| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23431447C>A | CA389052095 | MYH7 | c.767G>T (p.Gly256Val) n.873G>T | |
| 14 | g.23431447C= | CA2123451520 | MYH7 | c.767G= (p.Gly256=) n.873G= | |
| 14 | g.23431447C>G | CA389052096 | MYH7 | c.767G>C (p.Gly256Ala) n.873G>C | |
| 14 | g.23431447C>T | CA016810 | MYH7 | c.767G>A (p.Gly256Glu) n.873G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23431448C>A | CA389052097 | MYH7 | c.766G>T (p.Gly256Ter) n.872G>T | |
| 14 | g.23431448C>G | CA389052098 | MYH7 | c.766G>C (p.Gly256Arg) n.872G>C | |
| 14 | g.23431448C>T | CA389052099 | MYH7 | c.766G>A (p.Gly256Arg) n.872G>A | |
| 14 | g.23431449T>A | CA485767253 | MYH7 | c.765A>T (p.Thr255=) n.871A>T | ClinVar dbSNP |
| 14 | g.23431449T>C | CA485767255 | MYH7 | c.765A>G (p.Thr255=) n.871A>G | |
| 14 | g.23431449T>G | CA485767254 | MYH7 | c.765A>C (p.Thr255=) n.871A>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23431449T= | CA2123451523 | MYH7 | c.765A= (p.Thr255=) n.871A= | |
| 14 | g.23431450G>A | CA389052100 | MYH7 | c.764C>T (p.Thr255Ile) n.870C>T | dbSNP gnomAD v4 |
| 14 | g.23431450G>C | CA389052101 | MYH7 | c.764C>G (p.Thr255Arg) n.870C>G | |
| 14 | g.23431450G= | CA2123451531 | MYH7 | c.764C= (p.Thr255=) n.870C= | |
| 14 | g.23431450G>T | CA389052102 | MYH7 | c.764C>A (p.Thr255Lys) n.870C>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23431451T>A | CA389052105 | MYH7 | c.763A>T (p.Thr255Ser) n.869A>T | |
| 14 | g.23431451T>C | CA389052103 | MYH7 | c.763A>G (p.Thr255Ala) n.869A>G | |
| 14 | g.23431451T>G | CA389052104 | MYH7 | c.763A>C (p.Thr255Pro) n.869A>C | |
| 14 | g.23431452T>A | CA485767259 | MYH7 | c.762A>T (p.Ala254=) n.868A>T | |
| 14 | g.23431452T>C | CA485767260 | MYH7 | c.762A>G (p.Ala254=) n.868A>G | |
| 14 | g.23431452T>G | CA485767261 | MYH7 | c.762A>C (p.Ala254=) n.868A>C | |
| 14 | g.23431453G>A | CA389052106 | MYH7 | c.761C>T (p.Ala254Val) n.867C>T | |
| 14 | g.23431453G>C | CA389052107 | MYH7 | c.761C>G (p.Ala254Gly) n.867C>G | |
| 14 | g.23431453G= | CA2123451540 | MYH7 | c.761C= (p.Ala254=) n.867C= | |
| 14 | g.23431453G>T | CA10583172 | MYH7 | c.761C>A (p.Ala254Glu) n.867C>A | ClinVar dbSNP |
| 14 | g.23431454C>A | CA389052108 | MYH7 | c.760G>T (p.Ala254Ser) n.866G>T | |
| 14 | g.23431454C= | CA2123451549 | MYH7 | c.760G= (p.Ala254=) n.866G= | |
| 14 | g.23431454C>G | CA389052109 | MYH7 | c.760G>C (p.Ala254Pro) n.866G>C | |
| 14 | g.23431454C>T | CA389052110 | MYH7 | c.760G>A (p.Ala254Thr) n.866G>A | dbSNP |
| 14 | g.23431455C>A | CA485767266 | MYH7 | c.759G>T (p.Gly253=) n.865G>T | |
| 14 | g.23431455C= | CA2123451552 | MYH7 | c.759G= (p.Gly253=) n.865G= | |
| 14 | g.23431455C>G | CA485767267 | MYH7 | c.759G>C (p.Gly253=) n.865G>C | |
| 14 | g.23431455C>T | CA485767269 | MYH7 | c.759G>A (p.Gly253=) n.865G>A | dbSNP gnomAD v4 |
| 14 | g.23431456C>A | CA016808 | MYH7 | c.758G>T (p.Gly253Val) n.864G>T | ClinVar dbSNP |
| 14 | g.23431456C= | CA2123451561 | MYH7 | c.758G= (p.Gly253=) n.864G= | |
| 14 | g.23431456C>G | CA389052111 | MYH7 | c.758G>C (p.Gly253Ala) n.864G>C | |
| 14 | g.23431456C>T | CA389052112 | MYH7 | c.758G>A (p.Gly253Glu) n.864G>A | ClinVar dbSNP |
| 14 | g.23431457C>A | CA389052113 | MYH7 | c.757G>T (p.Gly253Trp) n.863G>T | |
| 14 | g.23431457C>G | CA389052114 | MYH7 | c.757G>C (p.Gly253Arg) n.863G>C | ClinVar dbSNP |
| 14 | g.23431457C>T | CA389052115 | MYH7 | c.757G>A (p.Gly253Arg) n.863G>A | |
| 14 | g.23431458A>C | CA389052117 | MYH7 | c.756T>G (p.Phe252Leu) n.862T>G | |
| 14 | g.23431458A>G | CA485767275 | MYH7 | c.756T>C (p.Phe252=) n.862T>C | |
| 14 | g.23431458A>T | CA389052116 | MYH7 | c.756T>A (p.Phe252Leu) n.862T>A | |
| 14 | g.23431459A= | CA2123451585 | MYH7 | c.755T= (p.Phe252=) n.861T= | |
| 14 | g.23431459A>C | CA277662 | MYH7 | c.755T>G (p.Phe252Cys) n.861T>G | ClinVar dbSNP |
| 14 | g.23431459A>G | CA016801 | MYH7 | c.755T>C (p.Phe252Ser) n.861T>C | ClinVar dbSNP |
| 14 | g.23431459A>T | CA389052118 | MYH7 | c.755T>A (p.Phe252Tyr) n.861T>A | |
| 14 | g.23431460A>C | CA389052119 | MYH7 | c.754T>G (p.Phe252Val) n.860T>G | |
| 14 | g.23431460A>G | CA389052120 | MYH7 | c.754T>C (p.Phe252Leu) n.860T>C | ClinVar |
| 14 | g.23431460A>T | CA389052121 | MYH7 | c.754T>A (p.Phe252Ile) n.860T>A |