| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.150974731A= | CA1752461862 | KCNH2 | c.287T= (p.Ile96=) c.110T= (p.Ile37=) n.510T= | |
| 7 | g.150974731A>C | CA369865335 | KCNH2 | c.287T>G (p.Ile96Ser) c.110T>G (p.Ile37Ser) n.510T>G | |
| 7 | g.150974731A>G | CA007567 | KCNH2 | c.287T>C (p.Ile96Thr) c.110T>C (p.Ile37Thr) n.510T>C | ClinVar dbSNP |
| 7 | g.150974731A>T | CA369865337 | KCNH2 | c.287T>A (p.Ile96Asn) c.110T>A (p.Ile37Asn) n.510T>A | |
| 7 | g.150974732T>A | CA369865339 | KCNH2 | c.286A>T (p.Ile96Phe) c.109A>T (p.Ile37Phe) n.509A>T | |
| 7 | g.150974732T>C | CA007547 | KCNH2 | c.286A>G (p.Ile96Val) c.109A>G (p.Ile37Val) n.509A>G | ClinVar dbSNP |
| 7 | g.150974732T>G | CA369865341 | KCNH2 | c.286A>C (p.Ile96Leu) c.109A>C (p.Ile37Leu) n.509A>C | |
| 7 | g.150974732T= | CA1752461868 | KCNH2 | c.286A= (p.Ile96=) c.109A= (p.Ile37=) n.509A= | |
| 7 | g.150974733T>A | CA369865343 | KCNH2 | c.285A>T (p.Glu95Asp) c.108A>T (p.Glu36Asp) n.508A>T | |
| 7 | g.150974733T>C | CA458871725 | KCNH2 | c.285A>G (p.Glu95=) c.108A>G (p.Glu36=) n.508A>G | gnomAD v4 |
| 7 | g.150974733T>G | CA369865345 | KCNH2 | c.285A>C (p.Glu95Asp) c.108A>C (p.Glu36Asp) n.508A>C | |
| 7 | g.150974734T>A | CA369865346 | KCNH2 | c.284A>T (p.Glu95Val) c.107A>T (p.Glu36Val) n.507A>T | |
| 7 | g.150974734T>C | CA369865348 | KCNH2 | c.284A>G (p.Glu95Gly) c.107A>G (p.Glu36Gly) n.507A>G | gnomAD v4 |
| 7 | g.150974734T>G | CA007512 | KCNH2 | c.284A>C (p.Glu95Ala) c.107A>C (p.Glu36Ala) n.507A>C | ClinVar dbSNP |
| 7 | g.150974734T= | CA1752461875 | KCNH2 | c.284A= (p.Glu95=) c.107A= (p.Glu36=) n.507A= | |
| 7 | g.150974735C>A | CA369865351 | KCNH2 | c.283G>T (p.Glu95Ter) c.106G>T (p.Glu36Ter) n.506G>T | |
| 7 | g.150974735C= | CA1752461881 | KCNH2 | c.283G= (p.Glu95=) c.106G= (p.Glu36=) n.506G= | |
| 7 | g.150974735C>G | CA369865353 | KCNH2 | c.283G>C (p.Glu95Gln) c.106G>C (p.Glu36Gln) n.506G>C | |
| 7 | g.150974735C>T | CA035006 | KCNH2 | c.283G>A (p.Glu95Lys) c.106G>A (p.Glu36Lys) n.506G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.150974736C>A | CA458871726 | KCNH2 | c.282G>T (p.Val94=) c.105G>T (p.Val35=) n.505G>T | |
| 7 | g.150974736C>G | CA458871727 | KCNH2 | c.282G>C (p.Val94=) c.105G>C (p.Val35=) n.505G>C | |
| 7 | g.150974736C>T | CA458871728 | KCNH2 | c.282G>A (p.Val94=) c.105G>A (p.Val35=) n.505G>A | |
| 7 | g.150974737del | CA2695208649 | KCNH2 | c.281del (p.Val94GlyfsTer22) c.104del (p.Val35GlyfsTer22) n.504del | |
| 7 | g.150974737A= | CA1752461883 | KCNH2 | c.281T= (p.Val94=) c.104T= (p.Val35=) n.504T= | |
| 7 | g.150974737A>C | CA007478 | KCNH2 | c.281T>G (p.Val94Gly) c.104T>G (p.Val35Gly) n.504T>G | ClinVar dbSNP |
| 7 | g.150974737A>G | CA369865356 | KCNH2 | c.281T>C (p.Val94Ala) c.104T>C (p.Val35Ala) n.504T>C | gnomAD v4 |
| 7 | g.150974737A>T | CA369865358 | KCNH2 | c.281T>A (p.Val94Glu) c.104T>A (p.Val35Glu) n.504T>A | |
| 7 | g.150974738C>A | CA369865360 | KCNH2 | c.280G>T (p.Val94Leu) c.103G>T (p.Val35Leu) n.503G>T | |
| 7 | g.150974738C= | CA1752461890 | KCNH2 | c.280G= (p.Val94=) c.103G= (p.Val35=) n.503G= | |
| 7 | g.150974738C>G | CA034895 | KCNH2 | c.280G>C (p.Val94Leu) c.103G>C (p.Val35Leu) n.503G>C | ClinVar dbSNP ExAC gnomAD v4 |
| 7 | g.150974738C>T | CA072383 | KCNH2 | c.280G>A (p.Val94Met) c.103G>A (p.Val35Met) n.503G>A | ClinVar dbSNP |
| 7 | g.150974739T>A | CA369865364 | KCNH2 | c.279A>T (p.Lys93Asn) c.102A>T (p.Lys34Asn) n.502A>T | |
| 7 | g.150974739T>C | CA458871729 | KCNH2 | c.279A>G (p.Lys93=) c.102A>G (p.Lys34=) n.502A>G | ClinVar dbSNP |
| 7 | g.150974739T>G | CA369865365 | KCNH2 | c.279A>C (p.Lys93Asn) c.102A>C (p.Lys34Asn) n.502A>C | |
| 7 | g.150974740T>A | CA369865367 | KCNH2 | c.278A>T (p.Lys93Ile) c.101A>T (p.Lys34Ile) n.501A>T | |
| 7 | g.150974740T>C | CA034847 | KCNH2 | c.278A>G (p.Lys93Arg) c.101A>G (p.Lys34Arg) n.501A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.150974740T>G | CA369865370 | KCNH2 | c.278A>C (p.Lys93Thr) c.101A>C (p.Lys34Thr) n.501A>C | |
| 7 | g.150974740T= | CA1752461892 | KCNH2 | c.278A= (p.Lys93=) c.101A= (p.Lys34=) n.501A= | |
| 7 | g.150974741T>A | CA369865372 | KCNH2 | c.277A>T (p.Lys93Ter) c.100A>T (p.Lys34Ter) n.500A>T | |
| 7 | g.150974741T>C | CA369865374 | KCNH2 | c.277A>G (p.Lys93Glu) c.100A>G (p.Lys34Glu) n.500A>G | |
| 7 | g.150974741T>G | CA369865376 | KCNH2 | c.277A>C (p.Lys93Gln) c.100A>C (p.Lys34Gln) n.500A>C | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.150974741T= | CA1752461898 | KCNH2 | c.277A= (p.Lys93=) c.100A= (p.Lys34=) n.500A= | |
| 7 | g.150974742G>A | CA034744 | KCNH2 | c.276C>T (p.Arg92=) c.99C>T (p.Arg33=) n.499C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.150974742G>C | CA458871730 | KCNH2 | c.276C>G (p.Arg92=) c.99C>G (p.Arg33=) n.499C>G | |
| 7 | g.150974742G= | CA1752461904 | KCNH2 | c.276C= (p.Arg92=) c.99C= (p.Arg33=) n.499C= | |
| 7 | g.150974742G>T | CA458871731 | KCNH2 | c.276C>A (p.Arg92=) c.99C>A (p.Arg33=) n.499C>A | gnomAD v4 |
| 7 | g.150974743C>A | CA007325 | KCNH2 | c.275G>T (p.Arg92Leu) c.98G>T (p.Arg33Leu) n.498G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.150974743C= | CA1752461915 | KCNH2 | c.275G= (p.Arg92=) c.98G= (p.Arg33=) n.498G= | |
| 7 | g.150974743C>G | CA369865378 | KCNH2 | c.275G>C (p.Arg92Pro) c.98G>C (p.Arg33Pro) n.498G>C | ClinVar dbSNP |
| 7 | g.150974743C>T | CA369865380 | KCNH2 | c.275G>A (p.Arg92His) c.98G>A (p.Arg33His) n.498G>A | gnomAD v4 |