Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.110911096T>ACA386696718MYL2c.482A>T (p.His161Leu)
c.425A>T (p.His142Leu)
c.440A>T (p.His147Leu)
12g.110911096T>CCA010425MYL2c.482A>G (p.His161Arg)
c.425A>G (p.His142Arg)
c.440A>G (p.His147Arg)
 ClinVar dbSNP
12g.110911096T>GCA386696719MYL2c.482A>C (p.His161Pro)
c.425A>C (p.His142Pro)
c.440A>C (p.His147Pro)
12g.110911096T=CA2063066665MYL2c.482A= (p.His161=)
c.425A= (p.His142=)
c.440A= (p.His147=)
12g.110911097G>ACA386696720MYL2c.481C>T (p.His161Tyr)
c.424C>T (p.His142Tyr)
c.439C>T (p.His147Tyr)
12g.110911097G>CCA386696722MYL2c.481C>G (p.His161Asp)
c.424C>G (p.His142Asp)
c.439C>G (p.His147Asp)
12g.110911097G>TCA386696721MYL2c.481C>A (p.His161Asn)
c.424C>A (p.His142Asn)
c.439C>A (p.His147Asn)
 COSMIC
12g.110911098G>ACA010418MYL2c.480C>T (p.Thr160=)
c.423C>T (p.Thr141=)
c.438C>T (p.Thr146=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.110911098G>CCA481750671MYL2c.480C>G (p.Thr160=)
c.423C>G (p.Thr141=)
c.438C>G (p.Thr146=)
12g.110911098G=CA2063066670MYL2c.480C= (p.Thr160=)
c.423C= (p.Thr141=)
c.438C= (p.Thr146=)
12g.110911098G>TCA481750673MYL2c.480C>A (p.Thr160=)
c.423C>A (p.Thr141=)
c.438C>A (p.Thr146=)
12g.110911099G>ACA386696723MYL2c.479C>T (p.Thr160Ile)
c.422C>T (p.Thr141Ile)
c.437C>T (p.Thr146Ile)
 gnomAD v4
12g.110911099G>CCA386696724MYL2c.479C>G (p.Thr160Ser)
c.422C>G (p.Thr141Ser)
c.437C>G (p.Thr146Ser)
 ClinVar dbSNP gnomAD v4
12g.110911099G=CA2063066675MYL2c.479C= (p.Thr160=)
c.422C= (p.Thr141=)
c.437C= (p.Thr146=)
12g.110911099G>TCA386696725MYL2c.479C>A (p.Thr160Asn)
c.422C>A (p.Thr141Asn)
c.437C>A (p.Thr146Asn)
 ClinVar
12g.110911100T>ACA386696726MYL2c.478A>T (p.Thr160Ser)
c.421A>T (p.Thr141Ser)
c.436A>T (p.Thr146Ser)
12g.110911100T>CCA386696727MYL2c.478A>G (p.Thr160Ala)
c.421A>G (p.Thr141Ala)
c.436A>G (p.Thr146Ala)
12g.110911100T>GCA386696728MYL2c.478A>C (p.Thr160Pro)
c.421A>C (p.Thr141Pro)
c.436A>C (p.Thr146Pro)
12g.110911105_110911107dupCA891844540MYL2c.476_478dup (p.Ile159_Thr160insIle)
c.419_421dup (p.Ile140_Thr141insIle)
c.434_436dup (p.Ile145_Thr146insIle)
 ClinVar dbSNP
12g.110911101G>ACA481750679MYL2c.477C>T (p.Ile159=)
c.420C>T (p.Ile140=)
c.435C>T (p.Ile145=)
12g.110911101G>CCA386696729MYL2c.477C>G (p.Ile159Met)
c.420C>G (p.Ile140Met)
c.435C>G (p.Ile145Met)
12g.110911101G>TCA481750681MYL2c.477C>A (p.Ile159=)
c.420C>A (p.Ile140=)
c.435C>A (p.Ile145=)
12g.110911102A=CA2063066690MYL2c.476T= (p.Ile159=)
c.419T= (p.Ile140=)
c.434T= (p.Ile145=)
12g.110911102A>CCA386696730MYL2c.476T>G (p.Ile159Ser)
c.419T>G (p.Ile140Ser)
c.434T>G (p.Ile145Ser)
 ClinVar
12g.110911102A>GCA386696731MYL2c.476T>C (p.Ile159Thr)
c.419T>C (p.Ile140Thr)
c.434T>C (p.Ile145Thr)
 ClinVar dbSNP
12g.110911102A>TCA386696732MYL2c.476T>A (p.Ile159Asn)
c.419T>A (p.Ile140Asn)
c.434T>A (p.Ile145Asn)
12g.110911103T>ACA386696734MYL2c.475A>T (p.Ile159Phe)
c.418A>T (p.Ile140Phe)
c.433A>T (p.Ile145Phe)
12g.110911103T>CCA043353MYL2c.475A>G (p.Ile159Val)
c.418A>G (p.Ile140Val)
c.433A>G (p.Ile145Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.110911103T>GCA386696733MYL2c.475A>C (p.Ile159Leu)
c.418A>C (p.Ile140Leu)
c.433A>C (p.Ile145Leu)
12g.110911103T=CA2063066695MYL2c.475A= (p.Ile159=)
c.418A= (p.Ile140=)
c.433A= (p.Ile145=)
12g.110911104G>ACA481750686MYL2c.474C>T (p.Ile158=)
c.417C>T (p.Ile139=)
c.432C>T (p.Ile144=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.110911104G>CCA386696735MYL2c.474C>G (p.Ile158Met)
c.417C>G (p.Ile139Met)
c.432C>G (p.Ile144Met)
12g.110911104G=CA2063066701MYL2c.474C= (p.Ile158=)
c.417C= (p.Ile139=)
c.432C= (p.Ile144=)
12g.110911104G>TCA481750688MYL2c.474C>A (p.Ile158=)
c.417C>A (p.Ile139=)
c.432C>A (p.Ile144=)
12g.110911105A>CCA386696736MYL2c.473T>G (p.Ile158Ser)
c.416T>G (p.Ile139Ser)
c.431T>G (p.Ile144Ser)
12g.110911105A>GCA386696737MYL2c.473T>C (p.Ile158Thr)
c.416T>C (p.Ile139Thr)
c.431T>C (p.Ile144Thr)
 ClinVar dbSNP
12g.110911105A>TCA386696738MYL2c.473T>A (p.Ile158Asn)
c.416T>A (p.Ile139Asn)
c.431T>A (p.Ile144Asn)
12g.110911106T>ACA386696739MYL2c.472A>T (p.Ile158Phe)
c.415A>T (p.Ile139Phe)
c.430A>T (p.Ile144Phe)
12g.110911106T>CCA386696740MYL2c.472A>G (p.Ile158Val)
c.415A>G (p.Ile139Val)
c.430A>G (p.Ile144Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
12g.110911106T>GCA386696741MYL2c.472A>C (p.Ile158Leu)
c.415A>C (p.Ile139Leu)
c.430A>C (p.Ile144Leu)
12g.110911106T=CA2063066708MYL2c.472A= (p.Ile158=)
c.415A= (p.Ile139=)
c.430A= (p.Ile144=)
12g.110911107G>ACA043304MYL2c.471C>T (p.His157=)
c.414C>T (p.His138=)
c.429C>T (p.His143=)
 dbSNP ExAC gnomAD v2 gnomAD v4
12g.110911107G>CCA386696742MYL2c.471C>G (p.His157Gln)
c.414C>G (p.His138Gln)
c.429C>G (p.His143Gln)
12g.110911107G=CA2063066717MYL2c.471C= (p.His157=)
c.414C= (p.His138=)
c.429C= (p.His143=)
12g.110911107G>TCA386696743MYL2c.471C>A (p.His157Gln)
c.414C>A (p.His138Gln)
c.429C>A (p.His143Gln)
12g.110911108T>ACA386696745MYL2c.470A>T (p.His157Leu)
c.413A>T (p.His138Leu)
c.428A>T (p.His143Leu)
12g.110911108T>CCA010412MYL2c.470A>G (p.His157Arg)
c.413A>G (p.His138Arg)
c.428A>G (p.His143Arg)
 ClinVar dbSNP
12g.110911108T>GCA386696744MYL2c.470A>C (p.His157Pro)
c.413A>C (p.His138Pro)
c.428A>C (p.His143Pro)
 dbSNP
12g.110911108T=CA2063066724MYL2c.470A= (p.His157=)
c.413A= (p.His138=)
c.428A= (p.His143=)
12g.110911109G>ACA043261MYL2c.469C>T (p.His157Tyr)
c.412C>T (p.His138Tyr)
c.427C>T (p.His143Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched