Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23413754C>ACA2580087897MYH7c.5790+5G>T (n.5790+5G>T)
ClinVar
14g.23413754C>TCA2575486117MYH7c.5790+5G>A (n.5790+5G>A)
gnomAD v4
14g.23413755C>ACA048326MYH7c.5790+4G>T (n.5790+4G>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413755C=CA2123457831MYH7c.5790+4G= (n.5790+4G=)
14g.23413756C=CA2123457843MYH7c.5790+3G= (n.5790+3G=)
14g.23413756C>GCA2123457845MYH7c.5790+3G>C (n.5790+3G>C)
dbSNP
14g.23413757delCA2697553891MYH7c.5790+2del (n.5790+2del)
ClinVar
14g.23413757A>CCA389034471MYH7c.5790+2T>G (n.5790+2T>G)
14g.23413757A>GCA389034473MYH7c.5790+2T>C (n.5790+2T>C)
gnomAD v4
14g.23413757A>TCA389034472MYH7c.5790+2T>A (n.5790+2T>A)
14g.23413758C>ACA389034474MYH7c.5790+1G>T (n.5790+1G>T)
14g.23413758C=CA2123457852MYH7c.5790+1G= (n.5790+1G=)
14g.23413758C>GCA389034475MYH7c.5790+1G>C (n.5790+1G>C)
14g.23413758C>TCA048284MYH7c.5790+1G>A (n.5790+1G>A)
dbSNP ExAC gnomAD v3 gnomAD v4
14g.23413759C>ACA389034476MYH7c.5790G>T (p.Lys1930Asn)
14g.23413759C>GCA389034477MYH7c.5790G>C (p.Lys1930Asn)
14g.23413759C>TCA485616043MYH7c.5790G>A (p.Lys1930=)
gnomAD v4
14g.23413760T>ACA389034478MYH7c.5789A>T (p.Lys1930Met)
14g.23413760T>CCA389034479MYH7c.5789A>G (p.Lys1930Arg)
dbSNP gnomAD v4
14g.23413760T>GCA389034480MYH7c.5789A>C (p.Lys1930Thr)
ClinVar
14g.23413760T=CA2123457861MYH7c.5789A= (p.Lys1930=)
14g.23413761T>ACA389034481MYH7c.5788A>T (p.Lys1930Ter)
14g.23413761T>CCA389034482MYH7c.5788A>G (p.Lys1930Glu)
14g.23413761T>GCA389034483MYH7c.5788A>C (p.Lys1930Gln)
14g.23413762C>ACA485616044MYH7c.5787G>T (p.Thr1929=)
ClinVar
14g.23413762C=CA2123457888MYH7c.5787G= (p.Thr1929=)
14g.23413762C>GCA485616045MYH7c.5787G>C (p.Thr1929=)
dbSNP
14g.23413762C>TCA016484MYH7c.5787G>A (p.Thr1929=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413763G>ACA016477MYH7c.5786C>T (p.Thr1929Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413763G>CCA389034484MYH7c.5786C>G (p.Thr1929Arg)
14g.23413763G=CA2123457899MYH7c.5786C= (p.Thr1929=)
14g.23413763G>TCA389034485MYH7c.5786C>A (p.Thr1929Lys)
14g.23413764T>ACA389034486MYH7c.5785A>T (p.Thr1929Ser)
14g.23413764T>CCA389034488MYH7c.5785A>G (p.Thr1929Ala)
dbSNP gnomAD v4
14g.23413764T>GCA389034487MYH7c.5785A>C (p.Thr1929Pro)
14g.23413764T=CA2123457911MYH7c.5785A= (p.Thr1929=)
14g.23413765G>ACA485616049MYH7c.5784C>T (p.Gly1928=)
14g.23413765G>CCA485616052MYH7c.5784C>G (p.Gly1928=)
14g.23413765G>TCA485616053MYH7c.5784C>A (p.Gly1928=)
14g.23413766C>ACA389034489MYH7c.5783G>T (p.Gly1928Val)
14g.23413766C=CA2123457921MYH7c.5783G= (p.Gly1928=)
14g.23413766C>GCA389034490MYH7c.5783G>C (p.Gly1928Ala)
14g.23413766C>TCA048231MYH7c.5783G>A (p.Gly1928Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23413767C>ACA389034491MYH7c.5782G>T (p.Gly1928Cys)
dbSNP gnomAD v2
14g.23413767C=CA2123457935MYH7c.5782G= (p.Gly1928=)
14g.23413767C>GCA389034492MYH7c.5782G>C (p.Gly1928Arg)
14g.23413767C>TCA389034493MYH7c.5782G>A (p.Gly1928Ser)
ClinVar
14g.23413768A>CCA389034494MYH7c.5781T>G (p.Ile1927Met)
14g.23413768A>GCA485616058MYH7c.5781T>C (p.Ile1927=)
ClinVar dbSNP
14g.23413768A>TCA485616057MYH7c.5781T>A (p.Ile1927=)
14g.23413769A=CA2123457938MYH7c.5780T= (p.Ile1927=)
14g.23413769A>CCA389034497MYH7c.5780T>G (p.Ile1927Ser)
14g.23413769A>GCA389034495MYH7c.5780T>C (p.Ile1927Thr)
dbSNP gnomAD v3 gnomAD v4
14g.23413769A>TCA389034496MYH7c.5780T>A (p.Ile1927Asn)
14g.23413770T>ACA048224MYH7c.5779A>T (p.Ile1927Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413770T>CCA389034498MYH7c.5779A>G (p.Ile1927Val)
14g.23413770T>GCA389034499MYH7c.5779A>C (p.Ile1927Leu)
dbSNP gnomAD v3 gnomAD v4
14g.23413770T=CA2123457950MYH7c.5779A= (p.Ile1927=)
14g.23413771G>ACA485616064MYH7c.5778C>T (p.Asp1926=)
14g.23413771G>CCA389034500MYH7c.5778C>G (p.Asp1926Glu)
14g.23413771G>TCA389034501MYH7c.5778C>A (p.Asp1926Glu)
14g.23413772T>ACA389034502MYH7c.5777A>T (p.Asp1926Val)
14g.23413772T>CCA389034504MYH7c.5777A>G (p.Asp1926Gly)
dbSNP
14g.23413772T>GCA389034503MYH7c.5777A>C (p.Asp1926Ala)
14g.23413772T=CA2123457963MYH7c.5777A= (p.Asp1926=)
14g.23413773C>ACA389034505MYH7c.5776G>T (p.Asp1926Tyr)
14g.23413773C>GCA389034506MYH7c.5776G>C (p.Asp1926His)
14g.23413773C>TCA389034507MYH7c.5776G>A (p.Asp1926Asn)
14g.23413774A>CCA485616067MYH7c.5775T>G (p.Arg1925=)
14g.23413774A>GCA485616069MYH7c.5775T>C (p.Arg1925=)
14g.23413774A>TCA485616068MYH7c.5775T>A (p.Arg1925=)
14g.23413775C>ACA389034508MYH7c.5774G>T (p.Arg1925Leu)
dbSNP
14g.23413775C=CA2123457972MYH7c.5774G= (p.Arg1925=)
14g.23413775C>GCA389034509MYH7c.5774G>C (p.Arg1925Pro)
14g.23413775C>TCA048213MYH7c.5774G>A (p.Arg1925His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413776G>ACA048205MYH7c.5773C>T (p.Arg1925Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23413776G>CCA257807342MYH7c.5773C>G (p.Arg1925Gly)
ClinVar dbSNP
14g.23413776G=CA2123457983MYH7c.5773C= (p.Arg1925=)
14g.23413776G>TCA389034510MYH7c.5773C>A (p.Arg1925Ser)
14g.23413777G>ACA485616071MYH7c.5772C>T (p.Ser1924=)
14g.23413777G>CCA389034511MYH7c.5772C>G (p.Ser1924Arg)
14g.23413777G>TCA389034512MYH7c.5772C>A (p.Ser1924Arg)
gnomAD v4
14g.23413778C>ACA016469MYH7c.5771G>T (p.Ser1924Ile)
ClinVar dbSNP gnomAD v4
14g.23413778C=CA2123458001MYH7c.5771G= (p.Ser1924=)
14g.23413778C>GCA389034514MYH7c.5771G>C (p.Ser1924Thr)
ClinVar
14g.23413778C>TCA389034513MYH7c.5771G>A (p.Ser1924Asn)
14g.23413779T>ACA389034515MYH7c.5770A>T (p.Ser1924Cys)
14g.23413779T>CCA389034516MYH7c.5770A>G (p.Ser1924Gly)
14g.23413779T>GCA389034517MYH7c.5770A>C (p.Ser1924Arg)
14g.23413779_23413780delinsTCCA2123458015MYH7c.5769_5770delinsGA (p.Lys1923=)
14g.23413780delCA1139663370MYH7c.5769del (p.Ser1924AlafsTer9)
ClinVar dbSNP gnomAD v4
14g.23413780C>ACA389034518MYH7c.5769G>T (p.Lys1923Asn)
14g.23413780C=CA2123458026MYH7c.5769G= (p.Lys1923=)
14g.23413780C>GCA389034519MYH7c.5769G>C (p.Lys1923Asn)
14g.23413780C>TCA485616075MYH7c.5769G>A (p.Lys1923=)
dbSNP gnomAD v2 gnomAD v4
14g.23413781T>ACA389034520MYH7c.5768A>T (p.Lys1923Met)
14g.23413781T>CCA389034521MYH7c.5768A>G (p.Lys1923Arg)
14g.23413781T>GCA389034522MYH7c.5768A>C (p.Lys1923Thr)
14g.23413784_23413798delCA2695219124MYH7c.5754_5768del (p.Asn1918_Ala1922del)
14g.23413782T>ACA389034523MYH7c.5767A>T (p.Lys1923Ter)
14g.23413782T>CCA389034524MYH7c.5767A>G (p.Lys1923Glu)
ClinVar dbSNP
14g.23413782T>GCA389034525MYH7c.5767A>C (p.Lys1923Gln)
14g.23413782T=CA2123458047MYH7c.5767A= (p.Lys1923=)
14g.23413783G>ACA485616079MYH7c.5766C>T (p.Ala1922=)
14g.23413783G>CCA485616080MYH7c.5766C>G (p.Ala1922=)
dbSNP
14g.23413783G=CA2123458056MYH7c.5766C= (p.Ala1922=)
14g.23413783G>TCA485616081MYH7c.5766C>A (p.Ala1922=)
14g.23413784G>ACA048194MYH7c.5765C>T (p.Ala1922Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23413784G>CCA389034527MYH7c.5765C>G (p.Ala1922Gly)
14g.23413784G=CA2123458063MYH7c.5765C= (p.Ala1922=)
14g.23413784G>TCA389034526MYH7c.5765C>A (p.Ala1922Asp)
14g.23413785C>ACA389034528MYH7c.5764G>T (p.Ala1922Ser)
14g.23413785C>GCA389034529MYH7c.5764G>C (p.Ala1922Pro)
14g.23413785C>TCA389034530MYH7c.5764G>A (p.Ala1922Thr)
gnomAD v4
14g.23413786C>ACA485616084MYH7c.5763G>T (p.Arg1921=)
14g.23413786C=CA2123458069MYH7c.5763G= (p.Arg1921=)
14g.23413786C>GCA485616085MYH7c.5763G>C (p.Arg1921=)
14g.23413786C>TCA485616086MYH7c.5763G>A (p.Arg1921=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23413787C>ACA257807344MYH7c.5762G>T (p.Arg1921Leu)
dbSNP
14g.23413787C=CA2123458081MYH7c.5762G= (p.Arg1921=)
14g.23413787C>GCA10576950MYH7c.5762G>C (p.Arg1921Pro)
ClinVar dbSNP
14g.23413787C>TCA016464MYH7c.5762G>A (p.Arg1921Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413788G>ACA016457MYH7c.5761C>T (p.Arg1921Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413788G>CCA16614381MYH7c.5761C>G (p.Arg1921Gly)
ClinVar dbSNP gnomAD v4
14g.23413788G=CA2123458102MYH7c.5761C= (p.Arg1921=)
14g.23413788G>TCA048169MYH7c.5761C>A (p.Arg1921=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413789C>ACA485616091MYH7c.5760G>T (p.Leu1920=)
ClinVar dbSNP
14g.23413789C>GCA485616089MYH7c.5760G>C (p.Leu1920=)
14g.23413789C>TCA485616090MYH7c.5760G>A (p.Leu1920=)
14g.23413790A>CCA389034531MYH7c.5759T>G (p.Leu1920Arg)
14g.23413790A>GCA389034532MYH7c.5759T>C (p.Leu1920Pro)
14g.23413790A>TCA389034533MYH7c.5759T>A (p.Leu1920Gln)
14g.23413791G>ACA485616092MYH7c.5758C>T (p.Leu1920=)
gnomAD v4
14g.23413791G>CCA389034535MYH7c.5758C>G (p.Leu1920Val)
14g.23413791G>TCA389034534MYH7c.5758C>A (p.Leu1920Met)
14g.23413792C>ACA389034536MYH7c.5757G>T (p.Lys1919Asn)
14g.23413792C=CA2123458129MYH7c.5757G= (p.Lys1919=)
14g.23413792C>GCA389034537MYH7c.5757G>C (p.Lys1919Asn)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23413792C>TCA485616094MYH7c.5757G>A (p.Lys1919=)
14g.23413792_23413795delinsCTTGCA2123458133MYH7c.5754_5757delinsCAAG (p.Asn1918=)
14g.23413793T>ACA389034538MYH7c.5756A>T (p.Lys1919Met)
14g.23413793T>CCA389034539MYH7c.5756A>G (p.Lys1919Arg)
14g.23413793T>GCA389034540MYH7c.5756A>C (p.Lys1919Thr)
14g.23413796_23413798delCA2123458139MYH7c.5754_5756del (p.Asn1918del)
ClinVar dbSNP
14g.23413794T>ACA389034541MYH7c.5755A>T (p.Lys1919Ter)
14g.23413794T>CCA389034542MYH7c.5755A>G (p.Lys1919Glu)
14g.23413794T>GCA389034543MYH7c.5755A>C (p.Lys1919Gln)
14g.23413795G>ACA048157MYH7c.5754C>T (p.Asn1918=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413795G>CCA389034544MYH7c.5754C>G (p.Asn1918Lys)
ClinVar dbSNP
14g.23413795G=CA2123458149MYH7c.5754C= (p.Asn1918=)
14g.23413795G>TCA389034545MYH7c.5754C>A (p.Asn1918Lys)
COSMIC
14g.23413796T>ACA389034546MYH7c.5753A>T (p.Asn1918Ile)
14g.23413796T>CCA389034547MYH7c.5753A>G (p.Asn1918Ser)
14g.23413796T>GCA389034548MYH7c.5753A>C (p.Asn1918Thr)
14g.23413797T>ACA389034551MYH7c.5752A>T (p.Asn1918Tyr)
14g.23413797T>CCA389034550MYH7c.5752A>G (p.Asn1918Asp)
14g.23413797T>GCA389034549MYH7c.5752A>C (p.Asn1918His)
gnomAD v4
14g.23413798G>ACA485616099MYH7c.5751C>T (p.Val1917=)
14g.23413798G>CCA485616100MYH7c.5751C>G (p.Val1917=)
14g.23413798G>TCA485616102MYH7c.5751C>A (p.Val1917=)
14g.23413799A>CCA389034552MYH7c.5750T>G (p.Val1917Gly)
14g.23413799A>GCA389034553MYH7c.5750T>C (p.Val1917Ala)
14g.23413799A>TCA389034554MYH7c.5750T>A (p.Val1917Asp)
14g.23413800C>ACA016449MYH7c.5749G>T (p.Val1917Phe)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23413800C=CA2123458161MYH7c.5749G= (p.Val1917=)
14g.23413800C>GCA389034555MYH7c.5749G>C (p.Val1917Leu)
14g.23413800C>TCA389034556MYH7c.5749G>A (p.Val1917Ile)
14g.23413801C>ACA389034557MYH7c.5748G>T (p.Gln1916His)
14g.23413801C>GCA389034558MYH7c.5748G>C (p.Gln1916His)
ClinVar
14g.23413801C>TCA485616105MYH7c.5748G>A (p.Gln1916=)
14g.23413803_23413808delCA2573053875MYH7c.5743_5748del (p.Ser1915_Gln1916del)
ClinVar dbSNP
14g.23413802T>ACA389034559MYH7c.5747A>T (p.Gln1916Leu)
14g.23413802T>CCA389034560MYH7c.5747A>G (p.Gln1916Arg)
14g.23413802T>GCA389034561MYH7c.5747A>C (p.Gln1916Pro)
14g.23413803G>ACA389034562MYH7c.5746C>T (p.Gln1916Ter)
ClinVar dbSNP
14g.23413803G>CCA389034563MYH7c.5746C>G (p.Gln1916Glu)
14g.23413803G=CA2123458178MYH7c.5746C= (p.Gln1916=)
14g.23413803G>TCA389034564MYH7c.5746C>A (p.Gln1916Lys)
14g.23413804G>ACA485616110MYH7c.5745C>T (p.Ser1915=)
ClinVar dbSNP
14g.23413804G>CCA485616111MYH7c.5745C>G (p.Ser1915=)
14g.23413804G>TCA485616109MYH7c.5745C>A (p.Ser1915=)
14g.23413804_23413808delinsGGACTCA2123458186MYH7c.5741_5745delinsAGTCC (p.Glu1914=)
14g.23413805G>ACA389034565MYH7c.5744C>T (p.Ser1915Phe)
14g.23413805G>CCA389034566MYH7c.5744C>G (p.Ser1915Cys)
ClinVar
14g.23413805G>TCA389034567MYH7c.5744C>A (p.Ser1915Tyr)
14g.23413805_23413808delinsACA351898MYH7c.5741_5744delinsT (p.Glu1914_Ser1915delinsVal)
ClinVar dbSNP
14g.23413806A>CCA389034568MYH7c.5743T>G (p.Ser1915Ala)
14g.23413806A>GCA389034569MYH7c.5743T>C (p.Ser1915Pro)
14g.23413806A>TCA389034570MYH7c.5743T>A (p.Ser1915Thr)
14g.23413807C>ACA389034571MYH7c.5742G>T (p.Glu1914Asp)
ClinVar dbSNP gnomAD v4
14g.23413807C>GCA389034572MYH7c.5742G>C (p.Glu1914Asp)
14g.23413807C>TCA485616115MYH7c.5742G>A (p.Glu1914=)
ClinVar dbSNP gnomAD v4 COSMIC
14g.23413808T>ACA389034575MYH7c.5741A>T (p.Glu1914Val)
14g.23413808T>CCA389034573MYH7c.5741A>G (p.Glu1914Gly)
14g.23413808T>GCA389034574MYH7c.5741A>C (p.Glu1914Ala)
gnomAD v4
14g.23413809C>ACA389034576MYH7c.5740G>T (p.Glu1914Ter)
ClinVar dbSNP
14g.23413809C=CA2123458197MYH7c.5740G= (p.Glu1914=)
14g.23413809C>GCA389034577MYH7c.5740G>C (p.Glu1914Gln)
14g.23413809C>TCA016441MYH7c.5740G>A (p.Glu1914Lys)
ClinVar dbSNP
14g.23413810G>ACA016434MYH7c.5739C>T (p.Ala1913=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413810G>CCA048139MYH7c.5739C>G (p.Ala1913=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413810G=CA2123458210MYH7c.5739C= (p.Ala1913=)
14g.23413810G>TCA485616117MYH7c.5739C>A (p.Ala1913=)
dbSNP
14g.23413811G>ACA389034578MYH7c.5738C>T (p.Ala1913Val)
dbSNP gnomAD v2
14g.23413811G>CCA389034580MYH7c.5738C>G (p.Ala1913Gly)
14g.23413811G=CA2123458218MYH7c.5738C= (p.Ala1913=)
14g.23413811G>TCA389034579MYH7c.5738C>A (p.Ala1913Asp)
14g.23413812C>ACA389034581MYH7c.5737G>T (p.Ala1913Ser)
14g.23413812C=CA2123458224MYH7c.5737G= (p.Ala1913=)
14g.23413812C>GCA389034582MYH7c.5737G>C (p.Ala1913Pro)
14g.23413812C>TCA048119MYH7c.5737G>A (p.Ala1913Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413813G>ACA016427MYH7c.5736C>T (p.Ile1912=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413813G>CCA389034583MYH7c.5736C>G (p.Ile1912Met)
14g.23413813G=CA2123458229MYH7c.5736C= (p.Ile1912=)
14g.23413813G>TCA485616119MYH7c.5736C>A (p.Ile1912=)
dbSNP
14g.23413814delCA2573053876MYH7c.5735del (p.Ile1912ThrfsTer21)
ClinVar dbSNP
14g.23413814A=CA2123458232MYH7c.5735T= (p.Ile1912=)
14g.23413814A>CCA389034584MYH7c.5735T>G (p.Ile1912Ser)
14g.23413814A>GCA389034585MYH7c.5735T>C (p.Ile1912Thr)
14g.23413814A>TCA389034586MYH7c.5735T>A (p.Ile1912Asn)
ClinVar dbSNP
14g.23413815T>ACA389034587MYH7c.5734A>T (p.Ile1912Phe)
ClinVar dbSNP gnomAD v4
14g.23413815T>CCA389034588MYH7c.5734A>G (p.Ile1912Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23413815T>GCA389034589MYH7c.5734A>C (p.Ile1912Leu)
14g.23413815T=CA2123458238MYH7c.5734A= (p.Ile1912=)
14g.23413816G>ACA485616121MYH7c.5733C>T (p.Asp1911=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23413816G>CCA389034590MYH7c.5733C>G (p.Asp1911Glu)
14g.23413816G=CA2123458263MYH7c.5733C= (p.Asp1911=)
14g.23413816G>TCA389034591MYH7c.5733C>A (p.Asp1911Glu)
14g.23413817T>ACA389034592MYH7c.5732A>T (p.Asp1911Val)
14g.23413817T>CCA389034594MYH7c.5732A>G (p.Asp1911Gly)
14g.23413817T>GCA389034593MYH7c.5732A>C (p.Asp1911Ala)
14g.23413818C>ACA389034595MYH7c.5731G>T (p.Asp1911Tyr)
COSMIC
14g.23413818C>GCA389034597MYH7c.5731G>C (p.Asp1911His)
14g.23413818C>TCA389034596MYH7c.5731G>A (p.Asp1911Asn)
14g.23413819delCA2800863467MYH7c.5731del (p.Asp1911ThrfsTer22)
14g.23413819C>ACA485616122MYH7c.5730G>T (p.Ala1910=)
14g.23413819C=CA2123458271MYH7c.5730G= (p.Ala1910=)
14g.23413819C>GCA485616124MYH7c.5730G>C (p.Ala1910=)
14g.23413819C>TCA048097MYH7c.5730G>A (p.Ala1910=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413820G>ACA389034598MYH7c.5729C>T (p.Ala1910Val)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
14g.23413820G>CCA389034599MYH7c.5729C>G (p.Ala1910Gly)
14g.23413820G=CA2123458286MYH7c.5729C= (p.Ala1910=)
14g.23413820G>TCA389034600MYH7c.5729C>A (p.Ala1910Glu)
14g.23413821C>ACA389034601MYH7c.5728G>T (p.Ala1910Ser)
14g.23413821C>GCA389034602MYH7c.5728G>C (p.Ala1910Pro)
14g.23413821C>TCA389034603MYH7c.5728G>A (p.Ala1910Thr)
ClinVar dbSNP
14g.23413822C>ACA485616126MYH7c.5727G>T (p.Arg1909=)
14g.23413822C=CA2123458297MYH7c.5727G= (p.Arg1909=)
14g.23413822C>GCA485616127MYH7c.5727G>C (p.Arg1909=)
14g.23413822C>TCA048076MYH7c.5727G>A (p.Arg1909=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413823C>ACA389034604MYH7c.5726G>T (p.Arg1909Leu)
COSMIC
14g.23413823C=CA2123458307MYH7c.5726G= (p.Arg1909=)
14g.23413823C>GCA016422MYH7c.5726G>C (p.Arg1909Pro)
ClinVar dbSNP
14g.23413823C>TCA016417MYH7c.5726G>A (p.Arg1909Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23413824G>ACA048061MYH7c.5725C>T (p.Arg1909Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413824G>CCA389034605MYH7c.5725C>G (p.Arg1909Gly)
ClinVar dbSNP
14g.23413824G=CA2123458325MYH7c.5725C= (p.Arg1909=)
14g.23413824G>TCA016414MYH7c.5725C>A (p.Arg1909=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413825C>ACA389034606MYH7c.5724G>T (p.Glu1908Asp)
14g.23413825C=CA2123458335MYH7c.5724G= (p.Glu1908=)
14g.23413825C>GCA389034607MYH7c.5724G>C (p.Glu1908Asp)
14g.23413825C>TCA485616128MYH7c.5724G>A (p.Glu1908=)
ClinVar dbSNP
14g.23413826T>ACA389034608MYH7c.5723A>T (p.Glu1908Val)
ClinVar dbSNP
14g.23413826T>CCA389034609MYH7c.5723A>G (p.Glu1908Gly)
14g.23413826T>GCA389034610MYH7c.5723A>C (p.Glu1908Ala)
14g.23413826T=CA2123458354MYH7c.5723A= (p.Glu1908=)
14g.23413827C>ACA389034611MYH7c.5722G>T (p.Glu1908Ter)
14g.23413827C=CA2123458362MYH7c.5722G= (p.Glu1908=)
14g.23413827C>GCA389034612MYH7c.5722G>C (p.Glu1908Gln)
14g.23413827C>TCA389034613MYH7c.5722G>A (p.Glu1908Lys)
dbSNP
14g.23413828C>ACA389034614MYH7c.5721G>T (p.Glu1907Asp)
14g.23413828C>GCA389034615MYH7c.5721G>C (p.Glu1907Asp)
14g.23413828C>TCA485616129MYH7c.5721G>A (p.Glu1907=)
14g.23413829T>ACA389034617MYH7c.5720A>T (p.Glu1907Val)
14g.23413829T>CCA389034618MYH7c.5720A>G (p.Glu1907Gly)
14g.23413829T>GCA389034616MYH7c.5720A>C (p.Glu1907Ala)
14g.23413830C>ACA389034619MYH7c.5719G>T (p.Glu1907Ter)
14g.23413830C=CA2123458374MYH7c.5719G= (p.Glu1907=)
14g.23413830C>GCA389034620MYH7c.5719G>C (p.Glu1907Gln)
dbSNP gnomAD v4
14g.23413830C>TCA389034621MYH7c.5719G>A (p.Glu1907Lys)
14g.23413831T>ACA485616132MYH7c.5718A>T (p.Ala1906=)
14g.23413831T>CCA485616131MYH7c.5718A>G (p.Ala1906=)
dbSNP gnomAD v4
14g.23413831T>GCA016408MYH7c.5718A>C (p.Ala1906=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413831T=CA2123458388MYH7c.5718A= (p.Ala1906=)
14g.23413832G>ACA389034622MYH7c.5717C>T (p.Ala1906Val)
14g.23413832G>CCA016404MYH7c.5717C>G (p.Ala1906Gly)
ClinVar dbSNP
14g.23413832G=CA2123458406MYH7c.5717C= (p.Ala1906=)
14g.23413832G>TCA389034623MYH7c.5717C>A (p.Ala1906Glu)
14g.23413833C>ACA389034624MYH7c.5716G>T (p.Ala1906Ser)
14g.23413833C>GCA389034625MYH7c.5716G>C (p.Ala1906Pro)
14g.23413833C>TCA389034626MYH7c.5716G>A (p.Ala1906Thr)
14g.23413834C>ACA389034627MYH7c.5715G>T (p.Glu1905Asp)
14g.23413834C=CA2123458412MYH7c.5715G= (p.Glu1905=)
14g.23413834C>GCA389034628MYH7c.5715G>C (p.Glu1905Asp)
14g.23413834C>TCA485616133MYH7c.5715G>A (p.Glu1905=)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
14g.23413835T>ACA389034630MYH7c.5714A>T (p.Glu1905Val)
14g.23413835T>CCA389034631MYH7c.5714A>G (p.Glu1905Gly)
14g.23413835T>GCA389034629MYH7c.5714A>C (p.Glu1905Ala)
14g.23413836C>ACA389034632MYH7c.5713G>T (p.Glu1905Ter)
14g.23413836C>GCA389034633MYH7c.5713G>C (p.Glu1905Gln)
14g.23413836C>TCA389034634MYH7c.5713G>A (p.Glu1905Lys)
14g.23413837A>CCA389034635MYH7c.5712T>G (p.Asp1904Glu)
14g.23413837A>GCA485616134MYH7c.5712T>C (p.Asp1904=)
dbSNP
14g.23413837A>TCA389034636MYH7c.5712T>A (p.Asp1904Glu)
14g.23413838T>ACA389034639MYH7c.5711A>T (p.Asp1904Val)
14g.23413838T>CCA389034637MYH7c.5711A>G (p.Asp1904Gly)
14g.23413838T>GCA389034638MYH7c.5711A>C (p.Asp1904Ala)
14g.23413839C>ACA389034640MYH7c.5710G>T (p.Asp1904Tyr)
14g.23413839C>GCA389034641MYH7c.5710G>C (p.Asp1904His)
14g.23413839C>TCA389034642MYH7c.5710G>A (p.Asp1904Asn)
14g.23413840C>ACA485616135MYH7c.5709G>T (p.Leu1903=)
14g.23413840C=CA2123458424MYH7c.5709G= (p.Leu1903=)
14g.23413840C>GCA485616136MYH7c.5709G>C (p.Leu1903=)
14g.23413840C>TCA257807464MYH7c.5709G>A (p.Leu1903=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23413841A>CCA389034643MYH7c.5708T>G (p.Leu1903Arg)
14g.23413841A>GCA389034644MYH7c.5708T>C (p.Leu1903Pro)
14g.23413841A>TCA389034645MYH7c.5708T>A (p.Leu1903Gln)
14g.23413842G>ACA485616137MYH7c.5707C>T (p.Leu1903=)
COSMIC
14g.23413842G>CCA389034647MYH7c.5707C>G (p.Leu1903Val)
14g.23413842G>TCA389034646MYH7c.5707C>A (p.Leu1903Met)
14g.23413843C>ACA389034648MYH7c.5706G>T (p.Glu1902Asp)
14g.23413843C>GCA389034649MYH7c.5706G>C (p.Glu1902Asp)
14g.23413843C>TCA485616138MYH7c.5706G>A (p.Glu1902=)
ClinVar dbSNP
14g.23413844T>ACA389034650MYH7c.5705A>T (p.Glu1902Val)
14g.23413844T>CCA389034651MYH7c.5705A>G (p.Glu1902Gly)
14g.23413844T>GCA389034652MYH7c.5705A>C (p.Glu1902Ala)
14g.23413845C>ACA389034653MYH7c.5704G>T (p.Glu1902Ter)
14g.23413845C=CA2123458435MYH7c.5704G= (p.Glu1902=)
14g.23413845C>GCA016398MYH7c.5704G>C (p.Glu1902Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413845C>TCA016392MYH7c.5704G>A (p.Glu1902Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23413846G>ACA016386MYH7c.5703C>T (p.His1901=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413846G>CCA257807514MYH7c.5703C>G (p.His1901Gln)
dbSNP gnomAD v4
14g.23413846G=CA2123458461MYH7c.5703C= (p.His1901=)
14g.23413846G>TCA389034654MYH7c.5703C>A (p.His1901Gln)
14g.23413847T>ACA016379MYH7c.5702A>T (p.His1901Leu)
ClinVar dbSNP
14g.23413847T>CCA389034655MYH7c.5702A>G (p.His1901Arg)
14g.23413847T>GCA389034656MYH7c.5702A>C (p.His1901Pro)
14g.23413847T=CA2123458469MYH7c.5702A= (p.His1901=)
14g.23413848G>ACA389034658MYH7c.5701C>T (p.His1901Tyr)
14g.23413848G>CCA389034659MYH7c.5701C>G (p.His1901Asp)
14g.23413848G>TCA389034657MYH7c.5701C>A (p.His1901Asn)
14g.23413849C>ACA389034660MYH7c.5700G>T (p.Gln1900His)
14g.23413849C>GCA389034661MYH7c.5700G>C (p.Gln1900His)
14g.23413849C>TCA485616140MYH7c.5700G>A (p.Gln1900=)
14g.23413850T>ACA048008MYH7c.5699A>T (p.Gln1900Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23413850T>CCA389034662MYH7c.5699A>G (p.Gln1900Arg)
14g.23413850T>GCA389034663MYH7c.5699A>C (p.Gln1900Pro)
14g.23413850T=CA2123458480MYH7c.5699A= (p.Gln1900=)
14g.23413851G>ACA389034666MYH7c.5698C>T (p.Gln1900Ter)
14g.23413851G>CCA389034664MYH7c.5698C>G (p.Gln1900Glu)
14g.23413851G>TCA389034665MYH7c.5698C>A (p.Gln1900Lys)
14g.23413852C>ACA485616141MYH7c.5697G>T (p.Val1899=)
14g.23413852C=CA2123458486MYH7c.5697G= (p.Val1899=)
14g.23413852C>GCA485616142MYH7c.5697G>C (p.Val1899=)
14g.23413852C>TCA485616143MYH7c.5697G>A (p.Val1899=)
ClinVar dbSNP
14g.23413853A=CA2123458501MYH7c.5696T= (p.Val1899=)
14g.23413853A>CCA389034667MYH7c.5696T>G (p.Val1899Gly)
14g.23413853A>GCA016376MYH7c.5696T>C (p.Val1899Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23413853A>TCA389034668MYH7c.5696T>A (p.Val1899Glu)
14g.23413854C>ACA389034669MYH7c.5695G>T (p.Val1899Leu)
gnomAD v4
14g.23413854C>GCA389034670MYH7c.5695G>C (p.Val1899Leu)
gnomAD v4
14g.23413854C>TCA389034671MYH7c.5695G>A (p.Val1899Met)
ClinVar

Number of alleles fetched