Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73322905_73322920del | CA2629370534 | HCN4 | c.3177_3192del (p.Ser1059ArgfsTer?) c.1959_1974del (p.Ser653ArgfsTer?) | gnomAD v4 |
15 | g.73322904_73322924dup | CA619410586 | HCN4 | c.3169_3189dup (p.Pro1063_Gln1064insAlaSerSerProProProPro) c.1951_1971dup (p.Pro657_Gln658insAlaSerSerProProProPro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322910_73322920del | CA2629370536 | HCN4 | c.3176_3186del (p.Ser1059ThrfsTer?) c.1958_1968del (p.Ser653ThrfsTer?) | gnomAD v4 |
15 | g.73322913_73322930del | CA2629370537 | HCN4 | c.3168_3185del (p.Ala1057_Pro1062del) c.1950_1967del (p.Ala651_Pro656del) | gnomAD v4 |
15 | g.73322917C>A | CA393086066 | HCN4 | c.3176G>T (p.Ser1059Ile) c.1958G>T (p.Ser653Ile) | gnomAD v4 |
15 | g.73322917C>G | CA393086067 | HCN4 | c.3176G>C (p.Ser1059Thr) c.1958G>C (p.Ser653Thr) | gnomAD v4 |
15 | g.73322917C>T | CA393086068 | HCN4 | c.3176G>A (p.Ser1059Asn) c.1958G>A (p.Ser653Asn) | gnomAD v4 |
15 | g.73322918T>A | CA393086069 | HCN4 | c.3175A>T (p.Ser1059Cys) c.1957A>T (p.Ser653Cys) | |
15 | g.73322918T>C | CA393086070 | HCN4 | c.3175A>G (p.Ser1059Gly) c.1957A>G (p.Ser653Gly) | gnomAD v4 |
15 | g.73322918T>G | CA393086071 | HCN4 | c.3175A>C (p.Ser1059Arg) c.1957A>C (p.Ser653Arg) | gnomAD v3 gnomAD v4 |
15 | g.73322919G>A | CA491477974 | HCN4 | c.3174C>T (p.Ser1058=) c.1956C>T (p.Ser652=) | ClinVar dbSNP gnomAD v4 |
15 | g.73322919G>C | CA491477975 | HCN4 | c.3174C>G (p.Ser1058=) c.1956C>G (p.Ser652=) | |
15 | g.73322919G>T | CA491477976 | HCN4 | c.3174C>A (p.Ser1058=) c.1956C>A (p.Ser652=) | gnomAD v4 |
15 | g.73322920del | CA2575783822 | HCN4 | c.3174del (p.Ser1059AlafsTer?) c.1956del (p.Ser653AlafsTer?) | |
15 | g.73322920G>A | CA393086072 | HCN4 | c.3173C>T (p.Ser1058Phe) c.1955C>T (p.Ser652Phe) | gnomAD v4 |
15 | g.73322920G>C | CA393086073 | HCN4 | c.3173C>G (p.Ser1058Cys) c.1955C>G (p.Ser652Cys) | |
15 | g.73322920G>T | CA393086074 | HCN4 | c.3173C>A (p.Ser1058Tyr) c.1955C>A (p.Ser652Tyr) | gnomAD v4 |
15 | g.73322921A= | CA2187186995 | HCN4 | c.3172T= (p.Ser1058=) c.1954T= (p.Ser652=) | |
15 | g.73322921A>C | CA16620005 | HCN4 | c.3172T>G (p.Ser1058Ala) c.1954T>G (p.Ser652Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322921A>G | CA393086075 | HCN4 | c.3172T>C (p.Ser1058Pro) c.1954T>C (p.Ser652Pro) | gnomAD v4 |
15 | g.73322921A>T | CA393086076 | HCN4 | c.3172T>A (p.Ser1058Thr) c.1954T>A (p.Ser652Thr) | |
15 | g.73322922T>A | CA491477980 | HCN4 | c.3171A>T (p.Ala1057=) c.1953A>T (p.Ala651=) | |
15 | g.73322922T>C | CA491477981 | HCN4 | c.3171A>G (p.Ala1057=) c.1953A>G (p.Ala651=) | ClinVar dbSNP gnomAD v4 |
15 | g.73322922T>G | CA16607864 | HCN4 | c.3171A>C (p.Ala1057=) c.1953A>C (p.Ala651=) | ClinVar dbSNP |
15 | g.73322922T= | CA2187186999 | HCN4 | c.3171A= (p.Ala1057=) c.1953A= (p.Ala651=) | |
15 | g.73322922dup | CA2575783823 | HCN4 | c.3171dup (p.Ser1058IlefsTer?) c.1953dup (p.Ser652IlefsTer?) | |
15 | g.73322923G>A | CA393086079 | HCN4 | c.3170C>T (p.Ala1057Val) c.1952C>T (p.Ala651Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322923G>C | CA393086078 | HCN4 | c.3170C>G (p.Ala1057Gly) c.1952C>G (p.Ala651Gly) | |
15 | g.73322923G= | CA2187187005 | HCN4 | c.3170C= (p.Ala1057=) c.1952C= (p.Ala651=) | |
15 | g.73322923G>T | CA393086077 | HCN4 | c.3170C>A (p.Ala1057Glu) c.1952C>A (p.Ala651Glu) | gnomAD v4 |
15 | g.73322924C>A | CA393086080 | HCN4 | c.3169G>T (p.Ala1057Ser) c.1951G>T (p.Ala651Ser) | gnomAD v4 |
15 | g.73322924C>G | CA393086081 | HCN4 | c.3169G>C (p.Ala1057Pro) c.1951G>C (p.Ala651Pro) | gnomAD v4 |
15 | g.73322924C>T | CA393086082 | HCN4 | c.3169G>A (p.Ala1057Thr) c.1951G>A (p.Ala651Thr) | gnomAD v4 |
15 | g.73322925A= | CA2187187007 | HCN4 | c.3168T= (p.Pro1056=) c.1950T= (p.Pro650=) | |
15 | g.73322925A>C | CA491477982 | HCN4 | c.3168T>G (p.Pro1056=) c.1950T>G (p.Pro650=) | |
15 | g.73322925A>G | CA491477983 | HCN4 | c.3168T>C (p.Pro1056=) c.1950T>C (p.Pro650=) | dbSNP gnomAD v4 |
15 | g.73322925A>T | CA491477985 | HCN4 | c.3168T>A (p.Pro1056=) c.1950T>A (p.Pro650=) | gnomAD v4 |
15 | g.73322925_73322927delinsGGGTGGTGGGGGGCTGGATGCAGT | CA2580089971 | HCN4 | c.3166_3168delinsACTGCATCCAGCCCCCCACCACCC (p.Pro1055_Pro1056insThrAlaSerSerProProPro) c.1948_1950delinsACTGCATCCAGCCCCCCACCACCC (p.Pro649_Pro650insThrAlaSerSerProProPro) | ClinVar |
15 | g.73322926G>A | CA393086083 | HCN4 | c.3167C>T (p.Pro1056Leu) c.1949C>T (p.Pro650Leu) | gnomAD v4 |
15 | g.73322926G>C | CA393086084 | HCN4 | c.3167C>G (p.Pro1056Arg) c.1949C>G (p.Pro650Arg) | dbSNP |
15 | g.73322926G= | CA2187187010 | HCN4 | c.3167C= (p.Pro1056=) c.1949C= (p.Pro650=) | |
15 | g.73322926G>T | CA393086085 | HCN4 | c.3167C>A (p.Pro1056His) c.1949C>A (p.Pro650His) | gnomAD v4 |
15 | g.73322927G>A | CA393086086 | HCN4 | c.3166C>T (p.Pro1056Ser) c.1948C>T (p.Pro650Ser) | gnomAD v4 |
15 | g.73322927G>C | CA393086087 | HCN4 | c.3166C>G (p.Pro1056Ala) c.1948C>G (p.Pro650Ala) | ClinVar gnomAD v4 |
15 | g.73322927G= | CA2187187014 | HCN4 | c.3166C= (p.Pro1056=) c.1948C= (p.Pro650=) | |
15 | g.73322927G>T | CA272663675 | HCN4 | c.3166C>A (p.Pro1056Thr) c.1948C>A (p.Pro650Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322928T>A | CA491477991 | HCN4 | c.3165A>T (p.Pro1055=) c.1947A>T (p.Pro649=) | gnomAD v4 |
15 | g.73322928T>C | CA491477990 | HCN4 | c.3165A>G (p.Pro1055=) c.1947A>G (p.Pro649=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322928T>G | CA491477989 | HCN4 | c.3165A>C (p.Pro1055=) c.1947A>C (p.Pro649=) | gnomAD v4 |
15 | g.73322928T= | CA2187187018 | HCN4 | c.3165A= (p.Pro1055=) c.1947A= (p.Pro649=) | |
15 | g.73322929G>A | CA393086088 | HCN4 | c.3164C>T (p.Pro1055Leu) c.1946C>T (p.Pro649Leu) | gnomAD v4 |
15 | g.73322929G>C | CA393086089 | HCN4 | c.3164C>G (p.Pro1055Arg) c.1946C>G (p.Pro649Arg) | |
15 | g.73322929G>T | CA393086090 | HCN4 | c.3164C>A (p.Pro1055Gln) c.1946C>A (p.Pro649Gln) | gnomAD v4 |
15 | g.73322930G>A | CA393086093 | HCN4 | c.3163C>T (p.Pro1055Ser) c.1945C>T (p.Pro649Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322930G>C | CA393086092 | HCN4 | c.3163C>G (p.Pro1055Ala) c.1945C>G (p.Pro649Ala) | |
15 | g.73322930G= | CA2187187020 | HCN4 | c.3163C= (p.Pro1055=) c.1945C= (p.Pro649=) | |
15 | g.73322930G>T | CA393086091 | HCN4 | c.3163C>A (p.Pro1055Thr) c.1945C>A (p.Pro649Thr) | gnomAD v4 |
15 | g.73322931C>A | CA491477995 | HCN4 | c.3162G>T (p.Leu1054=) c.1944G>T (p.Leu648=) | gnomAD v4 |
15 | g.73322931C>G | CA491477996 | HCN4 | c.3162G>C (p.Leu1054=) c.1944G>C (p.Leu648=) | gnomAD v4 |
15 | g.73322931C>T | CA491477997 | HCN4 | c.3162G>A (p.Leu1054=) c.1944G>A (p.Leu648=) | gnomAD v4 |
15 | g.73322932A>C | CA393086094 | HCN4 | c.3161T>G (p.Leu1054Arg) c.1943T>G (p.Leu648Arg) | |
15 | g.73322932A>G | CA393086096 | HCN4 | c.3161T>C (p.Leu1054Pro) c.1943T>C (p.Leu648Pro) | gnomAD v4 |
15 | g.73322932A>T | CA393086095 | HCN4 | c.3161T>A (p.Leu1054Gln) c.1943T>A (p.Leu648Gln) | gnomAD v4 |
15 | g.73322933G>A | CA491478001 | HCN4 | c.3160C>T (p.Leu1054=) c.1942C>T (p.Leu648=) | gnomAD v4 |
15 | g.73322933G>C | CA393086097 | HCN4 | c.3160C>G (p.Leu1054Val) c.1942C>G (p.Leu648Val) | |
15 | g.73322933G>T | CA393086098 | HCN4 | c.3160C>A (p.Leu1054Met) c.1942C>A (p.Leu648Met) | gnomAD v4 |
15 | g.73322934G>A | CA491478002 | HCN4 | c.3159C>T (p.Leu1053=) c.1941C>T (p.Leu647=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322934G>C | CA491478004 | HCN4 | c.3159C>G (p.Leu1053=) c.1941C>G (p.Leu647=) | |
15 | g.73322934G= | CA2187187022 | HCN4 | c.3159C= (p.Leu1053=) c.1941C= (p.Leu647=) | |
15 | g.73322934G>T | CA491478003 | HCN4 | c.3159C>A (p.Leu1053=) c.1941C>A (p.Leu647=) | gnomAD v4 |
15 | g.73322935A= | CA2187187027 | HCN4 | c.3158T= (p.Leu1053=) c.1940T= (p.Leu647=) | |
15 | g.73322935A>C | CA393086099 | HCN4 | c.3158T>G (p.Leu1053Arg) c.1940T>G (p.Leu647Arg) | |
15 | g.73322935A>G | CA393086100 | HCN4 | c.3158T>C (p.Leu1053Pro) c.1940T>C (p.Leu647Pro) | ClinVar dbSNP gnomAD v4 |
15 | g.73322935A>T | CA393086101 | HCN4 | c.3158T>A (p.Leu1053His) c.1940T>A (p.Leu647His) | gnomAD v4 |
15 | g.73322936G>A | CA393086102 | HCN4 | c.3157C>T (p.Leu1053Phe) c.1939C>T (p.Leu647Phe) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322936G>C | CA393086103 | HCN4 | c.3157C>G (p.Leu1053Val) c.1939C>G (p.Leu647Val) | gnomAD v4 |
15 | g.73322936G= | CA2187187029 | HCN4 | c.3157C= (p.Leu1053=) c.1939C= (p.Leu647=) | |
15 | g.73322936G>T | CA393086104 | HCN4 | c.3157C>A (p.Leu1053Ile) c.1939C>A (p.Leu647Ile) | gnomAD v4 |
15 | g.73322937C>A | CA393086105 | HCN4 | c.3156G>T (p.Leu1052Phe) c.1938G>T (p.Leu646Phe) | dbSNP gnomAD v4 |
15 | g.73322937C= | CA2187187033 | HCN4 | c.3156G= (p.Leu1052=) c.1938G= (p.Leu646=) | |
15 | g.73322937C>G | CA393086106 | HCN4 | c.3156G>C (p.Leu1052Phe) c.1938G>C (p.Leu646Phe) | |
15 | g.73322937C>T | CA491478008 | HCN4 | c.3156G>A (p.Leu1052=) c.1938G>A (p.Leu646=) | gnomAD v4 |
15 | g.73322938A>C | CA393086109 | HCN4 | c.3155T>G (p.Leu1052Trp) c.1937T>G (p.Leu646Trp) | |
15 | g.73322938A>G | CA393086108 | HCN4 | c.3155T>C (p.Leu1052Ser) c.1937T>C (p.Leu646Ser) | |
15 | g.73322938A>T | CA393086107 | HCN4 | c.3155T>A (p.Leu1052Ter) c.1937T>A (p.Leu646Ter) | gnomAD v4 |
15 | g.73322939A>C | CA393086110 | HCN4 | c.3154T>G (p.Leu1052Val) c.1936T>G (p.Leu646Val) | |
15 | g.73322939A>G | CA491478010 | HCN4 | c.3154T>C (p.Leu1052=) c.1936T>C (p.Leu646=) | gnomAD v4 |
15 | g.73322939A>T | CA393086111 | HCN4 | c.3154T>A (p.Leu1052Met) c.1936T>A (p.Leu646Met) | |
15 | g.73322940G>A | CA491478011 | HCN4 | c.3153C>T (p.Ser1051=) c.1935C>T (p.Ser645=) | gnomAD v4 COSMIC |
15 | g.73322940G>C | CA491478012 | HCN4 | c.3153C>G (p.Ser1051=) c.1935C>G (p.Ser645=) | |
15 | g.73322940G>T | CA491478013 | HCN4 | c.3153C>A (p.Ser1051=) c.1935C>A (p.Ser645=) | gnomAD v4 |
15 | g.73322941G>A | CA393086112 | HCN4 | c.3152C>T (p.Ser1051Phe) c.1934C>T (p.Ser645Phe) | |
15 | g.73322941G>C | CA393086113 | HCN4 | c.3152C>G (p.Ser1051Cys) c.1934C>G (p.Ser645Cys) | ClinVar dbSNP |
15 | g.73322941G>T | CA393086114 | HCN4 | c.3152C>A (p.Ser1051Tyr) c.1934C>A (p.Ser645Tyr) | gnomAD v4 |
15 | g.73322942A>C | CA393086115 | HCN4 | c.3151T>G (p.Ser1051Ala) c.1933T>G (p.Ser645Ala) | |
15 | g.73322942A>G | CA393086116 | HCN4 | c.3151T>C (p.Ser1051Pro) c.1933T>C (p.Ser645Pro) | gnomAD v4 |
15 | g.73322942A>T | CA393086117 | HCN4 | c.3151T>A (p.Ser1051Thr) c.1933T>A (p.Ser645Thr) | gnomAD v4 |
15 | g.73322943T>A | CA491478015 | HCN4 | c.3150A>T (p.Gly1050=) c.1932A>T (p.Gly644=) | |
15 | g.73322943T>C | CA491478016 | HCN4 | c.3150A>G (p.Gly1050=) c.1932A>G (p.Gly644=) | |
15 | g.73322943T>G | CA7648876 | HCN4 | c.3150A>C (p.Gly1050=) c.1932A>C (p.Gly644=) | dbSNP ExAC gnomAD v4 |
15 | g.73322943T= | CA2187187035 | HCN4 | c.3150A= (p.Gly1050=) c.1932A= (p.Gly644=) | |
15 | g.73322944C>A | CA393086118 | HCN4 | c.3149G>T (p.Gly1050Val) c.1931G>T (p.Gly644Val) | gnomAD v4 |
15 | g.73322944C>G | CA393086119 | HCN4 | c.3149G>C (p.Gly1050Ala) c.1931G>C (p.Gly644Ala) | |
15 | g.73322944C>T | CA393086120 | HCN4 | c.3149G>A (p.Gly1050Glu) c.1931G>A (p.Gly644Glu) | gnomAD v4 |
15 | g.73322945C>A | CA393086122 | HCN4 | c.3148G>T (p.Gly1050Ter) c.1930G>T (p.Gly644Ter) | gnomAD v4 |
15 | g.73322945C= | CA2187187038 | HCN4 | c.3148G= (p.Gly1050=) c.1930G= (p.Gly644=) | |
15 | g.73322945C>G | CA393086123 | HCN4 | c.3148G>C (p.Gly1050Arg) c.1930G>C (p.Gly644Arg) | |
15 | g.73322945C>T | CA393086121 | HCN4 | c.3148G>A (p.Gly1050Arg) c.1930G>A (p.Gly644Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322946G>A | CA7648877 | HCN4 | c.3147C>T (p.His1049=) c.1929C>T (p.His643=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322946G>C | CA393086124 | HCN4 | c.3147C>G (p.His1049Gln) c.1929C>G (p.His643Gln) | |
15 | g.73322946G= | CA2187187045 | HCN4 | c.3147C= (p.His1049=) c.1929C= (p.His643=) | |
15 | g.73322946G>T | CA393086125 | HCN4 | c.3147C>A (p.His1049Gln) c.1929C>A (p.His643Gln) | gnomAD v4 |
15 | g.73322947T>A | CA393086126 | HCN4 | c.3146A>T (p.His1049Leu) c.1928A>T (p.His643Leu) | |
15 | g.73322947T>C | CA393086127 | HCN4 | c.3146A>G (p.His1049Arg) c.1928A>G (p.His643Arg) | |
15 | g.73322947T>G | CA393086128 | HCN4 | c.3146A>C (p.His1049Pro) c.1928A>C (p.His643Pro) | gnomAD v4 |
15 | g.73322948G>A | CA393086129 | HCN4 | c.3145C>T (p.His1049Tyr) c.1927C>T (p.His643Tyr) | gnomAD v4 |
15 | g.73322948G>C | CA393086130 | HCN4 | c.3145C>G (p.His1049Asp) c.1927C>G (p.His643Asp) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322948G= | CA2187187048 | HCN4 | c.3145C= (p.His1049=) c.1927C= (p.His643=) | |
15 | g.73322948G>T | CA393086131 | HCN4 | c.3145C>A (p.His1049Asn) c.1927C>A (p.His643Asn) | gnomAD v4 |
15 | g.73322950del | CA2575783824 | HCN4 | c.3145del (p.His1049ThrfsTer?) c.1927del (p.His643ThrfsTer?) | gnomAD v4 |
15 | g.73322949G>A | CA491478025 | HCN4 | c.3144C>T (p.Ser1048=) c.1926C>T (p.Ser642=) | ClinVar dbSNP gnomAD v4 |
15 | g.73322949G>C | CA491478027 | HCN4 | c.3144C>G (p.Ser1048=) c.1926C>G (p.Ser642=) | |
15 | g.73322949G>T | CA491478029 | HCN4 | c.3144C>A (p.Ser1048=) c.1926C>A (p.Ser642=) | gnomAD v4 |
15 | g.73322950G>A | CA393086132 | HCN4 | c.3143C>T (p.Ser1048Phe) c.1925C>T (p.Ser642Phe) | gnomAD v4 |
15 | g.73322950G>C | CA393086133 | HCN4 | c.3143C>G (p.Ser1048Cys) c.1925C>G (p.Ser642Cys) | |
15 | g.73322950G>T | CA393086134 | HCN4 | c.3143C>A (p.Ser1048Tyr) c.1925C>A (p.Ser642Tyr) | gnomAD v4 |
15 | g.73322951A>C | CA393086136 | HCN4 | c.3142T>G (p.Ser1048Ala) c.1924T>G (p.Ser642Ala) | |
15 | g.73322951A>G | CA393086137 | HCN4 | c.3142T>C (p.Ser1048Pro) c.1924T>C (p.Ser642Pro) | gnomAD v4 |
15 | g.73322951A>T | CA393086135 | HCN4 | c.3142T>A (p.Ser1048Thr) c.1924T>A (p.Ser642Thr) | gnomAD v4 |
15 | g.73322952G>A | CA491478033 | HCN4 | c.3141C>T (p.Gly1047=) c.1923C>T (p.Gly641=) | gnomAD v4 |
15 | g.73322952G>C | CA491478034 | HCN4 | c.3141C>G (p.Gly1047=) c.1923C>G (p.Gly641=) | |
15 | g.73322952G>T | CA491478036 | HCN4 | c.3141C>A (p.Gly1047=) c.1923C>A (p.Gly641=) | gnomAD v4 |
15 | g.73322953C>A | CA393086138 | HCN4 | c.3140G>T (p.Gly1047Val) c.1922G>T (p.Gly641Val) | gnomAD v4 |
15 | g.73322953C>G | CA393086139 | HCN4 | c.3140G>C (p.Gly1047Ala) c.1922G>C (p.Gly641Ala) | |
15 | g.73322953C>T | CA393086140 | HCN4 | c.3140G>A (p.Gly1047Asp) c.1922G>A (p.Gly641Asp) | gnomAD v4 |
15 | g.73322954C>A | CA393086141 | HCN4 | c.3139G>T (p.Gly1047Cys) c.1921G>T (p.Gly641Cys) | gnomAD v4 |
15 | g.73322954C>G | CA393086142 | HCN4 | c.3139G>C (p.Gly1047Arg) c.1921G>C (p.Gly641Arg) | |
15 | g.73322954C>T | CA393086143 | HCN4 | c.3139G>A (p.Gly1047Ser) c.1921G>A (p.Gly641Ser) | gnomAD v4 COSMIC |
15 | g.73322955A>C | CA491478041 | HCN4 | c.3138T>G (p.Ser1046=) c.1920T>G (p.Ser640=) | |
15 | g.73322955A>G | CA491478042 | HCN4 | c.3138T>C (p.Ser1046=) c.1920T>C (p.Ser640=) | gnomAD v4 |
15 | g.73322955A>T | CA491478039 | HCN4 | c.3138T>A (p.Ser1046=) c.1920T>A (p.Ser640=) | gnomAD v4 |
15 | g.73322956G>A | CA393086146 | HCN4 | c.3137C>T (p.Ser1046Phe) c.1919C>T (p.Ser640Phe) | |
15 | g.73322956G>C | CA393086144 | HCN4 | c.3137C>G (p.Ser1046Cys) c.1919C>G (p.Ser640Cys) | gnomAD v4 |
15 | g.73322956G>T | CA393086145 | HCN4 | c.3137C>A (p.Ser1046Tyr) c.1919C>A (p.Ser640Tyr) | gnomAD v4 COSMIC |
15 | g.73322957A>C | CA393086147 | HCN4 | c.3136T>G (p.Ser1046Ala) c.1918T>G (p.Ser640Ala) | |
15 | g.73322957A>G | CA393086148 | HCN4 | c.3136T>C (p.Ser1046Pro) c.1918T>C (p.Ser640Pro) | gnomAD v4 |
15 | g.73322957A>T | CA393086149 | HCN4 | c.3136T>A (p.Ser1046Thr) c.1918T>A (p.Ser640Thr) | gnomAD v4 |
15 | g.73322958G>A | CA491478045 | HCN4 | c.3135C>T (p.Ala1045=) c.1917C>T (p.Ala639=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322958G>C | CA491478044 | HCN4 | c.3135C>G (p.Ala1045=) c.1917C>G (p.Ala639=) | |
15 | g.73322958G= | CA2187187051 | HCN4 | c.3135C= (p.Ala1045=) c.1917C= (p.Ala639=) | |
15 | g.73322958G>T | CA491478043 | HCN4 | c.3135C>A (p.Ala1045=) c.1917C>A (p.Ala639=) | gnomAD v4 |
15 | g.73322958_73322959insCCCC | CA2838283602 | HCN4 | c.3134_3135insGGGG (p.Ser1046GlyfsTer?) c.1916_1917insGGGG (p.Ser640GlyfsTer?) | |
15 | g.73322959G>A | CA272663688 | HCN4 | c.3134C>T (p.Ala1045Val) c.1916C>T (p.Ala639Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322959G>C | CA393086150 | HCN4 | c.3134C>G (p.Ala1045Gly) c.1916C>G (p.Ala639Gly) | |
15 | g.73322959G= | CA2187187055 | HCN4 | c.3134C= (p.Ala1045=) c.1916C= (p.Ala639=) | |
15 | g.73322959G>T | CA393086151 | HCN4 | c.3134C>A (p.Ala1045Asp) c.1916C>A (p.Ala639Asp) | gnomAD v4 |
15 | g.73322960C>A | CA393086152 | HCN4 | c.3133G>T (p.Ala1045Ser) c.1915G>T (p.Ala639Ser) | gnomAD v4 |
15 | g.73322960C= | CA2187187061 | HCN4 | c.3133G= (p.Ala1045=) c.1915G= (p.Ala639=) | |
15 | g.73322960C>G | CA393086153 | HCN4 | c.3133G>C (p.Ala1045Pro) c.1915G>C (p.Ala639Pro) | |
15 | g.73322960C>T | CA7648878 | HCN4 | c.3133G>A (p.Ala1045Thr) c.1915G>A (p.Ala639Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322961C>A | CA491478047 | HCN4 | c.3132G>T (p.Arg1044=) c.1914G>T (p.Arg638=) | gnomAD v4 |
15 | g.73322961C>G | CA491478049 | HCN4 | c.3132G>C (p.Arg1044=) c.1914G>C (p.Arg638=) | |
15 | g.73322961C>T | CA491478048 | HCN4 | c.3132G>A (p.Arg1044=) c.1914G>A (p.Arg638=) | gnomAD v4 |
15 | g.73322962C>A | CA393086155 | HCN4 | c.3131G>T (p.Arg1044Leu) c.1913G>T (p.Arg638Leu) | gnomAD v4 |
15 | g.73322962C= | CA2187187064 | HCN4 | c.3131G= (p.Arg1044=) c.1913G= (p.Arg638=) | |
15 | g.73322962C>G | CA393086154 | HCN4 | c.3131G>C (p.Arg1044Pro) c.1913G>C (p.Arg638Pro) | gnomAD v4 |
15 | g.73322962C>T | CA247663 | HCN4 | c.3131G>A (p.Arg1044Gln) c.1913G>A (p.Arg638Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322963G>A | CA7648879 | HCN4 | c.3130C>T (p.Arg1044Trp) c.1912C>T (p.Arg638Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322963G>C | CA393086156 | HCN4 | c.3130C>G (p.Arg1044Gly) c.1912C>G (p.Arg638Gly) | gnomAD v4 |
15 | g.73322963G= | CA2187187070 | HCN4 | c.3130C= (p.Arg1044=) c.1912C= (p.Arg638=) | |
15 | g.73322963G>T | CA491478053 | HCN4 | c.3130C>A (p.Arg1044=) c.1912C>A (p.Arg638=) | gnomAD v4 |
15 | g.73322966del | CA2629370541 | HCN4 | c.3130del (p.Arg1044GlyfsTer?) c.1912del (p.Arg638GlyfsTer?) | gnomAD v4 |
15 | g.73322964G>A | CA491478054 | HCN4 | c.3129C>T (p.Pro1043=) c.1911C>T (p.Pro637=) | ClinVar gnomAD v4 |
15 | g.73322964G>C | CA491478055 | HCN4 | c.3129C>G (p.Pro1043=) c.1911C>G (p.Pro637=) | gnomAD v4 |
15 | g.73322964G>T | CA491478056 | HCN4 | c.3129C>A (p.Pro1043=) c.1911C>A (p.Pro637=) | gnomAD v4 |
15 | g.73322965G>A | CA393086157 | HCN4 | c.3128C>T (p.Pro1043Leu) c.1910C>T (p.Pro637Leu) | gnomAD v4 |
15 | g.73322965G>C | CA393086158 | HCN4 | c.3128C>G (p.Pro1043Arg) c.1910C>G (p.Pro637Arg) | |
15 | g.73322965G>T | CA393086159 | HCN4 | c.3128C>A (p.Pro1043His) c.1910C>A (p.Pro637His) | gnomAD v4 |
15 | g.73322966G>A | CA393086160 | HCN4 | c.3127C>T (p.Pro1043Ser) c.1909C>T (p.Pro637Ser) | |
15 | g.73322966G>C | CA393086161 | HCN4 | c.3127C>G (p.Pro1043Ala) c.1909C>G (p.Pro637Ala) | |
15 | g.73322966G= | CA2187187075 | HCN4 | c.3127C= (p.Pro1043=) c.1909C= (p.Pro637=) | |
15 | g.73322966G>T | CA393086162 | HCN4 | c.3127C>A (p.Pro1043Thr) c.1909C>A (p.Pro637Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322967C>A | CA491478059 | HCN4 | c.3126G>T (p.Pro1042=) c.1908G>T (p.Pro636=) | gnomAD v4 |
15 | g.73322967C= | CA2187187078 | HCN4 | c.3126G= (p.Pro1042=) c.1908G= (p.Pro636=) | |
15 | g.73322967C>G | CA491478060 | HCN4 | c.3126G>C (p.Pro1042=) c.1908G>C (p.Pro636=) | gnomAD v4 |
15 | g.73322967C>T | CA16606777 | HCN4 | c.3126G>A (p.Pro1042=) c.1908G>A (p.Pro636=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322968G>A | CA393086163 | HCN4 | c.3125C>T (p.Pro1042Leu) c.1907C>T (p.Pro636Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322968G>C | CA393086164 | HCN4 | c.3125C>G (p.Pro1042Arg) c.1907C>G (p.Pro636Arg) | gnomAD v4 |
15 | g.73322968G= | CA2187187085 | HCN4 | c.3125C= (p.Pro1042=) c.1907C= (p.Pro636=) | |
15 | g.73322968G>T | CA393086165 | HCN4 | c.3125C>A (p.Pro1042Gln) c.1907C>A (p.Pro636Gln) | gnomAD v4 |
15 | g.73322971del | CA2575783825 | HCN4 | c.3125del (p.Pro1042ArgfsTer?) c.1907del (p.Pro636ArgfsTer?) | gnomAD v4 |
15 | g.73322970_73322971del | CA2575783826 | HCN4 | c.3124_3125del (p.Pro1042AlafsTer?) c.1906_1907del (p.Pro636AlafsTer?) | |
15 | g.73322969G>A | CA393086167 | HCN4 | c.3124C>T (p.Pro1042Ser) c.1906C>T (p.Pro636Ser) | gnomAD v4 |
15 | g.73322969G>C | CA393086168 | HCN4 | c.3124C>G (p.Pro1042Ala) c.1906C>G (p.Pro636Ala) | dbSNP |
15 | g.73322969G= | CA2187187088 | HCN4 | c.3124C= (p.Pro1042=) c.1906C= (p.Pro636=) | |
15 | g.73322969G>T | CA393086166 | HCN4 | c.3124C>A (p.Pro1042Thr) c.1906C>A (p.Pro636Thr) | gnomAD v4 |
15 | g.73322970G>A | CA491478063 | HCN4 | c.3123C>T (p.Ala1041=) c.1905C>T (p.Ala635=) | gnomAD v4 |
15 | g.73322970G>C | CA491478064 | HCN4 | c.3123C>G (p.Ala1041=) c.1905C>G (p.Ala635=) | |
15 | g.73322970G>T | CA491478065 | HCN4 | c.3123C>A (p.Ala1041=) c.1905C>A (p.Ala635=) | gnomAD v4 |
15 | g.73322971G>A | CA393086169 | HCN4 | c.3122C>T (p.Ala1041Val) c.1904C>T (p.Ala635Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322971G>C | CA393086170 | HCN4 | c.3122C>G (p.Ala1041Gly) c.1904C>G (p.Ala635Gly) | |
15 | g.73322971G= | CA2187187092 | HCN4 | c.3122C= (p.Ala1041=) c.1904C= (p.Ala635=) | |
15 | g.73322971G>T | CA393086171 | HCN4 | c.3122C>A (p.Ala1041Asp) c.1904C>A (p.Ala635Asp) | gnomAD v4 |
15 | g.73322972C>A | CA393086172 | HCN4 | c.3121G>T (p.Ala1041Ser) c.1903G>T (p.Ala635Ser) | gnomAD v4 |
15 | g.73322972C= | CA2187187100 | HCN4 | c.3121G= (p.Ala1041=) c.1903G= (p.Ala635=) | |
15 | g.73322972C>G | CA393086173 | HCN4 | c.3121G>C (p.Ala1041Pro) c.1903G>C (p.Ala635Pro) | |
15 | g.73322972C>T | CA7648880 | HCN4 | c.3121G>A (p.Ala1041Thr) c.1903G>A (p.Ala635Thr) | dbSNP ExAC gnomAD v4 |
15 | g.73322973A>C | CA393086174 | HCN4 | c.3120T>G (p.Ser1040Arg) c.1902T>G (p.Ser634Arg) | |
15 | g.73322973A>G | CA491478069 | HCN4 | c.3120T>C (p.Ser1040=) c.1902T>C (p.Ser634=) | gnomAD v4 |
15 | g.73322973A>T | CA393086175 | HCN4 | c.3120T>A (p.Ser1040Arg) c.1902T>A (p.Ser634Arg) | COSMIC |
15 | g.73322974del | CA2838290808 | HCN4 | c.3119del (p.Ser1040MetfsTer?) c.1901del (p.Ser634MetfsTer?) | |
15 | g.73322974C>A | CA393086176 | HCN4 | c.3119G>T (p.Ser1040Ile) c.1901G>T (p.Ser634Ile) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322974C= | CA2187187103 | HCN4 | c.3119G= (p.Ser1040=) c.1901G= (p.Ser634=) | |
15 | g.73322974C>G | CA393086177 | HCN4 | c.3119G>C (p.Ser1040Thr) c.1901G>C (p.Ser634Thr) | |
15 | g.73322974C>T | CA393086178 | HCN4 | c.3119G>A (p.Ser1040Asn) c.1901G>A (p.Ser634Asn) | |
15 | g.73322975T>A | CA393086179 | HCN4 | c.3118A>T (p.Ser1040Cys) c.1900A>T (p.Ser634Cys) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322975T>C | CA393086180 | HCN4 | c.3118A>G (p.Ser1040Gly) c.1900A>G (p.Ser634Gly) | gnomAD v4 |
15 | g.73322975T>G | CA393086181 | HCN4 | c.3118A>C (p.Ser1040Arg) c.1900A>C (p.Ser634Arg) | |
15 | g.73322975T= | CA2187187106 | HCN4 | c.3118A= (p.Ser1040=) c.1900A= (p.Ser634=) | |
15 | g.73322976C>A | CA491478073 | HCN4 | c.3117G>T (p.Pro1039=) c.1899G>T (p.Pro633=) | gnomAD v4 |
15 | g.73322976C= | CA2187187110 | HCN4 | c.3117G= (p.Pro1039=) c.1899G= (p.Pro633=) | |
15 | g.73322976C>G | CA491478074 | HCN4 | c.3117G>C (p.Pro1039=) c.1899G>C (p.Pro633=) | gnomAD v4 |
15 | g.73322976C>T | CA7648881 | HCN4 | c.3117G>A (p.Pro1039=) c.1899G>A (p.Pro633=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322977G>A | CA7648882 | HCN4 | c.3116C>T (p.Pro1039Leu) c.1898C>T (p.Pro633Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322977G>C | CA393086182 | HCN4 | c.3116C>G (p.Pro1039Arg) c.1898C>G (p.Pro633Arg) | ClinVar dbSNP |
15 | g.73322977G= | CA2187187118 | HCN4 | c.3116C= (p.Pro1039=) c.1898C= (p.Pro633=) | |
15 | g.73322977G>T | CA393086183 | HCN4 | c.3116C>A (p.Pro1039Gln) c.1898C>A (p.Pro633Gln) | gnomAD v4 |
15 | g.73322978_73322979del | CA2575783827 | HCN4 | c.3115_3116del (p.Pro1039GlufsTer?) c.1897_1898del (p.Pro633GlufsTer?) | |
15 | g.73322978G>A | CA393086184 | HCN4 | c.3115C>T (p.Pro1039Ser) c.1897C>T (p.Pro633Ser) | gnomAD v4 COSMIC |
15 | g.73322978G>C | CA393086185 | HCN4 | c.3115C>G (p.Pro1039Ala) c.1897C>G (p.Pro633Ala) | |
15 | g.73322978G>T | CA393086186 | HCN4 | c.3115C>A (p.Pro1039Thr) c.1897C>A (p.Pro633Thr) | gnomAD v4 |
15 | g.73322979G>A | CA491478076 | HCN4 | c.3114C>T (p.Phe1038=) c.1896C>T (p.Phe632=) | |
15 | g.73322979G>C | CA393086187 | HCN4 | c.3114C>G (p.Phe1038Leu) c.1896C>G (p.Phe632Leu) | |
15 | g.73322979G= | CA2187187131 | HCN4 | c.3114C= (p.Phe1038=) c.1896C= (p.Phe632=) | |
15 | g.73322979G>T | CA393086188 | HCN4 | c.3114C>A (p.Phe1038Leu) c.1896C>A (p.Phe632Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322980A>C | CA393086189 | HCN4 | c.3113T>G (p.Phe1038Cys) c.1895T>G (p.Phe632Cys) | |
15 | g.73322980A>G | CA393086190 | HCN4 | c.3113T>C (p.Phe1038Ser) c.1895T>C (p.Phe632Ser) | |
15 | g.73322980A>T | CA393086191 | HCN4 | c.3113T>A (p.Phe1038Tyr) c.1895T>A (p.Phe632Tyr) | |
15 | g.73322981A= | CA2187187135 | HCN4 | c.3112T= (p.Phe1038=) c.1894T= (p.Phe632=) | |
15 | g.73322981A>C | CA393086192 | HCN4 | c.3112T>G (p.Phe1038Val) c.1894T>G (p.Phe632Val) | |
15 | g.73322981A>G | CA393086193 | HCN4 | c.3112T>C (p.Phe1038Leu) c.1894T>C (p.Phe632Leu) | dbSNP gnomAD v4 |
15 | g.73322981A>T | CA393086194 | HCN4 | c.3112T>A (p.Phe1038Ile) c.1894T>A (p.Phe632Ile) | |
15 | g.73322982G>A | CA491478079 | HCN4 | c.3111C>T (p.Thr1037=) c.1893C>T (p.Thr631=) | gnomAD v4 |
15 | g.73322982G>C | CA491478080 | HCN4 | c.3111C>G (p.Thr1037=) c.1893C>G (p.Thr631=) | |
15 | g.73322982G>T | CA491478081 | HCN4 | c.3111C>A (p.Thr1037=) c.1893C>A (p.Thr631=) | ClinVar gnomAD v4 |
15 | g.73322983G>A | CA393086196 | HCN4 | c.3110C>T (p.Thr1037Ile) c.1892C>T (p.Thr631Ile) | |
15 | g.73322983G>C | CA393086197 | HCN4 | c.3110C>G (p.Thr1037Ser) c.1892C>G (p.Thr631Ser) | |
15 | g.73322983G>T | CA393086195 | HCN4 | c.3110C>A (p.Thr1037Asn) c.1892C>A (p.Thr631Asn) | ClinVar gnomAD v4 |
15 | g.73322984T>A | CA393086198 | HCN4 | c.3109A>T (p.Thr1037Ser) c.1891A>T (p.Thr631Ser) | |
15 | g.73322984T>C | CA393086199 | HCN4 | c.3109A>G (p.Thr1037Ala) c.1891A>G (p.Thr631Ala) | gnomAD v4 |
15 | g.73322984T>G | CA393086200 | HCN4 | c.3109A>C (p.Thr1037Pro) c.1891A>C (p.Thr631Pro) | |
15 | g.73322985T>A | CA393086201 | HCN4 | c.3108A>T (p.Arg1036Ser) c.1890A>T (p.Arg630Ser) | ClinVar |
15 | g.73322985T>C | CA491478084 | HCN4 | c.3108A>G (p.Arg1036=) c.1890A>G (p.Arg630=) | |
15 | g.73322985T>G | CA393086202 | HCN4 | c.3108A>C (p.Arg1036Ser) c.1890A>C (p.Arg630Ser) | |
15 | g.73322986C>A | CA393086205 | HCN4 | c.3107G>T (p.Arg1036Ile) c.1889G>T (p.Arg630Ile) | gnomAD v4 |
15 | g.73322986C>G | CA393086203 | HCN4 | c.3107G>C (p.Arg1036Thr) c.1889G>C (p.Arg630Thr) | |
15 | g.73322986C>T | CA393086204 | HCN4 | c.3107G>A (p.Arg1036Lys) c.1889G>A (p.Arg630Lys) | |
15 | g.73322987T>A | CA393086206 | HCN4 | c.3106A>T (p.Arg1036Ter) c.1888A>T (p.Arg630Ter) | |
15 | g.73322987T>C | CA393086207 | HCN4 | c.3106A>G (p.Arg1036Gly) c.1888A>G (p.Arg630Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322987T>G | CA491478088 | HCN4 | c.3106A>C (p.Arg1036=) c.1888A>C (p.Arg630=) | |
15 | g.73322987T= | CA2187187138 | HCN4 | c.3106A= (p.Arg1036=) c.1888A= (p.Arg630=) | |
15 | g.73322988T>A | CA491478089 | HCN4 | c.3105A>T (p.Pro1035=) c.1887A>T (p.Pro629=) | |
15 | g.73322988T>C | CA491478090 | HCN4 | c.3105A>G (p.Pro1035=) c.1887A>G (p.Pro629=) | gnomAD v4 |
15 | g.73322988T>G | CA491478092 | HCN4 | c.3105A>C (p.Pro1035=) c.1887A>C (p.Pro629=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322988T= | CA2187187144 | HCN4 | c.3105A= (p.Pro1035=) c.1887A= (p.Pro629=) | |
15 | g.73322989G>A | CA393086208 | HCN4 | c.3104C>T (p.Pro1035Leu) c.1886C>T (p.Pro629Leu) | gnomAD v4 COSMIC |
15 | g.73322989G>C | CA393086209 | HCN4 | c.3104C>G (p.Pro1035Arg) c.1886C>G (p.Pro629Arg) | |
15 | g.73322989G>T | CA393086210 | HCN4 | c.3104C>A (p.Pro1035Gln) c.1886C>A (p.Pro629Gln) | gnomAD v4 |
15 | g.73322994dup | CA619410589 | HCN4 | c.3104dup (p.Arg1036LysfsTer?) c.1886dup (p.Arg630LysfsTer?) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322994del | CA2629370542 | HCN4 | c.3104del (p.Pro1035GlnfsTer?) c.1886del (p.Pro629GlnfsTer?) | gnomAD v4 |
15 | g.73322993_73322994del | CA2838283598 | HCN4 | c.3103_3104del (p.Pro1035LysfsTer?) c.1885_1886del (p.Pro629LysfsTer?) | |
15 | g.73322990G>A | CA393086212 | HCN4 | c.3103C>T (p.Pro1035Ser) c.1885C>T (p.Pro629Ser) | gnomAD v4 |
15 | g.73322990G>C | CA7648883 | HCN4 | c.3103C>G (p.Pro1035Ala) c.1885C>G (p.Pro629Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322990G= | CA2187187155 | HCN4 | c.3103C= (p.Pro1035=) c.1885C= (p.Pro629=) | |
15 | g.73322990G>T | CA393086211 | HCN4 | c.3103C>A (p.Pro1035Thr) c.1885C>A (p.Pro629Thr) | gnomAD v4 |
15 | g.73322991G>A | CA491478095 | HCN4 | c.3102C>T (p.Pro1034=) c.1884C>T (p.Pro628=) | gnomAD v4 COSMIC |
15 | g.73322991G>C | CA491478096 | HCN4 | c.3102C>G (p.Pro1034=) c.1884C>G (p.Pro628=) | |
15 | g.73322991G>T | CA491478097 | HCN4 | c.3102C>A (p.Pro1034=) c.1884C>A (p.Pro628=) | gnomAD v4 |
15 | g.73322992G>A | CA393086213 | HCN4 | c.3101C>T (p.Pro1034Leu) c.1883C>T (p.Pro628Leu) | ClinVar gnomAD v4 |
15 | g.73322992G>C | CA272663736 | HCN4 | c.3101C>G (p.Pro1034Arg) c.1883C>G (p.Pro628Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322992G= | CA2187187164 | HCN4 | c.3101C= (p.Pro1034=) c.1883C= (p.Pro628=) | |
15 | g.73322992G>T | CA393086214 | HCN4 | c.3101C>A (p.Pro1034His) c.1883C>A (p.Pro628His) | gnomAD v4 |
15 | g.73322993G>A | CA393086215 | HCN4 | c.3100C>T (p.Pro1034Ser) c.1882C>T (p.Pro628Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322993G>C | CA393086216 | HCN4 | c.3100C>G (p.Pro1034Ala) c.1882C>G (p.Pro628Ala) | |
15 | g.73322993G= | CA2187187173 | HCN4 | c.3100C= (p.Pro1034=) c.1882C= (p.Pro628=) | |
15 | g.73322993G>T | CA393086217 | HCN4 | c.3100C>A (p.Pro1034Thr) c.1882C>A (p.Pro628Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322994G>A | CA7648884 | HCN4 | c.3099C>T (p.Gly1033=) c.1881C>T (p.Gly627=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322994G>C | CA491478100 | HCN4 | c.3099C>G (p.Gly1033=) c.1881C>G (p.Gly627=) | dbSNP gnomAD v4 |
15 | g.73322994G= | CA2187187181 | HCN4 | c.3099C= (p.Gly1033=) c.1881C= (p.Gly627=) | |
15 | g.73322994G>T | CA491478101 | HCN4 | c.3099C>A (p.Gly1033=) c.1881C>A (p.Gly627=) | dbSNP gnomAD v4 |
15 | g.73322995C>A | CA393086218 | HCN4 | c.3098G>T (p.Gly1033Val) c.1880G>T (p.Gly627Val) | gnomAD v4 |
15 | g.73322995C= | CA2187187186 | HCN4 | c.3098G= (p.Gly1033=) c.1880G= (p.Gly627=) | |
15 | g.73322995C>G | CA393086219 | HCN4 | c.3098G>C (p.Gly1033Ala) c.1880G>C (p.Gly627Ala) | gnomAD v4 |
15 | g.73322995C>T | CA393086220 | HCN4 | c.3098G>A (p.Gly1033Asp) c.1880G>A (p.Gly627Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322996C>A | CA393086221 | HCN4 | c.3097G>T (p.Gly1033Cys) c.1879G>T (p.Gly627Cys) | gnomAD v4 |
15 | g.73322996C>G | CA393086222 | HCN4 | c.3097G>C (p.Gly1033Arg) c.1879G>C (p.Gly627Arg) | |
15 | g.73322996C>T | CA393086223 | HCN4 | c.3097G>A (p.Gly1033Ser) c.1879G>A (p.Gly627Ser) | |
15 | g.73322997T>A | CA491478106 | HCN4 | c.3096A>T (p.Pro1032=) c.1878A>T (p.Pro626=) | |
15 | g.73322997T>C | CA491478107 | HCN4 | c.3096A>G (p.Pro1032=) c.1878A>G (p.Pro626=) | ClinVar gnomAD v4 |
15 | g.73322997T>G | CA491478105 | HCN4 | c.3096A>C (p.Pro1032=) c.1878A>C (p.Pro626=) | dbSNP gnomAD v4 |
15 | g.73322997T= | CA2187187189 | HCN4 | c.3096A= (p.Pro1032=) c.1878A= (p.Pro626=) | |
15 | g.73322998G>A | CA393086224 | HCN4 | c.3095C>T (p.Pro1032Leu) c.1877C>T (p.Pro626Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322998G>C | CA393086225 | HCN4 | c.3095C>G (p.Pro1032Arg) c.1877C>G (p.Pro626Arg) | |
15 | g.73322998G= | CA2187187192 | HCN4 | c.3095C= (p.Pro1032=) c.1877C= (p.Pro626=) | |
15 | g.73322998G>T | CA393086226 | HCN4 | c.3095C>A (p.Pro1032Gln) c.1877C>A (p.Pro626Gln) | |
15 | g.73322999G>A | CA393086227 | HCN4 | c.3094C>T (p.Pro1032Ser) c.1876C>T (p.Pro626Ser) | gnomAD v3 gnomAD v4 |
15 | g.73322999G>C | CA393086228 | HCN4 | c.3094C>G (p.Pro1032Ala) c.1876C>G (p.Pro626Ala) | |
15 | g.73322999G= | CA2187187195 | HCN4 | c.3094C= (p.Pro1032=) c.1876C= (p.Pro626=) | |
15 | g.73322999G>T | CA7648885 | HCN4 | c.3094C>A (p.Pro1032Thr) c.1876C>A (p.Pro626Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323000G>A | CA491478110 | HCN4 | c.3093C>T (p.Ser1031=) c.1875C>T (p.Ser625=) | ClinVar gnomAD v4 |
15 | g.73323000G>C | CA393086229 | HCN4 | c.3093C>G (p.Ser1031Arg) c.1875C>G (p.Ser625Arg) | |
15 | g.73323000G= | CA2187187199 | HCN4 | c.3093C= (p.Ser1031=) c.1875C= (p.Ser625=) | |
15 | g.73323000G>T | CA393086230 | HCN4 | c.3093C>A (p.Ser1031Arg) c.1875C>A (p.Ser625Arg) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323001C>A | CA393086231 | HCN4 | c.3092G>T (p.Ser1031Ile) c.1874G>T (p.Ser625Ile) | gnomAD v4 |
15 | g.73323001C>G | CA393086232 | HCN4 | c.3092G>C (p.Ser1031Thr) c.1874G>C (p.Ser625Thr) | |
15 | g.73323001C>T | CA393086233 | HCN4 | c.3092G>A (p.Ser1031Asn) c.1874G>A (p.Ser625Asn) | gnomAD v4 |
15 | g.73323002T>A | CA393086234 | HCN4 | c.3091A>T (p.Ser1031Cys) c.1873A>T (p.Ser625Cys) | |
15 | g.73323002T>C | CA393086235 | HCN4 | c.3091A>G (p.Ser1031Gly) c.1873A>G (p.Ser625Gly) | gnomAD v4 |
15 | g.73323002T>G | CA393086236 | HCN4 | c.3091A>C (p.Ser1031Arg) c.1873A>C (p.Ser625Arg) | |
15 | g.73323003G>A | CA491478112 | HCN4 | c.3090C>T (p.His1030=) c.1872C>T (p.His624=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323003G>C | CA393086237 | HCN4 | c.3090C>G (p.His1030Gln) c.1872C>G (p.His624Gln) | |
15 | g.73323003G= | CA2187187202 | HCN4 | c.3090C= (p.His1030=) c.1872C= (p.His624=) | |
15 | g.73323003G>T | CA393086238 | HCN4 | c.3090C>A (p.His1030Gln) c.1872C>A (p.His624Gln) | gnomAD v4 |
15 | g.73323004T>A | CA393086241 | HCN4 | c.3089A>T (p.His1030Leu) c.1871A>T (p.His624Leu) | |
15 | g.73323004T>C | CA393086240 | HCN4 | c.3089A>G (p.His1030Arg) c.1871A>G (p.His624Arg) | |
15 | g.73323004T>G | CA393086239 | HCN4 | c.3089A>C (p.His1030Pro) c.1871A>C (p.His624Pro) | |
15 | g.73323005G>A | CA393086244 | HCN4 | c.3088C>T (p.His1030Tyr) c.1870C>T (p.His624Tyr) | |
15 | g.73323005G>C | CA393086242 | HCN4 | c.3088C>G (p.His1030Asp) c.1870C>G (p.His624Asp) | |
15 | g.73323005G>T | CA393086243 | HCN4 | c.3088C>A (p.His1030Asn) c.1870C>A (p.His624Asn) | gnomAD v4 |
15 | g.73323006G>A | CA491478116 | HCN4 | c.3087C>T (p.Gly1029=) c.1869C>T (p.Gly623=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323006G>C | CA491478118 | HCN4 | c.3087C>G (p.Gly1029=) c.1869C>G (p.Gly623=) | ClinVar dbSNP |
15 | g.73323006G= | CA2187187204 | HCN4 | c.3087C= (p.Gly1029=) c.1869C= (p.Gly623=) | |
15 | g.73323006G>T | CA491478120 | HCN4 | c.3087C>A (p.Gly1029=) c.1869C>A (p.Gly623=) | gnomAD v4 |
15 | g.73323007C>A | CA393086245 | HCN4 | c.3086G>T (p.Gly1029Val) c.1868G>T (p.Gly623Val) | gnomAD v4 |
15 | g.73323007C>G | CA393086246 | HCN4 | c.3086G>C (p.Gly1029Ala) c.1868G>C (p.Gly623Ala) | |
15 | g.73323007C>T | CA393086247 | HCN4 | c.3086G>A (p.Gly1029Asp) c.1868G>A (p.Gly623Asp) | gnomAD v4 |
15 | g.73323008C>A | CA393086250 | HCN4 | c.3085G>T (p.Gly1029Cys) c.1867G>T (p.Gly623Cys) | gnomAD v4 |
15 | g.73323008C>G | CA393086249 | HCN4 | c.3085G>C (p.Gly1029Arg) c.1867G>C (p.Gly623Arg) | |
15 | g.73323008C>T | CA393086248 | HCN4 | c.3085G>A (p.Gly1029Ser) c.1867G>A (p.Gly623Ser) | gnomAD v4 |
15 | g.73323009A>C | CA491478121 | HCN4 | c.3084T>G (p.Pro1028=) c.1866T>G (p.Pro622=) | |
15 | g.73323009A>G | CA491478122 | HCN4 | c.3084T>C (p.Pro1028=) c.1866T>C (p.Pro622=) | |
15 | g.73323009A>T | CA491478123 | HCN4 | c.3084T>A (p.Pro1028=) c.1866T>A (p.Pro622=) | |
15 | g.73323010G>A | CA393086251 | HCN4 | c.3083C>T (p.Pro1028Leu) c.1865C>T (p.Pro622Leu) | gnomAD v4 |
15 | g.73323010G>C | CA393086252 | HCN4 | c.3083C>G (p.Pro1028Arg) c.1865C>G (p.Pro622Arg) | ClinVar dbSNP gnomAD v4 |
15 | g.73323010G= | CA2187187206 | HCN4 | c.3083C= (p.Pro1028=) c.1865C= (p.Pro622=) | |
15 | g.73323010G>T | CA393086253 | HCN4 | c.3083C>A (p.Pro1028His) c.1865C>A (p.Pro622His) | gnomAD v4 |
15 | g.73323015dup | CA2575783828 | HCN4 | c.3083dup (p.Gly1029TrpfsTer?) c.1865dup (p.Gly623TrpfsTer?) | gnomAD v4 |
15 | g.73323015del | CA645586807 | HCN4 | c.3083del (p.Pro1028LeufsTer?) c.1865del (p.Pro622LeufsTer?) | gnomAD v4 COSMIC |
15 | g.73323011G>A | CA393086254 | HCN4 | c.3082C>T (p.Pro1028Ser) c.1864C>T (p.Pro622Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323011G>C | CA393086255 | HCN4 | c.3082C>G (p.Pro1028Ala) c.1864C>G (p.Pro622Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323011G= | CA2187187210 | HCN4 | c.3082C= (p.Pro1028=) c.1864C= (p.Pro622=) | |
15 | g.73323011G>T | CA393086256 | HCN4 | c.3082C>A (p.Pro1028Thr) c.1864C>A (p.Pro622Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323012G>A | CA491478124 | HCN4 | c.3081C>T (p.Pro1027=) c.1863C>T (p.Pro621=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323012G>C | CA491478125 | HCN4 | c.3081C>G (p.Pro1027=) c.1863C>G (p.Pro621=) | |
15 | g.73323012G= | CA2187187214 | HCN4 | c.3081C= (p.Pro1027=) c.1863C= (p.Pro621=) | |
15 | g.73323012G>T | CA491478126 | HCN4 | c.3081C>A (p.Pro1027=) c.1863C>A (p.Pro621=) | gnomAD v4 |
15 | g.73323013G>A | CA7648886 | HCN4 | c.3080C>T (p.Pro1027Leu) c.1862C>T (p.Pro621Leu) | dbSNP ExAC gnomAD v2 |
15 | g.73323013G>C | CA393086257 | HCN4 | c.3080C>G (p.Pro1027Arg) c.1862C>G (p.Pro621Arg) | |
15 | g.73323013G= | CA2187187223 | HCN4 | c.3080C= (p.Pro1027=) c.1862C= (p.Pro621=) | |
15 | g.73323013G>T | CA272663752 | HCN4 | c.3080C>A (p.Pro1027His) c.1862C>A (p.Pro621His) | dbSNP gnomAD v4 |
15 | g.73323014G>A | CA393086258 | HCN4 | c.3079C>T (p.Pro1027Ser) c.1861C>T (p.Pro621Ser) | ClinVar |
15 | g.73323014G>C | CA393086259 | HCN4 | c.3079C>G (p.Pro1027Ala) c.1861C>G (p.Pro621Ala) | gnomAD v4 |
15 | g.73323014G= | CA2187187225 | HCN4 | c.3079C= (p.Pro1027=) c.1861C= (p.Pro621=) | |
15 | g.73323014G>T | CA393086260 | HCN4 | c.3079C>A (p.Pro1027Thr) c.1861C>A (p.Pro621Thr) | dbSNP gnomAD v4 |
15 | g.73323015G>A | CA7648887 | HCN4 | c.3078C>T (p.Ser1026=) c.1860C>T (p.Ser620=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323015G>C | CA393086261 | HCN4 | c.3078C>G (p.Ser1026Arg) c.1860C>G (p.Ser620Arg) | gnomAD v4 |
15 | g.73323015G= | CA2187187229 | HCN4 | c.3078C= (p.Ser1026=) c.1860C= (p.Ser620=) | |
15 | g.73323015G>T | CA393086262 | HCN4 | c.3078C>A (p.Ser1026Arg) c.1860C>A (p.Ser620Arg) | gnomAD v4 |
15 | g.73323016C>A | CA393086263 | HCN4 | c.3077G>T (p.Ser1026Ile) c.1859G>T (p.Ser620Ile) | gnomAD v4 |
15 | g.73323016C= | CA2187187234 | HCN4 | c.3077G= (p.Ser1026=) c.1859G= (p.Ser620=) | |
15 | g.73323016C>G | CA393086264 | HCN4 | c.3077G>C (p.Ser1026Thr) c.1859G>C (p.Ser620Thr) | |
15 | g.73323016C>T | CA10587881 | HCN4 | c.3077G>A (p.Ser1026Asn) c.1859G>A (p.Ser620Asn) | ClinVar dbSNP gnomAD v4 |
15 | g.73323017T>A | CA393086265 | HCN4 | c.3076A>T (p.Ser1026Cys) c.1858A>T (p.Ser620Cys) | |
15 | g.73323017T>C | CA393086266 | HCN4 | c.3076A>G (p.Ser1026Gly) c.1858A>G (p.Ser620Gly) | gnomAD v4 |
15 | g.73323017T>G | CA393086267 | HCN4 | c.3076A>C (p.Ser1026Arg) c.1858A>C (p.Ser620Arg) | gnomAD v4 |