| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.1841468C>A | CA471992992 | TNNI2 | c.466C>A (p.Arg156=) | |
| 11 | g.1841468C= | CA1947878660 | TNNI2 | c.466C= (p.Arg156=) | |
| 11 | g.1841468C>G | CA379106826 | TNNI2 | c.466C>G (p.Arg156Gly) | |
| 11 | g.1841468C>T | CA122379 | TNNI2 | c.466C>T (p.Arg156Ter) | ClinVar dbSNP |
| 11 | g.1841469G>A | CA5815309 | TNNI2 | c.467G>A (p.Arg156Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 11 | g.1841469G>C | CA379106827 | TNNI2 | c.467G>C (p.Arg156Pro) | |
| 11 | g.1841469G= | CA1947878668 | TNNI2 | c.467G= (p.Arg156=) | |
| 11 | g.1841469G>T | CA379106828 | TNNI2 | c.467G>T (p.Arg156Leu) | |
| 11 | g.1841470A>C | CA471993013 | TNNI2 | c.468A>C (p.Arg156=) | |
| 11 | g.1841470A>G | CA471993016 | TNNI2 | c.468A>G (p.Arg156=) | |
| 11 | g.1841470A>T | CA471993018 | TNNI2 | c.468A>T (p.Arg156=) | |
| 11 | g.1841471G>A | CA379106829 | TNNI2 | c.469G>A (p.Asp157Asn) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.1841471G>C | CA379106830 | TNNI2 | c.469G>C (p.Asp157His) | |
| 11 | g.1841471G= | CA1947878672 | TNNI2 | c.469G= (p.Asp157=) | |
| 11 | g.1841471G>T | CA379106831 | TNNI2 | c.469G>T (p.Asp157Tyr) | |
| 11 | g.1841472A= | CA1947878674 | TNNI2 | c.470A= (p.Asp157=) | |
| 11 | g.1841472A>C | CA379106832 | TNNI2 | c.470A>C (p.Asp157Ala) | |
| 11 | g.1841472A>G | CA5815310 | TNNI2 | c.470A>G (p.Asp157Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.1841472A>T | CA379106833 | TNNI2 | c.470A>T (p.Asp157Val) | |
| 11 | g.1841473C>A | CA379106835 | TNNI2 | c.471C>A (p.Asp157Glu) | |
| 11 | g.1841473C= | CA1947878677 | TNNI2 | c.471C= (p.Asp157=) | |
| 11 | g.1841473C>G | CA379106834 | TNNI2 | c.471C>G (p.Asp157Glu) | |
| 11 | g.1841473C>T | CA5815311 | TNNI2 | c.471C>T (p.Asp157=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.1841474G>A | CA5815313 | TNNI2 | c.472G>A (p.Val158Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.1841474G>C | CA379106836 | TNNI2 | c.472G>C (p.Val158Leu) | |
| 11 | g.1841474G= | CA1947878682 | TNNI2 | c.472G= (p.Val158=) | |
| 11 | g.1841474G>T | CA5815312 | TNNI2 | c.472G>T (p.Val158Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.1841475T>A | CA379106837 | TNNI2 | c.473T>A (p.Val158Glu) | |
| 11 | g.1841475T>C | CA379106838 | TNNI2 | c.473T>C (p.Val158Ala) | |
| 11 | g.1841475T>G | CA379106839 | TNNI2 | c.473T>G (p.Val158Gly) | |
| 11 | g.1841476G>A | CA471993042 | TNNI2 | c.474G>A (p.Val158=) | |
| 11 | g.1841476G>C | CA471993043 | TNNI2 | c.474G>C (p.Val158=) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.1841476G= | CA1947878686 | TNNI2 | c.474G= (p.Val158=) | |
| 11 | g.1841476G>T | CA471993041 | TNNI2 | c.474G>T (p.Val158=) | |
| 11 | g.1841477G>A | CA379106840 | TNNI2 | c.475G>A (p.Gly159Ser) | |
| 11 | g.1841477G>C | CA379106841 | TNNI2 | c.475G>C (p.Gly159Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.1841477G= | CA1947878691 | TNNI2 | c.475G= (p.Gly159=) | |
| 11 | g.1841477G>T | CA379106842 | TNNI2 | c.475G>T (p.Gly159Cys) | |
| 11 | g.1841478G>A | CA379106843 | TNNI2 | c.476G>A (p.Gly159Asp) | |
| 11 | g.1841478G>C | CA379106844 | TNNI2 | c.476G>C (p.Gly159Ala) | gnomAD v4 |
| 11 | g.1841478G>T | CA379106845 | TNNI2 | c.476G>T (p.Gly159Val) | |
| 11 | g.1841479T>A | CA471993054 | TNNI2 | c.477T>A (p.Gly159=) | |
| 11 | g.1841479T>C | CA471993052 | TNNI2 | c.477T>C (p.Gly159=) | gnomAD v4 |
| 11 | g.1841479T>G | CA471993055 | TNNI2 | c.477T>G (p.Gly159=) | |
| 11 | g.1841480G>A | CA5815314 | TNNI2 | c.478G>A (p.Asp160Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.1841480G>C | CA379106847 | TNNI2 | c.478G>C (p.Asp160His) | |
| 11 | g.1841480G= | CA1947878695 | TNNI2 | c.478G= (p.Asp160=) | |
| 11 | g.1841480G>T | CA379106846 | TNNI2 | c.478G>T (p.Asp160Tyr) | |
| 11 | g.1841481A>C | CA379106850 | TNNI2 | c.479A>C (p.Asp160Ala) | |
| 11 | g.1841481A>G | CA379106848 | TNNI2 | c.479A>G (p.Asp160Gly) |