| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.1841523G>A | CA122377 | TNNI2 | c.521G>A (p.Arg174Gln) | ClinVar dbSNP |
| 11 | g.1841523G>C | CA379106951 | TNNI2 | c.521G>C (p.Arg174Pro) | |
| 11 | g.1841523G= | CA1947878771 | TNNI2 | c.521G= (p.Arg174=) | |
| 11 | g.1841523G>T | CA379106952 | TNNI2 | c.521G>T (p.Arg174Leu) | |
| 11 | g.1841523_1841526delinsGGAA | CA1947878773 | TNNI2 | c.521_524delinsGGAA (p.Arg174=) | |
| 11 | g.1841524G>A | CA471993249 | TNNI2 | c.522G>A (p.Arg174=) | gnomAD v4 |
| 11 | g.1841524G>C | CA471993246 | TNNI2 | c.522G>C (p.Arg174=) | |
| 11 | g.1841524G>T | CA471993247 | TNNI2 | c.522G>T (p.Arg174=) | |
| 11 | g.1841529_1841531del | CA122381 | TNNI2 | c.527_529del (p.Lys176del) | ClinVar dbSNP |
| 11 | g.1841525A>C | CA379106955 | TNNI2 | c.523A>C (p.Lys175Gln) | |
| 11 | g.1841525A>G | CA379106954 | TNNI2 | c.523A>G (p.Lys175Glu) | |
| 11 | g.1841525A>T | CA379106953 | TNNI2 | c.523A>T (p.Lys175Ter) | |
| 11 | g.1841526A>C | CA379106958 | TNNI2 | c.524A>C (p.Lys175Thr) | |
| 11 | g.1841526A>G | CA379106957 | TNNI2 | c.524A>G (p.Lys175Arg) | |
| 11 | g.1841526A>T | CA379106956 | TNNI2 | c.524A>T (p.Lys175Met) | |
| 11 | g.1841527G>A | CA471993255 | TNNI2 | c.525G>A (p.Lys175=) | dbSNP gnomAD v4 |
| 11 | g.1841527G>C | CA379106959 | TNNI2 | c.525G>C (p.Lys175Asn) | |
| 11 | g.1841527G= | CA1947878781 | TNNI2 | c.525G= (p.Lys175=) | |
| 11 | g.1841527G>T | CA206706 | TNNI2 | c.525G>T (p.Lys175Asn) | ClinVar dbSNP |
| 11 | g.1841528A>C | CA379106960 | TNNI2 | c.526A>C (p.Lys176Gln) | |
| 11 | g.1841528A>G | CA379106961 | TNNI2 | c.526A>G (p.Lys176Glu) | |
| 11 | g.1841528A>T | CA379106962 | TNNI2 | c.526A>T (p.Lys176Ter) | |
| 11 | g.1841529A>C | CA379106963 | TNNI2 | c.527A>C (p.Lys176Thr) | |
| 11 | g.1841529A>G | CA379106964 | TNNI2 | c.527A>G (p.Lys176Arg) | |
| 11 | g.1841529A>T | CA379106965 | TNNI2 | c.527A>T (p.Lys176Met) | |
| 11 | g.1841530G>A | CA471993261 | TNNI2 | c.528G>A (p.Lys176=) | |
| 11 | g.1841530G>C | CA379106966 | TNNI2 | c.528G>C (p.Lys176Asn) | |
| 11 | g.1841530G>T | CA379106967 | TNNI2 | c.528G>T (p.Lys176Asn) | |
| 11 | g.1841531A>C | CA379106968 | TNNI2 | c.529A>C (p.Met177Leu) | |
| 11 | g.1841531A>G | CA379106969 | TNNI2 | c.529A>G (p.Met177Val) | |
| 11 | g.1841531A>T | CA379106970 | TNNI2 | c.529A>T (p.Met177Leu) | |
| 11 | g.1841532T>A | CA379106973 | TNNI2 | c.530T>A (p.Met177Lys) | |
| 11 | g.1841532T>C | CA379106972 | TNNI2 | c.530T>C (p.Met177Thr) | ClinVar dbSNP |
| 11 | g.1841532T>G | CA379106971 | TNNI2 | c.530T>G (p.Met177Arg) | |
| 11 | g.1841532T= | CA1947878786 | TNNI2 | c.530T= (p.Met177=) | |
| 11 | g.1841533G>A | CA5815318 | TNNI2 | c.531G>A (p.Met177Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.1841533G>C | CA379106974 | TNNI2 | c.531G>C (p.Met177Ile) | |
| 11 | g.1841533G= | CA1947878791 | TNNI2 | c.531G= (p.Met177=) | |
| 11 | g.1841533G>T | CA379106975 | TNNI2 | c.531G>T (p.Met177Ile) | |
| 11 | g.1841534T>A | CA379106976 | TNNI2 | c.532T>A (p.Phe178Ile) | ClinVar dbSNP |
| 11 | g.1841534T>C | CA379106977 | TNNI2 | c.532T>C (p.Phe178Leu) | |
| 11 | g.1841534T>G | CA379106978 | TNNI2 | c.532T>G (p.Phe178Val) | |
| 11 | g.1841535T>A | CA379106979 | TNNI2 | c.533T>A (p.Phe178Tyr) | |
| 11 | g.1841535T>C | CA379106980 | TNNI2 | c.533T>C (p.Phe178Ser) | |
| 11 | g.1841535T>G | CA379106981 | TNNI2 | c.533T>G (p.Phe178Cys) | |
| 11 | g.1841536T>A | CA379106982 | TNNI2 | c.534T>A (p.Phe178Leu) | |
| 11 | g.1841536T>C | CA471993277 | TNNI2 | c.534T>C (p.Phe178=) | |
| 11 | g.1841536T>G | CA379106983 | TNNI2 | c.534T>G (p.Phe178Leu) | |
| 11 | g.1841537G>A | CA379106984 | TNNI2 | c.535G>A (p.Glu179Lys) | gnomAD v4 |
| 11 | g.1841537G>C | CA379106985 | TNNI2 | c.535G>C (p.Glu179Gln) |