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.47333596_47333810delinsGGCCTGGTACA2697548544MYBPC3c.2995-58_3151delinsTACCAGGCC
c.2977-58_3133delinsTACCAGGCC
c.2914-58_3070delinsTACCAGGCC
 ClinVar
11g.47333698_47333720delCA2695213944MYBPC3c.3029_3051del (p.Glu1010GlyfsTer?)
c.3011_3033del (p.Glu1004GlyfsTer?)
c.2948_2970del (p.Glu983GlyfsTer?)
11g.47333706delCA2695213947MYBPC3c.3041del (p.Leu1014ArgfsTer6)
c.3023del (p.Leu1008ArgfsTer6)
c.2960del (p.Leu987ArgfsTer6)
11g.47333706A>CCA380315503MYBPC3c.3041T>G (p.Leu1014Arg)
c.3023T>G (p.Leu1008Arg)
c.2960T>G (p.Leu987Arg)
11g.47333706A>GCA380315504MYBPC3c.3041T>C (p.Leu1014Pro)
c.3023T>C (p.Leu1008Pro)
c.2960T>C (p.Leu987Pro)
11g.47333706A>TCA380315506MYBPC3c.3041T>A (p.Leu1014Gln)
c.3023T>A (p.Leu1008Gln)
c.2960T>A (p.Leu987Gln)
11g.47333706_47333707delinsAGCA1969335930MYBPC3c.3040_3041delinsCT (p.Leu1014=)
c.3022_3023delinsCT (p.Leu1008=)
c.2959_2960delinsCT (p.Leu987=)
11g.47333707G>ACA474429278MYBPC3c.3040C>T (p.Leu1014=)
c.3022C>T (p.Leu1008=)
c.2959C>T (p.Leu987=)
 dbSNP gnomAD v2 gnomAD v4
11g.47333707G>CCA380315513MYBPC3c.3040C>G (p.Leu1014Val)
c.3022C>G (p.Leu1008Val)
c.2959C>G (p.Leu987Val)
11g.47333707G=CA1969335932MYBPC3c.3040C= (p.Leu1014=)
c.3022C= (p.Leu1008=)
c.2959C= (p.Leu987=)
11g.47333707G>TCA380315511MYBPC3c.3040C>A (p.Leu1014Met)
c.3022C>A (p.Leu1008Met)
c.2959C>A (p.Leu987Met)
 gnomAD v4
11g.47333710dupCA2613394080MYBPC3c.3040dup (p.Leu1014ProfsTer?)
c.3022dup (p.Leu1008ProfsTer?)
c.2959dup (p.Leu987ProfsTer?)
 gnomAD v4
11g.47333709_47333710dupCA2695213948MYBPC3c.3039_3040dup (p.Leu1014ProfsTer7)
c.3021_3022dup (p.Leu1008ProfsTer7)
c.2958_2959dup (p.Leu987ProfsTer7)
11g.47333710delCA013363MYBPC3c.3040del (p.Leu1014TrpfsTer6)
c.3022del (p.Leu1008TrpfsTer6)
c.2959del (p.Leu987TrpfsTer6)
 ClinVar dbSNP gnomAD v4
11g.47333708G>ACA474429279MYBPC3c.3039C>T (p.Pro1013=)
c.3021C>T (p.Pro1007=)
c.2958C>T (p.Pro986=)
 COSMIC COSMIC
11g.47333708G>CCA474429280MYBPC3c.3039C>G (p.Pro1013=)
c.3021C>G (p.Pro1007=)
c.2958C>G (p.Pro986=)
11g.47333708G=CA1969335933MYBPC3c.3039C= (p.Pro1013=)
c.3021C= (p.Pro1007=)
c.2958C= (p.Pro986=)
11g.47333708G>TCA474429281MYBPC3c.3039C>A (p.Pro1013=)
c.3021C>A (p.Pro1007=)
c.2958C>A (p.Pro986=)
 dbSNP gnomAD v4
11g.47333709G>ACA380315516MYBPC3c.3038C>T (p.Pro1013Leu)
c.3020C>T (p.Pro1007Leu)
c.2957C>T (p.Pro986Leu)
 gnomAD v4
11g.47333709G>CCA380315521MYBPC3c.3038C>G (p.Pro1013Arg)
c.3020C>G (p.Pro1007Arg)
c.2957C>G (p.Pro986Arg)
11g.47333709G>TCA380315519MYBPC3c.3038C>A (p.Pro1013His)
c.3020C>A (p.Pro1007His)
c.2957C>A (p.Pro986His)
 COSMIC COSMIC
11g.47333710G>ACA380315523MYBPC3c.3037C>T (p.Pro1013Ser)
c.3019C>T (p.Pro1007Ser)
c.2956C>T (p.Pro986Ser)
 gnomAD v4
11g.47333710G>CCA221682883MYBPC3c.3037C>G (p.Pro1013Ala)
c.3019C>G (p.Pro1007Ala)
c.2956C>G (p.Pro986Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47333710G=CA1969335934MYBPC3c.3037C= (p.Pro1013=)
c.3019C= (p.Pro1007=)
c.2956C= (p.Pro986=)
11g.47333710G>TCA380315526MYBPC3c.3037C>A (p.Pro1013Thr)
c.3019C>A (p.Pro1007Thr)
c.2956C>A (p.Pro986Thr)
 gnomAD v4
11g.47333711C>ACA380315532MYBPC3c.3036G>T (p.Gln1012His)
c.3018G>T (p.Gln1006His)
c.2955G>T (p.Gln985His)
11g.47333711C>GCA380315535MYBPC3c.3036G>C (p.Gln1012His)
c.3018G>C (p.Gln1006His)
c.2955G>C (p.Gln985His)
11g.47333711C>TCA474429282MYBPC3c.3036G>A (p.Gln1012=)
c.3018G>A (p.Gln1006=)
c.2955G>A (p.Gln985=)
11g.47333712T>ACA380315539MYBPC3c.3035A>T (p.Gln1012Leu)
c.3017A>T (p.Gln1006Leu)
c.2954A>T (p.Gln985Leu)
11g.47333712T>CCA380315540MYBPC3c.3035A>G (p.Gln1012Arg)
c.3017A>G (p.Gln1006Arg)
c.2954A>G (p.Gln985Arg)
11g.47333712T>GCA380315542MYBPC3c.3035A>C (p.Gln1012Pro)
c.3017A>C (p.Gln1006Pro)
c.2954A>C (p.Gln985Pro)
11g.47333713G>ACA013359MYBPC3c.3034C>T (p.Gln1012Ter)
c.3016C>T (p.Gln1006Ter)
c.2953C>T (p.Gln985Ter)
 ClinVar dbSNP gnomAD v4
11g.47333713G>CCA380315547MYBPC3c.3034C>G (p.Gln1012Glu)
c.3016C>G (p.Gln1006Glu)
c.2953C>G (p.Gln985Glu)
11g.47333713G=CA1969335938MYBPC3c.3034C= (p.Gln1012=)
c.3016C= (p.Gln1006=)
c.2953C= (p.Gln985=)
11g.47333713G>TCA380315549MYBPC3c.3034C>A (p.Gln1012Lys)
c.3016C>A (p.Gln1006Lys)
c.2953C>A (p.Gln985Lys)
 gnomAD v4
11g.47333714C>ACA474429283MYBPC3c.3033G>T (p.Gly1011=)
c.3015G>T (p.Gly1005=)
c.2952G>T (p.Gly984=)
 gnomAD v4
11g.47333714C=CA1969335939MYBPC3c.3033G= (p.Gly1011=)
c.3015G= (p.Gly1005=)
c.2952G= (p.Gly984=)
11g.47333714C>GCA474429284MYBPC3c.3033G>C (p.Gly1011=)
c.3015G>C (p.Gly1005=)
c.2952G>C (p.Gly984=)
11g.47333714C>TCA079091MYBPC3c.3033G>A (p.Gly1011=)
c.3015G>A (p.Gly1005=)
c.2952G>A (p.Gly984=)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.47333717delCA2613394101MYBPC3c.3033del (p.Gln1012SerfsTer8)
c.3015del (p.Gln1006SerfsTer8)
c.2952del (p.Gln985SerfsTer8)
 gnomAD v4
11g.47333715C>ACA380315553MYBPC3c.3032G>T (p.Gly1011Val)
c.3014G>T (p.Gly1005Val)
c.2951G>T (p.Gly984Val)
 gnomAD v4
11g.47333715C>GCA380315556MYBPC3c.3032G>C (p.Gly1011Ala)
c.3014G>C (p.Gly1005Ala)
c.2951G>C (p.Gly984Ala)
 gnomAD v4
11g.47333715C>TCA380315557MYBPC3c.3032G>A (p.Gly1011Glu)
c.3014G>A (p.Gly1005Glu)
c.2951G>A (p.Gly984Glu)
11g.47333716C>ACA380315562MYBPC3c.3031G>T (p.Gly1011Trp)
c.3013G>T (p.Gly1005Trp)
c.2950G>T (p.Gly984Trp)
11g.47333716C=CA1969335942MYBPC3c.3031G= (p.Gly1011=)
c.3013G= (p.Gly1005=)
c.2950G= (p.Gly984=)
11g.47333716C>GCA380315561MYBPC3c.3031G>C (p.Gly1011Arg)
c.3013G>C (p.Gly1005Arg)
c.2950G>C (p.Gly984Arg)
11g.47333716C>TCA079089MYBPC3c.3031G>A (p.Gly1011Arg)
c.3013G>A (p.Gly1005Arg)
c.2950G>A (p.Gly984Arg)
 dbSNP ExAC gnomAD v4
11g.47333716_47333718delinsCCTCA1969335941MYBPC3c.3029_3031delinsAGG (p.Glu1010=)
c.3011_3013delinsAGG (p.Glu1004=)
c.2948_2950delinsAGG (p.Glu983=)
11g.47333717C>ACA380315574MYBPC3c.3030G>T (p.Glu1010Asp)
c.3012G>T (p.Glu1004Asp)
c.2949G>T (p.Glu983Asp)
11g.47333717C>GCA380315577MYBPC3c.3030G>C (p.Glu1010Asp)
c.3012G>C (p.Glu1004Asp)
c.2949G>C (p.Glu983Asp)
 ClinVar
11g.47333717C>TCA052320MYBPC3c.3030G>A (p.Glu1010=)
c.3012G>A (p.Glu1004=)
c.2949G>A (p.Glu983=)
 ClinVar gnomAD v4
11g.47333719_47333720delCA013350MYBPC3c.3029_3030del (p.Glu1010GlyfsTer?)
c.3011_3012del (p.Glu1004GlyfsTer?)
c.2948_2949del (p.Glu983GlyfsTer?)
 ClinVar dbSNP
11g.47333718delCA2573130287MYBPC3c.3029del (p.Glu1010GlyfsTer10)
c.3011del (p.Glu1004GlyfsTer10)
c.2948del (p.Glu983GlyfsTer10)
11g.47333718T>ACA380315582MYBPC3c.3029A>T (p.Glu1010Val)
c.3011A>T (p.Glu1004Val)
c.2948A>T (p.Glu983Val)
11g.47333718T>CCA380315584MYBPC3c.3029A>G (p.Glu1010Gly)
c.3011A>G (p.Glu1004Gly)
c.2948A>G (p.Glu983Gly)
11g.47333718T>GCA380315586MYBPC3c.3029A>C (p.Glu1010Ala)
c.3011A>C (p.Glu1004Ala)
c.2948A>C (p.Glu983Ala)
11g.47333719delCA2573332625MYBPC3c.3028del (p.Glu1010ArgfsTer10)
c.3010del (p.Glu1004ArgfsTer10)
c.2947del (p.Glu983ArgfsTer10)
11g.47333719C>ACA380315588MYBPC3c.3028G>T (p.Glu1010Ter)
c.3010G>T (p.Glu1004Ter)
c.2947G>T (p.Glu983Ter)
11g.47333719C>GCA380315590MYBPC3c.3028G>C (p.Glu1010Gln)
c.3010G>C (p.Glu1004Gln)
c.2947G>C (p.Glu983Gln)
11g.47333719C>TCA052311MYBPC3c.3028G>A (p.Glu1010Lys)
c.3010G>A (p.Glu1004Lys)
c.2947G>A (p.Glu983Lys)
11g.47333720T>ACA380315592MYBPC3c.3027A>T (p.Lys1009Asn)
c.3009A>T (p.Lys1003Asn)
c.2946A>T (p.Lys982Asn)
11g.47333720T>CCA474429285MYBPC3c.3027A>G (p.Lys1009=)
c.3009A>G (p.Lys1003=)
c.2946A>G (p.Lys982=)
11g.47333720T>GCA380315594MYBPC3c.3027A>C (p.Lys1009Asn)
c.3009A>C (p.Lys1003Asn)
c.2946A>C (p.Lys982Asn)
11g.47333721T>ACA380315597MYBPC3c.3026A>T (p.Lys1009Ile)
c.3008A>T (p.Lys1003Ile)
c.2945A>T (p.Lys982Ile)
11g.47333721T>CCA380315599MYBPC3c.3026A>G (p.Lys1009Arg)
c.3008A>G (p.Lys1003Arg)
c.2945A>G (p.Lys982Arg)
 gnomAD v4
11g.47333721T>GCA380315595MYBPC3c.3026A>C (p.Lys1009Thr)
c.3008A>C (p.Lys1003Thr)
c.2945A>C (p.Lys982Thr)
11g.47333722T>ACA380315601MYBPC3c.3025A>T (p.Lys1009Ter)
c.3007A>T (p.Lys1003Ter)
c.2944A>T (p.Lys982Ter)
11g.47333722T>CCA380315603MYBPC3c.3025A>G (p.Lys1009Glu)
c.3007A>G (p.Lys1003Glu)
c.2944A>G (p.Lys982Glu)
11g.47333722T>GCA380315605MYBPC3c.3025A>C (p.Lys1009Gln)
c.3007A>C (p.Lys1003Gln)
c.2944A>C (p.Lys982Gln)
11g.47333723G>ACA474429286MYBPC3c.3024C>T (p.Thr1008=)
c.3006C>T (p.Thr1002=)
c.2943C>T (p.Thr981=)
 gnomAD v4
11g.47333723G>CCA474429287MYBPC3c.3024C>G (p.Thr1008=)
c.3006C>G (p.Thr1002=)
c.2943C>G (p.Thr981=)
11g.47333723G=CA1969335946MYBPC3c.3024C= (p.Thr1008=)
c.3006C= (p.Thr1002=)
c.2943C= (p.Thr981=)
11g.47333723G>TCA221682899MYBPC3c.3024C>A (p.Thr1008=)
c.3006C>A (p.Thr1002=)
c.2943C>A (p.Thr981=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47333724G>ACA380315607MYBPC3c.3023C>T (p.Thr1008Ile)
c.3005C>T (p.Thr1002Ile)
c.2942C>T (p.Thr981Ile)
11g.47333724G>CCA380315608MYBPC3c.3023C>G (p.Thr1008Ser)
c.3005C>G (p.Thr1002Ser)
c.2942C>G (p.Thr981Ser)
11g.47333724G>TCA380315609MYBPC3c.3023C>A (p.Thr1008Asn)
c.3005C>A (p.Thr1002Asn)
c.2942C>A (p.Thr981Asn)
 gnomAD v4
11g.47333725T>ACA380315612MYBPC3c.3022A>T (p.Thr1008Ser)
c.3004A>T (p.Thr1002Ser)
c.2941A>T (p.Thr981Ser)
 ClinVar
11g.47333725T>CCA380315614MYBPC3c.3022A>G (p.Thr1008Ala)
c.3004A>G (p.Thr1002Ala)
c.2941A>G (p.Thr981Ala)
 dbSNP gnomAD v4
11g.47333725T>GCA380315616MYBPC3c.3022A>C (p.Thr1008Pro)
c.3004A>C (p.Thr1002Pro)
c.2941A>C (p.Thr981Pro)
 gnomAD v4
11g.47333725T=CA1969335947MYBPC3c.3022A= (p.Thr1008=)
c.3004A= (p.Thr1002=)
c.2941A= (p.Thr981=)
11g.47333726C>ACA380315619MYBPC3c.3021G>T (p.Trp1007Cys)
c.3003G>T (p.Trp1001Cys)
c.2940G>T (p.Trp980Cys)
11g.47333726C=CA1969335949MYBPC3c.3021G= (p.Trp1007=)
c.3003G= (p.Trp1001=)
c.2940G= (p.Trp980=)
11g.47333726C>GCA380315621MYBPC3c.3021G>C (p.Trp1007Cys)
c.3003G>C (p.Trp1001Cys)
c.2940G>C (p.Trp980Cys)
 gnomAD v4
11g.47333726C>TCA013344MYBPC3c.3021G>A (p.Trp1007Ter)
c.3003G>A (p.Trp1001Ter)
c.2940G>A (p.Trp980Ter)
 ClinVar dbSNP
11g.47333727C>ACA380315626MYBPC3c.3020G>T (p.Trp1007Leu)
c.3002G>T (p.Trp1001Leu)
c.2939G>T (p.Trp980Leu)
11g.47333727C=CA1969335950MYBPC3c.3020G= (p.Trp1007=)
c.3002G= (p.Trp1001=)
c.2939G= (p.Trp980=)
11g.47333727C>GCA380315623MYBPC3c.3020G>C (p.Trp1007Ser)
c.3002G>C (p.Trp1001Ser)
c.2939G>C (p.Trp980Ser)
 dbSNP
11g.47333727C>TCA380315624MYBPC3c.3020G>A (p.Trp1007Ter)
c.3002G>A (p.Trp1001Ter)
c.2939G>A (p.Trp980Ter)
 ClinVar
11g.47333728A=CA1969335952MYBPC3c.3019T= (p.Trp1007=)
c.3001T= (p.Trp1001=)
c.2938T= (p.Trp980=)
11g.47333728A>CCA380315628MYBPC3c.3019T>G (p.Trp1007Gly)
c.3001T>G (p.Trp1001Gly)
c.2938T>G (p.Trp980Gly)
11g.47333728A>GCA013338MYBPC3c.3019T>C (p.Trp1007Arg)
c.3001T>C (p.Trp1001Arg)
c.2938T>C (p.Trp980Arg)
 ClinVar dbSNP
11g.47333728A>TCA380315630MYBPC3c.3019T>A (p.Trp1007Arg)
c.3001T>A (p.Trp1001Arg)
c.2938T>A (p.Trp980Arg)
11g.47333729G>ACA474429290MYBPC3c.3018C>T (p.Thr1006=)
c.3000C>T (p.Thr1000=)
c.2937C>T (p.Thr979=)
 dbSNP gnomAD v4
11g.47333729G>CCA474429289MYBPC3c.3018C>G (p.Thr1006=)
c.3000C>G (p.Thr1000=)
c.2937C>G (p.Thr979=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47333729G=CA1969335954MYBPC3c.3018C= (p.Thr1006=)
c.3000C= (p.Thr1000=)
c.2937C= (p.Thr979=)
11g.47333729G>TCA474429288MYBPC3c.3018C>A (p.Thr1006=)
c.3000C>A (p.Thr1000=)
c.2937C>A (p.Thr979=)
 gnomAD v4
11g.47333730delCA2695213949MYBPC3c.3018del (p.Trp1007GlyfsTer13)
c.3000del (p.Trp1001GlyfsTer13)
c.2937del (p.Trp980GlyfsTer13)
11g.47333730G>ACA380315633MYBPC3c.3017C>T (p.Thr1006Ile)
c.2999C>T (p.Thr1000Ile)
c.2936C>T (p.Thr979Ile)
 dbSNP gnomAD v4
11g.47333730G>CCA380315635MYBPC3c.3017C>G (p.Thr1006Ser)
c.2999C>G (p.Thr1000Ser)
c.2936C>G (p.Thr979Ser)
11g.47333730G=CA1969335955MYBPC3c.3017C= (p.Thr1006=)
c.2999C= (p.Thr1000=)
c.2936C= (p.Thr979=)
11g.47333730G>TCA013329MYBPC3c.3017C>A (p.Thr1006Asn)
c.2999C>A (p.Thr1000Asn)
c.2936C>A (p.Thr979Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47333731T>ACA380315638MYBPC3c.3016A>T (p.Thr1006Ser)
c.2998A>T (p.Thr1000Ser)
c.2935A>T (p.Thr979Ser)
11g.47333731T>CCA380315640MYBPC3c.3016A>G (p.Thr1006Ala)
c.2998A>G (p.Thr1000Ala)
c.2935A>G (p.Thr979Ala)
 dbSNP gnomAD v4
11g.47333731T>GCA380315642MYBPC3c.3016A>C (p.Thr1006Pro)
c.2998A>C (p.Thr1000Pro)
c.2935A>C (p.Thr979Pro)
 gnomAD v4
11g.47333731T=CA1969335956MYBPC3c.3016A= (p.Thr1006=)
c.2998A= (p.Thr1000=)
c.2935A= (p.Thr979=)
11g.47333732C>ACA474429291MYBPC3c.3015G>T (p.Val1005=)
c.2997G>T (p.Val999=)
c.2934G>T (p.Val978=)
 gnomAD v4
11g.47333732C>GCA474429292MYBPC3c.3015G>C (p.Val1005=)
c.2997G>C (p.Val999=)
c.2934G>C (p.Val978=)
11g.47333732C>TCA474429293MYBPC3c.3015G>A (p.Val1005=)
c.2997G>A (p.Val999=)
c.2934G>A (p.Val978=)
 ClinVar
11g.47333733A>CCA380315644MYBPC3c.3014T>G (p.Val1005Gly)
c.2996T>G (p.Val999Gly)
c.2933T>G (p.Val978Gly)
11g.47333733A>GCA380315647MYBPC3c.3014T>C (p.Val1005Ala)
c.2996T>C (p.Val999Ala)
c.2933T>C (p.Val978Ala)
11g.47333733A>TCA380315648MYBPC3c.3014T>A (p.Val1005Glu)
c.2996T>A (p.Val999Glu)
c.2933T>A (p.Val978Glu)
 ClinVar
11g.47333734C>ACA380315653MYBPC3c.3013G>T (p.Val1005Leu)
c.2995G>T (p.Val999Leu)
c.2932G>T (p.Val978Leu)
11g.47333734C>GCA380315655MYBPC3c.3013G>C (p.Val1005Leu)
c.2995G>C (p.Val999Leu)
c.2932G>C (p.Val978Leu)
11g.47333734C>TCA380315650MYBPC3c.3013G>A (p.Val1005Met)
c.2995G>A (p.Val999Met)
c.2932G>A (p.Val978Met)
 gnomAD v4
11g.47333741_47333758delCA915940866MYBPC3c.2996_3013del
c.2978_2995del
c.2915_2932del
11g.47333735C>ACA380315659MYBPC3c.3012G>T (p.Gln1004His)
c.2994G>T (p.Gln998His)
c.2931G>T (p.Gln977His)
 gnomAD v4
11g.47333735C=CA1969335958MYBPC3c.3012G= (p.Gln1004=)
c.2994G= (p.Gln998=)
c.2931G= (p.Gln977=)
11g.47333735C>GCA380315657MYBPC3c.3012G>C (p.Gln1004His)
c.2994G>C (p.Gln998His)
c.2931G>C (p.Gln977His)
 gnomAD v4
11g.47333735C>TCA474429294MYBPC3c.3012G>A (p.Gln1004=)
c.2994G>A (p.Gln998=)
c.2931G>A (p.Gln977=)
 dbSNP
11g.47333736T>ACA380315661MYBPC3c.3011A>T (p.Gln1004Leu)
c.2993A>T (p.Gln998Leu)
c.2930A>T (p.Gln977Leu)
11g.47333736T>CCA380315662MYBPC3c.3011A>G (p.Gln1004Arg)
c.2993A>G (p.Gln998Arg)
c.2930A>G (p.Gln977Arg)
 gnomAD v4
11g.47333736T>GCA380315663MYBPC3c.3011A>C (p.Gln1004Pro)
c.2993A>C (p.Gln998Pro)
c.2930A>C (p.Gln977Pro)
11g.47333736_47333738delinsTGACA1969335959MYBPC3c.3009_3011delinsTCA (p.Pro1003=)
c.2991_2993delinsTCA (p.Pro997=)
c.2928_2930delinsTCA (p.Pro976=)
11g.47333737G>ACA380315664MYBPC3c.3010C>T (p.Gln1004Ter)
c.2992C>T (p.Gln998Ter)
c.2929C>T (p.Gln977Ter)
11g.47333737G>CCA380315665MYBPC3c.3010C>G (p.Gln1004Glu)
c.2992C>G (p.Gln998Glu)
c.2929C>G (p.Gln977Glu)
11g.47333737G>TCA380315667MYBPC3c.3010C>A (p.Gln1004Lys)
c.2992C>A (p.Gln998Lys)
c.2929C>A (p.Gln977Lys)
 gnomAD v4
11g.47333738_47333739delCA1969335960MYBPC3c.3009_3010del (p.Gln1004GlyfsTer?)
c.2991_2992del (p.Gln998GlyfsTer?)
c.2928_2929del (p.Gln977GlyfsTer?)
 ClinVar dbSNP
11g.47333738A=CA1969335962MYBPC3c.3009T= (p.Pro1003=)
c.2991T= (p.Pro997=)
c.2928T= (p.Pro976=)
11g.47333738A>CCA079086MYBPC3c.3009T>G (p.Pro1003=)
c.2991T>G (p.Pro997=)
c.2928T>G (p.Pro976=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47333738A>GCA474429295MYBPC3c.3009T>C (p.Pro1003=)
c.2991T>C (p.Pro997=)
c.2928T>C (p.Pro976=)
11g.47333738A>TCA474429296MYBPC3c.3009T>A (p.Pro1003=)
c.2991T>A (p.Pro997=)
c.2928T>A (p.Pro976=)
11g.47333739G>ACA380315670MYBPC3c.3008C>T (p.Pro1003Leu)
c.2990C>T (p.Pro997Leu)
c.2927C>T (p.Pro976Leu)
 dbSNP gnomAD v4
11g.47333739G>CCA380315671MYBPC3c.3008C>G (p.Pro1003Arg)
c.2990C>G (p.Pro997Arg)
c.2927C>G (p.Pro976Arg)
11g.47333739G=CA1969335964MYBPC3c.3008C= (p.Pro1003=)
c.2990C= (p.Pro997=)
c.2927C= (p.Pro976=)
11g.47333739G>TCA380315673MYBPC3c.3008C>A (p.Pro1003His)
c.2990C>A (p.Pro997His)
c.2927C>A (p.Pro976His)
 gnomAD v4
11g.47333740G>ACA380315675MYBPC3c.3007C>T (p.Pro1003Ser)
c.2989C>T (p.Pro997Ser)
c.2926C>T (p.Pro976Ser)
11g.47333740G>CCA380315677MYBPC3c.3007C>G (p.Pro1003Ala)
c.2989C>G (p.Pro997Ala)
c.2926C>G (p.Pro976Ala)
11g.47333740G>TCA380315679MYBPC3c.3007C>A (p.Pro1003Thr)
c.2989C>A (p.Pro997Thr)
c.2926C>A (p.Pro976Thr)
 gnomAD v4
11g.47333741C>ACA474429297MYBPC3c.3006G>T (p.Arg1002=)
c.2988G>T (p.Arg996=)
c.2925G>T (p.Arg975=)
 gnomAD v4
11g.47333741C>GCA474429298MYBPC3c.3006G>C (p.Arg1002=)
c.2988G>C (p.Arg996=)
c.2925G>C (p.Arg975=)
11g.47333741C>TCA474429299MYBPC3c.3006G>A (p.Arg1002=)
c.2988G>A (p.Arg996=)
c.2925G>A (p.Arg975=)
 ClinVar gnomAD v4
11g.47333742C>ACA380315680MYBPC3c.3005G>T (p.Arg1002Leu)
c.2987G>T (p.Arg996Leu)
c.2924G>T (p.Arg975Leu)
11g.47333742C=CA1969335965MYBPC3c.3005G= (p.Arg1002=)
c.2987G= (p.Arg996=)
c.2924G= (p.Arg975=)
11g.47333742C>GCA380315682MYBPC3c.3005G>C (p.Arg1002Pro)
c.2987G>C (p.Arg996Pro)
c.2924G>C (p.Arg975Pro)
11g.47333742C>TCA013325MYBPC3c.3005G>A (p.Arg1002Gln)
c.2987G>A (p.Arg996Gln)
c.2924G>A (p.Arg975Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47333742_47333743delCA2697548545MYBPC3c.3004_3005del (p.Arg1002AlafsTer?)
c.2986_2987del (p.Arg996AlafsTer?)
c.2923_2924del (p.Arg975AlafsTer?)
 ClinVar
11g.47333743G>ACA013316MYBPC3c.3004C>T (p.Arg1002Trp)
c.2986C>T (p.Arg996Trp)
c.2923C>T (p.Arg975Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47333743G>CCA380315685MYBPC3c.3004C>G (p.Arg1002Gly)
c.2986C>G (p.Arg996Gly)
c.2923C>G (p.Arg975Gly)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47333743G=CA1969335968MYBPC3c.3004C= (p.Arg1002=)
c.2986C= (p.Arg996=)
c.2923C= (p.Arg975=)
11g.47333743G>TCA474429300MYBPC3c.3004C>A (p.Arg1002=)
c.2986C>A (p.Arg996=)
c.2923C>A (p.Arg975=)
 gnomAD v4
11g.47333746delCA2613394187MYBPC3c.3004del (p.Arg1002GlyfsTer4)
c.2986del (p.Arg996GlyfsTer4)
c.2923del (p.Arg975GlyfsTer4)
 gnomAD v4
11g.47333744G>ACA013310MYBPC3c.3003C>T (p.Pro1001=)
c.2985C>T (p.Pro995=)
c.2922C>T (p.Pro974=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47333744G>CCA474429301MYBPC3c.3003C>G (p.Pro1001=)
c.2985C>G (p.Pro995=)
c.2922C>G (p.Pro974=)
 dbSNP gnomAD v2 gnomAD v4
11g.47333744G=CA1969335970MYBPC3c.3003C= (p.Pro1001=)
c.2985C= (p.Pro995=)
c.2922C= (p.Pro974=)
11g.47333744G>TCA474429302MYBPC3c.3003C>A (p.Pro1001=)
c.2985C>A (p.Pro995=)
c.2922C>A (p.Pro974=)
11g.47333745G>ACA380315688MYBPC3c.3002C>T (p.Pro1001Leu)
c.2984C>T (p.Pro995Leu)
c.2921C>T (p.Pro974Leu)
 COSMIC COSMIC
11g.47333745G>CCA380315689MYBPC3c.3002C>G (p.Pro1001Arg)
c.2984C>G (p.Pro995Arg)
c.2921C>G (p.Pro974Arg)
11g.47333745G>TCA380315690MYBPC3c.3002C>A (p.Pro1001His)
c.2984C>A (p.Pro995His)
c.2921C>A (p.Pro974His)
 gnomAD v4
11g.47333746G>ACA052267MYBPC3c.3001C>T (p.Pro1001Ser)
c.2983C>T (p.Pro995Ser)
c.2920C>T (p.Pro974Ser)
 gnomAD v4
11g.47333746G>CCA380315692MYBPC3c.3001C>G (p.Pro1001Ala)
c.2983C>G (p.Pro995Ala)
c.2920C>G (p.Pro974Ala)
11g.47333746G=CA1969335972MYBPC3c.3001C= (p.Pro1001=)
c.2983C= (p.Pro995=)
c.2920C= (p.Pro974=)
11g.47333746G>TCA380315693MYBPC3c.3001C>A (p.Pro1001Thr)
c.2983C>A (p.Pro995Thr)
c.2920C>A (p.Pro974Thr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47333746_47333751delCA2613394204MYBPC3c.2996_3001del (p.Gly999_Pro1001delinsAla)
c.2978_2983del (p.Gly993_Pro995delinsAla)
c.2915_2920del (p.Gly972_Pro974delinsAla)
 gnomAD v4
11g.47333747C>ACA380315694MYBPC3c.3000G>T (p.Lys1000Asn)
c.2982G>T (p.Lys994Asn)
c.2919G>T (p.Lys973Asn)
 gnomAD v4
11g.47333747C=CA1969335974MYBPC3c.3000G= (p.Lys1000=)
c.2982G= (p.Lys994=)
c.2919G= (p.Lys973=)
11g.47333747C>GCA380315696MYBPC3c.3000G>C (p.Lys1000Asn)
c.2982G>C (p.Lys994Asn)
c.2919G>C (p.Lys973Asn)
11g.47333747C>TCA474429303MYBPC3c.3000G>A (p.Lys1000=)
c.2982G>A (p.Lys994=)
c.2919G>A (p.Lys973=)
 dbSNP gnomAD v4
11g.47333748T>ACA380315701MYBPC3c.2999A>T (p.Lys1000Met)
c.2981A>T (p.Lys994Met)
c.2918A>T (p.Lys973Met)
11g.47333748T>CCA380315700MYBPC3c.2999A>G (p.Lys1000Arg)
c.2981A>G (p.Lys994Arg)
c.2918A>G (p.Lys973Arg)
11g.47333748T>GCA380315698MYBPC3c.2999A>C (p.Lys1000Thr)
c.2981A>C (p.Lys994Thr)
c.2918A>C (p.Lys973Thr)
11g.47333749T>ACA380315703MYBPC3c.2998A>T (p.Lys1000Ter)
c.2980A>T (p.Lys994Ter)
c.2917A>T (p.Lys973Ter)
11g.47333749T>CCA380315705MYBPC3c.2998A>G (p.Lys1000Glu)
c.2980A>G (p.Lys994Glu)
c.2917A>G (p.Lys973Glu)
 COSMIC COSMIC
11g.47333749T>GCA380315707MYBPC3c.2998A>C (p.Lys1000Gln)
c.2980A>C (p.Lys994Gln)
c.2917A>C (p.Lys973Gln)
11g.47333750delCA2695213950MYBPC3c.2997del (p.Lys1000SerfsTer6)
c.2979del (p.Lys994SerfsTer6)
c.2916del (p.Lys973SerfsTer6)
11g.47333750G>ACA013301MYBPC3c.2997C>T (p.Gly999=)
c.2979C>T (p.Gly993=)
c.2916C>T (p.Gly972=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47333750G>CCA474429304MYBPC3c.2997C>G (p.Gly999=)
c.2979C>G (p.Gly993=)
c.2916C>G (p.Gly972=)
11g.47333750G=CA1969335976MYBPC3c.2997C= (p.Gly999=)
c.2979C= (p.Gly993=)
c.2916C= (p.Gly972=)
11g.47333750G>TCA474429305MYBPC3c.2997C>A (p.Gly999=)
c.2979C>A (p.Gly993=)
c.2916C>A (p.Gly972=)
 gnomAD v4
11g.47333751C>ACA380315708MYBPC3c.2996G>T (p.Gly999Val)
c.2978G>T (p.Gly993Val)
c.2915G>T (p.Gly972Val)
 gnomAD v4
11g.47333751C>GCA380315709MYBPC3c.2996G>C (p.Gly999Ala)
c.2978G>C (p.Gly993Ala)
c.2915G>C (p.Gly972Ala)
11g.47333751C>TCA380315710MYBPC3c.2996G>A (p.Gly999Asp)
c.2978G>A (p.Gly993Asp)
c.2915G>A (p.Gly972Asp)
 gnomAD v4
11g.47333753dupCA913187679MYBPC3c.2996dup
c.2978dup
c.2915dup
11g.47333752C>ACA380315712MYBPC3c.2995G>T (p.Gly999Cys)
c.2977G>T (p.Gly993Cys)
c.2914G>T (p.Gly972Cys)
11g.47333752C=CA1969335979MYBPC3c.2995G= (p.Gly999=)
c.2977G= (p.Gly993=)
c.2914G= (p.Gly972=)
11g.47333752C>GCA380315714MYBPC3c.2995G>C (p.Gly999Arg)
c.2977G>C (p.Gly993Arg)
c.2914G>C (p.Gly972Arg)
11g.47333752C>TCA380315715MYBPC3c.2995G>A (p.Gly999Ser)
c.2977G>A (p.Gly993Ser)
c.2914G>A (p.Gly972Ser)
 dbSNP
11g.47333753C>ACA380315717MYBPC3c.2995-1G>T (n.2995-1G>T)
c.2977-1G>T (n.2977-1G>T)
c.2914-1G>T (n.2914-1G>T)
 gnomAD v4
11g.47333753C=CA1969335981MYBPC3c.2995-1G= (n.2995-1G=)
c.2977-1G= (n.2977-1G=)
c.2914-1G= (n.2914-1G=)
11g.47333753C>GCA380315719MYBPC3c.2995-1G>C (n.2995-1G>C)
c.2977-1G>C (n.2977-1G>C)
c.2914-1G>C (n.2914-1G>C)
11g.47333753C>TCA013288MYBPC3c.2995-1G>A (n.2995-1G>A)
c.2977-1G>A (n.2977-1G>A)
c.2914-1G>A (n.2914-1G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47333753_47333754delCA2573053505MYBPC3c.2995-2_2995-1del (n.2995-2_2995-1del)
c.2977-2_2977-1del (n.2977-2_2977-1del)
c.2914-2_2914-1del (n.2914-2_2914-1del)
 ClinVar dbSNP
11g.47333754T>ACA380315725MYBPC3c.2995-2A>T (n.2995-2A>T)
c.2977-2A>T (n.2977-2A>T)
c.2914-2A>T (n.2914-2A>T)
11g.47333754T>CCA380315722MYBPC3c.2995-2A>G (n.2995-2A>G)
c.2977-2A>G (n.2977-2A>G)
c.2914-2A>G (n.2914-2A>G)
 dbSNP gnomAD v2 gnomAD v4
11g.47333754T>GCA380315724MYBPC3c.2995-2A>C (n.2995-2A>C)
c.2977-2A>C (n.2977-2A>C)
c.2914-2A>C (n.2914-2A>C)
11g.47333754T=CA1969335983MYBPC3c.2995-2A= (n.2995-2A=)
c.2977-2A= (n.2977-2A=)
c.2914-2A= (n.2914-2A=)
11g.47333755G>CCA676991690MYBPC3c.2995-3C>G (n.2995-3C>G)
c.2977-3C>G (n.2977-3C>G)
c.2914-3C>G (n.2914-3C>G)
 dbSNP
11g.47333755G=CA1969335984MYBPC3c.2995-3C= (n.2995-3C=)
c.2977-3C= (n.2977-3C=)
c.2914-3C= (n.2914-3C=)
11g.47333757G>CCA013296MYBPC3c.2995-5C>G (n.2995-5C>G)
c.2977-5C>G (n.2977-5C>G)
c.2914-5C>G (n.2914-5C>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47333757G=CA1969335986MYBPC3c.2995-5C= (n.2995-5C=)
c.2977-5C= (n.2977-5C=)
c.2914-5C= (n.2914-5C=)
11g.47333757G>TCA2613394228MYBPC3c.2995-5C>A (n.2995-5C>A)
c.2977-5C>A (n.2977-5C>A)
c.2914-5C>A (n.2914-5C>A)
 gnomAD v4
11g.47333760delCA2613394225MYBPC3c.2995-5del (n.2995-5del)
c.2977-5del (n.2977-5del)
c.2914-5del (n.2914-5del)
 gnomAD v4
11g.47333758G>ACA2613394230MYBPC3c.2995-6C>T (n.2995-6C>T)
c.2977-6C>T (n.2977-6C>T)
c.2914-6C>T (n.2914-6C>T)
 gnomAD v4
11g.47333759G>CCA2573146371MYBPC3c.2995-7C>G (n.2995-7C>G)
c.2977-7C>G (n.2977-7C>G)
c.2914-7C>G (n.2914-7C>G)
 ClinVar dbSNP
11g.47333759G>TCA2613394231MYBPC3c.2995-7C>A (n.2995-7C>A)
c.2977-7C>A (n.2977-7C>A)
c.2914-7C>A (n.2914-7C>A)
 gnomAD v4
11g.47333760G>ACA1969335988MYBPC3c.2995-8C>T (n.2995-8C>T)
c.2977-8C>T (n.2977-8C>T)
c.2914-8C>T (n.2914-8C>T)
 ClinVar dbSNP gnomAD v4
11g.47333760G=CA1969335987MYBPC3c.2995-8C= (n.2995-8C=)
c.2977-8C= (n.2977-8C=)
c.2914-8C= (n.2914-8C=)
11g.47333761A=CA1969335990MYBPC3c.2995-9T= (n.2995-9T=)
c.2977-9T= (n.2977-9T=)
c.2914-9T= (n.2914-9T=)
11g.47333761A>GCA2613394234MYBPC3c.2995-9T>C (n.2995-9T>C)
c.2977-9T>C (n.2977-9T>C)
c.2914-9T>C (n.2914-9T>C)
 gnomAD v4
11g.47333761A>TCA599374172MYBPC3c.2995-9T>A (n.2995-9T>A)
c.2977-9T>A (n.2977-9T>A)
c.2914-9T>A (n.2914-9T>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47333762G>ACA1139659392MYBPC3c.2995-10C>T (n.2995-10C>T)
c.2977-10C>T (n.2977-10C>T)
c.2914-10C>T (n.2914-10C>T)
 ClinVar dbSNP gnomAD v4
11g.47333762G>CCA2613394236MYBPC3c.2995-10C>G (n.2995-10C>G)
c.2977-10C>G (n.2977-10C>G)
c.2914-10C>G (n.2914-10C>G)
 gnomAD v4
11g.47333762G=CA1969335991MYBPC3c.2995-10C= (n.2995-10C=)
c.2977-10C= (n.2977-10C=)
c.2914-10C= (n.2914-10C=)
11g.47333762G>TCA2613394238MYBPC3c.2995-10C>A (n.2995-10C>A)
c.2977-10C>A (n.2977-10C>A)
c.2914-10C>A (n.2914-10C>A)
 gnomAD v4
11g.47333763G>TCA2613394239MYBPC3c.2995-11C>A (n.2995-11C>A)
c.2977-11C>A (n.2977-11C>A)
c.2914-11C>A (n.2914-11C>A)
 gnomAD v4
11g.47333764A=CA1969335992MYBPC3c.2995-12T= (n.2995-12T=)
c.2977-12T= (n.2977-12T=)
c.2914-12T= (n.2914-12T=)
11g.47333764A>GCA079072MYBPC3c.2995-12T>C (n.2995-12T>C)
c.2977-12T>C (n.2977-12T>C)
c.2914-12T>C (n.2914-12T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.47333767delCA2613394240MYBPC3c.2995-12del (n.2995-12del)
c.2977-12del (n.2977-12del)
c.2914-12del (n.2914-12del)
 gnomAD v4
11g.47333766A=CA1969335993MYBPC3c.2995-14T= (n.2995-14T=)
c.2977-14T= (n.2977-14T=)
c.2914-14T= (n.2914-14T=)
11g.47333766A>GCA1969335994MYBPC3c.2995-14T>C (n.2995-14T>C)
c.2977-14T>C (n.2977-14T>C)
c.2914-14T>C (n.2914-14T>C)
 ClinVar dbSNP
11g.47333768G>ACA2613394242MYBPC3c.2995-16C>T (n.2995-16C>T)
c.2977-16C>T (n.2977-16C>T)
c.2914-16C>T (n.2914-16C>T)
 gnomAD v4
11g.47333768G>TCA2613394244MYBPC3c.2995-16C>A (n.2995-16C>A)
c.2977-16C>A (n.2977-16C>A)
c.2914-16C>A (n.2914-16C>A)
 gnomAD v4
11g.47333769C>ACA2613394247MYBPC3c.2995-17G>T (n.2995-17G>T)
c.2977-17G>T (n.2977-17G>T)
c.2914-17G>T (n.2914-17G>T)
 gnomAD v4
11g.47333769C=CA1969335996MYBPC3c.2995-17G= (n.2995-17G=)
c.2977-17G= (n.2977-17G=)
c.2914-17G= (n.2914-17G=)
11g.47333769C>TCA599374173MYBPC3c.2995-17G>A (n.2995-17G>A)
c.2977-17G>A (n.2977-17G>A)
c.2914-17G>A (n.2914-17G>A)
 dbSNP gnomAD v2
11g.47333771T>GCA1969335998MYBPC3c.2995-19A>C (n.2995-19A>C)
c.2977-19A>C (n.2977-19A>C)
c.2914-19A>C (n.2914-19A>C)
 ClinVar dbSNP gnomAD v4
11g.47333771T=CA1969335997MYBPC3c.2995-19A= (n.2995-19A=)
c.2977-19A= (n.2977-19A=)
c.2914-19A= (n.2914-19A=)
11g.47333773A>TCA2613394251MYBPC3c.2995-21T>A (n.2995-21T>A)
c.2977-21T>A (n.2977-21T>A)
c.2914-21T>A (n.2914-21T>A)
 gnomAD v4
11g.47333774C>ACA2613394252MYBPC3c.2995-22G>T (n.2995-22G>T)
c.2977-22G>T (n.2977-22G>T)
c.2914-22G>T (n.2914-22G>T)
 gnomAD v4
11g.47333774C=CA1969335999MYBPC3c.2995-22G= (n.2995-22G=)
c.2977-22G= (n.2977-22G=)
c.2914-22G= (n.2914-22G=)
11g.47333774C>TCA937666372MYBPC3c.2995-22G>A (n.2995-22G>A)
c.2977-22G>A (n.2977-22G>A)
c.2914-22G>A (n.2914-22G>A)
 dbSNP gnomAD v3 gnomAD v4
11g.47333775C>ACA2613394253MYBPC3c.2995-23G>T (n.2995-23G>T)
c.2977-23G>T (n.2977-23G>T)
c.2914-23G>T (n.2914-23G>T)
 gnomAD v4
11g.47333775C>TCA2499361063MYBPC3c.2995-23G>A (n.2995-23G>A)
c.2977-23G>A (n.2977-23G>A)
c.2914-23G>A (n.2914-23G>A)
 gnomAD v4
11g.47333776C>ACA2613394255MYBPC3c.2995-24G>T (n.2995-24G>T)
c.2977-24G>T (n.2977-24G>T)
c.2914-24G>T (n.2914-24G>T)
 gnomAD v4
11g.47333777T>CCA2613394257MYBPC3c.2995-25A>G (n.2995-25A>G)
c.2977-25A>G (n.2977-25A>G)
c.2914-25A>G (n.2914-25A>G)
 gnomAD v4
11g.47333778G>TCA2613394258MYBPC3c.2995-26C>A (n.2995-26C>A)
c.2977-26C>A (n.2977-26C>A)
c.2914-26C>A (n.2914-26C>A)
 gnomAD v4
11g.47333781C=CA1969336000MYBPC3c.2995-29G= (n.2995-29G=)
c.2977-29G= (n.2977-29G=)
c.2914-29G= (n.2914-29G=)
11g.47333781C>TCA1969336001MYBPC3c.2995-29G>A (n.2995-29G>A)
c.2977-29G>A (n.2977-29G>A)
c.2914-29G>A (n.2914-29G>A)
 dbSNP gnomAD v4
11g.47333782C>TCA2613394259MYBPC3c.2995-30G>A (n.2995-30G>A)
c.2977-30G>A (n.2977-30G>A)
c.2914-30G>A (n.2914-30G>A)
 gnomAD v4
11g.47333783T>GCA2724174500MYBPC3c.2995-31A>C (n.2995-31A>C)
c.2977-31A>C (n.2977-31A>C)
c.2914-31A>C (n.2914-31A>C)
 dbSNP
11g.47333784G>TCA2613394261MYBPC3c.2995-32C>A (n.2995-32C>A)
c.2977-32C>A (n.2977-32C>A)
c.2914-32C>A (n.2914-32C>A)
 gnomAD v4
11g.47333785G>TCA2613394262MYBPC3c.2995-33C>A (n.2995-33C>A)
c.2977-33C>A (n.2977-33C>A)
c.2914-33C>A (n.2914-33C>A)
 gnomAD v4
11g.47333788C>ACA2565695536MYBPC3c.2995-36G>T (n.2995-36G>T)
c.2977-36G>T (n.2977-36G>T)
c.2914-36G>T (n.2914-36G>T)
11g.47333789A>CCA2613394263MYBPC3c.2995-37T>G (n.2995-37T>G)
c.2977-37T>G (n.2977-37T>G)
c.2914-37T>G (n.2914-37T>G)
 gnomAD v4
11g.47333790C>ACA2613394264MYBPC3c.2995-38G>T (n.2995-38G>T)
c.2977-38G>T (n.2977-38G>T)
c.2914-38G>T (n.2914-38G>T)
 gnomAD v4
11g.47333790C=CA1969336002MYBPC3c.2995-38G= (n.2995-38G=)
c.2977-38G= (n.2977-38G=)
c.2914-38G= (n.2914-38G=)
11g.47333790C>TCA599374174MYBPC3c.2995-38G>A (n.2995-38G>A)
c.2977-38G>A (n.2977-38G>A)
c.2914-38G>A (n.2914-38G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47333791T>CCA079073MYBPC3c.2995-39A>G (n.2995-39A>G)
c.2977-39A>G (n.2977-39A>G)
c.2914-39A>G (n.2914-39A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47333791T=CA1969336003MYBPC3c.2995-39A= (n.2995-39A=)
c.2977-39A= (n.2977-39A=)
c.2914-39A= (n.2914-39A=)
11g.47333792C>ACA2613394267MYBPC3c.2995-40G>T (n.2995-40G>T)
c.2977-40G>T (n.2977-40G>T)
c.2914-40G>T (n.2914-40G>T)
 gnomAD v4
11g.47333792C>TCA2613394266MYBPC3c.2995-40G>A (n.2995-40G>A)
c.2977-40G>A (n.2977-40G>A)
c.2914-40G>A (n.2914-40G>A)
 gnomAD v4
11g.47333793C>GCA2613394268MYBPC3c.2995-41G>C (n.2995-41G>C)
c.2977-41G>C (n.2977-41G>C)
c.2914-41G>C (n.2914-41G>C)
 gnomAD v4
11g.47333796G>ACA2613394270MYBPC3c.2995-44C>T (n.2995-44C>T)
c.2977-44C>T (n.2977-44C>T)
c.2914-44C>T (n.2914-44C>T)
 gnomAD v4
11g.47333796G>TCA2613394272MYBPC3c.2995-44C>A (n.2995-44C>A)
c.2977-44C>A (n.2977-44C>A)
c.2914-44C>A (n.2914-44C>A)
 gnomAD v4
11g.47333798dupCA2613394271MYBPC3c.2995-44dup (n.2995-44dup)
c.2977-44dup (n.2977-44dup)
c.2914-44dup (n.2914-44dup)
 gnomAD v4
11g.47333797G>ACA079075MYBPC3c.2995-45C>T (n.2995-45C>T)
c.2977-45C>T (n.2977-45C>T)
c.2914-45C>T (n.2914-45C>T)
 dbSNP ExAC gnomAD v4
11g.47333797G=CA1969336005MYBPC3c.2995-45C= (n.2995-45C=)
c.2977-45C= (n.2977-45C=)
c.2914-45C= (n.2914-45C=)
11g.47333798G>ACA676991707MYBPC3c.2995-46C>T (n.2995-46C>T)
c.2977-46C>T (n.2977-46C>T)
c.2914-46C>T (n.2914-46C>T)
 dbSNP gnomAD v3 gnomAD v4
11g.47333798G=CA1969336006MYBPC3c.2995-46C= (n.2995-46C=)
c.2977-46C= (n.2977-46C=)
c.2914-46C= (n.2914-46C=)
11g.47333798G>TCA2613394276MYBPC3c.2995-46C>A (n.2995-46C>A)
c.2977-46C>A (n.2977-46C>A)
c.2914-46C>A (n.2914-46C>A)
 gnomAD v4
11g.47333799C>ACA2613394277MYBPC3c.2995-47G>T (n.2995-47G>T)
c.2977-47G>T (n.2977-47G>T)
c.2914-47G>T (n.2914-47G>T)
 gnomAD v4
11g.47333799C>TCA2791331136MYBPC3c.2995-47G>A (n.2995-47G>A)
c.2977-47G>A (n.2977-47G>A)
c.2914-47G>A (n.2914-47G>A)
11g.47333800C>ACA1969336008MYBPC3c.2995-48G>T (n.2995-48G>T)
c.2977-48G>T (n.2977-48G>T)
c.2914-48G>T (n.2914-48G>T)
 dbSNP gnomAD v4
11g.47333800C=CA1969336007MYBPC3c.2995-48G= (n.2995-48G=)
c.2977-48G= (n.2977-48G=)
c.2914-48G= (n.2914-48G=)
11g.47333800C>TCA079077MYBPC3c.2995-48G>A (n.2995-48G>A)
c.2977-48G>A (n.2977-48G>A)
c.2914-48G>A (n.2914-48G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47333801G>ACA079079MYBPC3c.2995-49C>T (n.2995-49C>T)
c.2977-49C>T (n.2977-49C>T)
c.2914-49C>T (n.2914-49C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47333801G=CA1969336010MYBPC3c.2995-49C= (n.2995-49C=)
c.2977-49C= (n.2977-49C=)
c.2914-49C= (n.2914-49C=)
11g.47333801G>TCA2613394280MYBPC3c.2995-49C>A (n.2995-49C>A)
c.2977-49C>A (n.2977-49C>A)
c.2914-49C>A (n.2914-49C>A)
 gnomAD v4
11g.47333802G>ACA599374175MYBPC3c.2995-50C>T (n.2995-50C>T)
c.2977-50C>T (n.2977-50C>T)
c.2914-50C>T (n.2914-50C>T)
 dbSNP gnomAD v2 gnomAD v4
11g.47333802G>CCA2596115253MYBPC3c.2995-50C>G (n.2995-50C>G)
c.2977-50C>G (n.2977-50C>G)
c.2914-50C>G (n.2914-50C>G)
 dbSNP gnomAD v3 gnomAD v4
11g.47333802G=CA1969336012MYBPC3c.2995-50C= (n.2995-50C=)
c.2977-50C= (n.2977-50C=)
c.2914-50C= (n.2914-50C=)
11g.47333802G>TCA2613394284MYBPC3c.2995-50C>A (n.2995-50C>A)
c.2977-50C>A (n.2977-50C>A)
c.2914-50C>A (n.2914-50C>A)
 gnomAD v4
11g.47333803C>ACA2613394285MYBPC3c.2995-51G>T (n.2995-51G>T)
c.2977-51G>T (n.2977-51G>T)
c.2914-51G>T (n.2914-51G>T)
 gnomAD v4
11g.47333803C>TCA2613394287MYBPC3c.2995-51G>A (n.2995-51G>A)
c.2977-51G>A (n.2977-51G>A)
c.2914-51G>A (n.2914-51G>A)
 gnomAD v4
11g.47333804C>ACA2613394288MYBPC3c.2995-52G>T (n.2995-52G>T)
c.2977-52G>T (n.2977-52G>T)
c.2914-52G>T (n.2914-52G>T)
 gnomAD v4
11g.47333804C=CA1969336014MYBPC3c.2995-52G= (n.2995-52G=)
c.2977-52G= (n.2977-52G=)
c.2914-52G= (n.2914-52G=)
11g.47333804C>TCA221682985MYBPC3c.2995-52G>A (n.2995-52G>A)
c.2977-52G>A (n.2977-52G>A)
c.2914-52G>A (n.2914-52G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47333805G>ACA676991715MYBPC3c.2995-53C>T (n.2995-53C>T)
c.2977-53C>T (n.2977-53C>T)
c.2914-53C>T (n.2914-53C>T)
 dbSNP gnomAD v3 gnomAD v4
11g.47333805G=CA1969336016MYBPC3c.2995-53C= (n.2995-53C=)
c.2977-53C= (n.2977-53C=)
c.2914-53C= (n.2914-53C=)
11g.47333805G>TCA2613394293MYBPC3c.2995-53C>A (n.2995-53C>A)
c.2977-53C>A (n.2977-53C>A)
c.2914-53C>A (n.2914-53C>A)
 gnomAD v4
11g.47333805_47333808dupCA2613394292MYBPC3c.2995-56_2995-53dup (n.2995-56_2995-53dup)
c.2977-56_2977-53dup (n.2977-56_2977-53dup)
c.2914-56_2914-53dup (n.2914-56_2914-53dup)
 gnomAD v4
11g.47333806C>ACA2613394295MYBPC3c.2995-54G>T (n.2995-54G>T)
c.2977-54G>T (n.2977-54G>T)
c.2914-54G>T (n.2914-54G>T)
 gnomAD v4

Number of alleles fetched