Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38606133C>A | CA352149089 | SCN5A | c.1156G>T (p.Gly386Trp) c.1027G>T (p.Gly343Trp) | |
3 | g.38606133C= | CA1358586001 | SCN5A | c.1156G= (p.Gly386=) c.1027G= (p.Gly343=) | |
3 | g.38606133C>G | CA352149091 | SCN5A | c.1156G>C (p.Gly386Arg) c.1027G>C (p.Gly343Arg) | |
3 | g.38606133C>T | CA014429 | SCN5A | c.1156G>A (p.Gly386Arg) c.1027G>A (p.Gly343Arg) | ClinVar dbSNP |
3 | g.38606134T>A | CA433137651 | SCN5A | c.1155A>T (p.Ala385=) c.1026A>T (p.Ala342=) | |
3 | g.38606134T>C | CA433137654 | SCN5A | c.1155A>G (p.Ala385=) c.1026A>G (p.Ala342=) | |
3 | g.38606134T>G | CA433137652 | SCN5A | c.1155A>C (p.Ala385=) c.1026A>C (p.Ala342=) | |
3 | g.38606135G>A | CA352149094 | SCN5A | c.1154C>T (p.Ala385Val) c.1025C>T (p.Ala342Val) | |
3 | g.38606135G>C | CA352149095 | SCN5A | c.1154C>G (p.Ala385Gly) c.1025C>G (p.Ala342Gly) | |
3 | g.38606135G>T | CA352149098 | SCN5A | c.1154C>A (p.Ala385Glu) c.1025C>A (p.Ala342Glu) | |
3 | g.38606136C>A | CA352149100 | SCN5A | c.1153G>T (p.Ala385Ser) c.1024G>T (p.Ala342Ser) | ClinVar dbSNP |
3 | g.38606136C= | CA1358586002 | SCN5A | c.1153G= (p.Ala385=) c.1024G= (p.Ala342=) | |
3 | g.38606136C>G | CA352149101 | SCN5A | c.1153G>C (p.Ala385Pro) c.1024G>C (p.Ala342Pro) | |
3 | g.38606136C>T | CA057314 | SCN5A | c.1153G>A (p.Ala385Thr) c.1024G>A (p.Ala342Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38606137G>A | CA014423 | SCN5A | c.1152C>T (p.Ser384=) c.1023C>T (p.Ser341=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38606137G>C | CA433137659 | SCN5A | c.1152C>G (p.Ser384=) c.1023C>G (p.Ser341=) | dbSNP |
3 | g.38606137G= | CA1358586003 | SCN5A | c.1152C= (p.Ser384=) c.1023C= (p.Ser341=) | |
3 | g.38606137G>T | CA433137657 | SCN5A | c.1152C>A (p.Ser384=) c.1023C>A (p.Ser341=) | gnomAD v4 |
3 | g.38606138G>A | CA352149107 | SCN5A | c.1151C>T (p.Ser384Phe) c.1022C>T (p.Ser341Phe) | |
3 | g.38606138G>C | CA352149105 | SCN5A | c.1151C>G (p.Ser384Cys) c.1022C>G (p.Ser341Cys) | |
3 | g.38606138G>T | CA352149109 | SCN5A | c.1151C>A (p.Ser384Tyr) c.1022C>A (p.Ser341Tyr) | |
3 | g.38606139A= | CA1358586004 | SCN5A | c.1150T= (p.Ser384=) c.1021T= (p.Ser341=) | |
3 | g.38606139A>C | CA352149111 | SCN5A | c.1150T>G (p.Ser384Ala) c.1021T>G (p.Ser341Ala) | |
3 | g.38606139A>G | CA352149112 | SCN5A | c.1150T>C (p.Ser384Pro) c.1021T>C (p.Ser341Pro) | |
3 | g.38606139A>T | CA057286 | SCN5A | c.1150T>A (p.Ser384Thr) c.1021T>A (p.Ser341Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38606140C>A | CA352149116 | SCN5A | c.1149G>T (p.Arg383Ser) c.1020G>T (p.Arg340Ser) | |
3 | g.38606140C>G | CA352149118 | SCN5A | c.1149G>C (p.Arg383Ser) c.1020G>C (p.Arg340Ser) | |
3 | g.38606140C>T | CA433137661 | SCN5A | c.1149G>A (p.Arg383=) c.1020G>A (p.Arg340=) | ClinVar |
3 | g.38606141C>A | CA352149121 | SCN5A | c.1148G>T (p.Arg383Met) c.1019G>T (p.Arg340Met) | |
3 | g.38606141C= | CA1358586005 | SCN5A | c.1148G= (p.Arg383=) c.1019G= (p.Arg340=) | |
3 | g.38606141C>G | CA352149122 | SCN5A | c.1148G>C (p.Arg383Thr) c.1019G>C (p.Arg340Thr) | |
3 | g.38606141C>T | CA352149124 | SCN5A | c.1148G>A (p.Arg383Lys) c.1019G>A (p.Arg340Lys) | ClinVar dbSNP |
3 | g.38606142T>A | CA352149126 | SCN5A | c.1147A>T (p.Arg383Trp) c.1018A>T (p.Arg340Trp) | |
3 | g.38606142T>C | CA352149127 | SCN5A | c.1147A>G (p.Arg383Gly) c.1018A>G (p.Arg340Gly) | |
3 | g.38606142T>G | CA433137664 | SCN5A | c.1147A>C (p.Arg383=) c.1018A>C (p.Arg340=) | |
3 | g.38606143G>A | CA433137666 | SCN5A | c.1146C>T (p.Leu382=) c.1017C>T (p.Leu339=) | |
3 | g.38606143G>C | CA433137667 | SCN5A | c.1146C>G (p.Leu382=) c.1017C>G (p.Leu339=) | |
3 | g.38606143G>T | CA433137668 | SCN5A | c.1146C>A (p.Leu382=) c.1017C>A (p.Leu339=) | |
3 | g.38606144A>C | CA352149130 | SCN5A | c.1145T>G (p.Leu382Arg) c.1016T>G (p.Leu339Arg) | |
3 | g.38606144A>G | CA352149132 | SCN5A | c.1145T>C (p.Leu382Pro) c.1016T>C (p.Leu339Pro) | |
3 | g.38606144A>T | CA352149133 | SCN5A | c.1145T>A (p.Leu382His) c.1016T>A (p.Leu339His) | |
3 | g.38606145G>A | CA352149139 | SCN5A | c.1144C>T (p.Leu382Phe) c.1015C>T (p.Leu339Phe) | ClinVar |
3 | g.38606145G>C | CA352149136 | SCN5A | c.1144C>G (p.Leu382Val) c.1015C>G (p.Leu339Val) | gnomAD v4 |
3 | g.38606145G>T | CA352149138 | SCN5A | c.1144C>A (p.Leu382Ile) c.1015C>A (p.Leu339Ile) | COSMIC COSMIC COSMIC |
3 | g.38606146G>A | CA433137670 | SCN5A | c.1143C>T (p.Thr381=) c.1014C>T (p.Thr338=) | |
3 | g.38606146G>C | CA433137671 | SCN5A | c.1143C>G (p.Thr381=) c.1014C>G (p.Thr338=) | |
3 | g.38606146G= | CA1358586006 | SCN5A | c.1143C= (p.Thr381=) c.1014C= (p.Thr338=) | |
3 | g.38606146G>T | CA433137672 | SCN5A | c.1143C>A (p.Thr381=) c.1014C>A (p.Thr338=) | dbSNP gnomAD v4 |
3 | g.38606147G>A | CA352149141 | SCN5A | c.1142C>T (p.Thr381Ile) c.1013C>T (p.Thr338Ile) | |
3 | g.38606147G>C | CA352149143 | SCN5A | c.1142C>G (p.Thr381Ser) c.1013C>G (p.Thr338Ser) |