Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23415187_23415190delinsGGTC | CA2123462368 | MYH7 | c.5364_5367delinsGACC (p.Gln1788=) | |
14 | g.23415188G>A | CA389035714 | MYH7 | c.5366C>T (p.Thr1789Ile) | |
14 | g.23415188G>C | CA389035715 | MYH7 | c.5366C>G (p.Thr1789Ser) | |
14 | g.23415188G>T | CA389035716 | MYH7 | c.5366C>A (p.Thr1789Asn) | |
14 | g.23415188_23415190del | CA10577513 | MYH7 | c.5364_5366del (p.Gln1788_Thr1789delinsHis) | ClinVar dbSNP |
14 | g.23415189T>A | CA389035718 | MYH7 | c.5365A>T (p.Thr1789Ser) | |
14 | g.23415189T>C | CA389035717 | MYH7 | c.5365A>G (p.Thr1789Ala) | ClinVar |
14 | g.23415189T>G | CA389035719 | MYH7 | c.5365A>C (p.Thr1789Pro) | |
14 | g.23415190C>A | CA389035720 | MYH7 | c.5364G>T (p.Gln1788His) | |
14 | g.23415190C= | CA2123462377 | MYH7 | c.5364G= (p.Gln1788=) | |
14 | g.23415190C>G | CA389035721 | MYH7 | c.5364G>C (p.Gln1788His) | |
14 | g.23415190C>T | CA257809113 | MYH7 | c.5364G>A (p.Gln1788=) | dbSNP |
14 | g.23415191T>A | CA389035722 | MYH7 | c.5363A>T (p.Gln1788Leu) | |
14 | g.23415191T>C | CA046577 | MYH7 | c.5363A>G (p.Gln1788Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23415191T>G | CA389035723 | MYH7 | c.5363A>C (p.Gln1788Pro) | |
14 | g.23415191T= | CA2123462380 | MYH7 | c.5363A= (p.Gln1788=) | |
14 | g.23415192G>A | CA389035724 | MYH7 | c.5362C>T (p.Gln1788Ter) | |
14 | g.23415192G>C | CA389035725 | MYH7 | c.5362C>G (p.Gln1788Glu) | dbSNP |
14 | g.23415192G= | CA2123462383 | MYH7 | c.5362C= (p.Gln1788=) | |
14 | g.23415192G>T | CA389035726 | MYH7 | c.5362C>A (p.Gln1788Lys) | |
14 | g.23415193T>A | CA389035727 | MYH7 | c.5361A>T (p.Glu1787Asp) | |
14 | g.23415193T>C | CA016008 | MYH7 | c.5361A>G (p.Glu1787=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23415193T>G | CA389035728 | MYH7 | c.5361A>C (p.Glu1787Asp) | ClinVar |
14 | g.23415193T= | CA2123462389 | MYH7 | c.5361A= (p.Glu1787=) | |
14 | g.23415194T>A | CA389035731 | MYH7 | c.5360A>T (p.Glu1787Val) | |
14 | g.23415194T>C | CA389035729 | MYH7 | c.5360A>G (p.Glu1787Gly) | ClinVar |
14 | g.23415194T>G | CA389035730 | MYH7 | c.5360A>C (p.Glu1787Ala) | |
14 | g.23415195C>A | CA389035732 | MYH7 | c.5359G>T (p.Glu1787Ter) | |
14 | g.23415195C= | CA2123462409 | MYH7 | c.5359G= (p.Glu1787=) | |
14 | g.23415195C>G | CA389035733 | MYH7 | c.5359G>C (p.Glu1787Gln) | ClinVar dbSNP |
14 | g.23415195C>T | CA389035734 | MYH7 | c.5359G>A (p.Glu1787Lys) | ClinVar COSMIC |
14 | g.23415196C>A | CA389035735 | MYH7 | c.5358G>T (p.Met1786Ile) | |
14 | g.23415196C>G | CA389035736 | MYH7 | c.5358G>C (p.Met1786Ile) | |
14 | g.23415196C>T | CA389035737 | MYH7 | c.5358G>A (p.Met1786Ile) | ClinVar |
14 | g.23415197A>C | CA389035738 | MYH7 | c.5357T>G (p.Met1786Arg) | |
14 | g.23415197A>G | CA389035739 | MYH7 | c.5357T>C (p.Met1786Thr) | |
14 | g.23415197A>T | CA389035740 | MYH7 | c.5357T>A (p.Met1786Lys) | |
14 | g.23415198T>A | CA389035741 | MYH7 | c.5356A>T (p.Met1786Leu) | |
14 | g.23415198T>C | CA389035742 | MYH7 | c.5356A>G (p.Met1786Val) | |
14 | g.23415198T>G | CA389035743 | MYH7 | c.5356A>C (p.Met1786Leu) | |
14 | g.23415199G>A | CA485765832 | MYH7 | c.5355C>T (p.Asn1785=) | ClinVar |
14 | g.23415199G>C | CA389035744 | MYH7 | c.5355C>G (p.Asn1785Lys) | |
14 | g.23415199G>T | CA389035745 | MYH7 | c.5355C>A (p.Asn1785Lys) | |
14 | g.23415199_23415202delinsGTTC | CA2123462414 | MYH7 | c.5352_5355delinsGAAC (p.Lys1784=) | |
14 | g.23415200T>A | CA389035746 | MYH7 | c.5354A>T (p.Asn1785Ile) | |
14 | g.23415200T>C | CA389035747 | MYH7 | c.5354A>G (p.Asn1785Ser) | |
14 | g.23415200T>G | CA389035748 | MYH7 | c.5354A>C (p.Asn1785Thr) | |
14 | g.23415206_23415208del | CA016003 | MYH7 | c.5352_5354del (p.Lys1784del) | ClinVar dbSNP gnomAD v4 |
14 | g.23415201T>A | CA389035749 | MYH7 | c.5353A>T (p.Asn1785Tyr) | |
14 | g.23415201T>C | CA389035750 | MYH7 | c.5353A>G (p.Asn1785Asp) | ClinVar |