Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.10392859T>ACA398091665MYH8,MYHASc.5435A>T (p.Lys1812Met)
n.76+9652T>A
c.5531A>T (p.Lys1844Met)
17g.10392859T>CCA8387044MYH8,MYHASc.5435A>G (p.Lys1812Arg)
n.76+9652T>C
c.5531A>G (p.Lys1844Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.10392859T>GCA398091669MYH8,MYHASc.5435A>C (p.Lys1812Thr)
n.76+9652T>G
c.5531A>C (p.Lys1844Thr)
17g.10392859T=CA2247204670MYH8,MYHASc.5435A= (p.Lys1812=)
n.76+9652T=
c.5531A= (p.Lys1844=)
17g.10392860T>ACA398091672MYH8,MYHASc.5434A>T (p.Lys1812Ter)
n.76+9653T>A
c.5530A>T (p.Lys1844Ter)
17g.10392860T>CCA398091675MYH8,MYHASc.5434A>G (p.Lys1812Glu)
n.76+9653T>C
c.5530A>G (p.Lys1844Glu)
17g.10392860T>GCA398091677MYH8,MYHASc.5434A>C (p.Lys1812Gln)
n.76+9653T>G
c.5530A>C (p.Lys1844Gln)
17g.10392861C>ACA497837342MYH8,MYHASc.5433G>T (p.Gly1811=)
n.76+9654C>A
c.5529G>T (p.Gly1843=)
17g.10392861C>GCA497837340MYH8,MYHASc.5433G>C (p.Gly1811=)
n.76+9654C>G
c.5529G>C (p.Gly1843=)
17g.10392861C>TCA497837339MYH8,MYHASc.5433G>A (p.Gly1811=)
n.76+9654C>T
c.5529G>A (p.Gly1843=)
COSMIC
17g.10392862C>ACA398091680MYH8,MYHASc.5432G>T (p.Gly1811Val)
n.76+9655C>A
c.5528G>T (p.Gly1843Val)
17g.10392862C=CA2247204679MYH8,MYHASc.5432G= (p.Gly1811=)
n.76+9655C=
c.5528G= (p.Gly1843=)
17g.10392862C>GCA398091686MYH8,MYHASc.5432G>C (p.Gly1811Ala)
n.76+9655C>G
c.5528G>C (p.Gly1843Ala)
dbSNP gnomAD v2 gnomAD v4
17g.10392862C>TCA398091683MYH8,MYHASc.5432G>A (p.Gly1811Glu)
n.76+9655C>T
c.5528G>A (p.Gly1843Glu)
COSMIC
17g.10392863C>ACA398091691MYH8,MYHASc.5431G>T (p.Gly1811Trp)
n.76+9656C>A
c.5527G>T (p.Gly1843Trp)
17g.10392863C>GCA398091716MYH8,MYHASc.5431G>C (p.Gly1811Arg)
n.76+9656C>G
c.5527G>C (p.Gly1843Arg)
17g.10392863C>TCA398091694MYH8,MYHASc.5431G>A (p.Gly1811Arg)
n.76+9656C>T
c.5527G>A (p.Gly1843Arg)
gnomAD v4 COSMIC
17g.10392864A=CA2247204685MYH8,MYHASc.5430T= (p.Gly1810=)
n.76+9657A=
c.5526T= (p.Gly1842=)
17g.10392864A>CCA497837347MYH8,MYHASc.5430T>G (p.Gly1810=)
n.76+9657A>C
c.5526T>G (p.Gly1842=)
dbSNP
17g.10392864A>GCA497837348MYH8,MYHASc.5430T>C (p.Gly1810=)
n.76+9657A>G
c.5526T>C (p.Gly1842=)
dbSNP gnomAD v4 COSMIC
17g.10392864A>TCA497837349MYH8,MYHASc.5430T>A (p.Gly1810=)
n.76+9657A>T
c.5526T>A (p.Gly1842=)
17g.10392865C>ACA287717719MYH8,MYHASc.5429G>T (p.Gly1810Val)
n.76+9658C>A
c.5525G>T (p.Gly1842Val)
dbSNP
17g.10392865C=CA2247204694MYH8,MYHASc.5429G= (p.Gly1810=)
n.76+9658C=
c.5525G= (p.Gly1842=)
17g.10392865C>GCA398091720MYH8,MYHASc.5429G>C (p.Gly1810Ala)
n.76+9658C>G
c.5525G>C (p.Gly1842Ala)
17g.10392865C>TCA398091724MYH8,MYHASc.5429G>A (p.Gly1810Asp)
n.76+9658C>T
c.5525G>A (p.Gly1842Asp)
17g.10392866C>ACA398091727MYH8,MYHASc.5428G>T (p.Gly1810Cys)
n.76+9659C>A
c.5524G>T (p.Gly1842Cys)
dbSNP gnomAD v3 gnomAD v4
17g.10392866C=CA2247204699MYH8,MYHASc.5428G= (p.Gly1810=)
n.76+9659C=
c.5524G= (p.Gly1842=)
17g.10392866C>GCA398091730MYH8,MYHASc.5428G>C (p.Gly1810Arg)
n.76+9659C>G
c.5524G>C (p.Gly1842Arg)
gnomAD v4
17g.10392866C>TCA398091732MYH8,MYHASc.5428G>A (p.Gly1810Ser)
n.76+9659C>T
c.5524G>A (p.Gly1842Ser)
dbSNP gnomAD v4
17g.10392867C>ACA398091736MYH8,MYHASc.5427G>T (p.Lys1809Asn)
n.76+9660C>A
c.5523G>T (p.Lys1841Asn)
17g.10392867C=CA2247204711MYH8,MYHASc.5427G= (p.Lys1809=)
n.76+9660C=
c.5523G= (p.Lys1841=)
17g.10392867C>GCA398091753MYH8,MYHASc.5427G>C (p.Lys1809Asn)
n.76+9660C>G
c.5523G>C (p.Lys1841Asn)
17g.10392867C>TCA8387045MYH8,MYHASc.5427G>A (p.Lys1809=)
n.76+9660C>T
c.5523G>A (p.Lys1841=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.10392868T>ACA398091767MYH8,MYHASc.5426A>T (p.Lys1809Met)
n.76+9661T>A
c.5522A>T (p.Lys1841Met)
17g.10392868T>CCA398091768MYH8,MYHASc.5426A>G (p.Lys1809Arg)
n.76+9661T>C
c.5522A>G (p.Lys1841Arg)
17g.10392868T>GCA398091771MYH8,MYHASc.5426A>C (p.Lys1809Thr)
n.76+9661T>G
c.5522A>C (p.Lys1841Thr)
17g.10392869T>ACA398091778MYH8,MYHASc.5425A>T (p.Lys1809Ter)
n.76+9662T>A
c.5521A>T (p.Lys1841Ter)
17g.10392869T>CCA398091775MYH8,MYHASc.5425A>G (p.Lys1809Glu)
n.76+9662T>C
c.5521A>G (p.Lys1841Glu)
17g.10392869T>GCA398091777MYH8,MYHASc.5425A>C (p.Lys1809Gln)
n.76+9662T>G
c.5521A>C (p.Lys1841Gln)
dbSNP gnomAD v3 gnomAD v4
17g.10392869T=CA2247204714MYH8,MYHASc.5425A= (p.Lys1809=)
n.76+9662T=
c.5521A= (p.Lys1841=)
17g.10392870C>ACA497837355MYH8,MYHASc.5424G>T (p.Leu1808=)
n.76+9663C>A
c.5520G>T (p.Leu1840=)
17g.10392870C=CA2247204719MYH8,MYHASc.5424G= (p.Leu1808=)
n.76+9663C=
c.5520G= (p.Leu1840=)
17g.10392870C>GCA497837357MYH8,MYHASc.5424G>C (p.Leu1808=)
n.76+9663C>G
c.5520G>C (p.Leu1840=)
17g.10392870C>TCA497837359MYH8,MYHASc.5424G>A (p.Leu1808=)
n.76+9663C>T
c.5520G>A (p.Leu1840=)
dbSNP
17g.10392871A>CCA398091781MYH8,MYHASc.5423T>G (p.Leu1808Arg)
n.76+9664A>C
c.5519T>G (p.Leu1840Arg)
17g.10392871A>GCA398091783MYH8,MYHASc.5423T>C (p.Leu1808Pro)
n.76+9664A>G
c.5519T>C (p.Leu1840Pro)
17g.10392871A>TCA398091788MYH8,MYHASc.5423T>A (p.Leu1808Gln)
n.76+9664A>T
c.5519T>A (p.Leu1840Gln)
17g.10392872G>ACA497837361MYH8,MYHASc.5422C>T (p.Leu1808=)
n.76+9665G>A
c.5518C>T (p.Leu1840=)
17g.10392872G>CCA398091792MYH8,MYHASc.5422C>G (p.Leu1808Val)
n.76+9665G>C
c.5518C>G (p.Leu1840Val)
17g.10392872G>TCA398091796MYH8,MYHASc.5422C>A (p.Leu1808Met)
n.76+9665G>T
c.5518C>A (p.Leu1840Met)
17g.10392873C>ACA497837362MYH8,MYHASc.5421G>T (p.Ala1807=)
n.76+9666C>A
c.5517G>T (p.Ala1839=)
17g.10392873C=CA2247204727MYH8,MYHASc.5421G= (p.Ala1807=)
n.76+9666C=
c.5517G= (p.Ala1839=)
17g.10392873C>GCA287717728MYH8,MYHASc.5421G>C (p.Ala1807=)
n.76+9666C>G
c.5517G>C (p.Ala1839=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392873C>TCA8387046MYH8,MYHASc.5421G>A (p.Ala1807=)
n.76+9666C>T
c.5517G>A (p.Ala1839=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.10392874G>ACA398091804MYH8,MYHASc.5420C>T (p.Ala1807Val)
n.76+9667G>A
c.5516C>T (p.Ala1839Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.10392874G>CCA398091807MYH8,MYHASc.5420C>G (p.Ala1807Gly)
n.76+9667G>C
c.5516C>G (p.Ala1839Gly)
17g.10392874G=CA2247204734MYH8,MYHASc.5420C= (p.Ala1807=)
n.76+9667G=
c.5516C= (p.Ala1839=)
17g.10392874G>TCA398091811MYH8,MYHASc.5420C>A (p.Ala1807Glu)
n.76+9667G>T
c.5516C>A (p.Ala1839Glu)
dbSNP gnomAD v3 gnomAD v4
17g.10392875C>ACA398091821MYH8,MYHASc.5419G>T (p.Ala1807Ser)
n.76+9668C>A
c.5515G>T (p.Ala1839Ser)
dbSNP gnomAD v3 gnomAD v4 COSMIC
17g.10392875C=CA2247204740MYH8,MYHASc.5419G= (p.Ala1807=)
n.76+9668C=
c.5515G= (p.Ala1839=)
17g.10392875C>GCA398091817MYH8,MYHASc.5419G>C (p.Ala1807Pro)
n.76+9668C>G
c.5515G>C (p.Ala1839Pro)
17g.10392875C>TCA398091814MYH8,MYHASc.5419G>A (p.Ala1807Thr)
n.76+9668C>T
c.5515G>A (p.Ala1839Thr)
17g.10392876C>ACA497837370MYH8,MYHASc.5418G>T (p.Leu1806=)
n.76+9669C>A
c.5514G>T (p.Leu1838=)
17g.10392876C=CA2247204747MYH8,MYHASc.5418G= (p.Leu1806=)
n.76+9669C=
c.5514G= (p.Leu1838=)
17g.10392876C>GCA497837369MYH8,MYHASc.5418G>C (p.Leu1806=)
n.76+9669C>G
c.5514G>C (p.Leu1838=)
17g.10392876C>TCA8387047MYH8,MYHASc.5418G>A (p.Leu1806=)
n.76+9669C>T
c.5514G>A (p.Leu1838=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.10392877A>CCA398091828MYH8,MYHASc.5417T>G (p.Leu1806Arg)
n.76+9670A>C
c.5513T>G (p.Leu1838Arg)
17g.10392877A>GCA398091831MYH8,MYHASc.5417T>C (p.Leu1806Pro)
n.76+9670A>G
c.5513T>C (p.Leu1838Pro)
17g.10392877A>TCA398091834MYH8,MYHASc.5417T>A (p.Leu1806Gln)
n.76+9670A>T
c.5513T>A (p.Leu1838Gln)
17g.10392878G>ACA497837372MYH8,MYHASc.5416C>T (p.Leu1806=)
n.76+9671G>A
c.5512C>T (p.Leu1838=)
17g.10392878G>CCA398091838MYH8,MYHASc.5416C>G (p.Leu1806Val)
n.76+9671G>C
c.5512C>G (p.Leu1838Val)
17g.10392878G>TCA398091842MYH8,MYHASc.5416C>A (p.Leu1806Met)
n.76+9671G>T
c.5512C>A (p.Leu1838Met)
17g.10392879C>ACA398091846MYH8,MYHASc.5415G>T (p.Gln1805His)
n.76+9672C>A
c.5511G>T (p.Gln1837His)
dbSNP
17g.10392879C=CA2247204749MYH8,MYHASc.5415G= (p.Gln1805=)
n.76+9672C=
c.5511G= (p.Gln1837=)
17g.10392879C>GCA398091848MYH8,MYHASc.5415G>C (p.Gln1805His)
n.76+9672C>G
c.5511G>C (p.Gln1837His)
17g.10392879C>TCA497837376MYH8,MYHASc.5415G>A (p.Gln1805=)
n.76+9672C>T
c.5511G>A (p.Gln1837=)
gnomAD v4
17g.10392880T>ACA398091854MYH8,MYHASc.5414A>T (p.Gln1805Leu)
n.76+9673T>A
c.5510A>T (p.Gln1837Leu)
COSMIC
17g.10392880T>CCA398091857MYH8,MYHASc.5414A>G (p.Gln1805Arg)
n.76+9673T>C
c.5510A>G (p.Gln1837Arg)
17g.10392880T>GCA398091860MYH8,MYHASc.5414A>C (p.Gln1805Pro)
n.76+9673T>G
c.5510A>C (p.Gln1837Pro)
17g.10392881G>ACA398091864MYH8,MYHASc.5413C>T (p.Gln1805Ter)
n.76+9674G>A
c.5509C>T (p.Gln1837Ter)
gnomAD v4
17g.10392881G>CCA398091870MYH8,MYHASc.5413C>G (p.Gln1805Glu)
n.76+9674G>C
c.5509C>G (p.Gln1837Glu)
17g.10392881G=CA2247204752MYH8,MYHASc.5413C= (p.Gln1805=)
n.76+9674G=
c.5509C= (p.Gln1837=)
17g.10392881G>TCA398091873MYH8,MYHASc.5413C>A (p.Gln1805Lys)
n.76+9674G>T
c.5509C>A (p.Gln1837Lys)
dbSNP gnomAD v3 gnomAD v4
17g.10392882C>ACA398091878MYH8,MYHASc.5412G>T (p.Glu1804Asp)
n.76+9675C>A
c.5508G>T (p.Glu1836Asp)
dbSNP gnomAD v2 gnomAD v4
17g.10392882C=CA2247204760MYH8,MYHASc.5412G= (p.Glu1804=)
n.76+9675C=
c.5508G= (p.Glu1836=)
17g.10392882C>GCA398091882MYH8,MYHASc.5412G>C (p.Glu1804Asp)
n.76+9675C>G
c.5508G>C (p.Glu1836Asp)
17g.10392882C>TCA497837380MYH8,MYHASc.5412G>A (p.Glu1804=)
n.76+9675C>T
c.5508G>A (p.Glu1836=)
17g.10392883T>ACA398091886MYH8,MYHASc.5411A>T (p.Glu1804Val)
n.76+9676T>A
c.5507A>T (p.Glu1836Val)
17g.10392883T>CCA398091890MYH8,MYHASc.5411A>G (p.Glu1804Gly)
n.76+9676T>C
c.5507A>G (p.Glu1836Gly)
gnomAD v4
17g.10392883T>GCA398091894MYH8,MYHASc.5411A>C (p.Glu1804Ala)
n.76+9676T>G
c.5507A>C (p.Glu1836Ala)
17g.10392884C>ACA398091899MYH8,MYHASc.5410G>T (p.Glu1804Ter)
n.76+9677C>A
c.5506G>T (p.Glu1836Ter)
COSMIC
17g.10392884C=CA2247204766MYH8,MYHASc.5410G= (p.Glu1804=)
n.76+9677C=
c.5506G= (p.Glu1836=)
17g.10392884C>GCA398091902MYH8,MYHASc.5410G>C (p.Glu1804Gln)
n.76+9677C>G
c.5506G>C (p.Glu1836Gln)
17g.10392884C>TCA8387048MYH8,MYHASc.5410G>A (p.Glu1804Lys)
n.76+9677C>T
c.5506G>A (p.Glu1836Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.10392885G>ACA287717731MYH8,MYHASc.5409C>T (p.Ala1803=)
n.76+9678G>A
c.5505C>T (p.Ala1835=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392885G>CCA497837384MYH8,MYHASc.5409C>G (p.Ala1803=)
n.76+9678G>C
c.5505C>G (p.Ala1835=)
17g.10392885G=CA2247204775MYH8,MYHASc.5409C= (p.Ala1803=)
n.76+9678G=
c.5505C= (p.Ala1835=)
17g.10392885G>TCA497837385MYH8,MYHASc.5409C>A (p.Ala1803=)
n.76+9678G>T
c.5505C>A (p.Ala1835=)
gnomAD v3 gnomAD v4
17g.10392886delCA2576170790MYH8,MYHASc.5409del (p.Glu1804SerfsTer5)
n.76+9679del
c.5505del (p.Glu1836SerfsTer5)
17g.10392886G>ACA398091921MYH8,MYHASc.5408C>T (p.Ala1803Val)
n.76+9679G>A
c.5504C>T (p.Ala1835Val)
COSMIC
17g.10392886G>CCA398091924MYH8,MYHASc.5408C>G (p.Ala1803Gly)
n.76+9679G>C
c.5504C>G (p.Ala1835Gly)
17g.10392886G>TCA398091926MYH8,MYHASc.5408C>A (p.Ala1803Asp)
n.76+9679G>T
c.5504C>A (p.Ala1835Asp)
17g.10392887C>ACA398091931MYH8,MYHASc.5407G>T (p.Ala1803Ser)
n.76+9680C>A
c.5503G>T (p.Ala1835Ser)
17g.10392887C>GCA398091933MYH8,MYHASc.5407G>C (p.Ala1803Pro)
n.76+9680C>G
c.5503G>C (p.Ala1835Pro)
17g.10392887C>TCA398091936MYH8,MYHASc.5407G>A (p.Ala1803Thr)
n.76+9680C>T
c.5503G>A (p.Ala1835Thr)
17g.10392888C>ACA398091943MYH8,MYHASc.5406G>T (p.Glu1802Asp)
n.76+9681C>A
c.5502G>T (p.Glu1834Asp)
COSMIC
17g.10392888C>GCA398091939MYH8,MYHASc.5406G>C (p.Glu1802Asp)
n.76+9681C>G
c.5502G>C (p.Glu1834Asp)
gnomAD v4
17g.10392888C>TCA497837392MYH8,MYHASc.5406G>A (p.Glu1802=)
n.76+9681C>T
c.5502G>A (p.Glu1834=)
dbSNP
17g.10392889T>ACA398091947MYH8,MYHASc.5405A>T (p.Glu1802Val)
n.76+9682T>A
c.5501A>T (p.Glu1834Val)
dbSNP gnomAD v3 gnomAD v4
17g.10392889T>CCA398091952MYH8,MYHASc.5405A>G (p.Glu1802Gly)
n.76+9682T>C
c.5501A>G (p.Glu1834Gly)
17g.10392889T>GCA398091949MYH8,MYHASc.5405A>C (p.Glu1802Ala)
n.76+9682T>G
c.5501A>C (p.Glu1834Ala)
17g.10392889T=CA2247204783MYH8,MYHASc.5405A= (p.Glu1802=)
n.76+9682T=
c.5501A= (p.Glu1834=)
17g.10392890C>ACA398091956MYH8,MYHASc.5404G>T (p.Glu1802Ter)
n.76+9683C>A
c.5500G>T (p.Glu1834Ter)
17g.10392890C>GCA398091962MYH8,MYHASc.5404G>C (p.Glu1802Gln)
n.76+9683C>G
c.5500G>C (p.Glu1834Gln)
17g.10392890C>TCA398091959MYH8,MYHASc.5404G>A (p.Glu1802Lys)
n.76+9683C>T
c.5500G>A (p.Glu1834Lys)
gnomAD v4
17g.10392891A>CCA398091965MYH8,MYHASc.5403T>G (p.Asp1801Glu)
n.76+9684A>C
c.5499T>G (p.Asp1833Glu)
17g.10392891A>GCA497837394MYH8,MYHASc.5403T>C (p.Asp1801=)
n.76+9684A>G
c.5499T>C (p.Asp1833=)
17g.10392891A>TCA398091968MYH8,MYHASc.5403T>A (p.Asp1801Glu)
n.76+9684A>T
c.5499T>A (p.Asp1833Glu)
17g.10392892T>ACA398091972MYH8,MYHASc.5402A>T (p.Asp1801Val)
n.76+9685T>A
c.5498A>T (p.Asp1833Val)
17g.10392892T>CCA398091979MYH8,MYHASc.5402A>G (p.Asp1801Gly)
n.76+9685T>C
c.5498A>G (p.Asp1833Gly)
17g.10392892T>GCA398091975MYH8,MYHASc.5402A>C (p.Asp1801Ala)
n.76+9685T>G
c.5498A>C (p.Asp1833Ala)
17g.10392893C>ACA398091983MYH8,MYHASc.5401G>T (p.Asp1801Tyr)
n.76+9686C>A
c.5497G>T (p.Asp1833Tyr)
17g.10392893C>GCA398091986MYH8,MYHASc.5401G>C (p.Asp1801His)
n.76+9686C>G
c.5497G>C (p.Asp1833His)
gnomAD v4
17g.10392893C>TCA398091989MYH8,MYHASc.5401G>A (p.Asp1801Asn)
n.76+9686C>T
c.5497G>A (p.Asp1833Asn)
17g.10392894T>ACA497837398MYH8,MYHASc.5400A>T (p.Leu1800=)
n.76+9687T>A
c.5496A>T (p.Leu1832=)
17g.10392894T>CCA8387049MYH8,MYHASc.5400A>G (p.Leu1800=)
n.76+9687T>C
c.5496A>G (p.Leu1832=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.10392894T>GCA497837399MYH8,MYHASc.5400A>C (p.Leu1800=)
n.76+9687T>G
c.5496A>C (p.Leu1832=)
17g.10392894T=CA2247204794MYH8,MYHASc.5400A= (p.Leu1800=)
n.76+9687T=
c.5496A= (p.Leu1832=)
17g.10392895A>CCA398091996MYH8,MYHASc.5399T>G (p.Leu1800Arg)
n.76+9688A>C
c.5495T>G (p.Leu1832Arg)
17g.10392895A>GCA398091998MYH8,MYHASc.5399T>C (p.Leu1800Pro)
n.76+9688A>G
c.5495T>C (p.Leu1832Pro)
17g.10392895A>TCA398092001MYH8,MYHASc.5399T>A (p.Leu1800Gln)
n.76+9688A>T
c.5495T>A (p.Leu1832Gln)
17g.10392896G>ACA497837400MYH8,MYHASc.5398C>T (p.Leu1800=)
n.76+9689G>A
c.5494C>T (p.Leu1832=)
17g.10392896G>CCA398092005MYH8,MYHASc.5398C>G (p.Leu1800Val)
n.76+9689G>C
c.5494C>G (p.Leu1832Val)
17g.10392896G=CA2247204814MYH8,MYHASc.5398C= (p.Leu1800=)
n.76+9689G=
c.5494C= (p.Leu1832=)
17g.10392896G>TCA8387050MYH8,MYHASc.5398C>A (p.Leu1800Ile)
n.76+9689G>T
c.5494C>A (p.Leu1832Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.10392897A=CA2247204821MYH8,MYHASc.5397T= (p.Arg1799=)
n.76+9690A=
c.5493T= (p.Arg1831=)
17g.10392897A>CCA497837403MYH8,MYHASc.5397T>G (p.Arg1799=)
n.76+9690A>C
c.5493T>G (p.Arg1831=)
17g.10392897A>GCA497837402MYH8,MYHASc.5397T>C (p.Arg1799=)
n.76+9690A>G
c.5493T>C (p.Arg1831=)
dbSNP
17g.10392897A>TCA497837401MYH8,MYHASc.5397T>A (p.Arg1799=)
n.76+9690A>T
c.5493T>A (p.Arg1831=)
17g.10392898C>ACA398092012MYH8,MYHASc.5396G>T (p.Arg1799Leu)
n.76+9691C>A
c.5492G>T (p.Arg1831Leu)
17g.10392898C=CA2247204828MYH8,MYHASc.5396G= (p.Arg1799=)
n.76+9691C=
c.5492G= (p.Arg1831=)
17g.10392898C>GCA398092015MYH8,MYHASc.5396G>C (p.Arg1799Pro)
n.76+9691C>G
c.5492G>C (p.Arg1831Pro)
17g.10392898C>TCA8387051MYH8,MYHASc.5396G>A (p.Arg1799His)
n.76+9691C>T
c.5492G>A (p.Arg1831His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.10392899G>ACA398092027MYH8,MYHASc.5395C>T (p.Arg1799Cys)
n.76+9692G>A
c.5491C>T (p.Arg1831Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.10392899G>CCA398092023MYH8,MYHASc.5395C>G (p.Arg1799Gly)
n.76+9692G>C
c.5491C>G (p.Arg1831Gly)
dbSNP
17g.10392899G=CA2247204836MYH8,MYHASc.5395C= (p.Arg1799=)
n.76+9692G=
c.5491C= (p.Arg1831=)
17g.10392899G>TCA398092025MYH8,MYHASc.5395C>A (p.Arg1799Ser)
n.76+9692G>T
c.5491C>A (p.Arg1831Ser)
dbSNP gnomAD v4
17g.10392900A=CA2247204841MYH8,MYHASc.5394T= (p.His1798=)
n.76+9693A=
c.5490T= (p.His1830=)
17g.10392900A>CCA398092030MYH8,MYHASc.5394T>G (p.His1798Gln)
n.76+9693A>C
c.5490T>G (p.His1830Gln)
17g.10392900A>GCA497837404MYH8,MYHASc.5394T>C (p.His1798=)
n.76+9693A>G
c.5490T>C (p.His1830=)
dbSNP gnomAD v2 gnomAD v4
17g.10392900A>TCA8387052MYH8,MYHASc.5394T>A (p.His1798Gln)
n.76+9693A>T
c.5490T>A (p.His1830Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.10392901T>ACA398092034MYH8,MYHASc.5393A>T (p.His1798Leu)
n.76+9694T>A
c.5489A>T (p.His1830Leu)
dbSNP gnomAD v2 gnomAD v4
17g.10392901T>CCA398092035MYH8,MYHASc.5393A>G (p.His1798Arg)
n.76+9694T>C
c.5489A>G (p.His1830Arg)
17g.10392901T>GCA398092039MYH8,MYHASc.5393A>C (p.His1798Pro)
n.76+9694T>G
c.5489A>C (p.His1830Pro)
17g.10392901T=CA2247204853MYH8,MYHASc.5393A= (p.His1798=)
n.76+9694T=
c.5489A= (p.His1830=)
17g.10392902G>ACA398092043MYH8,MYHASc.5392C>T (p.His1798Tyr)
n.76+9695G>A
c.5488C>T (p.His1830Tyr)
gnomAD v4
17g.10392902G>CCA398092046MYH8,MYHASc.5392C>G (p.His1798Asp)
n.76+9695G>C
c.5488C>G (p.His1830Asp)
17g.10392902G>TCA398092049MYH8,MYHASc.5392C>A (p.His1798Asn)
n.76+9695G>T
c.5488C>A (p.His1830Asn)
17g.10392903C>ACA398092053MYH8,MYHASc.5391G>T (p.Gln1797His)
n.76+9696C>A
c.5487G>T (p.Gln1829His)
17g.10392903C>GCA398092056MYH8,MYHASc.5391G>C (p.Gln1797His)
n.76+9696C>G
c.5487G>C (p.Gln1829His)
17g.10392903C>TCA497837405MYH8,MYHASc.5391G>A (p.Gln1797=)
n.76+9696C>T
c.5487G>A (p.Gln1829=)
COSMIC
17g.10392904T>ACA398092065MYH8,MYHASc.5390A>T (p.Gln1797Leu)
n.76+9697T>A
c.5486A>T (p.Gln1829Leu)
17g.10392904T>CCA398092063MYH8,MYHASc.5390A>G (p.Gln1797Arg)
n.76+9697T>C
c.5486A>G (p.Gln1829Arg)
dbSNP gnomAD v2 gnomAD v4
17g.10392904T>GCA398092060MYH8,MYHASc.5390A>C (p.Gln1797Pro)
n.76+9697T>G
c.5486A>C (p.Gln1829Pro)
17g.10392904T=CA2247204867MYH8,MYHASc.5390A= (p.Gln1797=)
n.76+9697T=
c.5486A= (p.Gln1829=)
17g.10392905G>ACA398092070MYH8,MYHASc.5389C>T (p.Gln1797Ter)
n.76+9698G>A
c.5485C>T (p.Gln1829Ter)
gnomAD v4
17g.10392905G>CCA398092073MYH8,MYHASc.5389C>G (p.Gln1797Glu)
n.76+9698G>C
c.5485C>G (p.Gln1829Glu)
17g.10392905G=CA2247204872MYH8,MYHASc.5389C= (p.Gln1797=)
n.76+9698G=
c.5485C= (p.Gln1829=)
17g.10392905G>TCA398092074MYH8,MYHASc.5389C>A (p.Gln1797Lys)
n.76+9698G>T
c.5485C>A (p.Gln1829Lys)
dbSNP gnomAD v3 gnomAD v4
17g.10392906C>ACA497837406MYH8,MYHASc.5388G>T (p.Leu1796=)
n.76+9699C>A
c.5484G>T (p.Leu1828=)
17g.10392906C>GCA497837407MYH8,MYHASc.5388G>C (p.Leu1796=)
n.76+9699C>G
c.5484G>C (p.Leu1828=)
17g.10392906C>TCA497837408MYH8,MYHASc.5388G>A (p.Leu1796=)
n.76+9699C>T
c.5484G>A (p.Leu1828=)
17g.10392907A=CA2247204877MYH8,MYHASc.5387T= (p.Leu1796=)
n.76+9700A=
c.5483T= (p.Leu1828=)
17g.10392907A>CCA398092076MYH8,MYHASc.5387T>G (p.Leu1796Arg)
n.76+9700A>C
c.5483T>G (p.Leu1828Arg)
17g.10392907A>GCA398092085MYH8,MYHASc.5387T>C (p.Leu1796Pro)
n.76+9700A>G
c.5483T>C (p.Leu1828Pro)
dbSNP
17g.10392907A>TCA398092088MYH8,MYHASc.5387T>A (p.Leu1796Gln)
n.76+9700A>T
c.5483T>A (p.Leu1828Gln)
17g.10392908G>ACA8387053MYH8,MYHASc.5386C>T (p.Leu1796=)
n.76+9701G>A
c.5482C>T (p.Leu1828=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.10392908G>CCA287717749MYH8,MYHASc.5386C>G (p.Leu1796Val)
n.76+9701G>C
c.5482C>G (p.Leu1828Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392908G=CA2247204885MYH8,MYHASc.5386C= (p.Leu1796=)
n.76+9701G=
c.5482C= (p.Leu1828=)
17g.10392908G>TCA398092097MYH8,MYHASc.5386C>A (p.Leu1796Met)
n.76+9701G>T
c.5482C>A (p.Leu1828Met)
17g.10392909G>ACA497837409MYH8,MYHASc.5385C>T (p.Asp1795=)
n.76+9702G>A
c.5481C>T (p.Asp1827=)
17g.10392909G>CCA398092100MYH8,MYHASc.5385C>G (p.Asp1795Glu)
n.76+9702G>C
c.5481C>G (p.Asp1827Glu)
17g.10392909G>TCA398092102MYH8,MYHASc.5385C>A (p.Asp1795Glu)
n.76+9702G>T
c.5481C>A (p.Asp1827Glu)
17g.10392910T>ACA398092115MYH8,MYHASc.5384A>T (p.Asp1795Val)
n.76+9703T>A
c.5480A>T (p.Asp1827Val)
17g.10392910T>CCA398092112MYH8,MYHASc.5384A>G (p.Asp1795Gly)
n.76+9703T>C
c.5480A>G (p.Asp1827Gly)
17g.10392910T>GCA398092108MYH8,MYHASc.5384A>C (p.Asp1795Ala)
n.76+9703T>G
c.5480A>C (p.Asp1827Ala)
dbSNP
17g.10392910T=CA2247204894MYH8,MYHASc.5384A= (p.Asp1795=)
n.76+9703T=
c.5480A= (p.Asp1827=)
17g.10392911C>ACA398092119MYH8,MYHASc.5383G>T (p.Asp1795Tyr)
n.76+9704C>A
c.5479G>T (p.Asp1827Tyr)
17g.10392911C=CA2247204896MYH8,MYHASc.5383G= (p.Asp1795=)
n.76+9704C=
c.5479G= (p.Asp1827=)
17g.10392911C>GCA398092124MYH8,MYHASc.5383G>C (p.Asp1795His)
n.76+9704C>G
c.5479G>C (p.Asp1827His)
17g.10392911C>TCA398092128MYH8,MYHASc.5383G>A (p.Asp1795Asn)
n.76+9704C>T
c.5479G>A (p.Asp1827Asn)
dbSNP gnomAD v4
17g.10392912C>ACA398092131MYH8,MYHASc.5382G>T (p.Lys1794Asn)
n.76+9705C>A
c.5478G>T (p.Lys1826Asn)
gnomAD v4
17g.10392912C=CA2247204911MYH8,MYHASc.5382G= (p.Lys1794=)
n.76+9705C=
c.5478G= (p.Lys1826=)
17g.10392912C>GCA398092133MYH8,MYHASc.5382G>C (p.Lys1794Asn)
n.76+9705C>G
c.5478G>C (p.Lys1826Asn)
17g.10392912C>TCA287717754MYH8,MYHASc.5382G>A (p.Lys1794=)
n.76+9705C>T
c.5478G>A (p.Lys1826=)
dbSNP
17g.10392913T>ACA398092140MYH8,MYHASc.5381A>T (p.Lys1794Met)
n.76+9706T>A
c.5477A>T (p.Lys1826Met)
17g.10392913T>CCA398092142MYH8,MYHASc.5381A>G (p.Lys1794Arg)
n.76+9706T>C
c.5477A>G (p.Lys1826Arg)
17g.10392913T>GCA398092145MYH8,MYHASc.5381A>C (p.Lys1794Thr)
n.76+9706T>G
c.5477A>C (p.Lys1826Thr)
17g.10392914T>ACA398092148MYH8,MYHASc.5380A>T (p.Lys1794Ter)
n.76+9707T>A
c.5476A>T (p.Lys1826Ter)
17g.10392914T>CCA398092150MYH8,MYHASc.5380A>G (p.Lys1794Glu)
n.76+9707T>C
c.5476A>G (p.Lys1826Glu)
dbSNP gnomAD v3 gnomAD v4
17g.10392914T>GCA398092155MYH8,MYHASc.5380A>C (p.Lys1794Gln)
n.76+9707T>G
c.5476A>C (p.Lys1826Gln)
17g.10392914T=CA2247204914MYH8,MYHASc.5380A= (p.Lys1794=)
n.76+9707T=
c.5476A= (p.Lys1826=)
17g.10392915C>ACA497837410MYH8,MYHASc.5379G>T (p.Val1793=)
n.76+9708C>A
c.5475G>T (p.Val1825=)
17g.10392915C>GCA497837411MYH8,MYHASc.5379G>C (p.Val1793=)
n.76+9708C>G
c.5475G>C (p.Val1825=)
17g.10392915C>TCA497837412MYH8,MYHASc.5379G>A (p.Val1793=)
n.76+9708C>T
c.5475G>A (p.Val1825=)
17g.10392916A=CA2247204916MYH8,MYHASc.5378T= (p.Val1793=)
n.76+9709A=
c.5474T= (p.Val1825=)
17g.10392916A>CCA398092163MYH8,MYHASc.5378T>G (p.Val1793Gly)
n.76+9709A>C
c.5474T>G (p.Val1825Gly)
dbSNP gnomAD v4
17g.10392916A>GCA398092161MYH8,MYHASc.5378T>C (p.Val1793Ala)
n.76+9709A>G
c.5474T>C (p.Val1825Ala)
17g.10392916A>TCA398092159MYH8,MYHASc.5378T>A (p.Val1793Glu)
n.76+9709A>T
c.5474T>A (p.Val1825Glu)
17g.10392917C>ACA398092169MYH8,MYHASc.5377G>T (p.Val1793Leu)
n.76+9710C>A
c.5473G>T (p.Val1825Leu)
gnomAD v4
17g.10392917C=CA2247204919MYH8,MYHASc.5377G= (p.Val1793=)
n.76+9710C=
c.5473G= (p.Val1825=)
17g.10392917C>GCA398092176MYH8,MYHASc.5377G>C (p.Val1793Leu)
n.76+9710C>G
c.5473G>C (p.Val1825Leu)
17g.10392917C>TCA398092172MYH8,MYHASc.5377G>A (p.Val1793Met)
n.76+9710C>T
c.5473G>A (p.Val1825Met)
dbSNP gnomAD v4 COSMIC
17g.10392918C>ACA287717759MYH8,MYHASc.5376G>T (p.Thr1792=)
n.76+9711C>A
c.5472G>T (p.Thr1824=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392918C=CA2247204923MYH8,MYHASc.5376G= (p.Thr1792=)
n.76+9711C=
c.5472G= (p.Thr1824=)
17g.10392918C>GCA497837413MYH8,MYHASc.5376G>C (p.Thr1792=)
n.76+9711C>G
c.5472G>C (p.Thr1824=)
17g.10392918C>TCA8387054MYH8,MYHASc.5376G>A (p.Thr1792=)
n.76+9711C>T
c.5472G>A (p.Thr1824=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.10392919G>ACA8387055MYH8,MYHASc.5375C>T (p.Thr1792Met)
n.76+9712G>A
c.5471C>T (p.Thr1824Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.10392919G>CCA398092190MYH8,MYHASc.5375C>G (p.Thr1792Arg)
n.76+9712G>C
c.5471C>G (p.Thr1824Arg)
17g.10392919G=CA2247204926MYH8,MYHASc.5375C= (p.Thr1792=)
n.76+9712G=
c.5471C= (p.Thr1824=)
17g.10392919G>TCA398092195MYH8,MYHASc.5375C>A (p.Thr1792Lys)
n.76+9712G>T
c.5471C>A (p.Thr1824Lys)
17g.10392920T>ACA398092200MYH8,MYHASc.5374A>T (p.Thr1792Ser)
n.76+9713T>A
c.5470A>T (p.Thr1824Ser)
17g.10392920T>CCA398092203MYH8,MYHASc.5374A>G (p.Thr1792Ala)
n.76+9713T>C
c.5470A>G (p.Thr1824Ala)
17g.10392920T>GCA398092207MYH8,MYHASc.5374A>C (p.Thr1792Pro)
n.76+9713T>G
c.5470A>C (p.Thr1824Pro)
17g.10392921C>ACA398092213MYH8,MYHASc.5373G>T (p.Gln1791His)
n.76+9714C>A
c.5469G>T (p.Gln1823His)
17g.10392921C>GCA398092217MYH8,MYHASc.5373G>C (p.Gln1791His)
n.76+9714C>G
c.5469G>C (p.Gln1823His)
17g.10392921C>TCA497837414MYH8,MYHASc.5373G>A (p.Gln1791=)
n.76+9714C>T
c.5469G>A (p.Gln1823=)
17g.10392922T>ACA398092227MYH8,MYHASc.5372A>T (p.Gln1791Leu)
n.76+9715T>A
c.5468A>T (p.Gln1823Leu)
17g.10392922T>CCA398092224MYH8,MYHASc.5372A>G (p.Gln1791Arg)
n.76+9715T>C
c.5468A>G (p.Gln1823Arg)
17g.10392922T>GCA398092219MYH8,MYHASc.5372A>C (p.Gln1791Pro)
n.76+9715T>G
c.5468A>C (p.Gln1823Pro)
17g.10392923G>ACA398092231MYH8,MYHASc.5371C>T (p.Gln1791Ter)
n.76+9716G>A
c.5467C>T (p.Gln1823Ter)
17g.10392923G>CCA398092234MYH8,MYHASc.5371C>G (p.Gln1791Glu)
n.76+9716G>C
c.5467C>G (p.Gln1823Glu)
17g.10392923G>TCA398092238MYH8,MYHASc.5371C>A (p.Gln1791Lys)
n.76+9716G>T
c.5467C>A (p.Gln1823Lys)
17g.10392924C>ACA398092242MYH8,MYHASc.5370G>T (p.Glu1790Asp)
n.76+9717C>A
c.5466G>T (p.Glu1822Asp)
17g.10392924C=CA2247204929MYH8,MYHASc.5370G= (p.Glu1790=)
n.76+9717C=
c.5466G= (p.Glu1822=)
17g.10392924C>GCA398092245MYH8,MYHASc.5370G>C (p.Glu1790Asp)
n.76+9717C>G
c.5466G>C (p.Glu1822Asp)
17g.10392924C>TCA497837465MYH8,MYHASc.5370G>A (p.Glu1790=)
n.76+9717C>T
c.5466G>A (p.Glu1822=)
dbSNP gnomAD v2 gnomAD v4
17g.10392925T>ACA398092249MYH8,MYHASc.5369A>T (p.Glu1790Val)
n.76+9718T>A
c.5465A>T (p.Glu1822Val)
17g.10392925T>CCA398092250MYH8,MYHASc.5369A>G (p.Glu1790Gly)
n.76+9718T>C
c.5465A>G (p.Glu1822Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392925T>GCA398092251MYH8,MYHASc.5369A>C (p.Glu1790Ala)
n.76+9718T>G
c.5465A>C (p.Glu1822Ala)
17g.10392925T=CA2247204933MYH8,MYHASc.5369A= (p.Glu1790=)
n.76+9718T=
c.5465A= (p.Glu1822=)
17g.10392926C>ACA398092253MYH8,MYHASc.5368G>T (p.Glu1790Ter)
n.76+9719C>A
c.5464G>T (p.Glu1822Ter)
17g.10392926C=CA2247204936MYH8,MYHASc.5368G= (p.Glu1790=)
n.76+9719C=
c.5464G= (p.Glu1822=)
17g.10392926C>GCA398092254MYH8,MYHASc.5368G>C (p.Glu1790Gln)
n.76+9719C>G
c.5464G>C (p.Glu1822Gln)
17g.10392926C>TCA398092255MYH8,MYHASc.5368G>A (p.Glu1790Lys)
n.76+9719C>T
c.5464G>A (p.Glu1822Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392927C>ACA497837466MYH8,MYHASc.5367G>T (p.Leu1789=)
n.76+9720C>A
c.5463G>T (p.Leu1821=)
17g.10392927C>GCA497837467MYH8,MYHASc.5367G>C (p.Leu1789=)
n.76+9720C>G
c.5463G>C (p.Leu1821=)
17g.10392927C>TCA497837468MYH8,MYHASc.5367G>A (p.Leu1789=)
n.76+9720C>T
c.5463G>A (p.Leu1821=)
17g.10392928A=CA2247204940MYH8,MYHASc.5366T= (p.Leu1789=)
n.76+9721A=
c.5462T= (p.Leu1821=)
17g.10392928A>CCA398092257MYH8,MYHASc.5366T>G (p.Leu1789Arg)
n.76+9721A>C
c.5462T>G (p.Leu1821Arg)
dbSNP
17g.10392928A>GCA398092258MYH8,MYHASc.5366T>C (p.Leu1789Pro)
n.76+9721A>G
c.5462T>C (p.Leu1821Pro)
17g.10392928A>TCA398092256MYH8,MYHASc.5366T>A (p.Leu1789Gln)
n.76+9721A>T
c.5462T>A (p.Leu1821Gln)
17g.10392929G>ACA497837469MYH8,MYHASc.5365C>T (p.Leu1789=)
n.76+9722G>A
c.5461C>T (p.Leu1821=)
17g.10392929G>CCA398092259MYH8,MYHASc.5365C>G (p.Leu1789Val)
n.76+9722G>C
c.5461C>G (p.Leu1821Val)
gnomAD v4
17g.10392929G>TCA398092261MYH8,MYHASc.5365C>A (p.Leu1789Met)
n.76+9722G>T
c.5461C>A (p.Leu1821Met)
17g.10392930G>ACA497837470MYH8,MYHASc.5364C>T (p.Asn1788=)
n.76+9723G>A
c.5460C>T (p.Asn1820=)
17g.10392930G>CCA398092266MYH8,MYHASc.5364C>G (p.Asn1788Lys)
n.76+9723G>C
c.5460C>G (p.Asn1820Lys)
17g.10392930G>TCA398092267MYH8,MYHASc.5364C>A (p.Asn1788Lys)
n.76+9723G>T
c.5460C>A (p.Asn1820Lys)
gnomAD v4
17g.10392930_10392933delinsGTTCCA2247204942MYH8,MYHASc.5361_5364delinsGAAC (p.Lys1787=)
n.76+9723_76+9726delinsGTTC
c.5457_5460delinsGAAC (p.Lys1819=)
17g.10392931T>ACA398092279MYH8,MYHASc.5363A>T (p.Asn1788Ile)
n.76+9724T>A
c.5459A>T (p.Asn1820Ile)
17g.10392931T>CCA398092277MYH8,MYHASc.5363A>G (p.Asn1788Ser)
n.76+9724T>C
c.5459A>G (p.Asn1820Ser)
17g.10392931T>GCA398092272MYH8,MYHASc.5363A>C (p.Asn1788Thr)
n.76+9724T>G
c.5459A>C (p.Asn1820Thr)
dbSNP
17g.10392931T=CA2247204943MYH8,MYHASc.5363A= (p.Asn1788=)
n.76+9724T=
c.5459A= (p.Asn1820=)
17g.10392937_10392939delCA8387056MYH8,MYHASc.5361_5363del (p.Lys1787del)
n.76+9730_76+9732del
c.5457_5459del (p.Lys1819del)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.10392932T>ACA398092284MYH8,MYHASc.5362A>T (p.Asn1788Tyr)
n.76+9725T>A
c.5458A>T (p.Asn1820Tyr)
17g.10392932T>CCA398092287MYH8,MYHASc.5362A>G (p.Asn1788Asp)
n.76+9725T>C
c.5458A>G (p.Asn1820Asp)
17g.10392932T>GCA398092290MYH8,MYHASc.5362A>C (p.Asn1788His)
n.76+9725T>G
c.5458A>C (p.Asn1820His)
17g.10392933C>ACA398092294MYH8,MYHASc.5361G>T (p.Lys1787Asn)
n.76+9726C>A
c.5457G>T (p.Lys1819Asn)
17g.10392933C>GCA398092296MYH8,MYHASc.5361G>C (p.Lys1787Asn)
n.76+9726C>G
c.5457G>C (p.Lys1819Asn)
COSMIC
17g.10392933C>TCA497837471MYH8,MYHASc.5361G>A (p.Lys1787=)
n.76+9726C>T
c.5457G>A (p.Lys1819=)
17g.10392934T>ACA398092299MYH8,MYHASc.5360A>T (p.Lys1787Met)
n.76+9727T>A
c.5456A>T (p.Lys1819Met)
17g.10392934T>CCA398092303MYH8,MYHASc.5360A>G (p.Lys1787Arg)
n.76+9727T>C
c.5456A>G (p.Lys1819Arg)
17g.10392934T>GCA398092302MYH8,MYHASc.5360A>C (p.Lys1787Thr)
n.76+9727T>G
c.5456A>C (p.Lys1819Thr)
17g.10392935T>ACA398092306MYH8,MYHASc.5359A>T (p.Lys1787Ter)
n.76+9728T>A
c.5455A>T (p.Lys1819Ter)
17g.10392935T>CCA398092308MYH8,MYHASc.5359A>G (p.Lys1787Glu)
n.76+9728T>C
c.5455A>G (p.Lys1819Glu)
17g.10392935T>GCA398092311MYH8,MYHASc.5359A>C (p.Lys1787Gln)
n.76+9728T>G
c.5455A>C (p.Lys1819Gln)
17g.10392936C>ACA398092315MYH8,MYHASc.5358G>T (p.Lys1786Asn)
n.76+9729C>A
c.5454G>T (p.Lys1818Asn)
17g.10392936C=CA2247204944MYH8,MYHASc.5358G= (p.Lys1786=)
n.76+9729C=
c.5454G= (p.Lys1818=)
17g.10392936C>GCA398092317MYH8,MYHASc.5358G>C (p.Lys1786Asn)
n.76+9729C>G
c.5454G>C (p.Lys1818Asn)
17g.10392936C>TCA8387057MYH8,MYHASc.5358G>A (p.Lys1786=)
n.76+9729C>T
c.5454G>A (p.Lys1818=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.10392937T>ACA398092326MYH8,MYHASc.5357A>T (p.Lys1786Met)
n.76+9730T>A
c.5453A>T (p.Lys1818Met)
17g.10392937T>CCA398092329MYH8,MYHASc.5357A>G (p.Lys1786Arg)
n.76+9730T>C
c.5453A>G (p.Lys1818Arg)
17g.10392937T>GCA398092332MYH8,MYHASc.5357A>C (p.Lys1786Thr)
n.76+9730T>G
c.5453A>C (p.Lys1818Thr)
17g.10392938T>ACA398092336MYH8,MYHASc.5356A>T (p.Lys1786Ter)
n.76+9731T>A
c.5452A>T (p.Lys1818Ter)
17g.10392938T>CCA398092339MYH8,MYHASc.5356A>G (p.Lys1786Glu)
n.76+9731T>C
c.5452A>G (p.Lys1818Glu)
17g.10392938T>GCA398092342MYH8,MYHASc.5356A>C (p.Lys1786Gln)
n.76+9731T>G
c.5452A>C (p.Lys1818Gln)
17g.10392939C>ACA398092349MYH8,MYHASc.5355G>T (p.Met1785Ile)
n.76+9732C>A
c.5451G>T (p.Met1817Ile)
17g.10392939C>GCA398092351MYH8,MYHASc.5355G>C (p.Met1785Ile)
n.76+9732C>G
c.5451G>C (p.Met1817Ile)
17g.10392939C>TCA398092347MYH8,MYHASc.5355G>A (p.Met1785Ile)
n.76+9732C>T
c.5451G>A (p.Met1817Ile)
17g.10392940A>CCA398092361MYH8,MYHASc.5354T>G (p.Met1785Arg)
n.76+9733A>C
c.5450T>G (p.Met1817Arg)
17g.10392940A>GCA398092355MYH8,MYHASc.5354T>C (p.Met1785Thr)
n.76+9733A>G
c.5450T>C (p.Met1817Thr)
dbSNP
17g.10392940A>TCA398092359MYH8,MYHASc.5354T>A (p.Met1785Lys)
n.76+9733A>T
c.5450T>A (p.Met1817Lys)
17g.10392941T>ACA398092364MYH8,MYHASc.5353A>T (p.Met1785Leu)
n.76+9734T>A
c.5449A>T (p.Met1817Leu)
gnomAD v4
17g.10392941T>CCA398092367MYH8,MYHASc.5353A>G (p.Met1785Val)
n.76+9734T>C
c.5449A>G (p.Met1817Val)
17g.10392941T>GCA398092371MYH8,MYHASc.5353A>C (p.Met1785Leu)
n.76+9734T>G
c.5449A>C (p.Met1817Leu)
17g.10392942C>ACA497837472MYH8,MYHASc.5352G>T (p.Arg1784=)
n.76+9735C>A
c.5448G>T (p.Arg1816=)
17g.10392942C=CA2247204947MYH8,MYHASc.5352G= (p.Arg1784=)
n.76+9735C=
c.5448G= (p.Arg1816=)
17g.10392942C>GCA8387058MYH8,MYHASc.5352G>C (p.Arg1784=)
n.76+9735C>G
c.5448G>C (p.Arg1816=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.10392942C>TCA497837473MYH8,MYHASc.5352G>A (p.Arg1784=)
n.76+9735C>T
c.5448G>A (p.Arg1816=)
dbSNP gnomAD v2 gnomAD v4
17g.10392943C>ACA398092382MYH8,MYHASc.5351G>T (p.Arg1784Leu)
n.76+9736C>A
c.5447G>T (p.Arg1816Leu)
17g.10392943C=CA2247204953MYH8,MYHASc.5351G= (p.Arg1784=)
n.76+9736C=
c.5447G= (p.Arg1816=)
17g.10392943C>GCA398092379MYH8,MYHASc.5351G>C (p.Arg1784Pro)
n.76+9736C>G
c.5447G>C (p.Arg1816Pro)
gnomAD v4
17g.10392943C>TCA8387059MYH8,MYHASc.5351G>A (p.Arg1784Gln)
n.76+9736C>T
c.5447G>A (p.Arg1816Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.10392944G>ACA398092387MYH8,MYHASc.5350C>T (p.Arg1784Trp)
n.76+9737G>A
c.5446C>T (p.Arg1816Trp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392944G>CCA207949MYH8,MYHASc.5350C>G (p.Arg1784Gly)
n.76+9737G>C
c.5446C>G (p.Arg1816Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.10392944G=CA2247204968MYH8,MYHASc.5350C= (p.Arg1784=)
n.76+9737G=
c.5446C= (p.Arg1816=)
17g.10392944G>TCA497837474MYH8,MYHASc.5350C>A (p.Arg1784=)
n.76+9737G>T
c.5446C>A (p.Arg1816=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392945C>ACA398092393MYH8,MYHASc.5349G>T (p.Glu1783Asp)
n.76+9738C>A
c.5445G>T (p.Glu1815Asp)
17g.10392945C=CA2247204979MYH8,MYHASc.5349G= (p.Glu1783=)
n.76+9738C=
c.5445G= (p.Glu1815=)
17g.10392945C>GCA398092396MYH8,MYHASc.5349G>C (p.Glu1783Asp)
n.76+9738C>G
c.5445G>C (p.Glu1815Asp)
17g.10392945C>TCA8387060MYH8,MYHASc.5349G>A (p.Glu1783=)
n.76+9738C>T
c.5445G>A (p.Glu1815=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.10392946T>ACA398092407MYH8,MYHASc.5348A>T (p.Glu1783Val)
n.76+9739T>A
c.5444A>T (p.Glu1815Val)
17g.10392946T>CCA398092403MYH8,MYHASc.5348A>G (p.Glu1783Gly)
n.76+9739T>C
c.5444A>G (p.Glu1815Gly)
17g.10392946T>GCA398092405MYH8,MYHASc.5348A>C (p.Glu1783Ala)
n.76+9739T>G
c.5444A>C (p.Glu1815Ala)
17g.10392947C>ACA398092409MYH8,MYHASc.5347G>T (p.Glu1783Ter)
n.76+9740C>A
c.5443G>T (p.Glu1815Ter)
17g.10392947C=CA2247204987MYH8,MYHASc.5347G= (p.Glu1783=)
n.76+9740C=
c.5443G= (p.Glu1815=)
17g.10392947C>GCA398092410MYH8,MYHASc.5347G>C (p.Glu1783Gln)
n.76+9740C>G
c.5443G>C (p.Glu1815Gln)
17g.10392947C>TCA398092411MYH8,MYHASc.5347G>A (p.Glu1783Lys)
n.76+9740C>T
c.5443G>A (p.Glu1815Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392948C>ACA497837475MYH8,MYHASc.5346G>T (p.Leu1782=)
n.76+9741C>A
c.5442G>T (p.Leu1814=)
17g.10392948C>GCA497837476MYH8,MYHASc.5346G>C (p.Leu1782=)
n.76+9741C>G
c.5442G>C (p.Leu1814=)
17g.10392948C>TCA497837477MYH8,MYHASc.5346G>A (p.Leu1782=)
n.76+9741C>T
c.5442G>A (p.Leu1814=)
17g.10392949A=CA2247204995MYH8,MYHASc.5345T= (p.Leu1782=)
n.76+9742A=
c.5441T= (p.Leu1814=)
17g.10392949A>CCA398092413MYH8,MYHASc.5345T>G (p.Leu1782Arg)
n.76+9742A>C
c.5441T>G (p.Leu1814Arg)
dbSNP gnomAD v2
17g.10392949A>GCA398092416MYH8,MYHASc.5345T>C (p.Leu1782Pro)
n.76+9742A>G
c.5441T>C (p.Leu1814Pro)
17g.10392949A>TCA398092419MYH8,MYHASc.5345T>A (p.Leu1782Gln)
n.76+9742A>T
c.5441T>A (p.Leu1814Gln)
17g.10392950G>ACA497837479MYH8,MYHASc.5344C>T (p.Leu1782=)
n.76+9743G>A
c.5440C>T (p.Leu1814=)
17g.10392950G>CCA398092420MYH8,MYHASc.5344C>G (p.Leu1782Val)
n.76+9743G>C
c.5440C>G (p.Leu1814Val)
17g.10392950G>TCA398092421MYH8,MYHASc.5344C>A (p.Leu1782Met)
n.76+9743G>T
c.5440C>A (p.Leu1814Met)
gnomAD v4
17g.10392951G>ACA497837480MYH8,MYHASc.5343C>T (p.His1781=)
n.76+9744G>A
c.5439C>T (p.His1813=)
COSMIC
17g.10392951G>CCA398092423MYH8,MYHASc.5343C>G (p.His1781Gln)
n.76+9744G>C
c.5439C>G (p.His1813Gln)
gnomAD v4
17g.10392951G>TCA398092425MYH8,MYHASc.5343C>A (p.His1781Gln)
n.76+9744G>T
c.5439C>A (p.His1813Gln)
17g.10392952T>ACA398092428MYH8,MYHASc.5342A>T (p.His1781Leu)
n.76+9745T>A
c.5438A>T (p.His1813Leu)
17g.10392952T>CCA398092431MYH8,MYHASc.5342A>G (p.His1781Arg)
n.76+9745T>C
c.5438A>G (p.His1813Arg)
17g.10392952T>GCA398092434MYH8,MYHASc.5342A>C (p.His1781Pro)
n.76+9745T>G
c.5438A>C (p.His1813Pro)
dbSNP
17g.10392952T=CA2247205002MYH8,MYHASc.5342A= (p.His1781=)
n.76+9745T=
c.5438A= (p.His1813=)
17g.10392953G>ACA398092437MYH8,MYHASc.5341C>T (p.His1781Tyr)
n.76+9746G>A
c.5437C>T (p.His1813Tyr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.10392953G>CCA398092442MYH8,MYHASc.5341C>G (p.His1781Asp)
n.76+9746G>C
c.5437C>G (p.His1813Asp)
17g.10392953G=CA2247205018MYH8,MYHASc.5341C= (p.His1781=)
n.76+9746G=
c.5437C= (p.His1813=)
17g.10392953G>TCA398092440MYH8,MYHASc.5341C>A (p.His1781Asn)
n.76+9746G>T
c.5437C>A (p.His1813Asn)
17g.10392955delCA2636104662MYH8,MYHASc.5341del (p.His1781ThrfsTer5)
n.76+9748del
c.5437del (p.His1813ThrfsTer5)
gnomAD v4
17g.10392954G>ACA497837483MYH8,MYHASc.5340C>T (p.Ala1780=)
n.76+9747G>A
c.5436C>T (p.Ala1812=)
17g.10392954G>CCA497837484MYH8,MYHASc.5340C>G (p.Ala1780=)
n.76+9747G>C
c.5436C>G (p.Ala1812=)
17g.10392954G>TCA497837486MYH8,MYHASc.5340C>A (p.Ala1780=)
n.76+9747G>T
c.5436C>A (p.Ala1812=)
17g.10392955G>ACA398092447MYH8,MYHASc.5339C>T (p.Ala1780Val)
n.76+9748G>A
c.5435C>T (p.Ala1812Val)
gnomAD v4
17g.10392955G>CCA398092449MYH8,MYHASc.5339C>G (p.Ala1780Gly)
n.76+9748G>C
c.5435C>G (p.Ala1812Gly)
17g.10392955G>TCA398092453MYH8,MYHASc.5339C>A (p.Ala1780Asp)
n.76+9748G>T
c.5435C>A (p.Ala1812Asp)
17g.10392956C>ACA398092456MYH8,MYHASc.5338G>T (p.Ala1780Ser)
n.76+9749C>A
c.5434G>T (p.Ala1812Ser)
17g.10392956C=CA2247205037MYH8,MYHASc.5338G= (p.Ala1780=)
n.76+9749C=
c.5434G= (p.Ala1812=)
17g.10392956C>GCA398092460MYH8,MYHASc.5338G>C (p.Ala1780Pro)
n.76+9749C>G
c.5434G>C (p.Ala1812Pro)
17g.10392956C>TCA8387061MYH8,MYHASc.5338G>A (p.Ala1780Thr)
n.76+9749C>T
c.5434G>A (p.Ala1812Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.10392957G>ACA8387062MYH8,MYHASc.5337C>T (p.Ser1779=)
n.76+9750G>A
c.5433C>T (p.Ser1811=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.10392957G>CCA398092469MYH8,MYHASc.5337C>G (p.Ser1779Arg)
n.76+9750G>C
c.5433C>G (p.Ser1811Arg)
17g.10392957G=CA2247205044MYH8,MYHASc.5337C= (p.Ser1779=)
n.76+9750G=
c.5433C= (p.Ser1811=)
17g.10392957G>TCA398092471MYH8,MYHASc.5337C>A (p.Ser1779Arg)
n.76+9750G>T
c.5433C>A (p.Ser1811Arg)
17g.10392958C>ACA398092476MYH8,MYHASc.5336G>T (p.Ser1779Ile)
n.76+9751C>A
c.5432G>T (p.Ser1811Ile)
17g.10392958C>GCA398092480MYH8,MYHASc.5336G>C (p.Ser1779Thr)
n.76+9751C>G
c.5432G>C (p.Ser1811Thr)
17g.10392958C>TCA398092482MYH8,MYHASc.5336G>A (p.Ser1779Asn)
n.76+9751C>T
c.5432G>A (p.Ser1811Asn)
gnomAD v4
17g.10392959T>ACA398092492MYH8,MYHASc.5335A>T (p.Ser1779Cys)
n.76+9752T>A
c.5431A>T (p.Ser1811Cys)
17g.10392959T>CCA8387063MYH8,MYHASc.5335A>G (p.Ser1779Gly)
n.76+9752T>C
c.5431A>G (p.Ser1811Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.10392959T>GCA398092489MYH8,MYHASc.5335A>C (p.Ser1779Arg)
n.76+9752T>G
c.5431A>C (p.Ser1811Arg)
17g.10392959T=CA2247205053MYH8,MYHASc.5335A= (p.Ser1779=)
n.76+9752T=
c.5431A= (p.Ser1811=)

Number of alleles fetched