UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73343534A>C | CA393094937 | HCN4 | c.1060T>G (p.Tyr354Asp) | |
| 15 | g.73343534A>G | CA393094936 | HCN4 | c.1060T>C (p.Tyr354His) | |
| 15 | g.73343534A>T | CA393094935 | HCN4 | c.1060T>A (p.Tyr354Asn) | |
| 15 | g.73343535G>A | CA491479748 | HCN4 | c.1059C>T (p.Asp353=) | |
| 15 | g.73343535G>C | CA393094938 | HCN4 | c.1059C>G (p.Asp353Glu) | |
| 15 | g.73343535G>T | CA393094939 | HCN4 | c.1059C>A (p.Asp353Glu) | |
| 15 | g.73343536T>A | CA393094940 | HCN4 | c.1058A>T (p.Asp353Val) | |
| 15 | g.73343536T>C | CA393094941 | HCN4 | c.1058A>G (p.Asp353Gly) | gnomAD v4 |
| 15 | g.73343536T>G | CA393094942 | HCN4 | c.1058A>C (p.Asp353Ala) | gnomAD v4 |
| 15 | g.73343537C>A | CA393094943 | HCN4 | c.1057G>T (p.Asp353Tyr) | |
| 15 | g.73343537C>G | CA393094944 | HCN4 | c.1057G>C (p.Asp353His) | |
| 15 | g.73343537C>T | CA393094945 | HCN4 | c.1057G>A (p.Asp353Asn) | dbSNP |
| 15 | g.73343538C>A | CA491479752 | HCN4 | c.1056G>T (p.Val352=) | |
| 15 | g.73343538C>G | CA491479753 | HCN4 | c.1056G>C (p.Val352=) | |
| 15 | g.73343538C>T | CA491479754 | HCN4 | c.1056G>A (p.Val352=) | dbSNP |
| 15 | g.73343539A>C | CA393094946 | HCN4 | c.1055T>G (p.Val352Gly) | |
| 15 | g.73343539A>G | CA393094947 | HCN4 | c.1055T>C (p.Val352Ala) | |
| 15 | g.73343539A>T | CA393094948 | HCN4 | c.1055T>A (p.Val352Glu) | |
| 15 | g.73343540C>A | CA393094950 | HCN4 | c.1054G>T (p.Val352Leu) | |
| 15 | g.73343540C= | CA2187179859 | HCN4 | c.1054G= (p.Val352=) | |
| 15 | g.73343540C>G | CA393094951 | HCN4 | c.1054G>C (p.Val352Leu) | |
| 15 | g.73343540C>T | CA393094949 | HCN4 | c.1054G>A (p.Val352Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343541G>A | CA7649376 | HCN4 | c.1053C>T (p.Pro351=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343541G>C | CA491479755 | HCN4 | c.1053C>G (p.Pro351=) | |
| 15 | g.73343541G= | CA2187179865 | HCN4 | c.1053C= (p.Pro351=) | |
| 15 | g.73343541G>T | CA491479757 | HCN4 | c.1053C>A (p.Pro351=) | |
| 15 | g.73343544del | CA2697549204 | HCN4 | c.1053del (p.Val352TrpfsTer?) | ClinVar |
| 15 | g.73343542G>A | CA272684466 | HCN4 | c.1052C>T (p.Pro351Leu) | dbSNP |
| 15 | g.73343542G>C | CA393094952 | HCN4 | c.1052C>G (p.Pro351Arg) | gnomAD v4 |
| 15 | g.73343542G= | CA2187179868 | HCN4 | c.1052C= (p.Pro351=) | |
| 15 | g.73343542G>T | CA393094953 | HCN4 | c.1052C>A (p.Pro351His) | |
| 15 | g.73343543G>A | CA272684471 | HCN4 | c.1051C>T (p.Pro351Ser) | dbSNP COSMIC |
| 15 | g.73343543G>C | CA393094954 | HCN4 | c.1051C>G (p.Pro351Ala) | |
| 15 | g.73343543G= | CA2187179873 | HCN4 | c.1051C= (p.Pro351=) | |
| 15 | g.73343543G>T | CA393094955 | HCN4 | c.1051C>A (p.Pro351Thr) | |
| 15 | g.73343544G>A | CA491479758 | HCN4 | c.1050C>T (p.Ile350=) | |
| 15 | g.73343544G>C | CA272684488 | HCN4 | c.1050C>G (p.Ile350Met) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73343544G= | CA2187179879 | HCN4 | c.1050C= (p.Ile350=) | |
| 15 | g.73343544G>T | CA491479760 | HCN4 | c.1050C>A (p.Ile350=) | |
| 15 | g.73343545A>C | CA393094956 | HCN4 | c.1049T>G (p.Ile350Ser) | |
| 15 | g.73343545A>G | CA393094957 | HCN4 | c.1049T>C (p.Ile350Thr) | |
| 15 | g.73343545A>T | CA393094958 | HCN4 | c.1049T>A (p.Ile350Asn) | |
| 15 | g.73343546T>A | CA393094960 | HCN4 | c.1048A>T (p.Ile350Phe) | |
| 15 | g.73343546T>C | CA393094961 | HCN4 | c.1048A>G (p.Ile350Val) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73343546T>G | CA393094959 | HCN4 | c.1048A>C (p.Ile350Leu) | |
| 15 | g.73343546T= | CA2187179881 | HCN4 | c.1048A= (p.Ile350=) | |
| 15 | g.73343547G>A | CA7649377 | HCN4 | c.1047C>T (p.Ser349=) | dbSNP ExAC |
| 15 | g.73343547G>C | CA491479762 | HCN4 | c.1047C>G (p.Ser349=) | |
| 15 | g.73343547G= | CA2187179885 | HCN4 | c.1047C= (p.Ser349=) | |
| 15 | g.73343547G>T | CA491479763 | HCN4 | c.1047C>A (p.Ser349=) | |
| 15 | g.73343548G>A | CA393094962 | HCN4 | c.1046C>T (p.Ser349Phe) | COSMIC |
| 15 | g.73343548G>C | CA393094963 | HCN4 | c.1046C>G (p.Ser349Cys) | |
| 15 | g.73343548G>T | CA393094964 | HCN4 | c.1046C>A (p.Ser349Tyr) | |
| 15 | g.73343549A>C | CA393094967 | HCN4 | c.1045T>G (p.Ser349Ala) | |
| 15 | g.73343549A>G | CA393094966 | HCN4 | c.1045T>C (p.Ser349Pro) | |
| 15 | g.73343549A>T | CA393094965 | HCN4 | c.1045T>A (p.Ser349Thr) | |
| 15 | g.73343550G>A | CA491479765 | HCN4 | c.1044C>T (p.Ser348=) | ClinVar gnomAD v4 |
| 15 | g.73343550G>C | CA491479766 | HCN4 | c.1044C>G (p.Ser348=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73343550G>T | CA491479767 | HCN4 | c.1044C>A (p.Ser348=) | |
| 15 | g.73343551G>A | CA393094968 | HCN4 | c.1043C>T (p.Ser348Phe) | COSMIC |
| 15 | g.73343551G>C | CA393094969 | HCN4 | c.1043C>G (p.Ser348Cys) | |
| 15 | g.73343551G>T | CA393094970 | HCN4 | c.1043C>A (p.Ser348Tyr) | |
| 15 | g.73343552A>C | CA393094971 | HCN4 | c.1042T>G (p.Ser348Ala) | |
| 15 | g.73343552A>G | CA393094972 | HCN4 | c.1042T>C (p.Ser348Pro) | |
| 15 | g.73343552A>T | CA393094973 | HCN4 | c.1042T>A (p.Ser348Thr) | |
| 15 | g.73343553A>C | CA393094974 | HCN4 | c.1041T>G (p.Ile347Met) | |
| 15 | g.73343553A>G | CA491479770 | HCN4 | c.1041T>C (p.Ile347=) | |
| 15 | g.73343553A>T | CA491479771 | HCN4 | c.1041T>A (p.Ile347=) | |
| 15 | g.73343554A>C | CA393094976 | HCN4 | c.1040T>G (p.Ile347Ser) | |
| 15 | g.73343554A>G | CA393094977 | HCN4 | c.1040T>C (p.Ile347Thr) | |
| 15 | g.73343554A>T | CA393094975 | HCN4 | c.1040T>A (p.Ile347Asn) | |
| 15 | g.73343555T>A | CA393094978 | HCN4 | c.1039A>T (p.Ile347Phe) | |
| 15 | g.73343555T>C | CA393094979 | HCN4 | c.1039A>G (p.Ile347Val) | |
| 15 | g.73343555T>G | CA393094980 | HCN4 | c.1039A>C (p.Ile347Leu) | |
| 15 | g.73343556G>A | CA7649378 | HCN4 | c.1038C>T (p.Phe346=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73343556G>C | CA393094981 | HCN4 | c.1038C>G (p.Phe346Leu) | |
| 15 | g.73343556G= | CA2187179891 | HCN4 | c.1038C= (p.Phe346=) | |
| 15 | g.73343556G>T | CA393094982 | HCN4 | c.1038C>A (p.Phe346Leu) | |
| 15 | g.73343557A>C | CA393094985 | HCN4 | c.1037T>G (p.Phe346Cys) | |
| 15 | g.73343557A>G | CA393094983 | HCN4 | c.1037T>C (p.Phe346Ser) | |
| 15 | g.73343557A>T | CA393094984 | HCN4 | c.1037T>A (p.Phe346Tyr) | |
| 15 | g.73343558A>C | CA393094986 | HCN4 | c.1036T>G (p.Phe346Val) | |
| 15 | g.73343558A>G | CA393094987 | HCN4 | c.1036T>C (p.Phe346Leu) | |
| 15 | g.73343558A>T | CA393094988 | HCN4 | c.1036T>A (p.Phe346Ile) | |
| 15 | g.73343559A>C | CA393094989 | HCN4 | c.1035T>G (p.Asp345Glu) | |
| 15 | g.73343559A>G | CA491479773 | HCN4 | c.1035T>C (p.Asp345=) | |
| 15 | g.73343559A>T | CA393094990 | HCN4 | c.1035T>A (p.Asp345Glu) | |
| 15 | g.73343560T>A | CA393094993 | HCN4 | c.1034A>T (p.Asp345Val) | |
| 15 | g.73343560T>C | CA393094991 | HCN4 | c.1034A>G (p.Asp345Gly) | |
| 15 | g.73343560T>G | CA393094992 | HCN4 | c.1034A>C (p.Asp345Ala) | |
| 15 | g.73343561C>A | CA393094994 | HCN4 | c.1033G>T (p.Asp345Tyr) | |
| 15 | g.73343561C>G | CA393094995 | HCN4 | c.1033G>C (p.Asp345His) | |
| 15 | g.73343561C>T | CA393094996 | HCN4 | c.1033G>A (p.Asp345Asn) | |
| 15 | g.73343562T>A | CA491479774 | HCN4 | c.1032A>T (p.Val344=) | |
| 15 | g.73343562T>C | CA7649379 | HCN4 | c.1032A>G (p.Val344=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73343562T>G | CA491479775 | HCN4 | c.1032A>C (p.Val344=) | |
| 15 | g.73343562T= | CA2187179895 | HCN4 | c.1032A= (p.Val344=) | |
| 15 | g.73343563A>C | CA393094997 | HCN4 | c.1031T>G (p.Val344Gly) | |
| 15 | g.73343563A>G | CA393094998 | HCN4 | c.1031T>C (p.Val344Ala) | |
| 15 | g.73343563A>T | CA393094999 | HCN4 | c.1031T>A (p.Val344Glu) | |
| 15 | g.73343564C>A | CA393095000 | HCN4 | c.1030G>T (p.Val344Leu) | |
| 15 | g.73343564C>G | CA393095001 | HCN4 | c.1030G>C (p.Val344Leu) | |
| 15 | g.73343564C>T | CA393095002 | HCN4 | c.1030G>A (p.Val344Ile) | |
| 15 | g.73343565C>A | CA393095003 | HCN4 | c.1029G>T (p.Met343Ile) | |
| 15 | g.73343565C= | CA2187179898 | HCN4 | c.1029G= (p.Met343=) | |
| 15 | g.73343565C>G | CA393095004 | HCN4 | c.1029G>C (p.Met343Ile) | |
| 15 | g.73343565C>T | CA7649380 | HCN4 | c.1029G>A (p.Met343Ile) | dbSNP ExAC gnomAD v2 |
| 15 | g.73343566A>C | CA393095005 | HCN4 | c.1028T>G (p.Met343Arg) | |
| 15 | g.73343566A>G | CA393095007 | HCN4 | c.1028T>C (p.Met343Thr) | gnomAD v4 |
| 15 | g.73343566A>T | CA393095006 | HCN4 | c.1028T>A (p.Met343Lys) | |
| 15 | g.73343567T>A | CA393095008 | HCN4 | c.1027A>T (p.Met343Leu) | ClinVar gnomAD v4 |
| 15 | g.73343567T>C | CA7649381 | HCN4 | c.1027A>G (p.Met343Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343567T>G | CA393095009 | HCN4 | c.1027A>C (p.Met343Leu) | COSMIC |
| 15 | g.73343567T= | CA2187179904 | HCN4 | c.1027A= (p.Met343=) | |
| 15 | g.73343568G>A | CA491479776 | HCN4 | c.1026C>T (p.Phe342=) | |
| 15 | g.73343568G>C | CA393095010 | HCN4 | c.1026C>G (p.Phe342Leu) | ClinVar dbSNP |
| 15 | g.73343568G= | CA2187179907 | HCN4 | c.1026C= (p.Phe342=) | |
| 15 | g.73343568G>T | CA393095011 | HCN4 | c.1026C>A (p.Phe342Leu) | |
| 15 | g.73343569A>C | CA393095014 | HCN4 | c.1025T>G (p.Phe342Cys) | |
| 15 | g.73343569A>G | CA393095013 | HCN4 | c.1025T>C (p.Phe342Ser) | |
| 15 | g.73343569A>T | CA393095012 | HCN4 | c.1025T>A (p.Phe342Tyr) | |
| 15 | g.73343570A>C | CA393095015 | HCN4 | c.1024T>G (p.Phe342Val) | |
| 15 | g.73343570A>G | CA393095016 | HCN4 | c.1024T>C (p.Phe342Leu) | |
| 15 | g.73343570A>T | CA393095017 | HCN4 | c.1024T>A (p.Phe342Ile) | |
| 15 | g.73343571C>A | CA393095018 | HCN4 | c.1023G>T (p.Trp341Cys) | |
| 15 | g.73343571C= | CA2187179911 | HCN4 | c.1023G= (p.Trp341=) | |
| 15 | g.73343571C>G | CA393095019 | HCN4 | c.1023G>C (p.Trp341Cys) | ClinVar dbSNP |
| 15 | g.73343571C>T | CA393095020 | HCN4 | c.1023G>A (p.Trp341Ter) | |
| 15 | g.73343572C>A | CA393095021 | HCN4 | c.1022G>T (p.Trp341Leu) | |
| 15 | g.73343572C>G | CA393095023 | HCN4 | c.1022G>C (p.Trp341Ser) | |
| 15 | g.73343572C>T | CA393095022 | HCN4 | c.1022G>A (p.Trp341Ter) | |
| 15 | g.73343573A>C | CA393095024 | HCN4 | c.1021T>G (p.Trp341Gly) | |
| 15 | g.73343573A>G | CA393095025 | HCN4 | c.1021T>C (p.Trp341Arg) | |
| 15 | g.73343573A>T | CA393095026 | HCN4 | c.1021T>A (p.Trp341Arg) | |
| 15 | g.73343574G>A | CA491479777 | HCN4 | c.1020C>T (p.Ser340=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73343574G>C | CA393095027 | HCN4 | c.1020C>G (p.Ser340Arg) | ClinVar |
| 15 | g.73343574G= | CA2187179915 | HCN4 | c.1020C= (p.Ser340=) | |
| 15 | g.73343574G>T | CA393095028 | HCN4 | c.1020C>A (p.Ser340Arg) | |
| 15 | g.73343575C>A | CA393095029 | HCN4 | c.1019G>T (p.Ser340Ile) | |
| 15 | g.73343575C>G | CA393095030 | HCN4 | c.1019G>C (p.Ser340Thr) | |
| 15 | g.73343575C>T | CA393095031 | HCN4 | c.1019G>A (p.Ser340Asn) | |
| 15 | g.73343576T>A | CA393095032 | HCN4 | c.1018A>T (p.Ser340Cys) | |
| 15 | g.73343576T>C | CA393095033 | HCN4 | c.1018A>G (p.Ser340Gly) | ClinVar gnomAD v4 |
| 15 | g.73343576T>G | CA393095034 | HCN4 | c.1018A>C (p.Ser340Arg) | |
| 15 | g.73343577T>A | CA393095036 | HCN4 | c.1017A>T (p.Lys339Asn) | |
| 15 | g.73343577T>C | CA491479778 | HCN4 | c.1017A>G (p.Lys339=) | |
| 15 | g.73343577T>G | CA393095035 | HCN4 | c.1017A>C (p.Lys339Asn) | |
| 15 | g.73343578T>A | CA393095037 | HCN4 | c.1016A>T (p.Lys339Ile) | |
| 15 | g.73343578T>C | CA393095039 | HCN4 | c.1016A>G (p.Lys339Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343578T>G | CA393095038 | HCN4 | c.1016A>C (p.Lys339Thr) | |
| 15 | g.73343578T= | CA2187179918 | HCN4 | c.1016A= (p.Lys339=) | |
| 15 | g.73343579T>A | CA393095040 | HCN4 | c.1015A>T (p.Lys339Ter) | |
| 15 | g.73343579T>C | CA393095042 | HCN4 | c.1015A>G (p.Lys339Glu) | |
| 15 | g.73343579T>G | CA393095041 | HCN4 | c.1015A>C (p.Lys339Gln) | |
| 15 | g.73343580C>A | CA491479779 | HCN4 | c.1014G>T (p.Leu338=) | |
| 15 | g.73343580C= | CA2187179923 | HCN4 | c.1014G= (p.Leu338=) | |
| 15 | g.73343580C>G | CA7649382 | HCN4 | c.1014G>C (p.Leu338=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343580C>T | CA491479780 | HCN4 | c.1014G>A (p.Leu338=) | |
| 15 | g.73343581A>C | CA393095043 | HCN4 | c.1013T>G (p.Leu338Arg) | |
| 15 | g.73343581A>G | CA393095044 | HCN4 | c.1013T>C (p.Leu338Pro) | |
| 15 | g.73343581A>T | CA393095045 | HCN4 | c.1013T>A (p.Leu338Gln) | |
| 15 | g.73343582G>A | CA491479781 | HCN4 | c.1012C>T (p.Leu338=) | |
| 15 | g.73343582G>C | CA393095046 | HCN4 | c.1012C>G (p.Leu338Val) | |
| 15 | g.73343582G= | CA2187179926 | HCN4 | c.1012C= (p.Leu338=) | |
| 15 | g.73343582G>T | CA272684517 | HCN4 | c.1012C>A (p.Leu338Met) | dbSNP gnomAD v4 |
| 15 | g.73343583G>A | CA491479782 | HCN4 | c.1011C>T (p.Tyr337=) | |
| 15 | g.73343583G>C | CA393095047 | HCN4 | c.1011C>G (p.Tyr337Ter) | |
| 15 | g.73343583G>T | CA393095048 | HCN4 | c.1011C>A (p.Tyr337Ter) | |
| 15 | g.73343584T>A | CA393095049 | HCN4 | c.1010A>T (p.Tyr337Phe) | |
| 15 | g.73343584T>C | CA393095050 | HCN4 | c.1010A>G (p.Tyr337Cys) | |
| 15 | g.73343584T>G | CA393095051 | HCN4 | c.1010A>C (p.Tyr337Ser) | |
| 15 | g.73343585A>C | CA393095054 | HCN4 | c.1009T>G (p.Tyr337Asp) | |
| 15 | g.73343585A>G | CA393095052 | HCN4 | c.1009T>C (p.Tyr337His) | ClinVar |
| 15 | g.73343585A>T | CA393095053 | HCN4 | c.1009T>A (p.Tyr337Asn) | |
| 15 | g.73343586C>A | CA393095055 | HCN4 | c.1008G>T (p.Lys336Asn) | |
| 15 | g.73343586C= | CA2187179928 | HCN4 | c.1008G= (p.Lys336=) | |
| 15 | g.73343586C>G | CA393095056 | HCN4 | c.1008G>C (p.Lys336Asn) | |
| 15 | g.73343586C>T | CA491479783 | HCN4 | c.1008G>A (p.Lys336=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73343587T>A | CA393095057 | HCN4 | c.1007A>T (p.Lys336Met) | |
| 15 | g.73343587T>C | CA393095058 | HCN4 | c.1007A>G (p.Lys336Arg) | gnomAD v4 COSMIC |
| 15 | g.73343587T>G | CA393095059 | HCN4 | c.1007A>C (p.Lys336Thr) | |
| 15 | g.73343588T>A | CA393095060 | HCN4 | c.1006A>T (p.Lys336Ter) | |
| 15 | g.73343588T>C | CA393095061 | HCN4 | c.1006A>G (p.Lys336Glu) | |
| 15 | g.73343588T>G | CA393095062 | HCN4 | c.1006A>C (p.Lys336Gln) | |
| 15 | g.73343589C>A | CA393095063 | HCN4 | c.1005G>T (p.Met335Ile) | ClinVar dbSNP |
| 15 | g.73343589C= | CA2187179934 | HCN4 | c.1005G= (p.Met335=) | |
| 15 | g.73343589C>G | CA393095064 | HCN4 | c.1005G>C (p.Met335Ile) | |
| 15 | g.73343589C>T | CA7649383 | HCN4 | c.1005G>A (p.Met335Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343590A= | CA2187179942 | HCN4 | c.1004T= (p.Met335=) | |
| 15 | g.73343590A>C | CA272684521 | HCN4 | c.1004T>G (p.Met335Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343590A>G | CA393095066 | HCN4 | c.1004T>C (p.Met335Thr) | |
| 15 | g.73343590A>T | CA393095065 | HCN4 | c.1004T>A (p.Met335Lys) | |
| 15 | g.73343591T>A | CA393095067 | HCN4 | c.1003A>T (p.Met335Leu) | |
| 15 | g.73343591T>C | CA393095068 | HCN4 | c.1003A>G (p.Met335Val) | dbSNP gnomAD v4 |
| 15 | g.73343591T>G | CA393095069 | HCN4 | c.1003A>C (p.Met335Leu) | |
| 15 | g.73343591T= | CA2187179946 | HCN4 | c.1003A= (p.Met335=) | |
| 15 | g.73343592T>A | CA393095070 | HCN4 | c.1002A>T (p.Lys334Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343592T>C | CA491479784 | HCN4 | c.1002A>G (p.Lys334=) | |
| 15 | g.73343592T>G | CA393095071 | HCN4 | c.1002A>C (p.Lys334Asn) | |
| 15 | g.73343592T= | CA2187179949 | HCN4 | c.1002A= (p.Lys334=) | |
| 15 | g.73343593T>A | CA393095072 | HCN4 | c.1001A>T (p.Lys334Ile) | |
| 15 | g.73343593T>C | CA393095073 | HCN4 | c.1001A>G (p.Lys334Arg) | gnomAD v4 |
| 15 | g.73343593T>G | CA393095074 | HCN4 | c.1001A>C (p.Lys334Thr) | |
| 15 | g.73343594T>A | CA393095075 | HCN4 | c.1000A>T (p.Lys334Ter) | |
| 15 | g.73343594T>C | CA393095076 | HCN4 | c.1000A>G (p.Lys334Glu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343594T>G | CA393095077 | HCN4 | c.1000A>C (p.Lys334Gln) | |
| 15 | g.73343594T= | CA2187179951 | HCN4 | c.1000A= (p.Lys334=) | |
| 15 | g.73343595A>C | CA393095078 | HCN4 | c.999T>G (p.Ile333Met) | |
| 15 | g.73343595A>G | CA491479786 | HCN4 | c.999T>C (p.Ile333=) | gnomAD v4 |
| 15 | g.73343595A>T | CA491479785 | HCN4 | c.999T>A (p.Ile333=) | |
| 15 | g.73343596A>C | CA393095080 | HCN4 | c.998T>G (p.Ile333Ser) | |
| 15 | g.73343596A>G | CA393095081 | HCN4 | c.998T>C (p.Ile333Thr) | |
| 15 | g.73343596A>T | CA393095079 | HCN4 | c.998T>A (p.Ile333Asn) | |
| 15 | g.73343597T>A | CA393095082 | HCN4 | c.997A>T (p.Ile333Phe) | |
| 15 | g.73343597T>C | CA393095083 | HCN4 | c.997A>G (p.Ile333Val) | |
| 15 | g.73343597T>G | CA393095084 | HCN4 | c.997A>C (p.Ile333Leu) | |
| 15 | g.73343598C>A | CA491479787 | HCN4 | c.996G>T (p.Arg332=) | |
| 15 | g.73343598C>G | CA491479788 | HCN4 | c.996G>C (p.Arg332=) | |
| 15 | g.73343598C>T | CA491479789 | HCN4 | c.996G>A (p.Arg332=) | |
| 15 | g.73343599C>A | CA393095085 | HCN4 | c.995G>T (p.Arg332Leu) | |
| 15 | g.73343599C= | CA2187179956 | HCN4 | c.995G= (p.Arg332=) | |
| 15 | g.73343599C>G | CA393095086 | HCN4 | c.995G>C (p.Arg332Pro) | gnomAD v4 |
| 15 | g.73343599C>T | CA7649384 | HCN4 | c.995G>A (p.Arg332Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343600G>A | CA7649385 | HCN4 | c.994C>T (p.Arg332Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73343600G>C | CA393095087 | HCN4 | c.994C>G (p.Arg332Gly) | gnomAD v4 |
| 15 | g.73343600G= | CA2187179964 | HCN4 | c.994C= (p.Arg332=) | |
| 15 | g.73343600G>T | CA491479790 | HCN4 | c.994C>A (p.Arg332=) | gnomAD v4 |
| 15 | g.73343601C>A | CA393095088 | HCN4 | c.993G>T (p.Gln331His) | gnomAD v4 |
| 15 | g.73343601C>G | CA393095089 | HCN4 | c.993G>C (p.Gln331His) | |
| 15 | g.73343601C>T | CA491479791 | HCN4 | c.993G>A (p.Gln331=) | gnomAD v4 |
| 15 | g.73343602T>A | CA393095090 | HCN4 | c.992A>T (p.Gln331Leu) | |
| 15 | g.73343602T>C | CA393095091 | HCN4 | c.992A>G (p.Gln331Arg) | gnomAD v4 |
| 15 | g.73343602T>G | CA393095092 | HCN4 | c.992A>C (p.Gln331Pro) | |
| 15 | g.73343603G>A | CA393095094 | HCN4 | c.991C>T (p.Gln331Ter) | |
| 15 | g.73343603G>C | CA393095093 | HCN4 | c.991C>G (p.Gln331Glu) | |
| 15 | g.73343603G= | CA2187179969 | HCN4 | c.991C= (p.Gln331=) | |
| 15 | g.73343603G>T | CA7649386 | HCN4 | c.991C>A (p.Gln331Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343604C>A | CA16607014 | HCN4 | c.990G>T (p.Pro330=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343604C= | CA2187179978 | HCN4 | c.990G= (p.Pro330=) | |
| 15 | g.73343604C>G | CA7649388 | HCN4 | c.990G>C (p.Pro330=) | ClinVar dbSNP ExAC |
| 15 | g.73343604C>T | CA7649387 | HCN4 | c.990G>A (p.Pro330=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73343605G>A | CA7649389 | HCN4 | c.989C>T (p.Pro330Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343605G>C | CA393095095 | HCN4 | c.989C>G (p.Pro330Arg) | |
| 15 | g.73343605G= | CA2187179984 | HCN4 | c.989C= (p.Pro330=) | |
| 15 | g.73343605G>T | CA393095096 | HCN4 | c.989C>A (p.Pro330Gln) | |
| 15 | g.73343606G>A | CA393095097 | HCN4 | c.988C>T (p.Pro330Ser) | ClinVar dbSNP |
| 15 | g.73343606G>C | CA393095098 | HCN4 | c.988C>G (p.Pro330Ala) | |
| 15 | g.73343606G= | CA2187179994 | HCN4 | c.988C= (p.Pro330=) | |
| 15 | g.73343606G>T | CA393095099 | HCN4 | c.988C>A (p.Pro330Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73343607G>A | CA491479792 | HCN4 | c.987C>T (p.Asp329=) | |
| 15 | g.73343607G>C | CA393095101 | HCN4 | c.987C>G (p.Asp329Glu) | |
| 15 | g.73343607G= | CA2187179999 | HCN4 | c.987C= (p.Asp329=) | |
| 15 | g.73343607G>T | CA393095100 | HCN4 | c.987C>A (p.Asp329Glu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343608T>A | CA393095102 | HCN4 | c.986A>T (p.Asp329Val) | |
| 15 | g.73343608T>C | CA393095103 | HCN4 | c.986A>G (p.Asp329Gly) | gnomAD v4 |
| 15 | g.73343608T>G | CA393095104 | HCN4 | c.986A>C (p.Asp329Ala) | |
| 15 | g.73343609C>A | CA393095105 | HCN4 | c.985G>T (p.Asp329Tyr) | |
| 15 | g.73343609C>G | CA393095106 | HCN4 | c.985G>C (p.Asp329His) | |
| 15 | g.73343609C>T | CA393095107 | HCN4 | c.985G>A (p.Asp329Asn) | |
| 15 | g.73343610del | CA2629389086 | HCN4 | c.985del (p.Asp329ThrfsTer7) | gnomAD v4 |
| 15 | g.73343610C>A | CA491479793 | HCN4 | c.984G>T (p.Leu328=) | |
| 15 | g.73343610C= | CA2187180006 | HCN4 | c.984G= (p.Leu328=) | |
| 15 | g.73343610C>G | CA491479794 | HCN4 | c.984G>C (p.Leu328=) | |
| 15 | g.73343610C>T | CA272684533 | HCN4 | c.984G>A (p.Leu328=) | ClinVar dbSNP |
| 15 | g.73343611A>C | CA393095108 | HCN4 | c.983T>G (p.Leu328Arg) | |
| 15 | g.73343611A>G | CA393095110 | HCN4 | c.983T>C (p.Leu328Pro) | |
| 15 | g.73343611A>T | CA393095109 | HCN4 | c.983T>A (p.Leu328Gln) | |
| 15 | g.73343612G>A | CA491479795 | HCN4 | c.982C>T (p.Leu328=) | dbSNP COSMIC |
| 15 | g.73343612G>C | CA393095111 | HCN4 | c.982C>G (p.Leu328Val) | |
| 15 | g.73343612G= | CA2187180007 | HCN4 | c.982C= (p.Leu328=) | |
| 15 | g.73343612G>T | CA393095112 | HCN4 | c.982C>A (p.Leu328Met) | |
| 15 | g.73343613G>A | CA491479796 | HCN4 | c.981C>T (p.Ile327=) | |
| 15 | g.73343613G>C | CA393095113 | HCN4 | c.981C>G (p.Ile327Met) | |
| 15 | g.73343613G>T | CA491479797 | HCN4 | c.981C>A (p.Ile327=) | |
| 15 | g.73343614A>C | CA393095114 | HCN4 | c.980T>G (p.Ile327Ser) | |
| 15 | g.73343614A>G | CA393095115 | HCN4 | c.980T>C (p.Ile327Thr) | |
| 15 | g.73343614A>T | CA393095116 | HCN4 | c.980T>A (p.Ile327Asn) | |
| 15 | g.73343615T>A | CA393095117 | HCN4 | c.979A>T (p.Ile327Phe) | |
| 15 | g.73343615T>C | CA393095118 | HCN4 | c.979A>G (p.Ile327Val) | |
| 15 | g.73343615T>G | CA393095119 | HCN4 | c.979A>C (p.Ile327Leu) | |
| 15 | g.73343616G>A | CA491479798 | HCN4 | c.978C>T (p.Ile326=) | |
| 15 | g.73343616G>C | CA393095120 | HCN4 | c.978C>G (p.Ile326Met) | ClinVar |
| 15 | g.73343616G>T | CA491479799 | HCN4 | c.978C>A (p.Ile326=) | |
| 15 | g.73343617A>C | CA393095123 | HCN4 | c.977T>G (p.Ile326Ser) | |
| 15 | g.73343617A>G | CA393095122 | HCN4 | c.977T>C (p.Ile326Thr) | |
| 15 | g.73343617A>T | CA393095121 | HCN4 | c.977T>A (p.Ile326Asn) | |
| 15 | g.73343618T>A | CA393095124 | HCN4 | c.976A>T (p.Ile326Phe) | |
| 15 | g.73343618T>C | CA393095125 | HCN4 | c.976A>G (p.Ile326Val) | |
| 15 | g.73343618T>G | CA393095126 | HCN4 | c.976A>C (p.Ile326Leu) | |
| 15 | g.73343619C>A | CA7649390 | HCN4 | c.975G>T (p.Glu325Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343619C= | CA2187180013 | HCN4 | c.975G= (p.Glu325=) | |
| 15 | g.73343619C>G | CA393095127 | HCN4 | c.975G>C (p.Glu325Asp) | |
| 15 | g.73343619C>T | CA491479800 | HCN4 | c.975G>A (p.Glu325=) | |
| 15 | g.73343620T>A | CA393095128 | HCN4 | c.974A>T (p.Glu325Val) | |
| 15 | g.73343620T>C | CA393095129 | HCN4 | c.974A>G (p.Glu325Gly) | |
| 15 | g.73343620T>G | CA393095130 | HCN4 | c.974A>C (p.Glu325Ala) | |
| 15 | g.73343621C>A | CA393095131 | HCN4 | c.973G>T (p.Glu325Ter) | |
| 15 | g.73343621C>G | CA393095132 | HCN4 | c.973G>C (p.Glu325Gln) | |
| 15 | g.73343621C>T | CA393095133 | HCN4 | c.973G>A (p.Glu325Lys) | |
| 15 | g.73343622T>A | CA491479801 | HCN4 | c.972A>T (p.Thr324=) | |
| 15 | g.73343622T>C | CA7649391 | HCN4 | c.972A>G (p.Thr324=) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
| 15 | g.73343622T>G | CA491479802 | HCN4 | c.972A>C (p.Thr324=) | |
| 15 | g.73343622T= | CA2187180019 | HCN4 | c.972A= (p.Thr324=) | |
| 15 | g.73343623G>A | CA393095135 | HCN4 | c.971C>T (p.Thr324Ile) | |
| 15 | g.73343623G>C | CA393095136 | HCN4 | c.971C>G (p.Thr324Arg) | |
| 15 | g.73343623G>T | CA393095134 | HCN4 | c.971C>A (p.Thr324Lys) | |
| 15 | g.73343624T>A | CA393095137 | HCN4 | c.970A>T (p.Thr324Ser) | |
| 15 | g.73343624T>C | CA393095138 | HCN4 | c.970A>G (p.Thr324Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73343624T>G | CA393095139 | HCN4 | c.970A>C (p.Thr324Pro) | |
| 15 | g.73343624T= | CA2187180026 | HCN4 | c.970A= (p.Thr324=) | |
| 15 | g.73343625G>A | CA491479803 | HCN4 | c.969C>T (p.Asn323=) | |
| 15 | g.73343625G>C | CA393095140 | HCN4 | c.969C>G (p.Asn323Lys) | |
| 15 | g.73343625G>T | CA393095141 | HCN4 | c.969C>A (p.Asn323Lys) | |
| 15 | g.73343626T>A | CA393095144 | HCN4 | c.968A>T (p.Asn323Ile) | |
| 15 | g.73343626T>C | CA393095142 | HCN4 | c.968A>G (p.Asn323Ser) | |
| 15 | g.73343626T>G | CA393095143 | HCN4 | c.968A>C (p.Asn323Thr) | |
| 15 | g.73343627T>A | CA393095145 | HCN4 | c.967A>T (p.Asn323Tyr) | |
| 15 | g.73343627T>C | CA393095146 | HCN4 | c.967A>G (p.Asn323Asp) | |
| 15 | g.73343627T>G | CA393095147 | HCN4 | c.967A>C (p.Asn323His) | |
| 15 | g.73343628G>A | CA7649392 | HCN4 | c.966C>T (p.Asp322=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73343628G>C | CA393095148 | HCN4 | c.966C>G (p.Asp322Glu) | |
| 15 | g.73343628G= | CA2187180033 | HCN4 | c.966C= (p.Asp322=) | |
| 15 | g.73343628G>T | CA393095149 | HCN4 | c.966C>A (p.Asp322Glu) | |
| 15 | g.73343629T>A | CA393095151 | HCN4 | c.965A>T (p.Asp322Val) | |
| 15 | g.73343629T>C | CA393095152 | HCN4 | c.965A>G (p.Asp322Gly) | |
| 15 | g.73343629T>G | CA393095150 | HCN4 | c.965A>C (p.Asp322Ala) | |
| 15 | g.73343630C>A | CA393095154 | HCN4 | c.964G>T (p.Asp322Tyr) | |
| 15 | g.73343630C>G | CA393095153 | HCN4 | c.964G>C (p.Asp322His) | |
| 15 | g.73343630C>T | CA393095155 | HCN4 | c.964G>A (p.Asp322Asn) | |
| 15 | g.73343631C>A | CA393095156 | HCN4 | c.963G>T (p.Glu321Asp) | |
| 15 | g.73343631C>G | CA393095157 | HCN4 | c.963G>C (p.Glu321Asp) | |
| 15 | g.73343631C>T | CA491479804 | HCN4 | c.963G>A (p.Glu321=) | |
| 15 | g.73343632T>A | CA393095158 | HCN4 | c.962A>T (p.Glu321Val) | COSMIC |
| 15 | g.73343632T>C | CA393095159 | HCN4 | c.962A>G (p.Glu321Gly) | |
| 15 | g.73343632T>G | CA393095160 | HCN4 | c.962A>C (p.Glu321Ala) | |
| 15 | g.73343633C>A | CA393095161 | HCN4 | c.961G>T (p.Glu321Ter) | |
| 15 | g.73343633C>G | CA393095162 | HCN4 | c.961G>C (p.Glu321Gln) | |
| 15 | g.73343633C>T | CA393095163 | HCN4 | c.961G>A (p.Glu321Lys) | |
| 15 | g.73343634C>A | CA491479807 | HCN4 | c.960G>T (p.Val320=) | |
| 15 | g.73343634C= | CA2187180038 | HCN4 | c.960G= (p.Val320=) | |
| 15 | g.73343634C>G | CA491479806 | HCN4 | c.960G>C (p.Val320=) | |
| 15 | g.73343634C>T | CA491479805 | HCN4 | c.960G>A (p.Val320=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |