Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.202532603A>CCA350341715BMPR2c.1147A>C (p.Met383Leu)
c.1078A>C (p.Met360Leu)
2g.202532603A>GCA350341716BMPR2c.1147A>G (p.Met383Val)
c.1078A>G (p.Met360Val)
2g.202532603A>TCA350341717BMPR2c.1147A>T (p.Met383Leu)
c.1078A>T (p.Met360Leu)
2g.202532603_202532604delinsATCA1321545652BMPR2c.1147_1148delinsAT (p.Met383=)
c.1078_1079delinsAT (p.Met360=)
2g.202532604delCA658655725BMPR2c.1148del (p.Met383ArgfsTer6)
c.1079del (p.Met360ArgfsTer6)
 ClinVar dbSNP
2g.202532604T>ACA350341718BMPR2c.1148T>A (p.Met383Lys)
c.1079T>A (p.Met360Lys)
2g.202532604T>CCA350341719BMPR2c.1148T>C (p.Met383Thr)
c.1079T>C (p.Met360Thr)
2g.202532604T>GCA350341720BMPR2c.1148T>G (p.Met383Arg)
c.1079T>G (p.Met360Arg)
2g.202532604dupCA2586971100BMPR2c.1148dup (p.Met383IlefsTer16)
c.1079dup (p.Met360IlefsTer16)
2g.202532605G>ACA350341721BMPR2c.1149G>A (p.Met383Ile)
c.1080G>A (p.Met360Ile)
2g.202532605G>CCA350341723BMPR2c.1149G>C (p.Met383Ile)
c.1080G>C (p.Met360Ile)
2g.202532605G>TCA350341722BMPR2c.1149G>T (p.Met383Ile)
c.1080G>T (p.Met360Ile)
2g.202532606G>ACA350341724BMPR2c.1150G>A (p.Ala384Thr)
c.1081G>A (p.Ala361Thr)
2g.202532606G>CCA350341726BMPR2c.1150G>C (p.Ala384Pro)
c.1081G>C (p.Ala361Pro)
2g.202532606G>TCA350341725BMPR2c.1150G>T (p.Ala384Ser)
c.1081G>T (p.Ala361Ser)
2g.202532607C>ACA350341727BMPR2c.1151C>A (p.Ala384Glu)
c.1082C>A (p.Ala361Glu)
2g.202532607C=CA1321545653BMPR2c.1151C= (p.Ala384=)
c.1082C= (p.Ala361=)
2g.202532607C>GCA350341729BMPR2c.1151C>G (p.Ala384Gly)
c.1082C>G (p.Ala361Gly)
2g.202532607C>TCA350341728BMPR2c.1151C>T (p.Ala384Val)
c.1082C>T (p.Ala361Val)
 ClinVar dbSNP
2g.202532608A>CCA430849428BMPR2c.1152A>C (p.Ala384=)
c.1083A>C (p.Ala361=)
2g.202532608A>GCA430849429BMPR2c.1152A>G (p.Ala384=)
c.1083A>G (p.Ala361=)
2g.202532608A>TCA430849430BMPR2c.1152A>T (p.Ala384=)
c.1083A>T (p.Ala361=)
2g.202532609C>ACA350341730BMPR2c.1153C>A (p.Pro385Thr)
c.1084C>A (p.Pro362Thr)
2g.202532609C>GCA350341731BMPR2c.1153C>G (p.Pro385Ala)
c.1084C>G (p.Pro362Ala)
2g.202532609C>TCA350341732BMPR2c.1153C>T (p.Pro385Ser)
c.1084C>T (p.Pro362Ser)
2g.202532610C>ACA350341733BMPR2c.1154C>A (p.Pro385Gln)
c.1085C>A (p.Pro362Gln)
2g.202532610C>GCA350341734BMPR2c.1154C>G (p.Pro385Arg)
c.1085C>G (p.Pro362Arg)
 ClinVar dbSNP
2g.202532610C>TCA350341735BMPR2c.1154C>T (p.Pro385Leu)
c.1085C>T (p.Pro362Leu)
2g.202532611A>CCA430849440BMPR2c.1155A>C (p.Pro385=)
c.1086A>C (p.Pro362=)
2g.202532611A>GCA430849442BMPR2c.1155A>G (p.Pro385=)
c.1086A>G (p.Pro362=)
2g.202532611A>TCA430849441BMPR2c.1155A>T (p.Pro385=)
c.1086A>T (p.Pro362=)
2g.202532612G>ACA350341736BMPR2c.1156G>A (p.Glu386Lys)
c.1087G>A (p.Glu363Lys)
 ClinVar dbSNP
2g.202532612G>CCA350341737BMPR2c.1156G>C (p.Glu386Gln)
c.1087G>C (p.Glu363Gln)
 ClinVar dbSNP
2g.202532612G=CA1321545654BMPR2c.1156G= (p.Glu386=)
c.1087G= (p.Glu363=)
2g.202532612G>TCA350341738BMPR2c.1156G>T (p.Glu386Ter)
c.1087G>T (p.Glu363Ter)
2g.202532613A=CA1321545655BMPR2c.1157A= (p.Glu386=)
c.1088A= (p.Glu363=)
2g.202532613A>CCA350341739BMPR2c.1157A>C (p.Glu386Ala)
c.1088A>C (p.Glu363Ala)
 ClinVar dbSNP
2g.202532613A>GCA350341740BMPR2c.1157A>G (p.Glu386Gly)
c.1088A>G (p.Glu363Gly)
 ClinVar dbSNP COSMIC
2g.202532613A>TCA350341741BMPR2c.1157A>T (p.Glu386Val)
c.1088A>T (p.Glu363Val)
 ClinVar dbSNP
2g.202532614A>CCA350341742BMPR2c.1158A>C (p.Glu386Asp)
c.1089A>C (p.Glu363Asp)
2g.202532614A>GCA430849455BMPR2c.1158A>G (p.Glu386=)
c.1089A>G (p.Glu363=)
2g.202532614A>TCA350341743BMPR2c.1158A>T (p.Glu386Asp)
c.1089A>T (p.Glu363Asp)
2g.202532615G>ACA350341744BMPR2c.1159G>A (p.Val387Met)
c.1090G>A (p.Val364Met)
2g.202532615G>CCA350341745BMPR2c.1159G>C (p.Val387Leu)
c.1090G>C (p.Val364Leu)
2g.202532615G>TCA350341746BMPR2c.1159G>T (p.Val387Leu)
c.1090G>T (p.Val364Leu)
2g.202532616T>ACA350341747BMPR2c.1160T>A (p.Val387Glu)
c.1091T>A (p.Val364Glu)
2g.202532616T>CCA350341748BMPR2c.1160T>C (p.Val387Ala)
c.1091T>C (p.Val364Ala)
2g.202532616T>GCA350341749BMPR2c.1160T>G (p.Val387Gly)
c.1091T>G (p.Val364Gly)
2g.202532617delCA2586971101BMPR2c.1161del (p.Leu388Ter)
c.1092del (p.Leu365Ter)
2g.202532617G>ACA64029547BMPR2c.1161G>A (p.Val387=)
c.1092G>A (p.Val364=)
 dbSNP

Number of alleles fetched