Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47330388_47335387delCA2740090117
11g.47332259_47335041delCA2580084187MYBPC3c.2905+1_3628-1del
c.2887+1_3610-1del
c.2824+1_3547-1del
ClinVar
11g.47332677_47333963delCA2573051316MYBPC3c.2956_3519del
c.2938_3501del
c.2875_3438del
ClinVar
11g.47332675_47335092delCA2573051317MYBPC3c.2855_3518del
c.2837_3500del
c.2774_3437del
ClinVar
11g.47332894_47332897delinsAAGTCA1969334688MYBPC3c.3407_3410delinsACTT (p.Tyr1136=)
c.3389_3392delinsACTT (p.Tyr1130=)
c.3326_3329delinsACTT (p.Tyr1109=)
11g.47332900_47332902delCA014090MYBPC3c.3407_3409del (p.Tyr1136del)
c.3389_3391del (p.Tyr1130del)
c.3326_3328del (p.Tyr1109del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332896G>ACA079354MYBPC3c.3408C>T (p.Tyr1136=)
c.3390C>T (p.Tyr1130=)
c.3327C>T (p.Tyr1109=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47332896G>CCA380313523MYBPC3c.3408C>G (p.Tyr1136Ter)
c.3390C>G (p.Tyr1130Ter)
c.3327C>G (p.Tyr1109Ter)
ClinVar dbSNP
11g.47332896G=CA1969334691MYBPC3c.3408C= (p.Tyr1136=)
c.3390C= (p.Tyr1130=)
c.3327C= (p.Tyr1109=)
11g.47332896G>TCA014095MYBPC3c.3408C>A (p.Tyr1136Ter)
c.3390C>A (p.Tyr1130Ter)
c.3327C>A (p.Tyr1109Ter)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47332897T>ACA380313529MYBPC3c.3407A>T (p.Tyr1136Phe)
c.3389A>T (p.Tyr1130Phe)
c.3326A>T (p.Tyr1109Phe)
11g.47332897T>CCA380313532MYBPC3c.3407A>G (p.Tyr1136Cys)
c.3389A>G (p.Tyr1130Cys)
c.3326A>G (p.Tyr1109Cys)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47332897T>GCA380313535MYBPC3c.3407A>C (p.Tyr1136Ser)
c.3389A>C (p.Tyr1130Ser)
c.3326A>C (p.Tyr1109Ser)
11g.47332897T=CA1969334695MYBPC3c.3407A= (p.Tyr1136=)
c.3389A= (p.Tyr1130=)
c.3326A= (p.Tyr1109=)
11g.47332898A>CCA380313539MYBPC3c.3406T>G (p.Tyr1136Asp)
c.3388T>G (p.Tyr1130Asp)
c.3325T>G (p.Tyr1109Asp)
11g.47332898A>GCA380313544MYBPC3c.3406T>C (p.Tyr1136His)
c.3388T>C (p.Tyr1130His)
c.3325T>C (p.Tyr1109His)
gnomAD v4
11g.47332898A>TCA380313541MYBPC3c.3406T>A (p.Tyr1136Asn)
c.3388T>A (p.Tyr1130Asn)
c.3325T>A (p.Tyr1109Asn)
11g.47332899G>ACA053815MYBPC3c.3405C>T (p.Tyr1135=)
c.3387C>T (p.Tyr1129=)
c.3324C>T (p.Tyr1108=)
ClinVar gnomAD v4
11g.47332899G>CCA380313547MYBPC3c.3405C>G (p.Tyr1135Ter)
c.3387C>G (p.Tyr1129Ter)
c.3324C>G (p.Tyr1108Ter)
11g.47332899G>TCA380313549MYBPC3c.3405C>A (p.Tyr1135Ter)
c.3387C>A (p.Tyr1129Ter)
c.3324C>A (p.Tyr1108Ter)
gnomAD v4
11g.47332900T>ACA380313554MYBPC3c.3404A>T (p.Tyr1135Phe)
c.3386A>T (p.Tyr1129Phe)
c.3323A>T (p.Tyr1108Phe)
11g.47332900T>CCA380313557MYBPC3c.3404A>G (p.Tyr1135Cys)
c.3386A>G (p.Tyr1129Cys)
c.3323A>G (p.Tyr1108Cys)
11g.47332900T>GCA380313559MYBPC3c.3404A>C (p.Tyr1135Ser)
c.3386A>C (p.Tyr1129Ser)
c.3323A>C (p.Tyr1108Ser)
11g.47332901A>CCA380313564MYBPC3c.3403T>G (p.Tyr1135Asp)
c.3385T>G (p.Tyr1129Asp)
c.3322T>G (p.Tyr1108Asp)
11g.47332901A>GCA380313567MYBPC3c.3403T>C (p.Tyr1135His)
c.3385T>C (p.Tyr1129His)
c.3322T>C (p.Tyr1108His)
11g.47332901A>TCA380313569MYBPC3c.3403T>A (p.Tyr1135Asn)
c.3385T>A (p.Tyr1129Asn)
c.3322T>A (p.Tyr1108Asn)
11g.47332902delCA2580084218MYBPC3c.3402del (p.Tyr1135ThrfsTer?)
c.3384del (p.Tyr1129ThrfsTer?)
c.3321del (p.Tyr1108ThrfsTer?)
ClinVar
11g.47332902G>ACA474429045MYBPC3c.3402C>T (p.Gly1134=)
c.3384C>T (p.Gly1128=)
c.3321C>T (p.Gly1107=)
11g.47332902G>CCA474429046MYBPC3c.3402C>G (p.Gly1134=)
c.3384C>G (p.Gly1128=)
c.3321C>G (p.Gly1107=)
ClinVar dbSNP
11g.47332902G=CA1969334696MYBPC3c.3402C= (p.Gly1134=)
c.3384C= (p.Gly1128=)
c.3321C= (p.Gly1107=)
11g.47332902G>TCA474429047MYBPC3c.3402C>A (p.Gly1134=)
c.3384C>A (p.Gly1128=)
c.3321C>A (p.Gly1107=)
gnomAD v4
11g.47332903C>ACA380313571MYBPC3c.3401G>T (p.Gly1134Val)
c.3383G>T (p.Gly1128Val)
c.3320G>T (p.Gly1107Val)
11g.47332903C=CA1969334698MYBPC3c.3401G= (p.Gly1134=)
c.3383G= (p.Gly1128=)
c.3320G= (p.Gly1107=)
11g.47332903C>GCA380313575MYBPC3c.3401G>C (p.Gly1134Ala)
c.3383G>C (p.Gly1128Ala)
c.3320G>C (p.Gly1107Ala)
11g.47332903C>TCA221682263MYBPC3c.3401G>A (p.Gly1134Asp)
c.3383G>A (p.Gly1128Asp)
c.3320G>A (p.Gly1107Asp)
dbSNP gnomAD v4 COSMIC
11g.47332904C>ACA380313586MYBPC3c.3400G>T (p.Gly1134Cys)
c.3382G>T (p.Gly1128Cys)
c.3319G>T (p.Gly1107Cys)
11g.47332904C>GCA380313583MYBPC3c.3400G>C (p.Gly1134Arg)
c.3382G>C (p.Gly1128Arg)
c.3319G>C (p.Gly1107Arg)
11g.47332904C>TCA380313580MYBPC3c.3400G>A (p.Gly1134Ser)
c.3382G>A (p.Gly1128Ser)
c.3319G>A (p.Gly1107Ser)
gnomAD v4
11g.47332905A=CA1969334699MYBPC3c.3399T= (p.Asn1133=)
c.3381T= (p.Asn1127=)
c.3318T= (p.Asn1106=)
11g.47332905A>CCA380313589MYBPC3c.3399T>G (p.Asn1133Lys)
c.3381T>G (p.Asn1127Lys)
c.3318T>G (p.Asn1106Lys)
11g.47332905A>GCA474429048MYBPC3c.3399T>C (p.Asn1133=)
c.3381T>C (p.Asn1127=)
c.3318T>C (p.Asn1106=)
dbSNP gnomAD v4
11g.47332905A>TCA380313593MYBPC3c.3399T>A (p.Asn1133Lys)
c.3381T>A (p.Asn1127Lys)
c.3318T>A (p.Asn1106Lys)
gnomAD v4
11g.47332906T>ACA380313596MYBPC3c.3398A>T (p.Asn1133Ile)
c.3380A>T (p.Asn1127Ile)
c.3317A>T (p.Asn1106Ile)
11g.47332906T>CCA221682267MYBPC3c.3398A>G (p.Asn1133Ser)
c.3380A>G (p.Asn1127Ser)
c.3317A>G (p.Asn1106Ser)
dbSNP gnomAD v2
11g.47332906T>GCA380313600MYBPC3c.3398A>C (p.Asn1133Thr)
c.3380A>C (p.Asn1127Thr)
c.3317A>C (p.Asn1106Thr)
dbSNP gnomAD v3 gnomAD v4
11g.47332906T=CA1969334700MYBPC3c.3398A= (p.Asn1133=)
c.3380A= (p.Asn1127=)
c.3317A= (p.Asn1106=)
11g.47332907T>ACA380313605MYBPC3c.3397A>T (p.Asn1133Tyr)
c.3379A>T (p.Asn1127Tyr)
c.3316A>T (p.Asn1106Tyr)
11g.47332907T>CCA380313608MYBPC3c.3397A>G (p.Asn1133Asp)
c.3379A>G (p.Asn1127Asp)
c.3316A>G (p.Asn1106Asp)
11g.47332907T>GCA380313611MYBPC3c.3397A>C (p.Asn1133His)
c.3379A>C (p.Asn1127His)
c.3316A>C (p.Asn1106His)
11g.47332908G>ACA079350MYBPC3c.3396C>T (p.Gly1132=)
c.3378C>T (p.Gly1126=)
c.3315C>T (p.Gly1105=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched