>T (p.Arg187Met) | |
3 | g.122262184G>A | CA435424548 | CASR | c.1149G>A (p.Arg383=) c.666G>A (p.Arg222=) c.561G>A (p.Arg187=) | ClinVar |
3 | g.122262184G>C | CA82738910 | CASR | c.1149G>C (p.Arg383Ser) c.666G>C (p.Arg222Ser) c.561G>C (p.Arg187Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262184G= | CA1397873529 | CASR | c.1149G= (p.Arg383=) c.666G= (p.Arg222=) c.561G= (p.Arg187=) | |
3 | g.122262184G>T | CA354152695 | CASR | c.1149G>T (p.Arg383Ser) c.666G>T (p.Arg222Ser) c.561G>T (p.Arg187Ser) | |
3 | g.122262185T>A | CA354152696 | CASR | c.1150T>A (p.Phe384Ile) c.667T>A (p.Phe223Ile) c.562T>A (p.Phe188Ile) | |
3 | g.122262185T>C | CA354152697 | CASR | c.1150T>C (p.Phe384Leu) c.667T>C (p.Phe223Leu) c.562T>C (p.Phe188Leu) | |
3 | g.122262185T>G | CA354152698 | CASR | c.1150T>G (p.Phe384Val) c.667T>G (p.Phe223Val) c.562T>G (p.Phe188Val) | |
3 | g.122262186T>A | CA354152699 | CASR | c.1151T>A (p.Phe384Tyr) c.668T>A (p.Phe223Tyr) c.563T>A (p.Phe188Tyr) | |
3 | g.122262186T>C | CA354152700 | CASR | c.1151T>C (p.Phe384Ser) c.668T>C (p.Phe223Ser) c.563T>C (p.Phe188Ser) | |
3 | g.122262186T>G | CA354152701 | CASR | c.1151T>G (p.Phe384Cys) c.668T>G (p.Phe223Cys) c.563T>G (p.Phe188Cys) | |
3 | g.122262187T>A | CA354152702 | CASR | c.1152T>A (p.Phe384Leu) c.669T>A (p.Phe223Leu) c.564T>A (p.Phe188Leu) | |
3 | g.122262187T>C | CA435424552 | CASR | c.1152T>C (p.Phe384=) c.669T>C (p.Phe223=) c.564T>C (p.Phe188=) | |
3 | g.122262187T>G | CA354152703 | CASR | c.1152T>G (p.Phe384Leu) c.669T>G (p.Phe223Leu) c.564T>G (p.Phe188Leu) | |
3 | g.122262188A>C | CA354152704 | CASR | c.1153A>C (p.Ser385Arg) c.670A>C (p.Ser224Arg) c.565A>C (p.Ser189Arg) | gnomAD v4 |
3 | g.122262188A>G | CA354152705 | CASR | c.1153A>G (p.Ser385Gly) c.670A>G (p.Ser224Gly) c.565A>G (p.Ser189Gly) | |
3 | g.122262188A>T | CA354152706 | CASR | c.1153A>T (p.Ser385Cys) c.670A>T (p.Ser224Cys) c.565A>T (p.Ser189Cys) | |
3 | g.122262189G>A | CA354152707 | CASR | c.1154G>A (p.Ser385Asn) c.671G>A (p.Ser224Asn) c.566G>A (p.Ser189Asn) | ClinVar dbSNP |
3 | g.122262189G>C | CA354152709 | CASR | c.1154G>C (p.Ser385Thr) c.671G>C (p.Ser224Thr) c.566G>C (p.Ser189Thr) | |
3 | g.122262189G= | CA1397873536 | CASR | c.1154G= (p.Ser385=) c.671G= (p.Ser224=) c.566G= (p.Ser189=) | |
3 | g.122262189G>T | CA354152708 | CASR | c.1154G>T (p.Ser385Ile) c.671G>T (p.Ser224Ile) c.566G>T (p.Ser189Ile) | |
3 | g.122262190C>A | CA354152710 | CASR | c.1155C>A (p.Ser385Arg) c.672C>A (p.Ser224Arg) c.567C>A (p.Ser189Arg) | ClinVar COSMIC |
3 | g.122262190C= | CA1397873544 | CASR | c.1155C= (p.Ser385=) c.672C= (p.Ser224=) c.567C= (p.Ser189=) | |
3 | g.122262190C>G | CA354152711 | CASR | c.1155C>G (p.Ser385Arg) c.672C>G (p.Ser224Arg) c.567C>G (p.Ser189Arg) | |
3 | g.122262190C>T | CA435424562 | CASR | c.1155C>T (p.Ser385=) c.672C>T (p.Ser224=) c.567C>T (p.Ser189=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262191A>C | CA354152712 | CASR | c.1156A>C (p.Asn386His) c.673A>C (p.Asn225His) c.568A>C (p.Asn190His) | ClinVar dbSNP |
3 | g.122262191A>G | CA354152713 | CASR | c.1156A>G (p.Asn386Asp) c.673A>G (p.Asn225Asp) c.568A>G (p.Asn190Asp) | |
3 | g.122262191A>T | CA354152714 | CASR | c.1156A>T (p.Asn386Tyr) c.673A>T (p.Asn225Tyr) c.568A>T (p.Asn190Tyr) | |
3 | g.122262192A>C | CA354152715 | CASR | c.1157A>C (p.Asn386Thr) c.674A>C (p.Asn225Thr) c.569A>C (p.Asn190Thr) | |
3 | g.122262192A>G | CA354152716 | CASR | c.1157A>G (p.Asn386Ser) c.674A>G (p.Asn225Ser) c.569A>G (p.Asn190Ser) | |
3 | g.122262192A>T | CA354152717 | CASR | c.1157A>T (p.Asn386Ile) c.674A>T (p.Asn225Ile) c.569A>T (p.Asn190Ile) | |
3 | g.122262193C>A | CA354152718 | CASR | c.1158C>A (p.Asn386Lys) c.675C>A (p.Asn225Lys) c.570C>A (p.Asn190Lys) | |
3 | g.122262193C>G | CA354152719 | CASR | c.1158C>G (p.Asn386Lys) c.675C>G (p.Asn225Lys) c.570C>G (p.Asn190Lys) | |
3 | g.122262193C>T | CA435424571 | CASR | c.1158C>T (p.Asn386=) c.675C>T (p.Asn225=) c.570C>T (p.Asn190=) | |
3 | g.122262194A= | CA1397873548 | CASR | c.1159A= (p.Ser387=) c.676A= (p.Ser226=) c.571A= (p.Ser191=) | |
3 | g.122262194A>C | CA354152721 | CASR | c.1159A>C (p.Ser387Arg) c.676A>C (p.Ser226Arg) c.571A>C (p.Ser191Arg) | |
3 | g.122262194A>G | CA2569603 | CASR | c.1159A>G (p.Ser387Gly) c.676A>G (p.Ser226Gly) c.571A>G (p.Ser191Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.122262194A>T | CA354152720 | CASR | c.1159A>T (p.Ser387Cys) c.676A>T (p.Ser226Cys) c.571A>T (p.Ser191Cys) | |
3 | g.122262195G>A | CA354152722 | CASR | c.1160G>A (p.Ser387Asn) c.677G>A (p.Ser226Asn) c.572G>A (p.Ser191Asn) | COSMIC |
3 | g.122262195G>C | CA354152723 | CASR | c.1160G>C (p.Ser387Thr) c.677G>C (p.Ser226Thr) c.572G>C (p.Ser191Thr) | ClinVar |
3 | g.122262195G>T | CA354152724 | CASR | c.1160G>T (p.Ser387Ile) c.677G>T (p.Ser226Ile) c.572G>T (p.Ser191Ile) | |
3 | g.122262196C>A | CA354152725 | CASR | c.1161C>A (p.Ser387Arg) c.678C>A (p.Ser226Arg) c.573C>A (p.Ser191Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.122262196C= | CA1397873555 | CASR | c.1161C= (p.Ser387=) c.678C= (p.Ser226=) c.573C= (p.Ser191=) | |
3 | g.122262196C>G | CA354152726 | CASR | c.1161C>G (p.Ser387Arg) c.678C>G (p.Ser226Arg) c.573C>G (p.Ser191Arg) | |
3 | g.122262196C>T | CA435424577 | CASR | c.1161C>T (p.Ser387=) c.678C>T (p.Ser226=) c.573C>T (p.Ser191=) | |
3 | g.122262197T>A | CA354152727 | CASR | c.1162T>A (p.Ser388Thr) c.679T>A (p.Ser227Thr) c.574T>A (p.Ser192Thr) | |
3 | g.122262197T>C | CA354152728 | CASR | c.1162T>C (p.Ser388Pro) c.679T>C (p.Ser227Pro) c.574T>C (p.Ser192Pro) | |
3 | g.122262197T>G | CA354152729 | CASR | c.1162T>G (p.Ser388Ala) c.679T>G (p.Ser227Ala) c.574T>G (p.Ser192Ala) | |
3 | g.122262198C>A | CA354152730 | CASR | c.1163C>A (p.Ser388Ter) c.680C>A (p.Ser227Ter) c.575C>A (p.Ser192Ter) | COSMIC |
3 | g.122262198C= | CA1397873566 | CASR | c.1163C= (p.Ser388=) c.680C= (p.Ser227=) c.575C= (p.Ser192=) | |
3 | g.122262198C>G | CA2569604 | CASR | c.1163C>G (p.Ser388Trp) c.680C>G (p.Ser227Trp) c.575C>G (p.Ser192Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.122262198C>T | CA82738915 | CASR | c.1163C>T (p.Ser388Leu) c.680C>T (p.Ser227Leu) c.575C>T (p.Ser192Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.122262199G>A | CA2569605 | CASR | c.1164G>A (p.Ser388=) c.681G>A (p.Ser227=) c.576G>A (p.Ser192=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262199G>C | CA435424583 | CASR | c.1164G>C (p.Ser388=) c.681G>C (p.Ser227=) c.576G>C (p.Ser192=) | ClinVar dbSNP gnomAD v2 |
3 | g.122262199G= | CA1397873576 | CASR | c.1164G= (p.Ser388=) c.681G= (p.Ser227=) c.576G= (p.Ser192=) | |
3 | g.122262199G>T | CA435424584 | CASR | c.1164G>T (p.Ser388=) c.681G>T (p.Ser227=) c.576G>T (p.Ser192=) | ClinVar |
3 | g.122262199_122262200delinsGA | CA1397873574 | CASR | c.1164_1165delinsGA (p.Ser388=) c.681_682delinsGA (p.Ser227=) c.576_577delinsGA (p.Ser192=) | |
3 | g.122262200del | CA2569606 | CASR | c.1165del (p.Thr389GlnfsTer21) c.682del (p.Thr228GlnfsTer21) c.577del (p.Thr193GlnfsTer21) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.122262200A>C | CA354152733 | CASR | c.1165A>C (p.Thr389Pro) c.682A>C (p.Thr228Pro) c.577A>C (p.Thr193Pro) | |
3 | g.122262200A>G | CA354152732 | CASR | c.1165A>G (p.Thr389Ala) c.682A>G (p.Thr228Ala) c.577A>G (p.Thr193Ala) | ClinVar |
3 | g.122262200A>T | CA354152731 | CASR | c.1165A>T (p.Thr389Ser) c.682A>T (p.Thr228Ser) c.577A>T (p.Thr193Ser) | |
3 | g.122262201C>A | CA354152734 | CASR | c.1166C>A (p.Thr389Lys) c.683C>A (p.Thr228Lys) c.578C>A (p.Thr193Lys) | |
3 | g.122262201C>G | CA354152735 | CASR | c.1166C>G (p.Thr389Arg) c.683C>G (p.Thr228Arg) c.578C>G (p.Thr193Arg) | ClinVar dbSNP |
3 | g.122262201C>T | CA354152736 | CASR | c.1166C>T (p.Thr389Ile) c.683C>T (p.Thr228Ile) c.578C>T (p.Thr193Ile) | |
3 | g.122262202A>C | CA435424588 | CASR | c.1167A>C (p.Thr389=) c.684A>C (p.Thr228=) c.579A>C (p.Thr193=) | |
3 | g.122262202A>G | CA435424589 | CASR | c.1167A>G (p.Thr389=) c.684A>G (p.Thr228=) c.579A>G (p.Thr193=) | |
3 | g.122262202A>T | CA435424590 | CASR | c.1167A>T (p.Thr389=) c.684A>T (p.Thr228=) c.579A>T (p.Thr193=) | |
3 | g.122262203G>A | CA82738922 | CASR | c.1168G>A (p.Ala390Thr) c.685G>A (p.Ala229Thr) c.580G>A (p.Ala194Thr) | ClinVar dbSNP gnomAD v4 |
3 | g.122262203G>C | CA354152737 | CASR | c.1168G>C (p.Ala390Pro) c.685G>C (p.Ala229Pro) c.580G>C (p.Ala194Pro) | |
3 | g.122262203G= | CA1397873585 | CASR | c.1168G= (p.Ala390=) c.685G= (p.Ala229=) c.580G= (p.Ala194=) | |
3 | g.122262203G>T | CA354152738 | CASR | c.1168G>T (p.Ala390Ser) c.685G>T (p.Ala229Ser) c.580G>T (p.Ala194Ser) | |
3 | g.122262204C>A | CA354152739 | CASR | c.1169C>A (p.Ala390Asp) c.686C>A (p.Ala229Asp) c.581C>A (p.Ala194Asp) | ClinVar dbSNP |
3 | g.122262204C= | CA1397873596 | CASR | c.1169C= (p.Ala390=) c.686C= (p.Ala229=) c.581C= (p.Ala194=) | |
3 | g.122262204C>G | CA2569607 | CASR | c.1169C>G (p.Ala390Gly) c.686C>G (p.Ala229Gly) c.581C>G (p.Ala194Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.122262204C>T | CA354152740 | CASR | c.1169C>T (p.Ala390Val) c.686C>T (p.Ala229Val) c.581C>T (p.Ala194Val) | COSMIC |
3 | g.122262205C>A | CA435424598 | CASR | c.1170C>A (p.Ala390=) c.687C>A (p.Ala229=) c.582C>A (p.Ala194=) | |
3 | g.122262205C= | CA1397873600 | CASR | c.1170C= (p.Ala390=) c.687C= (p.Ala229=) c.582C= (p.Ala194=) | |
3 | g.122262205C>G | CA435424596 | CASR | c.1170C>G (p.Ala390=) c.687C>G (p.Ala229=) c.582C>G (p.Ala194=) | |
3 | g.122262205C>T | CA435424594 | CASR | c.1170C>T (p.Ala390=) c.687C>T (p.Ala229=) c.582C>T (p.Ala194=) | ClinVar dbSNP |
3 | g.122262206T>A | CA354152741 | CASR | c.1171T>A (p.Phe391Ile) c.688T>A (p.Phe230Ile) c.583T>A (p.Phe195Ile) | |
3 | g.122262206T>C | CA354152742 | CASR | c.1171T>C (p.Phe391Leu) c.688T>C (p.Phe230Leu) c.583T>C (p.Phe195Leu) | gnomAD v4 |
3 | g.122262206T>G | CA354152743 | CASR | c.1171T>G (p.Phe391Val) c.688T>G (p.Phe230Val) c.583T>G (p.Phe195Val) | |
3 | g.122262207T>A | CA354152746 | CASR | c.1172T>A (p.Phe391Tyr) c.689T>A (p.Phe230Tyr) c.584T>A (p.Phe195Tyr) | |
3 | g.122262207T>C | CA354152745 | CASR | c.1172T>C (p.Phe391Ser) c.689T>C (p.Phe230Ser) c.584T>C (p.Phe195Ser) | ClinVar dbSNP |
3 | g.122262207T>G | CA354152744 | CASR | c.1172T>G (p.Phe391Cys) c.689T>G (p.Phe230Cys) c.584T>G (p.Phe195Cys) | |
3 | g.122262207T= | CA1397873602 | CASR | c.1172T= (p.Phe391=) c.689T= (p.Phe230=) c.584T= (p.Phe195=) | |
3 | g.122262208C>A | CA354152747 | CASR | c.1173C>A (p.Phe391Leu) c.690C>A (p.Phe230Leu) c.585C>A (p.Phe195Leu) | |
3 | g.122262208C= | CA1397873607 | CASR | c.1173C= (p.Phe391=) c.690C= (p.Phe230=) c.585C= (p.Phe195=) | |
3 | g.122262208C>G | CA354152748 | CASR | c.1173C>G (p.Phe391Leu) c.690C>G (p.Phe230Leu) c.585C>G (p.Phe195Leu) | |
3 | g.122262208C>T | CA82738939 | CASR | c.1173C>T (p.Phe391=) c.690C>T (p.Phe230=) c.585C>T (p.Phe195=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.122262209C>A | CA435424607 | CASR | c.1174C>A (p.Arg392=) c.691C>A (p.Arg231=) c.586C>A (p.Arg196=) | ClinVar dbSNP |
3 | g.122262209C= | CA1397873611 | CASR | c.1174C= (p.Arg392=) c.691C= (p.Arg231=) c.586C= (p.Arg196=) | |
3 | g.122262209C>G | CA354152749 | CASR | c.1174C>G (p.Arg392Gly) c.691C>G (p.Arg231Gly) c.586C>G (p.Arg196Gly) | |
3 | g.122262209C>T | CA354152750 | CASR | c.1174C>T (p.Arg392Ter) c.691C>T (p.Arg231Ter) c.586C>T (p.Arg196Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
3 | g.122262210G>A | CA354152751 | CASR | c.1175G>A (p.Arg392Gln) c.692G>A (p.Arg231Gln) c.587G>A (p.Arg196Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
3 | g.122262210G>C | CA354152752 | CASR | c.1175G>C (p.Arg392Pro) c.692G>C (p.Arg231Pro) c.587G>C (p.Arg196Pro) | |
3 | g.122262210G= | CA1397873622 | CASR | c.1175G= (p.Arg392=) c.692G= (p.Arg231=) c.587G= (p.Arg196=) | |
3 | g.122262210G>T | CA354152753 | CASR | c.1175G>T (p.Arg392Leu) c.692G>T (p.Arg231Leu) c.587G>T (p.Arg196Leu) | ClinVar dbSNP gnomAD v4 |
3 | g.122262211A= | CA1397873630 | CASR | c.1176A= (p.Arg392=) c.693A= (p.Arg231=) c.588A= (p.Arg196=) | |
3 | g.122262211A>C | CA435424613 | CASR | c.1176A>C (p.Arg392=) c.693A>C (p.Arg231=) c.588A>C (p.Arg196=) | |
3 | g.122262211A>G | CA435424614 | CASR | c.1176A>G (p.Arg392=) c.693A>G (p.Arg231=) c.588A>G (p.Arg196=) | ClinVar |
3 | g.122262211A>T | CA435424615 | CASR | c.1176A>T (p.Arg392=) c.693A>T (p.Arg231=) c.588A>T (p.Arg196=) | ClinVar dbSNP |
3 | g.122262212C>A | CA354152754 | CASR | c.1177C>A (p.Pro393Thr) c.694C>A (p.Pro232Thr) c.589C>A (p.Pro197Thr) | ClinVar dbSNP gnomAD v4 |
3 | g.122262212C>G | CA354152755 | CASR | c.1177C>G (p.Pro393Ala) c.694C>G (p.Pro232Ala) c.589C>G (p.Pro197Ala) | |
3 | g.122262212C>T | CA354152756 | CASR | c.1177C>T (p.Pro393Ser) c.694C>T (p.Pro232Ser) c.589C>T (p.Pro197Ser) | COSMIC |
3 | g.122262213C>A | CA354152757 | CASR | c.1178C>A (p.Pro393His) c.695C>A (p.Pro232His) c.590C>A (p.Pro197His) | |
3 | g.122262213C>G | CA354152758 | CASR | c.1178C>G (p.Pro393Arg) c.695C>G (p.Pro232Arg) c.590C>G (p.Pro197Arg) | |
3 | g.122262213C>T | CA354152759 | CASR | c.1178C>T (p.Pro393Leu) c.695C>T (p.Pro232Leu) c.590C>T (p.Pro197Leu) | COSMIC |
3 | g.122262214C>A | CA435424620 | CASR | c.1179C>A (p.Pro393=) c.696C>A (p.Pro232=) c.591C>A (p.Pro197=) | ClinVar dbSNP |
3 | g.122262214C= | CA1397873636 | CASR | c.1179C= (p.Pro393=) c.696C= (p.Pro232=) c.591C= (p.Pro197=) | |
3 | g.122262214C>G | CA435424621 | CASR | c.1179C>G (p.Pro393=) c.696C>G (p.Pro232=) c.591C>G (p.Pro197=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.122262214C>T | CA435424622 | CASR | c.1179C>T (p.Pro393=) c.696C>T (p.Pro232=) c.591C>T (p.Pro197=) | ClinVar dbSNP |
3 | g.122262215C>A | CA354152760 | CASR | c.1180C>A (p.Leu394Ile) c.697C>A (p.Leu233Ile) c.592C>A (p.Leu198Ile) | |
3 | g.122262215C= | CA1397873644 | CASR | c.1180C= (p.Leu394=) c.697C= (p.Leu233=) c.592C= (p.Leu198=) | |
3 | g.122262215C>G | CA354152761 | CASR | c.1180C>G (p.Leu394Val) c.697C>G (p.Leu233Val) c.592C>G (p.Leu198Val) | ClinVar dbSNP |
3 | g.122262215C>T | CA354152762 | CASR | c.1180C>T (p.Leu394Phe) c.697C>T (p.Leu233Phe) c.592C>T (p.Leu198Phe) | ClinVar dbSNP |
3 | g.122262216T>A | CA354152765 | CASR | c.1181T>A (p.Leu394His) c.698T>A (p.Leu233His) c.593T>A (p.Leu198His) | ClinVar dbSNP gnomAD v4 |
3 | g.122262216T>C | CA354152763 | CASR | c.1181T>C (p.Leu394Pro) c.698T>C (p.Leu233Pro) c.593T>C (p.Leu198Pro) | |
3 | g.122262216T>G | CA354152764 | CASR | c.1181T>G (p.Leu394Arg) c.698T>G (p.Leu233Arg) c.593T>G (p.Leu198Arg) | |
3 | g.122262217C>A | CA435424632 | CASR | c.1182C>A (p.Leu394=) c.699C>A (p.Leu233=) c.594C>A (p.Leu198=) | |
3 | g.122262217C= | CA1397873649 | CASR | c.1182C= (p.Leu394=) c.699C= (p.Leu233=) c.594C= (p.Leu198=) | |
3 | g.122262217C>G | CA435424633 | CASR | c.1182C>G (p.Leu394=) c.699C>G (p.Leu233=) c.594C>G (p.Leu198=) | |
3 | g.122262217C>T | CA435424635 | CASR | c.1182C>T (p.Leu394=) c.699C>T (p.Leu233=) c.594C>T (p.Leu198=) | dbSNP |
3 | g.122262218T>A | CA354152766 | CASR | c.1183T>A (p.Cys395Ser) c.700T>A (p.Cys234Ser) c.595T>A (p.Cys199Ser) | |
3 | g.122262218T>C | CA16042449 | CASR | c.1183T>C (p.Cys395Arg) c.700T>C (p.Cys234Arg) c.595T>C (p.Cys199Arg) | ClinVar dbSNP gnomAD v4 |
3 | g.122262218T>G | CA354152767 | CASR | c.1183T>G (p.Cys395Gly) c.700T>G (p.Cys234Gly) c.595T>G (p.Cys199Gly) | |
3 | g.122262218T= | CA1397873651 | CASR | c.1183T= (p.Cys395=) c.700T= (p.Cys234=) c.595T= (p.Cys199=) | |
3 | g.122262219G>A | CA354152768 | CASR | c.1184G>A (p.Cys395Tyr) c.701G>A (p.Cys234Tyr) c.596G>A (p.Cys199Tyr) | |
3 | g.122262219G>C | CA354152769 | CASR | c.1184G>C (p.Cys395Ser) c.701G>C (p.Cys234Ser) c.596G>C (p.Cys199Ser) | |
3 | g.122262219G>T | CA354152770 | CASR | c.1184G>T (p.Cys395Phe) c.701G>T (p.Cys234Phe) c.596G>T (p.Cys199Phe) | COSMIC |
3 | g.122262220T>A | CA354152771 | CASR | c.1185T>A (p.Cys395Ter) c.702T>A (p.Cys234Ter) c.597T>A (p.Cys199Ter) | |
3 | g.122262220T>C | CA435424644 | CASR | c.1185T>C (p.Cys395=) c.702T>C (p.Cys234=) c.597T>C (p.Cys199=) | |
3 | g.122262220T>G | CA354152772 | CASR | c.1185T>G (p.Cys395Trp) c.702T>G (p.Cys234Trp) c.597T>G (p.Cys199Trp) | gnomAD v4 |
3 | g.122262221A>C | CA354152773 | CASR | c.1186A>C (p.Thr396Pro) c.703A>C (p.Thr235Pro) c.598A>C (p.Thr200Pro) | |
3 | g.122262221A>G | CA354152774 | CASR | c.1186A>G (p.Thr396Ala) c.703A>G (p.Thr235Ala) c.598A>G (p.Thr200Ala) | |
3 | g.122262221A>T | CA354152775 | CASR | c.1186A>T (p.Thr396Ser) c.703A>T (p.Thr235Ser) c.598A>T (p.Thr200Ser) | |
3 | g.122262222C>A | CA354152777 | CASR | c.1187C>A (p.Thr396Lys) c.704C>A (p.Thr235Lys) c.599C>A (p.Thr200Lys) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.122262222C= | CA1397873657 | CASR | c.1187C= (p.Thr396=) c.704C= (p.Thr235=) c.599C= (p.Thr200=) | |
3 | g.122262222C>G | CA354152778 | CASR | c.1187C>G (p.Thr396Arg) c.704C>G (p.Thr235Arg) c.599C>G (p.Thr200Arg) | ClinVar dbSNP |
3 | g.122262222C>T | CA354152776 | CASR | c.1187C>T (p.Thr396Ile) c.704C>T (p.Thr235Ile) c.599C>T (p.Thr200Ile) | |
3 | g.122262223A= | CA1397873662 | CASR | c.1188A= (p.Thr396=) c.705A= (p.Thr235=) c.600A= (p.Thr200=) | |
3 | g.122262223A>C | CA435424651 | CASR | c.1188A>C (p.Thr396=) c.705A>C (p.Thr235=) c.600A>C (p.Thr200=) | |
3 | g.122262223A>G | CA2569608 | CASR | c.1188A>G (p.Thr396=) c.705A>G (p.Thr235=) c.600A>G (p.Thr200=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262223A>T | CA435424652 | CASR | c.1188A>T (p.Thr396=) c.705A>T (p.Thr235=) c.600A>T (p.Thr200=) | |
3 | g.122262224G>A | CA16617817 | CASR | c.1189G>A (p.Gly397Arg) c.706G>A (p.Gly236Arg) c.601G>A (p.Gly201Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.122262224G>C | CA354152779 | CASR | c.1189G>C (p.Gly397Arg) c.706G>C (p.Gly236Arg) c.601G>C (p.Gly201Arg) | |
3 | g.122262224G= | CA1397873664 | CASR | c.1189G= (p.Gly397=) c.706G= (p.Gly236=) c.601G= (p.Gly201=) | |
3 | g.122262224G>T | CA354152780 | CASR | c.1189G>T (p.Gly397Trp) c.706G>T (p.Gly236Trp) c.601G>T (p.Gly201Trp) | |
3 | g.122262225G>A | CA354152781 | CASR | c.1190G>A (p.Gly397Glu) c.707G>A (p.Gly236Glu) c.602G>A (p.Gly201Glu) | ClinVar dbSNP |
3 | g.122262225G>C | CA354152782 | CASR | c.1190G>C (p.Gly397Ala) c.707G>C (p.Gly236Ala) c.602G>C (p.Gly201Ala) | |
3 | g.122262225G= | CA1397873669 | CASR | c.1190G= (p.Gly397=) c.707G= (p.Gly236=) c.602G= (p.Gly201=) | |
3 | g.122262225G>T | CA354152783 | CASR | c.1190G>T (p.Gly397Val) c.707G>T (p.Gly236Val) c.602G>T (p.Gly201Val) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.122262226G>A | CA2569609 | CASR | c.1191G>A (p.Gly397=) c.708G>A (p.Gly236=) c.603G>A (p.Gly201=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.122262226G>C | CA435424657 | CASR | c.1191G>C (p.Gly397=) c.708G>C (p.Gly236=) c.603G>C (p.Gly201=) | |
3 | g.122262226G= | CA1397873671 | CASR | c.1191G= (p.Gly397=) c.708G= (p.Gly236=) c.603G= (p.Gly201=) | |
3 | g.122262226G>T | CA435424656 | CASR | c.1191G>T (p.Gly397=) c.708G>T (p.Gly236=) c.603G>T (p.Gly201=) | gnomAD v4 |
3 | g.122262227G>A | CA216118 | CASR | c.1192G>A (p.Asp398Asn) c.709G>A (p.Asp237Asn) c.604G>A (p.Asp202Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262227G>C | CA354152784 | CASR | c.1192G>C (p.Asp398His) c.709G>C (p.Asp237His) c.604G>C (p.Asp202His) | |
3 | g.122262227G= | CA1397873674 | CASR | c.1192G= (p.Asp398=) c.709G= (p.Asp237=) c.604G= (p.Asp202=) | |
3 | g.122262227G>T | CA354152785 | CASR | c.1192G>T (p.Asp398Tyr) c.709G>T (p.Asp237Tyr) c.604G>T (p.Asp202Tyr) | ClinVar dbSNP |
3 | g.122262228A= | CA1397873680 | CASR | c.1193A= (p.Asp398=) c.710A= (p.Asp237=) c.605A= (p.Asp202=) | |
3 | g.122262228A>C | CA354152786 | CASR | c.1193A>C (p.Asp398Ala) c.710A>C (p.Asp237Ala) c.605A>C (p.Asp202Ala) | |
3 | g.122262228A>G | CA2569610 | CASR | c.1193A>G (p.Asp398Gly) c.710A>G (p.Asp237Gly) c.605A>G (p.Asp202Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262228A>T | CA354152787 | CASR | c.1193A>T (p.Asp398Val) c.710A>T (p.Asp237Val) c.605A>T (p.Asp202Val) | ClinVar dbSNP gnomAD v4 |
3 | g.122262229T>A | CA354152788 | CASR | c.1194T>A (p.Asp398Glu) c.711T>A (p.Asp237Glu) c.606T>A (p.Asp202Glu) | |
3 | g.122262229T>C | CA435424658 | CASR | c.1194T>C (p.Asp398=) c.711T>C (p.Asp237=) c.606T>C (p.Asp202=) | |
3 | g.122262229T>G | CA354152789 | CASR | c.1194T>G (p.Asp398Glu) c.711T>G (p.Asp237Glu) c.606T>G (p.Asp202Glu) | gnomAD v4 |
3 | g.122262230G>A | CA354152790 | CASR | c.1195G>A (p.Glu399Lys) c.712G>A (p.Glu238Lys) c.607G>A (p.Glu203Lys) | |
3 | g.122262230G>C | CA354152791 | CASR | c.1195G>C (p.Glu399Gln) c.712G>C (p.Glu238Gln) c.607G>C (p.Glu203Gln) | |
3 | g.122262230G>T | CA354152792 | CASR | c.1195G>T (p.Glu399Ter) c.712G>T (p.Glu238Ter) c.607G>T (p.Glu203Ter) | |
3 | g.122262231A>C | CA354152793 | CASR | c.1196A>C (p.Glu399Ala) c.713A>C (p.Glu238Ala) c.608A>C (p.Glu203Ala) | |
3 | g.122262231A>G | CA354152794 | CASR | c.1196A>G (p.Glu399Gly) c.713A>G (p.Glu238Gly) c.608A>G (p.Glu203Gly) | |
3 | g.122262231A>T | CA354152795 | CASR | c.1196A>T (p.Glu399Val) c.713A>T (p.Glu238Val) c.608A>T (p.Glu203Val) | |
3 | g.122262232G>A | CA435424663 | CASR | c.1197G>A (p.Glu399=) c.714G>A (p.Glu238=) c.609G>A (p.Glu203=) | |
3 | g.122262232G>C | CA354152796 | CASR | c.1197G>C (p.Glu399Asp) c.714G>C (p.Glu238Asp) c.609G>C (p.Glu203Asp) | COSMIC |
3 | g.122262232G>T | CA354152797 | CASR | c.1197G>T (p.Glu399Asp) c.714G>T (p.Glu238Asp) c.609G>T (p.Glu203Asp) | |
3 | g.122262233A= | CA1397873682 | CASR | c.1198A= (p.Asn400=) c.715A= (p.Asn239=) c.610A= (p.Asn204=) | |
3 | g.122262233A>C | CA354152798 | CASR | c.1198A>C (p.Asn400His) c.715A>C (p.Asn239His) c.610A>C (p.Asn204His) | |
3 | g.122262233A>G | CA354152799 | CASR | c.1198A>G (p.Asn400Asp) c.715A>G (p.Asn239Asp) c.610A>G (p.Asn204Asp) | ClinVar dbSNP |
3 | g.122262233A>T | CA354152800 | CASR | c.1198A>T (p.Asn400Tyr) c.715A>T (p.Asn239Tyr) c.610A>T (p.Asn204Tyr) | ClinVar |
3 | g.122262234A= | CA1397873686 | CASR | c.1199A= (p.Asn400=) c.716A= (p.Asn239=) c.611A= (p.Asn204=) | |
3 | g.122262234A>C | CA354152801 | CASR | c.1199A>C (p.Asn400Thr) c.716A>C (p.Asn239Thr) c.611A>C (p.Asn204Thr) | |
3 | g.122262234A>G | CA354152802 | CASR | c.1199A>G (p.Asn400Ser) c.716A>G (p.Asn239Ser) c.611A>G (p.Asn204Ser) | dbSNP |
3 | g.122262234A>T | CA2569611 | CASR | c.1199A>T (p.Asn400Ile) c.716A>T (p.Asn239Ile) c.611A>T (p.Asn204Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262235C>A | CA354152803 | CASR | c.1200C>A (p.Asn400Lys) c.717C>A (p.Asn239Lys) c.612C>A (p.Asn204Lys) | |
3 | g.122262235C>G | CA354152804 | CASR | c.1200C>G (p.Asn400Lys) c.717C>G (p.Asn239Lys) c.612C>G (p.Asn204Lys) | |
3 | g.122262235C>T | CA435424667 | CASR | c.1200C>T (p.Asn400=) c.717C>T (p.Asn239=) c.612C>T (p.Asn204=) | |
3 | g.122262236A>C | CA354152805 | CASR | c.1201A>C (p.Ile401Leu) c.718A>C (p.Ile240Leu) c.613A>C (p.Ile205Leu) | |
3 | g.122262236A>G | CA354152807 | CASR | c.1201A>G (p.Ile401Val) c.718A>G (p.Ile240Val) c.613A>G (p.Ile205Val) | |
3 | g.122262236A>T | CA354152806 | CASR | c.1201A>T (p.Ile401Phe) c.718A>T (p.Ile240Phe) c.613A>T (p.Ile205Phe) | |
3 | g.122262237T>A | CA354152808 | CASR | c.1202T>A (p.Ile401Asn) c.719T>A (p.Ile240Asn) c.614T>A (p.Ile205Asn) | |
3 | g.122262237T>C | CA354152809 | CASR | c.1202T>C (p.Ile401Thr) c.719T>C (p.Ile240Thr) c.614T>C (p.Ile205Thr) | |
3 | g.122262237T>G | CA354152810 | CASR | c.1202T>G (p.Ile401Ser) c.719T>G (p.Ile240Ser) c.614T>G (p.Ile205Ser) | |
3 | g.122262238C>A | CA435424674 | CASR | c.1203C>A (p.Ile401=) c.720C>A (p.Ile240=) c.615C>A (p.Ile205=) | |
3 | g.122262238C>G | CA354152811 | CASR | c.1203C>G (p.Ile401Met) c.720C>G (p.Ile240Met) c.615C>G (p.Ile205Met) | |
3 | g.122262238C>T | CA435424675 | CASR | c.1203C>T (p.Ile401=) c.720C>T (p.Ile240=) c.615C>T (p.Ile205=) | |
3 | g.122262239A>C | CA354152812 | CASR | c.1204A>C (p.Ser402Arg) c.721A>C (p.Ser241Arg) c.616A>C (p.Ser206Arg) | |
3 | g.122262239A>G | CA354152813 | CASR | c.1204A>G (p.Ser402Gly) c.721A>G (p.Ser241Gly) c.616A>G (p.Ser206Gly) | ClinVar gnomAD v4 |
3 | g.122262239A>T | CA354152814 | CASR | c.1204A>T (p.Ser402Cys) c.721A>T (p.Ser241Cys) c.616A>T (p.Ser206Cys) | |
3 | g.122262240G>A | CA354152815 | CASR | c.1205G>A (p.Ser402Asn) c.722G>A (p.Ser241Asn) c.617G>A (p.Ser206Asn) | ClinVar dbSNP gnomAD v4 |
3 | g.122262240G>C | CA354152816 | CASR | c.1205G>C (p.Ser402Thr) c.722G>C (p.Ser241Thr) c.617G>C (p.Ser206Thr) | |
3 | g.122262240G= | CA1397873689 | CASR | c.1205G= (p.Ser402=) c.722G= (p.Ser241=) c.617G= (p.Ser206=) | |
3 | g.122262240G>T | CA354152817 | CASR | c.1205G>T (p.Ser402Ile) c.722G>T (p.Ser241Ile) c.617G>T (p.Ser206Ile) | |
3 | g.122262241C>A | CA354152818 | CASR | c.1206C>A (p.Ser402Arg) c.723C>A (p.Ser241Arg) c.618C>A (p.Ser206Arg) | |
3 | g.122262241C= | CA1397873693 | CASR | c.1206C= (p.Ser402=) c.723C= (p.Ser241=) c.618C= (p.Ser206=) | |
3 | g.122262241C>G | CA2569612 | CASR | c.1206C>G (p.Ser402Arg) c.723C>G (p.Ser241Arg) c.618C>G (p.Ser206Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.122262241C>T | CA435424678 | CASR | c.1206C>T (p.Ser402=) c.723C>T (p.Ser241=) c.618C>T (p.Ser206=) | gnomAD v4 |
3 | g.122262242A= | CA1397873701 | CASR | c.1207A= (p.Ser403=) c.724A= (p.Ser242=) c.619A= (p.Ser207=) | |
3 | g.122262242A>C | CA354152820 | CASR | c.1207A>C (p.Ser403Arg) c.724A>C (p.Ser242Arg) c.619A>C (p.Ser207Arg) | ClinVar dbSNP gnomAD v4 |
3 | g.122262242A>G | CA354152819 | CASR | c.1207A>G (p.Ser403Gly) c.724A>G (p.Ser242Gly) c.619A>G (p.Ser207Gly) | ClinVar |
3 | g.122262242A>T | CA2569613 | CASR | c.1207A>T (p.Ser403Cys) c.724A>T (p.Ser242Cys) c.619A>T (p.Ser207Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.122262243G>A | CA354152821 | CASR | c.1208G>A (p.Ser403Asn) c.725G>A (p.Ser242Asn) c.620G>A (p.Ser207Asn) | gnomAD v4 |
3 | g.122262243G>C | CA354152822 | CASR | c.1208G>C (p.Ser403Thr) c.725G>C (p.Ser242Thr) c.620G>C (p.Ser207Thr) | |
3 | g.122262243G>T | CA354152823 | CASR | c.1208G>T (p.Ser403Ile) c.725G>T (p.Ser242Ile) c.620G>T (p.Ser207Ile) | |
3 | g.122262244T>A | CA354152824 | CASR | c.1209T>A (p.Ser403Arg) c.726T>A (p.Ser242Arg) c.621T>A (p.Ser207Arg) | |
3 | g.122262244T>C | CA216120 | CASR | c.1209T>C (p.Ser403=) c.726T>C (p.Ser242=) c.621T>C (p.Ser207=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.122262244T>G | CA354152825 | CASR | c.1209T>G (p.Ser403Arg) c.726T>G (p.Ser242Arg) c.621T>G (p.Ser207Arg) | ClinVar dbSNP gnomAD v4 |
3 | g.122262244T= | CA1397873708 | CASR | c.1209T= (p.Ser403=) c.726T= (p.Ser242=) c.621T= (p.Ser207=) | |
3 | g.122262245G>A | CA354152826 | CASR | c.1210G>A (p.Val404Ile) c.727G>A (p.Val243Ile) c.622G>A (p.Val208Ile) | |
3 | g.122262245G>C | CA354152827 | CASR | c.1210G>C (p.Val404Leu) c.727G>C (p.Val243Leu) c.622G>C (p.Val208Leu) | |
3 | g.122262245G>T | CA354152828 | CASR | c.1210G>T (p.Val404Phe) c.727G>T (p.Val243Phe) c.622G>T (p.Val208Phe) | |
3 | g.122262246T>A | CA354152829 | CASR | c.1211T>A (p.Val404Asp) c.728T>A (p.Val243Asp) c.623T>A (p.Val208Asp) | |
3 | g.122262246T>C | CA354152830 | CASR | c.1211T>C (p.Val404Ala) c.728T>C (p.Val243Ala) c.623T>C (p.Val208Ala) | |
3 | g.122262246T>G | CA354152831 | CASR | c.1211T>G (p.Val404Gly) c.728T>G (p.Val243Gly) c.623T>G (p.Val208Gly) | ClinVar dbSNP |
3 | g.122262246T= | CA1397873713 | CASR | c.1211T= (p.Val404=) c.728T= (p.Val243=) c.623T= (p.Val208=) | |
3 | g.122262247C>A | CA435424687 | CASR | c.1212C>A (p.Val404=) c.729C>A (p.Val243=) c.624C>A (p.Val208=) | |
3 | g.122262247C= | CA1397873720 | CASR | c.1212C= (p.Val404=) c.729C= (p.Val243=) c.624C= (p.Val208=) | |
3 | g.122262247C>G | CA16611297 | CASR | c.1212C>G (p.Val404=) c.729C>G (p.Val243=) c.624C>G (p.Val208=) | ClinVar dbSNP gnomAD v4 |
3 | g.122262247C>T | CA82739001 | CASR | c.1212C>T (p.Val404=) c.729C>T (p.Val243=) c.624C>T (p.Val208=) | ClinVar dbSNP gnomAD v4 COSMIC |
3 | g.122262248G>A | CA82739006 | CASR | c.1213G>A (p.Glu405Lys) c.730G>A (p.Glu244Lys) c.625G>A (p.Glu209Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.122262248G>C | CA354152833 | CASR | c.1213G>C (p.Glu405Gln) c.730G>C (p.Glu244Gln) c.625G>C (p.Glu209Gln) | |
3 | g.122262248G= | CA1397873728 | CASR | c.1213G= (p.Glu405=) c.730G= (p.Glu244=) c.625G= (p.Glu209=) | |
3 | g.122262248G>T | CA354152832 | CASR | c.1213G>T (p.Glu405Ter) c.730G>T (p.Glu244Ter) c.625G>T (p.Glu209Ter) | |
3 | g.122262249A= | CA1397873732 | CASR | c.1214A= (p.Glu405=) c.731A= (p.Glu244=) c.626A= (p.Glu209=) | |
3 | g.122262249A>C | CA354152834 | CASR | c.1214A>C (p.Glu405Ala) c.731A>C (p.Glu244Ala) c.626A>C (p.Glu209Ala) | |
3 | g.122262249A>G | CA354152835 | CASR | c.1214A>G (p.Glu405Gly) c.731A>G (p.Glu244Gly) c.626A>G (p.Glu209Gly) | ClinVar dbSNP |
3 | g.122262249A>T | CA354152836 | CASR | c.1214A>T (p.Glu405Val) c.731A>T (p.Glu244Val) c.626A>T (p.Glu209Val) | |
3 | g.122262250G>A | CA435424691 | CASR | c.1215G>A (p.Glu405=) c.732G>A (p.Glu244=) c.627G>A (p.Glu209=) | |
3 | g.122262250G>C | CA354152837 | CASR | c.1215G>C (p.Glu405Asp) c.732G>C (p.Glu244Asp) c.627G>C (p.Glu209Asp) | gnomAD v4 |
3 | g.122262250G>T | CA354152838 | CASR | c.1215G>T (p.Glu405Asp) c.732G>T (p.Glu244Asp) c.627G>T (p.Glu209Asp) | |
3 | g.122262251A>C | CA354152841 | CASR | c.1216A>C (p.Thr406Pro) c.733A>C (p.Thr245Pro) c.628A>C (p.Thr210Pro) | |
3 | g.122262251A>G | CA354152840 | CASR | c.1216A>G (p.Thr406Ala) c.733A>G (p.Thr245Ala) c.628A>G (p.Thr210Ala) | |
3 | g.122262251A>T | CA354152839 | CASR | c.1216A>T (p.Thr406Ser) c.733A>T (p.Thr245Ser) c.628A>T (p.Thr210Ser) | |
3 | g.122262252C>A | CA354152842 | CASR | c.1217C>A (p.Thr406Asn) c.734C>A (p.Thr245Asn) c.629C>A (p.Thr210Asn) | |
3 | g.122262252C>G | CA354152843 | CASR | c.1217C>G (p.Thr406Ser) c.734C>G (p.Thr245Ser) c.629C>G (p.Thr210Ser) | |
3 | g.122262252C>T | CA354152844 | CASR | c.1217C>T (p.Thr406Ile) c.734C>T (p.Thr245Ile) c.629C>T (p.Thr210Ile) | |
3 | g.122262253C>A | CA435424698 | CASR | c.1218C>A (p.Thr406=) c.735C>A (p.Thr245=) c.630C>A (p.Thr210=) | ClinVar gnomAD v4 |
3 | g.122262253C>G | CA435424697 | CASR | c.1218C>G (p.Thr406=) c.735C>G (p.Thr245=) c.630C>G (p.Thr210=) | ClinVar |
3 | g.122262253C>T | CA435424696 | CASR | c.1218C>T (p.Thr406=) c.735C>T (p.Thr245=) c.630C>T (p.Thr210=) | |
3 | g.122262253_122262254delinsAG | CA645532163 | CASR | c.1218_1219delinsAG (p.Pro407Ala) c.735_736delinsAG (p.Pro246Ala) c.630_631delinsAG (p.Pro211Ala) | COSMIC |
3 | g.122262254C>A | CA354152845 | CASR | c.1219C>A (p.Pro407Thr) c.736C>A (p.Pro246Thr) c.631C>A (p.Pro211Thr) | |
3 | g.122262254C= | CA1397873735 | CASR | c.1219C= (p.Pro407=) c.736C= (p.Pro246=) c.631C= (p.Pro211=) | |
3 | g.122262254C>G | CA82739012 | CASR | c.1219C>G (p.Pro407Ala) c.736C>G (p.Pro246Ala) c.631C>G (p.Pro211Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.122262254C>T | CA354152846 | CASR | c.1219C>T (p.Pro407Ser) c.736C>T (p.Pro246Ser) c.631C>T (p.Pro211Ser) | |
3 | g.122262255C>A | CA354152847 | CASR | c.1220C>A (p.Pro407His) c.737C>A (p.Pro246His) c.632C>A (p.Pro211His) | |
3 | g.122262255C>G | CA354152849 | CASR | c.1220C>G (p.Pro407Arg) c.737C>G (p.Pro246Arg) c.632C>G (p.Pro211Arg) | gnomAD v4 |
3 | g.122262255C>T | CA354152848 | CASR | c.1220C>T (p.Pro407Leu) c.737C>T (p.Pro246Leu) c.632C>T (p.Pro211Leu) | |
3 | g.122262256T>A | CA435424705 | CASR | c.1221T>A (p.Pro407=) c.738T>A (p.Pro246=) c.633T>A (p.Pro211=) | |
3 | g.122262256T>C | CA435424706 | CASR | c.1221T>C (p.Pro407=) c.738T>C (p.Pro246=) c.633T>C (p.Pro211=) | |
3 | g.122262256T>G | CA435424708 | CASR | c.1221T>G (p.Pro407=) c.738T>G (p.Pro246=) c.633T>G (p.Pro211=) | |
3 | g.122262257T>A | CA354152850 | CASR | c.1222T>A (p.Tyr408Asn) c.739T>A (p.Tyr247Asn) c.634T>A (p.Tyr212Asn) | |
3 | g.122262257T>C | CA354152851 | CASR | c.1222T>C (p.Tyr408His) c.739T>C (p.Tyr247His) c.634T>C (p.Tyr212His) | |
3 | g.122262257T>G | CA354152852 | CASR | c.1222T>G (p.Tyr408Asp) c.739T>G (p.Tyr247Asp) c.634T>G (p.Tyr212Asp) | |
3 | g.122262258A= | CA1397873741 | CASR | c.1223A= (p.Tyr408=) c.740A= (p.Tyr247=) c.635A= (p.Tyr212=) | |
3 | g.122262258A>C | CA354152853 | CASR | c.1223A>C (p.Tyr408Ser) c.740A>C (p.Tyr247Ser) c.635A>C (p.Tyr212Ser) | |
3 | g.122262258A>G | CA354152854 | CASR | c.1223A>G (p.Tyr408Cys) c.740A>G (p.Tyr247Cys) c.635A>G (p.Tyr212Cys) | ClinVar dbSNP |
3 | g.122262258A>T | CA354152855 | CASR | c.1223A>T (p.Tyr408Phe) c.740A>T (p.Tyr247Phe) c.635A>T (p.Tyr212Phe) | |
3 | g.122262259C>A | CA354152856 | CASR | c.1224C>A (p.Tyr408Ter) c.741C>A (p.Tyr247Ter) c.636C>A (p.Tyr212Ter) | |
3 | g.122262259C>G | CA354152857 | CASR | c.1224C>G (p.Tyr408Ter) c.741C>G (p.Tyr247Ter) c.636C>G (p.Tyr212Ter) | |
3 | g.122262259C>T | CA435424712 | CASR | c.1224C>T (p.Tyr408=) c.741C>T (p.Tyr247=) c.636C>T (p.Tyr212=) | ClinVar dbSNP |
3 | g.122262260A= | CA1397873744 | CASR | c.1225A= (p.Ile409=) c.742A= (p.Ile248=) c.637A= (p.Ile213=) | |
3 | g.122262260A>C | CA354152858 | CASR | c.1225A>C (p.Ile409Leu) c.742A>C (p.Ile248Leu) c.637A>C (p.Ile213Leu) | ClinVar gnomAD v4 |
3 | g.122262260A>G | CA354152859 | CASR | c.1225A>G (p.Ile409Val) c.742A>G (p.Ile248Val) c.637A>G (p.Ile213Val) | ClinVar dbSNP gnomAD v4 |
3 | g.122262260A>T | CA354152860 | CASR | c.1225A>T (p.Ile409Leu) c.742A>T (p.Ile248Leu) c.637A>T (p.Ile213Leu) | |
3 | g.122262261T>A | CA354152861 | CASR | c.1226T>A (p.Ile409Lys) c.743T>A (p.Ile248Lys) c.638T>A (p.Ile213Lys) | |
3 | g.122262261T>C | CA354152863 | CASR | c.1226T>C (p.Ile409Thr) c.743T>C (p.Ile248Thr) c.638T>C (p.Ile213Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.122262261T>G | CA354152862 | CASR | c.1226T>G (p.Ile409Arg) c.743T>G (p.Ile248Arg) c.638T>G (p.Ile213Arg) | |
3 | g.122262261T= | CA1397873751 | CASR | c.1226T= (p.Ile409=) c.743T= (p.Ile248=) c.638T= (p.Ile213=) | |
3 | g.122262262A>C | CA435424718 | CASR | c.1227A>C (p.Ile409=) c.744A>C (p.Ile248=) c.639A>C (p.Ile213=) | |
3 | g.122262262A>G | CA354152864 | CASR | c.1227A>G (p.Ile409Met) c.744A>G (p.Ile248Met) c.639A>G (p.Ile213Met) | |
3 | g.122262262A>T | CA435424719 | CASR | c.1227A>T (p.Ile409=) c.744A>T (p.Ile248=) c.639A>T (p.Ile213=) | |
3 | g.122262263G>A | CA354152866 | CASR | c.1228G>A (p.Asp410Asn) c.745G>A (p.Asp249Asn) c.640G>A (p.Asp214Asn) | |
3 | g.122262263G>C | CA354152865 | CASR | c.1228G>C (p.Asp410His) c.745G>C (p.Asp249His) c.640G>C (p.Asp214His) | |
3 | g.122262263G>T | CA354152867 | CASR | c.1228G>T (p.Asp410Tyr) c.745G>T (p.Asp249Tyr) c.640G>T (p.Asp214Tyr) | gnomAD v4 |
3 | g.122262264A>C | CA354152868 | CASR | c.1229A>C (p.Asp410Ala) c.746A>C (p.Asp249Ala) c.641A>C (p.Asp214Ala) | |
3 | g.122262264A>G | CA354152869 | CASR | c.1229A>G (p.Asp410Gly) c.746A>G (p.Asp249Gly) c.641A>G (p.Asp214Gly) | |
3 | g.122262264A>T | CA354152870 | CASR | c.1229A>T (p.Asp410Val) c.746A>T (p.Asp249Val) c.641A>T (p.Asp214Val) | |
3 | g.122262265T>A | CA354152871 | CASR | c.1230T>A (p.Asp410Glu) c.747T>A (p.Asp249Glu) c.642T>A (p.Asp214Glu) | |
3 | g.122262265T>C | CA435424725 | CASR | c.1230T>C (p.Asp410=) c.747T>C (p.Asp249=) c.642T>C (p.Asp214=) | |
3 | g.122262265T>G | CA354152872 | CASR | c.1230T>G (p.Asp410Glu) c.747T>G (p.Asp249Glu) c.642T>G (p.Asp214Glu) | |
3 | g.122262266T>A | CA354152873 | CASR | c.1231T>A (p.Tyr411Asn) c.748T>A (p.Tyr250Asn) c.643T>A (p.Tyr215Asn) | ClinVar |
3 | g.122262266T>C | CA354152874 | CASR | c.1231T>C (p.Tyr411His) c.748T>C (p.Tyr250His) c.643T>C (p.Tyr215His) | |
3 | g.122262266T>G | CA354152875 | CASR | c.1231T>G (p.Tyr411Asp) c.748T>G (p.Tyr250Asp) c.643T>G (p.Tyr215Asp) | ClinVar |
3 | g.122262267A>C | CA354152876 | CASR | c.1232A>C (p.Tyr411Ser) c.749A>C (p.Tyr250Ser) c.644A>C (p.Tyr215Ser) | ClinVar |
3 | g.122262267A>G | CA354152877 | CASR | c.1232A>G (p.Tyr411Cys) c.749A>G (p.Tyr250Cys) c.644A>G (p.Tyr215Cys) | ClinVar |
3 | g.122262267A>T | CA354152878 | CASR | c.1232A>T (p.Tyr411Phe) c.749A>T (p.Tyr250Phe) c.644A>T (p.Tyr215Phe) | |
3 | g.122262268C>A | CA354152879 | CASR | c.1233C>A (p.Tyr411Ter) c.750C>A (p.Tyr250Ter) c.645C>A (p.Tyr215Ter) | |
3 | g.122262268C>G | CA354152880 | CASR | c.1233C>G (p.Tyr411Ter) c.750C>G (p.Tyr250Ter) c.645C>G (p.Tyr215Ter) | |
3 | g.122262268C>T | CA435424730 | CASR | c.1233C>T (p.Tyr411=) c.750C>T (p.Tyr250=) c.645C>T (p.Tyr215=) | ClinVar dbSNP gnomAD v4 |
3 | g.122262269A= | CA1397873755 | CASR | c.1234A= (p.Thr412=) c.751A= (p.Thr251=) c.646A= (p.Thr216=) | |
3 | g.122262269A>C | CA354152881 | CASR | c.1234A>C (p.Thr412Pro) c.751A>C (p.Thr251Pro) c.646A>C (p.Thr216Pro) | |
3 | g.122262269A>G | CA354152883 | CASR | c.1234A>G (p.Thr412Ala) c.751A>G (p.Thr251Ala) c.646A>G (p.Thr216Ala) | ClinVar dbSNP gnomAD v4 |
3 | g.122262269A>T | CA354152882 | CASR | c.1234A>T (p.Thr412Ser) c.751A>T (p.Thr251Ser) c.646A>T (p.Thr216Ser) | |
3 | g.122262270C>A | CA354152884 | CASR | c.1235C>A (p.Thr412Lys) c.752C>A (p.Thr251Lys) c.647C>A (p.Thr216Lys) | |
3 | g.122262270C= | CA1397873758 | CASR | c.1235C= (p.Thr412=) c.752C= (p.Thr251=) c.647C= (p.Thr216=) | |
3 | g.122262270C>G | CA354152885 | CASR | c.1235C>G (p.Thr412Arg) c.752C>G (p.Thr251Arg) c.647C>G (p.Thr216Arg) | |
3 | g.122262270C>T | CA354152886 | CASR | c.1235C>T (p.Thr412Met) c.752C>T (p.Thr251Met) c.647C>T (p.Thr216Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262271G>A | CA435424731 | CASR | c.1236G>A (p.Thr412=) c.753G>A (p.Thr251=) c.648G>A (p.Thr216=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.122262271G>C | CA435424734 | CASR | c.1236G>C (p.Thr412=) c.753G>C (p.Thr251=) c.648G>C (p.Thr216=) | ClinVar |
3 | g.122262271G= | CA1397873766 | CASR | c.1236G= (p.Thr412=) c.753G= (p.Thr251=) c.648G= (p.Thr216=) | |
3 | g.122262271G>T | CA82739016 | CASR | c.1236G>T (p.Thr412=) c.753G>T (p.Thr251=) c.648G>T (p.Thr216=) | ClinVar dbSNP gnomAD v4 |
3 | g.122262272C>A | CA354152887 | CASR | c.1237C>A (p.His413Asn) c.754C>A (p.His252Asn) c.649C>A (p.His217Asn) | |
3 | g.122262272C>G | CA354152888 | CASR | c.1237C>G (p.His413Asp) c.754C>G (p.His252Asp) c.649C>G (p.His217Asp) | |
3 | g.122262272C>T | CA354152889 | CASR | c.1237C>T (p.His413Tyr) c.754C>T (p.His252Tyr) c.649C>T (p.His217Tyr) | ClinVar dbSNP |
3 | g.122262273A= | CA1397873773 | CASR | c.1238A= (p.His413=) c.755A= (p.His252=) c.650A= (p.His217=) | |
3 | g.122262273A>C | CA354152890 | CASR | c.1238A>C (p.His413Pro) c.755A>C (p.His252Pro) c.650A>C (p.His217Pro) | |
3 | g.122262273A>G | CA354152891 | CASR | c.1238A>G (p.His413Arg) c.755A>G (p.His252Arg) c.650A>G (p.His217Arg) | gnomAD v4 |
3 | g.122262273A>T | CA354152892 | CASR | c.1238A>T (p.His413Leu) c.755A>T (p.His252Leu) c.650A>T (p.His217Leu) | ClinVar dbSNP gnomAD v4 |
3 | g.122262274T>A | CA354152894 | CASR | c.1239T>A (p.His413Gln) c.756T>A (p.His252Gln) c.651T>A (p.His217Gln) | |
3 | g.122262274T>C | CA435424736 | CASR | c.1239T>C (p.His413=) c.756T>C (p.His252=) c.651T>C (p.His217=) | |
3 | g.122262274T>G | CA354152893 | CASR | c.1239T>G (p.His413Gln) c.756T>G (p.His252Gln) c.651T>G (p.His217Gln) |