| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23431424_23431425del | CA2575486794 | MYH7 | c.792_793del (p.Glu264AspfsTer28) n.898_899del | |
| 14 | g.23431424_23431426delinsCTA | CA2123451420 | MYH7 | c.788_790delinsTAG (p.Ile263=) n.894_896delinsTAG | |
| 14 | g.23431425T>A | CA485767208 | MYH7 | c.789A>T (p.Ile263=) n.895A>T | |
| 14 | g.23431425T>C | CA016828 | MYH7 | c.789A>G (p.Ile263Met) n.895A>G | ClinVar dbSNP |
| 14 | g.23431425T>G | CA485767211 | MYH7 | c.789A>C (p.Ile263=) n.895A>C | |
| 14 | g.23431425T= | CA2123451428 | MYH7 | c.789A= (p.Ile263=) n.895A= | |
| 14 | g.23431426_23431427del | CA2123451427 | MYH7 | c.788_789del (p.Ile263ArgfsTer29) n.894_895del | ClinVar dbSNP gnomAD v4 |
| 14 | g.23431426A= | CA2123451436 | MYH7 | c.788T= (p.Ile263=) n.894T= | |
| 14 | g.23431426A>C | CA389052051 | MYH7 | c.788T>G (p.Ile263Arg) n.894T>G | |
| 14 | g.23431426A>G | CA016824 | MYH7 | c.788T>C (p.Ile263Thr) n.894T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23431426A>T | CA389052052 | MYH7 | c.788T>A (p.Ile263Lys) n.894T>A | |
| 14 | g.23431427T>A | CA389052053 | MYH7 | c.787A>T (p.Ile263Leu) n.893A>T | |
| 14 | g.23431427T>C | CA389052054 | MYH7 | c.787A>G (p.Ile263Val) n.893A>G | |
| 14 | g.23431427T>G | CA389052055 | MYH7 | c.787A>C (p.Ile263Leu) n.893A>C | ClinVar dbSNP |
| 14 | g.23431428G>A | CA485767220 | MYH7 | c.786C>T (p.Asp262=) n.892C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23431428G>C | CA389052056 | MYH7 | c.786C>G (p.Asp262Glu) n.892C>G | |
| 14 | g.23431428G= | CA2123451447 | MYH7 | c.786C= (p.Asp262=) n.892C= | |
| 14 | g.23431428G>T | CA389052057 | MYH7 | c.786C>A (p.Asp262Glu) n.892C>A | |
| 14 | g.23431429T>A | CA389052058 | MYH7 | c.785A>T (p.Asp262Val) n.891A>T | |
| 14 | g.23431429T>C | CA389052060 | MYH7 | c.785A>G (p.Asp262Gly) n.891A>G | COSMIC |
| 14 | g.23431429T>G | CA389052059 | MYH7 | c.785A>C (p.Asp262Ala) n.891A>C | |
| 14 | g.23431430C>A | CA389052061 | MYH7 | c.784G>T (p.Asp262Tyr) n.890G>T | |
| 14 | g.23431430C= | CA2123451452 | MYH7 | c.784G= (p.Asp262=) n.890G= | |
| 14 | g.23431430C>G | CA389052063 | MYH7 | c.784G>C (p.Asp262His) n.890G>C | |
| 14 | g.23431430C>T | CA389052062 | MYH7 | c.784G>A (p.Asp262Asn) n.890G>A | ClinVar dbSNP |
| 14 | g.23431431T>A | CA485767226 | MYH7 | c.783A>T (p.Ala261=) n.889A>T | |
| 14 | g.23431431T>C | CA485767227 | MYH7 | c.783A>G (p.Ala261=) n.889A>G | |
| 14 | g.23431431T>G | CA485767228 | MYH7 | c.783A>C (p.Ala261=) n.889A>C | |
| 14 | g.23431432G>A | CA389052064 | MYH7 | c.782C>T (p.Ala261Val) n.888C>T | ClinVar dbSNP |
| 14 | g.23431432G>C | CA389052066 | MYH7 | c.782C>G (p.Ala261Gly) n.888C>G | |
| 14 | g.23431432G= | CA2123451464 | MYH7 | c.782C= (p.Ala261=) n.888C= | |
| 14 | g.23431432G>T | CA389052065 | MYH7 | c.782C>A (p.Ala261Glu) n.888C>A | |
| 14 | g.23431433C>A | CA389052067 | MYH7 | c.781G>T (p.Ala261Ser) n.887G>T | |
| 14 | g.23431433C>G | CA389052068 | MYH7 | c.781G>C (p.Ala261Pro) n.887G>C | |
| 14 | g.23431433C>T | CA389052069 | MYH7 | c.781G>A (p.Ala261Thr) n.887G>A | |
| 14 | g.23431434A>C | CA485767230 | MYH7 | c.780T>G (p.Ser260=) n.886T>G | |
| 14 | g.23431434A>G | CA485767231 | MYH7 | c.780T>C (p.Ser260=) n.886T>C | gnomAD v4 |
| 14 | g.23431434A>T | CA485767233 | MYH7 | c.780T>A (p.Ser260=) n.886T>A | |
| 14 | g.23431435G>A | CA389052070 | MYH7 | c.779C>T (p.Ser260Phe) n.885C>T | COSMIC |
| 14 | g.23431435G>C | CA389052071 | MYH7 | c.779C>G (p.Ser260Cys) n.885C>G | |
| 14 | g.23431435G>T | CA389052072 | MYH7 | c.779C>A (p.Ser260Tyr) n.885C>A | COSMIC |
| 14 | g.23431436A= | CA2123451469 | MYH7 | c.778T= (p.Ser260=) n.884T= | |
| 14 | g.23431436A>C | CA389052073 | MYH7 | c.778T>G (p.Ser260Ala) n.884T>G | |
| 14 | g.23431436A>G | CA389052074 | MYH7 | c.778T>C (p.Ser260Pro) n.884T>C | |
| 14 | g.23431436A>T | CA389052075 | MYH7 | c.778T>A (p.Ser260Thr) n.884T>A | ClinVar dbSNP |
| 14 | g.23431437T>A | CA485767235 | MYH7 | c.777A>T (p.Ala259=) n.883A>T | ClinVar dbSNP |
| 14 | g.23431437T>C | CA485767236 | MYH7 | c.777A>G (p.Ala259=) n.883A>G | |
| 14 | g.23431437T>G | CA485767238 | MYH7 | c.777A>C (p.Ala259=) n.883A>C | |
| 14 | g.23431437_23431438insATAGACATATCT | CA2624251096 | MYH7 | c.777_778insGATATGTCTATA (p.Ala259_Ser260insAspMetSerIle) n.883_884insGATATGTCTATA | gnomAD v4 |
| 14 | g.23431438G>A | CA389052076 | MYH7 | c.776C>T (p.Ala259Val) n.882C>T |