Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47341257_47344691delCA913203384MYBPC3c.1091-1066_1791-12del
c.1073-1066_1773-12del
11g.47341969T>CCA676999161MYBPC3c.1790+22A>G (n.1790+22A>G)
c.1772+22A>G (n.1772+22A>G)
 dbSNP gnomAD v3 gnomAD v4
11g.47341969T=CA1969335248MYBPC3c.1790+22A= (n.1790+22A=)
c.1772+22A= (n.1772+22A=)
11g.47341970C>TCA2613401441MYBPC3c.1790+21G>A (n.1790+21G>A)
c.1772+21G>A (n.1772+21G>A)
 gnomAD v4
11g.47341971C>GCA2574815923MYBPC3c.1790+20G>C (n.1790+20G>C)
c.1772+20G>C (n.1772+20G>C)
 ClinVar
11g.47341972A=CA1969335249MYBPC3c.1790+19T= (n.1790+19T=)
c.1772+19T= (n.1772+19T=)
11g.47341972A>GCA599374393MYBPC3c.1790+19T>C (n.1790+19T>C)
c.1772+19T>C (n.1772+19T>C)
 dbSNP gnomAD v2 gnomAD v4
11g.47341973C>TCA2596115346MYBPC3c.1790+18G>A (n.1790+18G>A)
c.1772+18G>A (n.1772+18G>A)
 dbSNP gnomAD v3 gnomAD v4
11g.47341974C>GCA2574815926MYBPC3c.1790+17G>C (n.1790+17G>C)
c.1772+17G>C (n.1772+17G>C)
 gnomAD v4
11g.47341975T>CCA2613401471MYBPC3c.1790+16A>G (n.1790+16A>G)
c.1772+16A>G (n.1772+16A>G)
 gnomAD v4
11g.47341975T>GCA2613401467MYBPC3c.1790+16A>C (n.1790+16A>C)
c.1772+16A>C (n.1772+16A>C)
 gnomAD v4
11g.47341975dupCA2613401474MYBPC3c.1790+16dup (n.1790+16dup)
c.1772+16dup (n.1772+16dup)
 gnomAD v4
11g.47341976G=CA1969335251MYBPC3c.1790+15C= (n.1790+15C=)
c.1772+15C= (n.1772+15C=)
11g.47341976dupCA2613401484MYBPC3c.1790+15dup (n.1790+15dup)
c.1772+15dup (n.1772+15dup)
 gnomAD v4
11g.47341976_47341977insGCCAACACACTCACCCA1969335252MYBPC3c.1790+14_1790+15insGGTGAGTGTGTTGGC (n.1790+14_1790+15insGGTGAGTGTGTTGGC)
c.1772+14_1772+15insGGTGAGTGTGTTGGC (n.1772+14_1772+15insGGTGAGTGTGTTGGC)
 dbSNP
11g.47341977C=CA1969335253MYBPC3c.1790+14G= (n.1790+14G=)
c.1772+14G= (n.1772+14G=)
11g.47341977C>GCA221694847MYBPC3c.1790+14G>C (n.1790+14G>C)
c.1772+14G>C (n.1772+14G>C)
 dbSNP
11g.47341978C=CA1969335255MYBPC3c.1790+13G= (n.1790+13G=)
c.1772+13G= (n.1772+13G=)
11g.47341978C>GCA599374394MYBPC3c.1790+13G>C (n.1790+13G>C)
c.1772+13G>C (n.1772+13G>C)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47341978C>TCA078290MYBPC3c.1790+13G>A (n.1790+13G>A)
c.1772+13G>A (n.1772+13G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341978_47341979insAACACACTCACCGCCA2613401503MYBPC3c.1790+13_1790+14insCGGTGAGTGTGTTG (n.1790+13_1790+14insCGGTGAGTGTGTTG)
c.1772+13_1772+14insCGGTGAGTGTGTTG (n.1772+13_1772+14insCGGTGAGTGTGTTG)
 gnomAD v4
11g.47341979C>GCA2574815938MYBPC3c.1790+12G>C (n.1790+12G>C)
c.1772+12G>C (n.1772+12G>C)
 ClinVar
11g.47341979C>TCA2613401512MYBPC3c.1790+12G>A (n.1790+12G>A)
c.1772+12G>A (n.1772+12G>A)
 gnomAD v4
11g.47341980T>CCA599374395MYBPC3c.1790+11A>G (n.1790+11A>G)
c.1772+11A>G (n.1772+11A>G)
 dbSNP gnomAD v2 gnomAD v4
11g.47341980T=CA1969335256MYBPC3c.1790+11A= (n.1790+11A=)
c.1772+11A= (n.1772+11A=)
11g.47341982delCA2613401542MYBPC3c.1790+9del (n.1790+9del)
c.1772+9del (n.1772+9del)
 gnomAD v4
11g.47341985_47341986delCA2580615686MYBPC3c.1790+8_1790+9del (n.1790+8_1790+9del)
c.1772+8_1772+9del (n.1772+8_1772+9del)
 ClinVar dbSNP
11g.47341983A=CA1969335257MYBPC3c.1790+8T= (n.1790+8T=)
c.1772+8T= (n.1772+8T=)
11g.47341983A>GCA2499220971MYBPC3c.1790+8T>C (n.1790+8T>C)
c.1772+8T>C (n.1772+8T>C)
 ClinVar dbSNP
11g.47341983A>TCA599374396MYBPC3c.1790+8T>A (n.1790+8T>A)
c.1772+8T>A (n.1772+8T>A)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47341984C>ACA2613401551MYBPC3c.1790+7G>T (n.1790+7G>T)
c.1772+7G>T (n.1772+7G>T)
 gnomAD v4
11g.47341984C=CA1969335258MYBPC3c.1790+7G= (n.1790+7G=)
c.1772+7G= (n.1772+7G=)
11g.47341984C>TCA011126MYBPC3c.1790+7G>A (n.1790+7G>A)
c.1772+7G>A (n.1772+7G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341985A=CA1969335259MYBPC3c.1790+6T= (n.1790+6T=)
c.1772+6T= (n.1772+6T=)
11g.47341985A>GCA2613401567MYBPC3c.1790+6T>C (n.1790+6T>C)
c.1772+6T>C (n.1772+6T>C)
 gnomAD v4
11g.47341985A>TCA676999173MYBPC3c.1790+6T>A (n.1790+6T>A)
c.1772+6T>A (n.1772+6T>A)
 dbSNP
11g.47341986C=CA1969335261MYBPC3c.1790+5G= (n.1790+5G=)
c.1772+5G= (n.1772+5G=)
11g.47341986C>GCA2695212782MYBPC3c.1790+5G>C (n.1790+5G>C)
c.1772+5G>C (n.1772+5G>C)
11g.47341986C>TCA011121MYBPC3c.1790+5G>A (n.1790+5G>A)
c.1772+5G>A (n.1772+5G>A)
 ClinVar dbSNP
11g.47341988C>ACA2613401570MYBPC3c.1790+3G>T (n.1790+3G>T)
c.1772+3G>T (n.1772+3G>T)
 gnomAD v4
11g.47341988C=CA1969335262MYBPC3c.1790+3G= (n.1790+3G=)
c.1772+3G= (n.1772+3G=)
11g.47341988C>TCA221694866MYBPC3c.1790+3G>A (n.1790+3G>A)
c.1772+3G>A (n.1772+3G>A)
 ClinVar dbSNP gnomAD v4
11g.47341989A>CCA380324150MYBPC3c.1790+2T>G (n.1790+2T>G)
c.1772+2T>G (n.1772+2T>G)
11g.47341989A>GCA380324149MYBPC3c.1790+2T>C (n.1790+2T>C)
c.1772+2T>C (n.1772+2T>C)
11g.47341989A>TCA380324148MYBPC3c.1790+2T>A (n.1790+2T>A)
c.1772+2T>A (n.1772+2T>A)
11g.47341990C>ACA380324152MYBPC3c.1790+1G>T (n.1790+1G>T)
c.1772+1G>T (n.1772+1G>T)
11g.47341990C=CA1969335264MYBPC3c.1790+1G= (n.1790+1G=)
c.1772+1G= (n.1772+1G=)
11g.47341990C>GCA380324151MYBPC3c.1790+1G>C (n.1790+1G>C)
c.1772+1G>C (n.1772+1G>C)
 ClinVar
11g.47341990C>TCA380324153MYBPC3c.1790+1G>A (n.1790+1G>A)
c.1772+1G>A (n.1772+1G>A)
 ClinVar dbSNP
11g.47341991C>ACA380324154MYBPC3c.1790G>T (p.Arg597Leu)
c.1772G>T (p.Arg591Leu)
11g.47341991C=CA1969335266MYBPC3c.1790G= (p.Arg597=)
c.1772G= (p.Arg591=)
11g.47341991C>GCA380324155MYBPC3c.1790G>C (p.Arg597Pro)
c.1772G>C (p.Arg591Pro)
11g.47341991C>TCA011138MYBPC3c.1790G>A (p.Arg597Gln)
c.1772G>A (p.Arg591Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341992G>ACA011112MYBPC3c.1789C>T (p.Arg597Trp)
c.1771C>T (p.Arg591Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341992G>CCA380324156MYBPC3c.1789C>G (p.Arg597Gly)
c.1771C>G (p.Arg591Gly)
11g.47341992G=CA1969335268MYBPC3c.1789C= (p.Arg597=)
c.1771C= (p.Arg591=)
11g.47341992G>TCA474218683MYBPC3c.1789C>A (p.Arg597=)
c.1771C>A (p.Arg591=)
11g.47341993C>ACA474218684MYBPC3c.1788G>T (p.Gly596=)
c.1770G>T (p.Gly590=)
11g.47341993C=CA1969335269MYBPC3c.1788G= (p.Gly596=)
c.1770G= (p.Gly590=)
11g.47341993C>GCA046709MYBPC3c.1788G>C (p.Gly596=)
c.1770G>C (p.Gly590=)
11g.47341993C>TCA474218685MYBPC3c.1788G>A (p.Gly596=)
c.1770G>A (p.Gly590=)
 dbSNP
11g.47341994C>ACA380324157MYBPC3c.1787G>T (p.Gly596Val)
c.1769G>T (p.Gly590Val)
11g.47341994C>GCA380324158MYBPC3c.1787G>C (p.Gly596Ala)
c.1769G>C (p.Gly590Ala)
11g.47341994C>TCA046677MYBPC3c.1787G>A (p.Gly596Glu)
c.1769G>A (p.Gly590Glu)
11g.47341995C>ACA380324159MYBPC3c.1786G>T (p.Gly596Trp)
c.1768G>T (p.Gly590Trp)
11g.47341995C=CA1969335271MYBPC3c.1786G= (p.Gly596=)
c.1768G= (p.Gly590=)
11g.47341995C>GCA380324160MYBPC3c.1786G>C (p.Gly596Arg)
c.1768G>C (p.Gly590Arg)
 gnomAD v4
11g.47341995C>TCA011102MYBPC3c.1786G>A (p.Gly596Arg)
c.1768G>A (p.Gly590Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341996delCA2613401593MYBPC3c.1785del (p.Ile595MetfsTer7)
c.1767del (p.Ile589MetfsTer7)
 gnomAD v4
11g.47341996G>ACA078286MYBPC3c.1785C>T (p.Ile595=)
c.1767C>T (p.Ile589=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341996G>CCA380324161MYBPC3c.1785C>G (p.Ile595Met)
c.1767C>G (p.Ile589Met)
11g.47341996G=CA1969335274MYBPC3c.1785C= (p.Ile595=)
c.1767C= (p.Ile589=)
11g.47341996G>TCA474218686MYBPC3c.1785C>A (p.Ile595=)
c.1767C>A (p.Ile589=)
 ClinVar dbSNP gnomAD v4
11g.47341997A=CA1969335275MYBPC3c.1784T= (p.Ile595=)
c.1766T= (p.Ile589=)
11g.47341997A>CCA380324164MYBPC3c.1784T>G (p.Ile595Ser)
c.1766T>G (p.Ile589Ser)
11g.47341997A>GCA380324162MYBPC3c.1784T>C (p.Ile595Thr)
c.1766T>C (p.Ile589Thr)
11g.47341997A>TCA380324163MYBPC3c.1784T>A (p.Ile595Asn)
c.1766T>A (p.Ile589Asn)
 dbSNP
11g.47341998T>ACA380324165MYBPC3c.1783A>T (p.Ile595Phe)
c.1765A>T (p.Ile589Phe)
11g.47341998T>CCA011094MYBPC3c.1783A>G (p.Ile595Val)
c.1765A>G (p.Ile589Val)
 ClinVar dbSNP gnomAD v4
11g.47341998T>GCA380324166MYBPC3c.1783A>C (p.Ile595Leu)
c.1765A>C (p.Ile589Leu)
11g.47341998T=CA1969335276MYBPC3c.1783A= (p.Ile595=)
c.1765A= (p.Ile589=)
11g.47341999G>ACA046608MYBPC3c.1782C>T (p.His594=)
c.1764C>T (p.His588=)
 dbSNP gnomAD v2 gnomAD v4
11g.47341999G>CCA380324167MYBPC3c.1782C>G (p.His594Gln)
c.1764C>G (p.His588Gln)
11g.47341999G=CA1969335277MYBPC3c.1782C= (p.His594=)
c.1764C= (p.His588=)
11g.47341999G>TCA380324168MYBPC3c.1782C>A (p.His594Gln)
c.1764C>A (p.His588Gln)
 gnomAD v4
11g.47342000T>ACA380324169MYBPC3c.1781A>T (p.His594Leu)
c.1763A>T (p.His588Leu)
11g.47342000T>CCA380324170MYBPC3c.1781A>G (p.His594Arg)
c.1763A>G (p.His588Arg)
11g.47342000T>GCA380324171MYBPC3c.1781A>C (p.His594Pro)
c.1763A>C (p.His588Pro)
11g.47342001G>ACA380324172MYBPC3c.1780C>T (p.His594Tyr)
c.1762C>T (p.His588Tyr)
 ClinVar dbSNP
11g.47342001G>CCA380324173MYBPC3c.1780C>G (p.His594Asp)
c.1762C>G (p.His588Asp)
11g.47342001G>TCA380324174MYBPC3c.1780C>A (p.His594Asn)
c.1762C>A (p.His588Asn)
11g.47342003delCA2695212783MYBPC3c.1780del (p.His594ThrfsTer8)
c.1762del (p.His588ThrfsTer8)
11g.47342002G>ACA474218687MYBPC3c.1779C>T (p.Ser593=)
c.1761C>T (p.Ser587=)
 gnomAD v4
11g.47342002G>CCA474218688MYBPC3c.1779C>G (p.Ser593=)
c.1761C>G (p.Ser587=)
11g.47342002G>TCA046698MYBPC3c.1779C>A (p.Ser593=)
c.1761C>A (p.Ser587=)
 gnomAD v4
11g.47342003G>ACA011087MYBPC3c.1778C>T (p.Ser593Phe)
c.1760C>T (p.Ser587Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342003G>CCA380324176MYBPC3c.1778C>G (p.Ser593Cys)
c.1760C>G (p.Ser587Cys)
11g.47342003G=CA1969335279MYBPC3c.1778C= (p.Ser593=)
c.1760C= (p.Ser587=)
11g.47342003G>TCA380324175MYBPC3c.1778C>A (p.Ser593Tyr)
c.1760C>A (p.Ser587Tyr)
11g.47342003_47342004delinsGACA1969335281MYBPC3c.1777_1778delinsTC (p.Ser593=)
c.1759_1760delinsTC (p.Ser587=)
11g.47342003_47342005delinsGACCA1969335280MYBPC3c.1776_1778delinsGTC (p.Val592=)
c.1758_1760delinsGTC (p.Val586=)
11g.47342004delCA1969335282MYBPC3c.1777del (p.Ser593ProfsTer9)
c.1759del (p.Ser587ProfsTer9)
 ClinVar dbSNP gnomAD v4
11g.47342004A>CCA380324177MYBPC3c.1777T>G (p.Ser593Ala)
c.1759T>G (p.Ser587Ala)
11g.47342004A>GCA380324178MYBPC3c.1777T>C (p.Ser593Pro)
c.1759T>C (p.Ser587Pro)
11g.47342004A>TCA380324179MYBPC3c.1777T>A (p.Ser593Thr)
c.1759T>A (p.Ser587Thr)
11g.47342006_47342007delCA011070MYBPC3c.1776_1777del (p.Ser593ProfsTer11)
c.1758_1759del (p.Ser587ProfsTer11)
 ClinVar dbSNP
11g.47342005C>ACA474218689MYBPC3c.1776G>T (p.Val592=)
c.1758G>T (p.Val586=)
11g.47342005C=CA1969335284MYBPC3c.1776G= (p.Val592=)
c.1758G= (p.Val586=)
11g.47342005C>GCA474218690MYBPC3c.1776G>C (p.Val592=)
c.1758G>C (p.Val586=)
11g.47342005C>TCA011078MYBPC3c.1776G>A (p.Val592=)
c.1758G>A (p.Val586=)
 ClinVar dbSNP
11g.47342006A=CA1969335286MYBPC3c.1775T= (p.Val592=)
c.1757T= (p.Val586=)
11g.47342006A>CCA380324180MYBPC3c.1775T>G (p.Val592Gly)
c.1757T>G (p.Val586Gly)
11g.47342006A>GCA10581159MYBPC3c.1775T>C (p.Val592Ala)
c.1757T>C (p.Val586Ala)
 ClinVar dbSNP
11g.47342006A>TCA380324181MYBPC3c.1775T>A (p.Val592Glu)
c.1757T>A (p.Val586Glu)
11g.47342006dupCA2580084225MYBPC3c.1775dup (p.Ser593ValfsTer12)
c.1757dup (p.Ser587ValfsTer12)
 ClinVar
11g.47342007C>ACA380324182MYBPC3c.1774G>T (p.Val592Leu)
c.1756G>T (p.Val586Leu)
 gnomAD v4
11g.47342007C=CA1969335288MYBPC3c.1774G= (p.Val592=)
c.1756G= (p.Val586=)
11g.47342007C>GCA380324183MYBPC3c.1774G>C (p.Val592Leu)
c.1756G>C (p.Val586Leu)
11g.47342007C>TCA380324184MYBPC3c.1774G>A (p.Val592Met)
c.1756G>A (p.Val586Met)
 dbSNP gnomAD v3 gnomAD v4
11g.47342008C>ACA078282MYBPC3c.1773G>T (p.Lys591Asn)
c.1755G>T (p.Lys585Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47342008C=CA1969335290MYBPC3c.1773G= (p.Lys591=)
c.1755G= (p.Lys585=)
11g.47342008C>GCA380324185MYBPC3c.1773G>C (p.Lys591Asn)
c.1755G>C (p.Lys585Asn)
11g.47342008C>TCA474218691MYBPC3c.1773G>A (p.Lys591=)
c.1755G>A (p.Lys585=)
 dbSNP gnomAD v4
11g.47342009T>ACA380324188MYBPC3c.1772A>T (p.Lys591Met)
c.1754A>T (p.Lys585Met)
11g.47342009T>CCA380324186MYBPC3c.1772A>G (p.Lys591Arg)
c.1754A>G (p.Lys585Arg)
 gnomAD v4
11g.47342009T>GCA380324187MYBPC3c.1772A>C (p.Lys591Thr)
c.1754A>C (p.Lys585Thr)
11g.47342010T>ACA380324189MYBPC3c.1771A>T (p.Lys591Ter)
c.1753A>T (p.Lys585Ter)
11g.47342010T>CCA380324190MYBPC3c.1771A>G (p.Lys591Glu)
c.1753A>G (p.Lys585Glu)
11g.47342010T>GCA380324191MYBPC3c.1771A>C (p.Lys591Gln)
c.1753A>C (p.Lys585Gln)
11g.47342011T>ACA474218692MYBPC3c.1770A>T (p.Ile590=)
c.1752A>T (p.Ile584=)
11g.47342011T>CCA380324192MYBPC3c.1770A>G (p.Ile590Met)
c.1752A>G (p.Ile584Met)
 gnomAD v4
11g.47342011T>GCA474218695MYBPC3c.1770A>C (p.Ile590=)
c.1752A>C (p.Ile584=)
11g.47342012A=CA1969335291MYBPC3c.1769T= (p.Ile590=)
c.1751T= (p.Ile584=)
11g.47342012A>CCA380324193MYBPC3c.1769T>G (p.Ile590Arg)
c.1751T>G (p.Ile584Arg)
11g.47342012A>GCA380324194MYBPC3c.1769T>C (p.Ile590Thr)
c.1751T>C (p.Ile584Thr)
 dbSNP gnomAD v2 gnomAD v4
11g.47342012A>TCA380324195MYBPC3c.1769T>A (p.Ile590Lys)
c.1751T>A (p.Ile584Lys)
 gnomAD v4
11g.47342013T>ACA380324196MYBPC3c.1768A>T (p.Ile590Leu)
c.1750A>T (p.Ile584Leu)
11g.47342013T>CCA221694896MYBPC3c.1768A>G (p.Ile590Val)
c.1750A>G (p.Ile584Val)
 ClinVar dbSNP gnomAD v4
11g.47342013T>GCA380324197MYBPC3c.1768A>C (p.Ile590Leu)
c.1750A>C (p.Ile584Leu)
11g.47342013T=CA1969335293MYBPC3c.1768A= (p.Ile590=)
c.1750A= (p.Ile584=)
11g.47342014G>ACA474218704MYBPC3c.1767C>T (p.Arg589=)
c.1749C>T (p.Arg583=)
 dbSNP
11g.47342014G>CCA474218703MYBPC3c.1767C>G (p.Arg589=)
c.1749C>G (p.Arg583=)
11g.47342014G=CA1969335294MYBPC3c.1767C= (p.Arg589=)
c.1749C= (p.Arg583=)
11g.47342014G>TCA474218701MYBPC3c.1767C>A (p.Arg589=)
c.1749C>A (p.Arg583=)
11g.47342015C>ACA380324198MYBPC3c.1766G>T (p.Arg589Leu)
c.1748G>T (p.Arg583Leu)
 ClinVar
11g.47342015C=CA1969335296MYBPC3c.1766G= (p.Arg589=)
c.1748G= (p.Arg583=)
11g.47342015C>GCA380324199MYBPC3c.1766G>C (p.Arg589Pro)
c.1748G>C (p.Arg583Pro)
11g.47342015C>TCA011050MYBPC3c.1766G>A (p.Arg589His)
c.1748G>A (p.Arg583His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342016G>ACA380324201MYBPC3c.1765C>T (p.Arg589Cys)
c.1747C>T (p.Arg583Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47342016G>CCA380324202MYBPC3c.1765C>G (p.Arg589Gly)
c.1747C>G (p.Arg583Gly)
 dbSNP gnomAD v4
11g.47342016G=CA1969335298MYBPC3c.1765C= (p.Arg589=)
c.1747C= (p.Arg583=)
11g.47342016G>TCA380324200MYBPC3c.1765C>A (p.Arg589Ser)
c.1747C>A (p.Arg583Ser)
11g.47342017G>ACA078279MYBPC3c.1764C>T (p.Ser588=)
c.1746C>T (p.Ser582=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342017G>CCA380324204MYBPC3c.1764C>G (p.Ser588Arg)
c.1746C>G (p.Ser582Arg)
11g.47342017G=CA1969335299MYBPC3c.1764C= (p.Ser588=)
c.1746C= (p.Ser582=)
11g.47342017G>TCA380324203MYBPC3c.1764C>A (p.Ser588Arg)
c.1746C>A (p.Ser582Arg)
11g.47342018C>ACA380324205MYBPC3c.1763G>T (p.Ser588Ile)
c.1745G>T (p.Ser582Ile)
11g.47342018C>GCA380324206MYBPC3c.1763G>C (p.Ser588Thr)
c.1745G>C (p.Ser582Thr)
11g.47342018C>TCA046574MYBPC3c.1763G>A (p.Ser588Asn)
c.1745G>A (p.Ser582Asn)
11g.47342019T>ACA380324207MYBPC3c.1762A>T (p.Ser588Cys)
c.1744A>T (p.Ser582Cys)
11g.47342019T>CCA380324208MYBPC3c.1762A>G (p.Ser588Gly)
c.1744A>G (p.Ser582Gly)
 ClinVar
11g.47342019T>GCA380324209MYBPC3c.1762A>C (p.Ser588Arg)
c.1744A>C (p.Ser582Arg)
11g.47342020G>ACA046556MYBPC3c.1761C>T (p.Asp587=)
c.1743C>T (p.Asp581=)
 ClinVar
11g.47342020G>CCA380324210MYBPC3c.1761C>G (p.Asp587Glu)
c.1743C>G (p.Asp581Glu)
 dbSNP gnomAD v4
11g.47342020G=CA1969335301MYBPC3c.1761C= (p.Asp587=)
c.1743C= (p.Asp581=)
11g.47342020G>TCA380324211MYBPC3c.1761C>A (p.Asp587Glu)
c.1743C>A (p.Asp581Glu)
11g.47342021T>ACA380324212MYBPC3c.1760A>T (p.Asp587Val)
c.1742A>T (p.Asp581Val)
11g.47342021T>CCA380324213MYBPC3c.1760A>G (p.Asp587Gly)
c.1742A>G (p.Asp581Gly)
11g.47342021T>GCA380324214MYBPC3c.1760A>C (p.Asp587Ala)
c.1742A>C (p.Asp581Ala)
11g.47342022C>ACA380324215MYBPC3c.1759G>T (p.Asp587Tyr)
c.1741G>T (p.Asp581Tyr)
 gnomAD v4
11g.47342022C=CA1969335303MYBPC3c.1759G= (p.Asp587=)
c.1741G= (p.Asp581=)
11g.47342022C>GCA380324216MYBPC3c.1759G>C (p.Asp587His)
c.1741G>C (p.Asp581His)
 ClinVar dbSNP
11g.47342022C>TCA011034MYBPC3c.1759G>A (p.Asp587Asn)
c.1741G>A (p.Asp581Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342023G>ACA011029MYBPC3c.1758C>T (p.Pro586=)
c.1740C>T (p.Pro580=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342023G>CCA474218728MYBPC3c.1758C>G (p.Pro586=)
c.1740C>G (p.Pro580=)
11g.47342023G=CA1969335305MYBPC3c.1758C= (p.Pro586=)
c.1740C= (p.Pro580=)
11g.47342023G>TCA474218730MYBPC3c.1758C>A (p.Pro586=)
c.1740C>A (p.Pro580=)
11g.47342024G>ACA380324217MYBPC3c.1757C>T (p.Pro586Leu)
c.1739C>T (p.Pro580Leu)
11g.47342024G>CCA380324219MYBPC3c.1757C>G (p.Pro586Arg)
c.1739C>G (p.Pro580Arg)
11g.47342024G>TCA380324218MYBPC3c.1757C>A (p.Pro586His)
c.1739C>A (p.Pro580His)
11g.47342025G>ACA380324220MYBPC3c.1756C>T (p.Pro586Ser)
c.1738C>T (p.Pro580Ser)
11g.47342025G>CCA380324221MYBPC3c.1756C>G (p.Pro586Ala)
c.1738C>G (p.Pro580Ala)
 dbSNP
11g.47342025G=CA1969335307MYBPC3c.1756C= (p.Pro586=)
c.1738C= (p.Pro580=)
11g.47342025G>TCA380324222MYBPC3c.1756C>A (p.Pro586Thr)
c.1738C>A (p.Pro580Thr)
11g.47342025_47342026delinsGCCA1969335308MYBPC3c.1755_1756delinsGC (p.Val585=)
c.1737_1738delinsGC (p.Val579=)
11g.47342026delCA915948155MYBPC3c.1755del (p.Asp587ThrfsTer4)
c.1737del (p.Asp581ThrfsTer4)
 ClinVar dbSNP
11g.47342026C>ACA474218737MYBPC3c.1755G>T (p.Val585=)
c.1737G>T (p.Val579=)
11g.47342026C>GCA474218739MYBPC3c.1755G>C (p.Val585=)
c.1737G>C (p.Val579=)
11g.47342026C>TCA474218740MYBPC3c.1755G>A (p.Val585=)
c.1737G>A (p.Val579=)
 ClinVar
11g.47342027A>CCA380324223MYBPC3c.1754T>G (p.Val585Gly)
c.1736T>G (p.Val579Gly)
11g.47342027A>GCA380324224MYBPC3c.1754T>C (p.Val585Ala)
c.1736T>C (p.Val579Ala)
11g.47342027A>TCA380324225MYBPC3c.1754T>A (p.Val585Glu)
c.1736T>A (p.Val579Glu)
11g.47342028C>ACA380324226MYBPC3c.1753G>T (p.Val585Leu)
c.1735G>T (p.Val579Leu)
 gnomAD v4
11g.47342028C>GCA380324227MYBPC3c.1753G>C (p.Val585Leu)
c.1735G>C (p.Val579Leu)
11g.47342028C>TCA380324228MYBPC3c.1753G>A (p.Val585Met)
c.1735G>A (p.Val579Met)
11g.47342029C>ACA474218752MYBPC3c.1752G>T (p.Leu584=)
c.1734G>T (p.Leu578=)
11g.47342029C=CA1969335311MYBPC3c.1752G= (p.Leu584=)
c.1734G= (p.Leu578=)
11g.47342029C>GCA474218754MYBPC3c.1752G>C (p.Leu584=)
c.1734G>C (p.Leu578=)
11g.47342029C>TCA474218756MYBPC3c.1752G>A (p.Leu584=)
c.1734G>A (p.Leu578=)
 dbSNP
11g.47342030A>CCA380324231MYBPC3c.1751T>G (p.Leu584Arg)
c.1733T>G (p.Leu578Arg)
11g.47342030A>GCA380324230MYBPC3c.1751T>C (p.Leu584Pro)
c.1733T>C (p.Leu578Pro)
11g.47342030A>TCA380324229MYBPC3c.1751T>A (p.Leu584Gln)
c.1733T>A (p.Leu578Gln)
11g.47342031G>ACA474218763MYBPC3c.1750C>T (p.Leu584=)
c.1732C>T (p.Leu578=)
 ClinVar dbSNP
11g.47342031G>CCA380324232MYBPC3c.1750C>G (p.Leu584Val)
c.1732C>G (p.Leu578Val)
11g.47342031G=CA1969335312MYBPC3c.1750C= (p.Leu584=)
c.1732C= (p.Leu578=)
11g.47342031G>TCA380324233MYBPC3c.1750C>A (p.Leu584Met)
c.1732C>A (p.Leu578Met)
11g.47342032C>ACA380324234MYBPC3c.1749G>T (p.Glu583Asp)
c.1731G>T (p.Glu577Asp)
11g.47342032C=CA1969335313MYBPC3c.1749G= (p.Glu583=)
c.1731G= (p.Glu577=)
11g.47342032C>GCA380324235MYBPC3c.1749G>C (p.Glu583Asp)
c.1731G>C (p.Glu577Asp)
11g.47342032C>TCA221694946MYBPC3c.1749G>A (p.Glu583=)
c.1731G>A (p.Glu577=)
 dbSNP gnomAD v2 gnomAD v4
11g.47342033T>ACA380324236MYBPC3c.1748A>T (p.Glu583Val)
c.1730A>T (p.Glu577Val)
 dbSNP gnomAD v2 gnomAD v4
11g.47342033T>CCA380324237MYBPC3c.1748A>G (p.Glu583Gly)
c.1730A>G (p.Glu577Gly)
11g.47342033T>GCA380324238MYBPC3c.1748A>C (p.Glu583Ala)
c.1730A>C (p.Glu577Ala)
11g.47342033T=CA1969335315MYBPC3c.1748A= (p.Glu583=)
c.1730A= (p.Glu577=)
11g.47342034C>ACA380324239MYBPC3c.1747G>T (p.Glu583Ter)
c.1729G>T (p.Glu577Ter)
11g.47342034C=CA1969335317MYBPC3c.1747G= (p.Glu583=)
c.1729G= (p.Glu577=)
11g.47342034C>GCA380324240MYBPC3c.1747G>C (p.Glu583Gln)
c.1729G>C (p.Glu577Gln)
11g.47342034C>TCA380324241MYBPC3c.1747G>A (p.Glu583Lys)
c.1729G>A (p.Glu577Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47342035C>ACA380324242MYBPC3c.1746G>T (p.Lys582Asn)
c.1728G>T (p.Lys576Asn)
11g.47342035C>GCA380324243MYBPC3c.1746G>C (p.Lys582Asn)
c.1728G>C (p.Lys576Asn)
11g.47342035C>TCA474218775MYBPC3c.1746G>A (p.Lys582=)
c.1728G>A (p.Lys576=)
11g.47342039_47342047delCA2613401771MYBPC3c.1738_1746del (p.Asn580_Lys582del)
c.1720_1728del (p.Asn574_Lys576del)
 gnomAD v4
11g.47342036T>ACA380324244MYBPC3c.1745A>T (p.Lys582Met)
c.1727A>T (p.Lys576Met)
11g.47342036T>CCA380324246MYBPC3c.1745A>G (p.Lys582Arg)
c.1727A>G (p.Lys576Arg)
11g.47342036T>GCA380324245MYBPC3c.1745A>C (p.Lys582Thr)
c.1727A>C (p.Lys576Thr)
11g.47342037T>ACA380324247MYBPC3c.1744A>T (p.Lys582Ter)
c.1726A>T (p.Lys576Ter)
11g.47342037T>CCA380324248MYBPC3c.1744A>G (p.Lys582Glu)
c.1726A>G (p.Lys576Glu)
11g.47342037T>GCA380324249MYBPC3c.1744A>C (p.Lys582Gln)
c.1726A>C (p.Lys576Gln)
11g.47342038C>ACA474218783MYBPC3c.1743G>T (p.Gly581=)
c.1725G>T (p.Gly575=)
11g.47342038C>GCA474218784MYBPC3c.1743G>C (p.Gly581=)
c.1725G>C (p.Gly575=)
11g.47342038C>TCA474218786MYBPC3c.1743G>A (p.Gly581=)
c.1725G>A (p.Gly575=)
 ClinVar dbSNP
11g.47342039C>ACA380324250MYBPC3c.1742G>T (p.Gly581Val)
c.1724G>T (p.Gly575Val)
11g.47342039C=CA1969335319MYBPC3c.1742G= (p.Gly581=)
c.1724G= (p.Gly575=)
11g.47342039C>GCA380324251MYBPC3c.1742G>C (p.Gly581Ala)
c.1724G>C (p.Gly575Ala)
11g.47342039C>TCA380324252MYBPC3c.1742G>A (p.Gly581Glu)
c.1724G>A (p.Gly575Glu)
 dbSNP
11g.47342040C>ACA380324253MYBPC3c.1741G>T (p.Gly581Trp)
c.1723G>T (p.Gly575Trp)
11g.47342040C>GCA380324254MYBPC3c.1741G>C (p.Gly581Arg)
c.1723G>C (p.Gly575Arg)
11g.47342040C>TCA380324255MYBPC3c.1741G>A (p.Gly581Arg)
c.1723G>A (p.Gly575Arg)
11g.47342041A>CCA380324256MYBPC3c.1740T>G (p.Asn580Lys)
c.1722T>G (p.Asn574Lys)
11g.47342041A>GCA474218793MYBPC3c.1740T>C (p.Asn580=)
c.1722T>C (p.Asn574=)
 ClinVar gnomAD v4
11g.47342041A>TCA380324257MYBPC3c.1740T>A (p.Asn580Lys)
c.1722T>A (p.Asn574Lys)
11g.47342042T>ACA380324259MYBPC3c.1739A>T (p.Asn580Ile)
c.1721A>T (p.Asn574Ile)
11g.47342042T>CCA380324260MYBPC3c.1739A>G (p.Asn580Ser)
c.1721A>G (p.Asn574Ser)
 gnomAD v4
11g.47342042T>GCA380324258MYBPC3c.1739A>C (p.Asn580Thr)
c.1721A>C (p.Asn574Thr)
11g.47342043T>ACA380324261MYBPC3c.1738A>T (p.Asn580Tyr)
c.1720A>T (p.Asn574Tyr)
11g.47342043T>CCA380324262MYBPC3c.1738A>G (p.Asn580Asp)
c.1720A>G (p.Asn574Asp)
11g.47342043T>GCA380324263MYBPC3c.1738A>C (p.Asn580His)
c.1720A>C (p.Asn574His)
11g.47342044C>ACA380324264MYBPC3c.1737G>T (p.Lys579Asn)
c.1719G>T (p.Lys573Asn)
11g.47342044C>GCA380324265MYBPC3c.1737G>C (p.Lys579Asn)
c.1719G>C (p.Lys573Asn)
11g.47342044C>TCA474218802MYBPC3c.1737G>A (p.Lys579=)
c.1719G>A (p.Lys573=)
11g.47342045T>ACA380324268MYBPC3c.1736A>T (p.Lys579Met)
c.1718A>T (p.Lys573Met)
11g.47342045T>CCA380324267MYBPC3c.1736A>G (p.Lys579Arg)
c.1718A>G (p.Lys573Arg)
 gnomAD v4
11g.47342045T>GCA380324266MYBPC3c.1736A>C (p.Lys579Thr)
c.1718A>C (p.Lys573Thr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47342045T=CA1969335321MYBPC3c.1736A= (p.Lys579=)
c.1718A= (p.Lys573=)
11g.47342046T>ACA380324269MYBPC3c.1735A>T (p.Lys579Ter)
c.1717A>T (p.Lys573Ter)
11g.47342046T>CCA380324270MYBPC3c.1735A>G (p.Lys579Glu)
c.1717A>G (p.Lys573Glu)
11g.47342046T>GCA380324271MYBPC3c.1735A>C (p.Lys579Gln)
c.1717A>C (p.Lys573Gln)
11g.47342046_47342047delinsTCCA1969335322MYBPC3c.1734_1735delinsGA (p.Leu578=)
c.1716_1717delinsGA (p.Leu572=)
11g.47342047delCA011021MYBPC3c.1734del (p.Lys579ArgfsTer12)
c.1716del (p.Lys573ArgfsTer12)
 ClinVar dbSNP
11g.47342047C>ACA474218814MYBPC3c.1734G>T (p.Leu578=)
c.1716G>T (p.Leu572=)
11g.47342047C>GCA474218809MYBPC3c.1734G>C (p.Leu578=)
c.1716G>C (p.Leu572=)
11g.47342047C>TCA474218812MYBPC3c.1734G>A (p.Leu578=)
c.1716G>A (p.Leu572=)
 gnomAD v4 COSMIC COSMIC
11g.47342048A>CCA380324272MYBPC3c.1733T>G (p.Leu578Arg)
c.1715T>G (p.Leu572Arg)
11g.47342048A>GCA380324273MYBPC3c.1733T>C (p.Leu578Pro)
c.1715T>C (p.Leu572Pro)
11g.47342048A>TCA380324274MYBPC3c.1733T>A (p.Leu578Gln)
c.1715T>A (p.Leu572Gln)
11g.47342049G>ACA078276MYBPC3c.1732C>T (p.Leu578=)
c.1714C>T (p.Leu572=)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.47342049G>CCA380324276MYBPC3c.1732C>G (p.Leu578Val)
c.1714C>G (p.Leu572Val)
11g.47342049G=CA1969335325MYBPC3c.1732C= (p.Leu578=)
c.1714C= (p.Leu572=)
11g.47342049G>TCA380324275MYBPC3c.1732C>A (p.Leu578Met)
c.1714C>A (p.Leu572Met)
11g.47342050C>ACA380324277MYBPC3c.1731G>T (p.Trp577Cys)
c.1713G>T (p.Trp571Cys)
11g.47342050C=CA1969335327MYBPC3c.1731G= (p.Trp577=)
c.1713G= (p.Trp571=)
11g.47342050C>GCA380324278MYBPC3c.1731G>C (p.Trp577Cys)
c.1713G>C (p.Trp571Cys)
11g.47342050C>TCA011017MYBPC3c.1731G>A (p.Trp577Ter)
c.1713G>A (p.Trp571Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47342050_47342052delinsCCACA1969335328MYBPC3c.1729_1731delinsTGG (p.Trp577=)
c.1711_1713delinsTGG (p.Trp571=)
11g.47342051C>ACA380324279MYBPC3c.1730G>T (p.Trp577Leu)
c.1712G>T (p.Trp571Leu)
11g.47342051C=CA1969335330MYBPC3c.1730G= (p.Trp577=)
c.1712G= (p.Trp571=)
11g.47342051C>GCA380324280MYBPC3c.1730G>C (p.Trp577Ser)
c.1712G>C (p.Trp571Ser)
11g.47342051C>TCA380324281MYBPC3c.1730G>A (p.Trp577Ter)
c.1712G>A (p.Trp571Ter)
 ClinVar dbSNP
11g.47342056_47342057delCA891842476MYBPC3c.1729_1730del (p.Trp577AlafsTer27)
c.1711_1712del (p.Trp571AlafsTer27)
 ClinVar dbSNP
11g.47342052A>CCA380324282MYBPC3c.1729T>G (p.Trp577Gly)
c.1711T>G (p.Trp571Gly)
11g.47342052A>GCA380324283MYBPC3c.1729T>C (p.Trp577Arg)
c.1711T>C (p.Trp571Arg)
11g.47342052A>TCA380324284MYBPC3c.1729T>A (p.Trp577Arg)
c.1711T>A (p.Trp571Arg)
11g.47342053C>ACA474218831MYBPC3c.1728G>T (p.Val576=)
c.1710G>T (p.Val570=)
11g.47342053C>GCA474218833MYBPC3c.1728G>C (p.Val576=)
c.1710G>C (p.Val570=)
11g.47342053C>TCA474218836MYBPC3c.1728G>A (p.Val576=)
c.1710G>A (p.Val570=)
11g.47342054A>CCA380324285MYBPC3c.1727T>G (p.Val576Gly)
c.1709T>G (p.Val570Gly)
11g.47342054A>GCA380324286MYBPC3c.1727T>C (p.Val576Ala)
c.1709T>C (p.Val570Ala)
11g.47342054A>TCA380324287MYBPC3c.1727T>A (p.Val576Glu)
c.1709T>A (p.Val570Glu)
11g.47342055C>ACA380324288MYBPC3c.1726G>T (p.Val576Leu)
c.1708G>T (p.Val570Leu)
11g.47342055C=CA1969335332MYBPC3c.1726G= (p.Val576=)
c.1708G= (p.Val570=)
11g.47342055C>GCA380324289MYBPC3c.1726G>C (p.Val576Leu)
c.1708G>C (p.Val570Leu)
11g.47342055C>TCA078274MYBPC3c.1726G>A (p.Val576Met)
c.1708G>A (p.Val570Met)
 dbSNP ExAC gnomAD v2
11g.47342056A>CCA474218844MYBPC3c.1725T>G (p.Gly575=)
c.1707T>G (p.Gly569=)
11g.47342056A>GCA474218842MYBPC3c.1725T>C (p.Gly575=)
c.1707T>C (p.Gly569=)
11g.47342056A>TCA474218841MYBPC3c.1725T>A (p.Gly575=)
c.1707T>A (p.Gly569=)
11g.47342057C>ACA380324290MYBPC3c.1724G>T (p.Gly575Val)
c.1706G>T (p.Gly569Val)
 dbSNP gnomAD v4
11g.47342057C=CA1969335333MYBPC3c.1724G= (p.Gly575=)
c.1706G= (p.Gly569=)
11g.47342057C>GCA380324291MYBPC3c.1724G>C (p.Gly575Ala)
c.1706G>C (p.Gly569Ala)
11g.47342057C>TCA380324292MYBPC3c.1724G>A (p.Gly575Asp)
c.1706G>A (p.Gly569Asp)
11g.47342060delCA2739270440MYBPC3c.1724del (p.Gly575ValfsTer4)
c.1706del (p.Gly569ValfsTer4)
 ClinVar
11g.47342058C>ACA380324293MYBPC3c.1723G>T (p.Gly575Cys)
c.1705G>T (p.Gly569Cys)
11g.47342058C>GCA380324294MYBPC3c.1723G>C (p.Gly575Arg)
c.1705G>C (p.Gly569Arg)
11g.47342058C>TCA046514MYBPC3c.1723G>A (p.Gly575Ser)
c.1705G>A (p.Gly569Ser)
 COSMIC COSMIC
11g.47342059C>ACA474218855MYBPC3c.1722G>T (p.Arg574=)
c.1704G>T (p.Arg568=)
11g.47342059C>GCA474218857MYBPC3c.1722G>C (p.Arg574=)
c.1704G>C (p.Arg568=)
11g.47342059C>TCA474218859MYBPC3c.1722G>A (p.Arg574=)
c.1704G>A (p.Arg568=)
 COSMIC COSMIC
11g.47342060C>ACA380324296MYBPC3c.1721G>T (p.Arg574Leu)
c.1703G>T (p.Arg568Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47342060C=CA1969335336MYBPC3c.1721G= (p.Arg574=)
c.1703G= (p.Arg568=)
11g.47342060C>GCA380324295MYBPC3c.1721G>C (p.Arg574Pro)
c.1703G>C (p.Arg568Pro)
 dbSNP gnomAD v2 gnomAD v4
11g.47342060C>TCA011002MYBPC3c.1721G>A (p.Arg574Gln)
c.1703G>A (p.Arg568Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342061G>ACA010995MYBPC3c.1720C>T (p.Arg574Trp)
c.1702C>T (p.Arg568Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342061G>CCA380324297MYBPC3c.1720C>G (p.Arg574Gly)
c.1702C>G (p.Arg568Gly)
 dbSNP
11g.47342061G=CA1969335339MYBPC3c.1720C= (p.Arg574=)
c.1702C= (p.Arg568=)
11g.47342061G>TCA010986MYBPC3c.1720C>A (p.Arg574=)
c.1702C>A (p.Arg568=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342062A=CA1969335344MYBPC3c.1719T= (p.Val573=)
c.1701T= (p.Val567=)
11g.47342062A>CCA010977MYBPC3c.1719T>G (p.Val573=)
c.1701T>G (p.Val567=)
 ClinVar dbSNP
11g.47342062A>GCA474218868MYBPC3c.1719T>C (p.Val573=)
c.1701T>C (p.Val567=)
 ClinVar dbSNP
11g.47342062A>TCA010969MYBPC3c.1719T>A (p.Val573=)
c.1701T>A (p.Val567=)
 ClinVar dbSNP gnomAD v4
11g.47342063A>CCA380324298MYBPC3c.1718T>G (p.Val573Gly)
c.1700T>G (p.Val567Gly)
11g.47342063A>GCA380324300MYBPC3c.1718T>C (p.Val573Ala)
c.1700T>C (p.Val567Ala)
11g.47342063A>TCA380324299MYBPC3c.1718T>A (p.Val573Asp)
c.1700T>A (p.Val567Asp)
11g.47342064C>ACA380324301MYBPC3c.1717G>T (p.Val573Phe)
c.1699G>T (p.Val567Phe)
11g.47342064C>GCA380324302MYBPC3c.1717G>C (p.Val573Leu)
c.1699G>C (p.Val567Leu)
11g.47342064C>TCA380324303MYBPC3c.1717G>A (p.Val573Ile)
c.1699G>A (p.Val567Ile)
 ClinVar
11g.47342065A=CA1969335347MYBPC3c.1716T= (p.Asn572=)
c.1698T= (p.Asn566=)
11g.47342065A>CCA380324304MYBPC3c.1716T>G (p.Asn572Lys)
c.1698T>G (p.Asn566Lys)
11g.47342065A>GCA474218889MYBPC3c.1716T>C (p.Asn572=)
c.1698T>C (p.Asn566=)
 ClinVar dbSNP gnomAD v4
11g.47342065A>TCA380324305MYBPC3c.1716T>A (p.Asn572Lys)
c.1698T>A (p.Asn566Lys)
 dbSNP gnomAD v2
11g.47342066T>ACA380324306MYBPC3c.1715A>T (p.Asn572Ile)
c.1697A>T (p.Asn566Ile)
 dbSNP gnomAD v2 gnomAD v4
11g.47342066T>CCA380324307MYBPC3c.1715A>G (p.Asn572Ser)
c.1697A>G (p.Asn566Ser)
11g.47342066T>GCA380324308MYBPC3c.1715A>C (p.Asn572Thr)
c.1697A>C (p.Asn566Thr)
11g.47342066T=CA1969335349MYBPC3c.1715A= (p.Asn572=)
c.1697A= (p.Asn566=)
11g.47342067T>ACA380324309MYBPC3c.1714A>T (p.Asn572Tyr)
c.1696A>T (p.Asn566Tyr)
11g.47342067T>CCA380324310MYBPC3c.1714A>G (p.Asn572Asp)
c.1696A>G (p.Asn566Asp)
 ClinVar
11g.47342067T>GCA380324311MYBPC3c.1714A>C (p.Asn572His)
c.1696A>C (p.Asn566His)
11g.47342068C>ACA380324312MYBPC3c.1713G>T (p.Glu571Asp)
c.1695G>T (p.Glu565Asp)
11g.47342068C=CA1969335350MYBPC3c.1713G= (p.Glu571=)
c.1695G= (p.Glu565=)
11g.47342068C>GCA380324313MYBPC3c.1713G>C (p.Glu571Asp)
c.1695G>C (p.Glu565Asp)
11g.47342068C>TCA16613619MYBPC3c.1713G>A (p.Glu571=)
c.1695G>A (p.Glu565=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47342069T>ACA380324314MYBPC3c.1712A>T (p.Glu571Val)
c.1694A>T (p.Glu565Val)
11g.47342069T>CCA380324316MYBPC3c.1712A>G (p.Glu571Gly)
c.1694A>G (p.Glu565Gly)
11g.47342069T>GCA380324315MYBPC3c.1712A>C (p.Glu571Ala)
c.1694A>C (p.Glu565Ala)

Number of alleles fetched