Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47337768_47337769delinsTGCA1969331609MYBPC3c.2334_2335delinsCA (p.Pro778=)
c.2316_2317delinsCA (p.Pro772=)
c.2253_2254delinsCA (p.Pro751=)
11g.47337769G>ACA474216451MYBPC3c.2334C>T (p.Pro778=)
c.2316C>T (p.Pro772=)
c.2253C>T (p.Pro751=)
ClinVar dbSNP gnomAD v4
11g.47337769G>CCA474216454MYBPC3c.2334C>G (p.Pro778=)
c.2316C>G (p.Pro772=)
c.2253C>G (p.Pro751=)
11g.47337769G=CA1969331611MYBPC3c.2334C= (p.Pro778=)
c.2316C= (p.Pro772=)
c.2253C= (p.Pro751=)
11g.47337769G>TCA474216457MYBPC3c.2334C>A (p.Pro778=)
c.2316C>A (p.Pro772=)
c.2253C>A (p.Pro751=)
gnomAD v4
11g.47337773dupCA1969331610MYBPC3c.2334dup (p.Lys779GlnfsTer?)
c.2334dup (p.Lys779GlnfsTer29)
c.2316dup (p.Lys773GlnfsTer?)
c.2253dup (p.Lys752GlnfsTer?)
ClinVar dbSNP
11g.47337773delCA16042829MYBPC3c.2334del (p.Lys779ArgfsTer?)
c.2316del (p.Lys773ArgfsTer?)
c.2253del (p.Lys752ArgfsTer?)
ClinVar dbSNP gnomAD v4
11g.47337771_47337773delCA2613392572MYBPC3c.2332_2334del (p.Pro778del)
c.2314_2316del (p.Pro772del)
c.2251_2253del (p.Pro751del)
gnomAD v4
11g.47337770G>ACA380319044MYBPC3c.2333C>T (p.Pro778Leu)
c.2315C>T (p.Pro772Leu)
c.2252C>T (p.Pro751Leu)
dbSNP gnomAD v2
11g.47337770G>CCA380319045MYBPC3c.2333C>G (p.Pro778Arg)
c.2315C>G (p.Pro772Arg)
c.2252C>G (p.Pro751Arg)
11g.47337770G=CA1969331612MYBPC3c.2333C= (p.Pro778=)
c.2315C= (p.Pro772=)
c.2252C= (p.Pro751=)
11g.47337770G>TCA380319048MYBPC3c.2333C>A (p.Pro778His)
c.2315C>A (p.Pro772His)
c.2252C>A (p.Pro751His)
gnomAD v4
11g.47337771G>ACA380319054MYBPC3c.2332C>T (p.Pro778Ser)
c.2314C>T (p.Pro772Ser)
c.2251C>T (p.Pro751Ser)
gnomAD v4
11g.47337771G>CCA380319049MYBPC3c.2332C>G (p.Pro778Ala)
c.2314C>G (p.Pro772Ala)
c.2251C>G (p.Pro751Ala)
11g.47337771G>TCA380319051MYBPC3c.2332C>A (p.Pro778Thr)
c.2314C>A (p.Pro772Thr)
c.2251C>A (p.Pro751Thr)
gnomAD v4
11g.47337772G>ACA474216477MYBPC3c.2331C>T (p.Ala777=)
c.2313C>T (p.Ala771=)
c.2250C>T (p.Ala750=)
11g.47337772G>CCA474216479MYBPC3c.2331C>G (p.Ala777=)
c.2313C>G (p.Ala771=)
c.2250C>G (p.Ala750=)
11g.47337772G>TCA474216481MYBPC3c.2331C>A (p.Ala777=)
c.2313C>A (p.Ala771=)
c.2250C>A (p.Ala750=)
gnomAD v4
11g.47337773G>ACA078651MYBPC3c.2330C>T (p.Ala777Val)
c.2312C>T (p.Ala771Val)
c.2249C>T (p.Ala750Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337773G>CCA380319058MYBPC3c.2330C>G (p.Ala777Gly)
c.2312C>G (p.Ala771Gly)
c.2249C>G (p.Ala750Gly)
11g.47337773G=CA1969331613MYBPC3c.2330C= (p.Ala777=)
c.2312C= (p.Ala771=)
c.2249C= (p.Ala750=)
11g.47337773G>TCA380319062MYBPC3c.2330C>A (p.Ala777Asp)
c.2312C>A (p.Ala771Asp)
c.2249C>A (p.Ala750Asp)
gnomAD v4
11g.47337774C>ACA380319066MYBPC3c.2329G>T (p.Ala777Ser)
c.2311G>T (p.Ala771Ser)
c.2248G>T (p.Ala750Ser)
gnomAD v4
11g.47337774C>GCA380319069MYBPC3c.2329G>C (p.Ala777Pro)
c.2311G>C (p.Ala771Pro)
c.2248G>C (p.Ala750Pro)
gnomAD v4
11g.47337774C>TCA380319072MYBPC3c.2329G>A (p.Ala777Thr)
c.2311G>A (p.Ala771Thr)
c.2248G>A (p.Ala750Thr)
dbSNP
11g.47337775dupCA2573051240MYBPC3c.2329dup (p.Ala777GlyfsTer?)
c.2311dup (p.Ala771GlyfsTer?)
c.2248dup (p.Ala750GlyfsTer?)
11g.47337775C>ACA474216491MYBPC3c.2328G>T (p.Ala776=)
c.2310G>T (p.Ala770=)
c.2247G>T (p.Ala749=)
gnomAD v4
11g.47337775C=CA1969331614MYBPC3c.2328G= (p.Ala776=)
c.2310G= (p.Ala770=)
c.2247G= (p.Ala749=)
11g.47337775C>GCA474216493MYBPC3c.2328G>C (p.Ala776=)
c.2310G>C (p.Ala770=)
c.2247G>C (p.Ala749=)
11g.47337775C>TCA474216495MYBPC3c.2328G>A (p.Ala776=)
c.2310G>A (p.Ala770=)
c.2247G>A (p.Ala749=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337776G>ACA049319MYBPC3c.2327C>T (p.Ala776Val)
c.2309C>T (p.Ala770Val)
c.2246C>T (p.Ala749Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337776G>CCA380319085MYBPC3c.2327C>G (p.Ala776Gly)
c.2309C>G (p.Ala770Gly)
c.2246C>G (p.Ala749Gly)
11g.47337776G=CA1969331615MYBPC3c.2327C= (p.Ala776=)
c.2309C= (p.Ala770=)
c.2246C= (p.Ala749=)
11g.47337776G>TCA380319089MYBPC3c.2327C>A (p.Ala776Glu)
c.2309C>A (p.Ala770Glu)
c.2246C>A (p.Ala749Glu)
gnomAD v4
11g.47337777C>ACA380319093MYBPC3c.2326G>T (p.Ala776Ser)
c.2308G>T (p.Ala770Ser)
c.2245G>T (p.Ala749Ser)
gnomAD v4
11g.47337777C=CA1969331616MYBPC3c.2326G= (p.Ala776=)
c.2308G= (p.Ala770=)
c.2245G= (p.Ala749=)
11g.47337777C>GCA380319095MYBPC3c.2326G>C (p.Ala776Pro)
c.2308G>C (p.Ala770Pro)
c.2245G>C (p.Ala749Pro)
11g.47337777C>TCA380319099MYBPC3c.2326G>A (p.Ala776Thr)
c.2308G>A (p.Ala770Thr)
c.2245G>A (p.Ala749Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47337778A>CCA474216506MYBPC3c.2325T>G (p.Pro775=)
c.2307T>G (p.Pro769=)
c.2244T>G (p.Pro748=)
11g.47337778A>GCA474216510MYBPC3c.2325T>C (p.Pro775=)
c.2307T>C (p.Pro769=)
c.2244T>C (p.Pro748=)
gnomAD v4
11g.47337778A>TCA474216508MYBPC3c.2325T>A (p.Pro775=)
c.2307T>A (p.Pro769=)
c.2244T>A (p.Pro748=)
gnomAD v4
11g.47337779G>ACA380319110MYBPC3c.2324C>T (p.Pro775Leu)
c.2306C>T (p.Pro769Leu)
c.2243C>T (p.Pro748Leu)
gnomAD v4
11g.47337779G>CCA012122MYBPC3c.2324C>G (p.Pro775Arg)
c.2306C>G (p.Pro769Arg)
c.2243C>G (p.Pro748Arg)
ClinVar dbSNP gnomAD v4
11g.47337779G=CA1969331617MYBPC3c.2324C= (p.Pro775=)
c.2306C= (p.Pro769=)
c.2243C= (p.Pro748=)
11g.47337779G>TCA380319105MYBPC3c.2324C>A (p.Pro775His)
c.2306C>A (p.Pro769His)
c.2243C>A (p.Pro748His)
gnomAD v4
11g.47337780G>ACA380319115MYBPC3c.2323C>T (p.Pro775Ser)
c.2305C>T (p.Pro769Ser)
c.2242C>T (p.Pro748Ser)
gnomAD v4
11g.47337780G>CCA380319122MYBPC3c.2323C>G (p.Pro775Ala)
c.2305C>G (p.Pro769Ala)
c.2242C>G (p.Pro748Ala)
11g.47337780G>TCA380319118MYBPC3c.2323C>A (p.Pro775Thr)
c.2305C>A (p.Pro769Thr)
c.2242C>A (p.Pro748Thr)
gnomAD v4
11g.47337781T>ACA474216515MYBPC3c.2322A>T (p.Ala774=)
c.2304A>T (p.Ala768=)
c.2241A>T (p.Ala747=)
11g.47337781T>CCA474216517MYBPC3c.2322A>G (p.Ala774=)
c.2304A>G (p.Ala768=)
c.2241A>G (p.Ala747=)
gnomAD v4

Number of alleles fetched