| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.46859529C>A | CA352496039 | MYL3 | c.427G>T (p.Glu143Ter) n.649G>T n.385G>T | |
| 3 | g.46859529C= | CA1362297104 | MYL3 | c.427G= (p.Glu143=) n.649G= n.385G= | |
| 3 | g.46859529C>G | CA352496041 | MYL3 | c.427G>C (p.Glu143Gln) n.649G>C n.385G>C | |
| 3 | g.46859529C>T | CA013774 | MYL3 | c.427G>A (p.Glu143Lys) n.649G>A n.385G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.46859530C>A | CA352496046 | MYL3 | c.426G>T (p.Lys142Asn) n.648G>T n.384G>T | |
| 3 | g.46859530C= | CA1362297105 | MYL3 | c.426G= (p.Lys142=) n.648G= n.384G= | |
| 3 | g.46859530C>G | CA352496049 | MYL3 | c.426G>C (p.Lys142Asn) n.648G>C n.384G>C | |
| 3 | g.46859530C>T | CA433474387 | MYL3 | c.426G>A (p.Lys142=) n.648G>A n.384G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.46859531T>A | CA352496052 | MYL3 | c.425A>T (p.Lys142Met) n.647A>T n.383A>T | |
| 3 | g.46859531T>C | CA352496054 | MYL3 | c.425A>G (p.Lys142Arg) n.647A>G n.383A>G | |
| 3 | g.46859531T>G | CA352496057 | MYL3 | c.425A>C (p.Lys142Thr) n.647A>C n.383A>C | |
| 3 | g.46859532T>A | CA352496065 | MYL3 | c.424A>T (p.Lys142Ter) n.646A>T n.382A>T | |
| 3 | g.46859532T>C | CA352496062 | MYL3 | c.424A>G (p.Lys142Glu) n.646A>G n.382A>G | ClinVar dbSNP |
| 3 | g.46859532T>G | CA352496059 | MYL3 | c.424A>C (p.Lys142Gln) n.646A>C n.382A>C | |
| 3 | g.46859532T= | CA1362297106 | MYL3 | c.424A= (p.Lys142=) n.646A= n.382A= | |
| 3 | g.46859533G>A | CA433474388 | MYL3 | c.423C>T (p.Asp141=) n.645C>T n.381C>T | dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.46859533G>C | CA352496067 | MYL3 | c.423C>G (p.Asp141Glu) n.645C>G n.381C>G | |
| 3 | g.46859533G= | CA1362297107 | MYL3 | c.423C= (p.Asp141=) n.645C= n.381C= | |
| 3 | g.46859533G>T | CA352496071 | MYL3 | c.423C>A (p.Asp141Glu) n.645C>A n.381C>A | |
| 3 | g.46859534T>A | CA352496073 | MYL3 | c.422A>T (p.Asp141Val) n.644A>T n.380A>T | |
| 3 | g.46859534T>C | CA352496075 | MYL3 | c.422A>G (p.Asp141Gly) n.644A>G n.380A>G | |
| 3 | g.46859534T>G | CA352496077 | MYL3 | c.422A>C (p.Asp141Ala) n.644A>C n.380A>C | |
| 3 | g.46859535C>A | CA352496080 | MYL3 | c.421G>T (p.Asp141Tyr) n.643G>T n.379G>T | ClinVar dbSNP |
| 3 | g.46859535C= | CA1362297108 | MYL3 | c.421G= (p.Asp141=) n.643G= n.379G= | |
| 3 | g.46859535C>G | CA352496082 | MYL3 | c.421G>C (p.Asp141His) n.643G>C n.379G>C | |
| 3 | g.46859535C>T | CA352496085 | MYL3 | c.421G>A (p.Asp141Asn) n.643G>A n.379G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 3 | g.46859536G>A | CA044119 | MYL3 | c.420C>T (p.Phe140=) n.642C>T n.378C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.46859536G>C | CA352496090 | MYL3 | c.420C>G (p.Phe140Leu) n.642C>G n.378C>G | gnomAD v4 |
| 3 | g.46859536G= | CA1362297109 | MYL3 | c.420C= (p.Phe140=) n.642C= n.378C= | |
| 3 | g.46859536G>T | CA352496092 | MYL3 | c.420C>A (p.Phe140Leu) n.642C>A n.378C>A | |
| 3 | g.46859537A= | CA1362297110 | MYL3 | c.419T= (p.Phe140=) n.641T= n.377T= | |
| 3 | g.46859537A>C | CA352496100 | MYL3 | c.419T>G (p.Phe140Cys) n.641T>G n.377T>G | ClinVar dbSNP gnomAD v4 |
| 3 | g.46859537A>G | CA352496097 | MYL3 | c.419T>C (p.Phe140Ser) n.641T>C n.377T>C | ClinVar |
| 3 | g.46859537A>T | CA352496094 | MYL3 | c.419T>A (p.Phe140Tyr) n.641T>A n.377T>A | |
| 3 | g.46859538A>C | CA352496102 | MYL3 | c.418T>G (p.Phe140Val) n.640T>G n.376T>G | |
| 3 | g.46859538A>G | CA352496105 | MYL3 | c.418T>C (p.Phe140Leu) n.640T>C n.376T>C | ClinVar |
| 3 | g.46859538A>T | CA352496107 | MYL3 | c.418T>A (p.Phe140Ile) n.640T>A n.376T>A | |
| 3 | g.46859539G>A | CA433474389 | MYL3 | c.417C>T (p.Val139=) n.639C>T n.375C>T | |
| 3 | g.46859539G>C | CA433474390 | MYL3 | c.417C>G (p.Val139=) n.639C>G n.375C>G | |
| 3 | g.46859539G>T | CA433474391 | MYL3 | c.417C>A (p.Val139=) n.639C>A n.375C>A | |
| 3 | g.46859540A= | CA1362297111 | MYL3 | c.416T= (p.Val139=) n.638T= n.374T= | |
| 3 | g.46859540A>C | CA352496110 | MYL3 | c.416T>G (p.Val139Gly) n.638T>G n.374T>G | dbSNP |
| 3 | g.46859540A>G | CA352496112 | MYL3 | c.416T>C (p.Val139Ala) n.638T>C n.374T>C | |
| 3 | g.46859540A>T | CA352496115 | MYL3 | c.416T>A (p.Val139Asp) n.638T>A n.374T>A | |
| 3 | g.46859541C>A | CA352496117 | MYL3 | c.415G>T (p.Val139Phe) n.637G>T n.373G>T | |
| 3 | g.46859541C>G | CA352496118 | MYL3 | c.415G>C (p.Val139Leu) n.637G>C n.373G>C | gnomAD v4 |
| 3 | g.46859541C>T | CA352496119 | MYL3 | c.415G>A (p.Val139Ile) n.637G>A n.373G>A | |
| 3 | g.46859542C>A | CA433474392 | MYL3 | c.414G>T (p.Arg138=) n.636G>T n.372G>T | |
| 3 | g.46859542C>G | CA433474393 | MYL3 | c.414G>C (p.Arg138=) n.636G>C n.372G>C | |
| 3 | g.46859542C>T | CA433474394 | MYL3 | c.414G>A (p.Arg138=) n.636G>A n.372G>A |