Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.77182139_77182141delCA918918632MYO7Ac.3093_3095del (p.Asp1031del)
c.1158_1160del (p.Asp386del)
c.934_936del
c.3060_3062del (p.Asp1020del)
c.636_638del (p.Asp212del)
n.636_638del
c.2874_2876del (p.Asp958del)
c.2862_2864del (p.Asp954del)
c.2835_2837del (p.Asp945del)
n.3413_3415del
n.3415_3417del
c.3183_3185del (p.Asp1061del)
c.2952_2954del (p.Asp984del)
n.3198_3200del
dbSNP
11g.77182138A>CCA381944318MYO7Ac.3092A>C (p.Asp1031Ala)
c.1157A>C (p.Asp386Ala)
c.933A>C
c.3059A>C (p.Asp1020Ala)
c.635A>C (p.Asp212Ala)
n.635A>C
c.2873A>C (p.Asp958Ala)
c.2861A>C (p.Asp954Ala)
c.2834A>C (p.Asp945Ala)
n.3412A>C
n.3414A>C
c.3182A>C (p.Asp1061Ala)
c.2951A>C (p.Asp984Ala)
n.3197A>C
11g.77182138A>GCA381944320MYO7Ac.3092A>G (p.Asp1031Gly)
c.1157A>G (p.Asp386Gly)
c.933A>G
c.3059A>G (p.Asp1020Gly)
c.635A>G (p.Asp212Gly)
n.635A>G
c.2873A>G (p.Asp958Gly)
c.2861A>G (p.Asp954Gly)
c.2834A>G (p.Asp945Gly)
n.3412A>G
n.3414A>G
c.3182A>G (p.Asp1061Gly)
c.2951A>G (p.Asp984Gly)
n.3197A>G
11g.77182138A>TCA381944321MYO7Ac.3092A>T (p.Asp1031Val)
c.1157A>T (p.Asp386Val)
c.933A>T
c.3059A>T (p.Asp1020Val)
c.635A>T (p.Asp212Val)
n.635A>T
c.2873A>T (p.Asp958Val)
c.2861A>T (p.Asp954Val)
c.2834A>T (p.Asp945Val)
n.3412A>T
n.3414A>T
c.3182A>T (p.Asp1061Val)
c.2951A>T (p.Asp984Val)
n.3197A>T
11g.77182139C>ACA381944323MYO7Ac.3093C>A (p.Asp1031Glu)
c.1158C>A (p.Asp386Glu)
c.934C>A
c.3060C>A (p.Asp1020Glu)
c.636C>A (p.Asp212Glu)
n.636C>A
c.2874C>A (p.Asp958Glu)
c.2862C>A (p.Asp954Glu)
c.2835C>A (p.Asp945Glu)
n.3413C>A
n.3415C>A
c.3183C>A (p.Asp1061Glu)
c.2952C>A (p.Asp984Glu)
n.3198C>A
11g.77182139C=CA1984113549MYO7Ac.3093C= (p.Asp1031=)
c.1158C= (p.Asp386=)
c.934C=
c.3060C= (p.Asp1020=)
c.636C= (p.Asp212=)
n.636C=
c.2874C= (p.Asp958=)
c.2862C= (p.Asp954=)
c.2835C= (p.Asp945=)
n.3413C=
n.3415C=
c.3183C= (p.Asp1061=)
c.2952C= (p.Asp984=)
n.3198C=
11g.77182139C>GCA381944325MYO7Ac.3093C>G (p.Asp1031Glu)
c.1158C>G (p.Asp386Glu)
c.934C>G
c.3060C>G (p.Asp1020Glu)
c.636C>G (p.Asp212Glu)
n.636C>G
c.2874C>G (p.Asp958Glu)
c.2862C>G (p.Asp954Glu)
c.2835C>G (p.Asp945Glu)
n.3413C>G
n.3415C>G
c.3183C>G (p.Asp1061Glu)
c.2952C>G (p.Asp984Glu)
n.3198C>G
11g.77182139C>TCA224841799MYO7Ac.3093C>T (p.Asp1031=)
c.1158C>T (p.Asp386=)
c.934C>T
c.3060C>T (p.Asp1020=)
c.636C>T (p.Asp212=)
n.636C>T
c.2874C>T (p.Asp958=)
c.2862C>T (p.Asp954=)
c.2835C>T (p.Asp945=)
n.3413C>T
n.3415C>T
c.3183C>T (p.Asp1061=)
c.2952C>T (p.Asp984=)
n.3198C>T
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
11g.77182140G>ACA381944328MYO7Ac.3094G>A (p.Glu1032Lys)
c.1159G>A (p.Glu387Lys)
c.935G>A
c.3061G>A (p.Glu1021Lys)
c.637G>A (p.Glu213Lys)
n.637G>A
c.2875G>A (p.Glu959Lys)
c.2863G>A (p.Glu955Lys)
c.2836G>A (p.Glu946Lys)
n.3414G>A
n.3416G>A
c.3184G>A (p.Glu1062Lys)
c.2953G>A (p.Glu985Lys)
n.3199G>A
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.77182140G>CCA381944330MYO7Ac.3094G>C (p.Glu1032Gln)
c.1159G>C (p.Glu387Gln)
c.935G>C
c.3061G>C (p.Glu1021Gln)
c.637G>C (p.Glu213Gln)
n.637G>C
c.2875G>C (p.Glu959Gln)
c.2863G>C (p.Glu955Gln)
c.2836G>C (p.Glu946Gln)
n.3414G>C
n.3416G>C
c.3184G>C (p.Glu1062Gln)
c.2953G>C (p.Glu985Gln)
n.3199G>C
11g.77182140G=CA1984113554MYO7Ac.3094G= (p.Glu1032=)
c.1159G= (p.Glu387=)
c.935G=
c.3061G= (p.Glu1021=)
c.637G= (p.Glu213=)
n.637G=
c.2875G= (p.Glu959=)
c.2863G= (p.Glu955=)
c.2836G= (p.Glu946=)
n.3414G=
n.3416G=
c.3184G= (p.Glu1062=)
c.2953G= (p.Glu985=)
n.3199G=
11g.77182140G>TCA381944332MYO7Ac.3094G>T (p.Glu1032Ter)
c.1159G>T (p.Glu387Ter)
c.935G>T
c.3061G>T (p.Glu1021Ter)
c.637G>T (p.Glu213Ter)
n.637G>T
c.2875G>T (p.Glu959Ter)
c.2863G>T (p.Glu955Ter)
c.2836G>T (p.Glu946Ter)
n.3414G>T
n.3416G>T
c.3184G>T (p.Glu1062Ter)
c.2953G>T (p.Glu985Ter)
n.3199G>T
gnomAD v4
11g.77182141A>CCA381944334MYO7Ac.3095A>C (p.Glu1032Ala)
c.1160A>C (p.Glu387Ala)
c.936A>C
c.3062A>C (p.Glu1021Ala)
c.638A>C (p.Glu213Ala)
n.638A>C
c.2876A>C (p.Glu959Ala)
c.2864A>C (p.Glu955Ala)
c.2837A>C (p.Glu946Ala)
n.3415A>C
n.3417A>C
c.3185A>C (p.Glu1062Ala)
c.2954A>C (p.Glu985Ala)
n.3200A>C
11g.77182141A>GCA381944336MYO7Ac.3095A>G (p.Glu1032Gly)
c.1160A>G (p.Glu387Gly)
c.936A>G
c.3062A>G (p.Glu1021Gly)
c.638A>G (p.Glu213Gly)
n.638A>G
c.2876A>G (p.Glu959Gly)
c.2864A>G (p.Glu955Gly)
c.2837A>G (p.Glu946Gly)
n.3415A>G
n.3417A>G
c.3185A>G (p.Glu1062Gly)
c.2954A>G (p.Glu985Gly)
n.3200A>G
11g.77182141A>TCA381944338MYO7Ac.3095A>T (p.Glu1032Val)
c.1160A>T (p.Glu387Val)
c.936A>T
c.3062A>T (p.Glu1021Val)
c.638A>T (p.Glu213Val)
n.638A>T
c.2876A>T (p.Glu959Val)
c.2864A>T (p.Glu955Val)
c.2837A>T (p.Glu946Val)
n.3415A>T
n.3417A>T
c.3185A>T (p.Glu1062Val)
c.2954A>T (p.Glu985Val)
n.3200A>T
11g.77182142G>ACA2574931389MYO7Ac.3096G>A (p.Glu1032=)
c.1161G>A (p.Glu387=)
c.937G>A
c.3063G>A (p.Glu1021=)
c.639G>A (p.Glu213=)
n.639G>A
c.2877G>A (p.Glu959=)
c.2865G>A (p.Glu955=)
c.2838G>A (p.Glu946=)
n.3416G>A
n.3418G>A
c.3186G>A (p.Glu1062=)
c.2955G>A (p.Glu985=)
n.3201G>A
11g.77182142G>CCA381944340MYO7Ac.3096G>C (p.Glu1032Asp)
c.1161G>C (p.Glu387Asp)
c.937G>C
c.3063G>C (p.Glu1021Asp)
c.639G>C (p.Glu213Asp)
n.639G>C
c.2877G>C (p.Glu959Asp)
c.2865G>C (p.Glu955Asp)
c.2838G>C (p.Glu946Asp)
n.3416G>C
n.3418G>C
c.3186G>C (p.Glu1062Asp)
c.2955G>C (p.Glu985Asp)
n.3201G>C
11g.77182142G>TCA381944342MYO7Ac.3096G>T (p.Glu1032Asp)
c.1161G>T (p.Glu387Asp)
c.937G>T
c.3063G>T (p.Glu1021Asp)
c.639G>T (p.Glu213Asp)
n.639G>T
c.2877G>T (p.Glu959Asp)
c.2865G>T (p.Glu955Asp)
c.2838G>T (p.Glu946Asp)
n.3416G>T
n.3418G>T
c.3186G>T (p.Glu1062Asp)
c.2955G>T (p.Glu985Asp)
n.3201G>T
11g.77182144dupCA2580084978MYO7Ac.3098dup (p.Asp1034Ter)
c.1163dup (p.Asp389Ter)
c.939dup
c.3065dup (p.Asp1023Ter)
c.641dup (p.Asp215Ter)
n.641dup
c.2879dup (p.Asp961Ter)
c.2867dup (p.Asp957Ter)
c.2840dup (p.Asp948Ter)
n.3418dup
n.3420dup
c.3188dup (p.Asp1064Ter)
c.2957dup (p.Asp987Ter)
n.3203dup
ClinVar gnomAD v4
11g.77182143G>ACA381944348MYO7Ac.3097G>A (p.Gly1033Ser)
c.1162G>A (p.Gly388Ser)
c.938G>A
c.3064G>A (p.Gly1022Ser)
c.640G>A (p.Gly214Ser)
n.640G>A
c.2878G>A (p.Gly960Ser)
c.2866G>A (p.Gly956Ser)
c.2839G>A (p.Gly947Ser)
n.3417G>A
n.3419G>A
c.3187G>A (p.Gly1063Ser)
c.2956G>A (p.Gly986Ser)
n.3202G>A
11g.77182143G>CCA381944349MYO7Ac.3097G>C (p.Gly1033Arg)
c.1162G>C (p.Gly388Arg)
c.938G>C
c.3064G>C (p.Gly1022Arg)
c.640G>C (p.Gly214Arg)
n.640G>C
c.2878G>C (p.Gly960Arg)
c.2866G>C (p.Gly956Arg)
c.2839G>C (p.Gly947Arg)
n.3417G>C
n.3419G>C
c.3187G>C (p.Gly1063Arg)
c.2956G>C (p.Gly986Arg)
n.3202G>C
11g.77182143G>TCA381944345MYO7Ac.3097G>T (p.Gly1033Cys)
c.1162G>T (p.Gly388Cys)
c.938G>T
c.3064G>T (p.Gly1022Cys)
c.640G>T (p.Gly214Cys)
n.640G>T
c.2878G>T (p.Gly960Cys)
c.2866G>T (p.Gly956Cys)
c.2839G>T (p.Gly947Cys)
n.3417G>T
n.3419G>T
c.3187G>T (p.Gly1063Cys)
c.2956G>T (p.Gly986Cys)
n.3202G>T
11g.77182144G>ACA224841802MYO7Ac.3098G>A (p.Gly1033Asp)
c.1163G>A (p.Gly388Asp)
c.939G>A
c.3065G>A (p.Gly1022Asp)
c.641G>A (p.Gly214Asp)
n.641G>A
c.2879G>A (p.Gly960Asp)
c.2867G>A (p.Gly956Asp)
c.2840G>A (p.Gly947Asp)
n.3418G>A
n.3420G>A
c.3188G>A (p.Gly1063Asp)
c.2957G>A (p.Gly986Asp)
n.3203G>A
dbSNP gnomAD v3 gnomAD v4
11g.77182144G>CCA381944350MYO7Ac.3098G>C (p.Gly1033Ala)
c.1163G>C (p.Gly388Ala)
c.939G>C
c.3065G>C (p.Gly1022Ala)
c.641G>C (p.Gly214Ala)
n.641G>C
c.2879G>C (p.Gly960Ala)
c.2867G>C (p.Gly956Ala)
c.2840G>C (p.Gly947Ala)
n.3418G>C
n.3420G>C
c.3188G>C (p.Gly1063Ala)
c.2957G>C (p.Gly986Ala)
n.3203G>C
11g.77182144G=CA1984113555MYO7Ac.3098G= (p.Gly1033=)
c.1163G= (p.Gly388=)
c.939G=
c.3065G= (p.Gly1022=)
c.641G= (p.Gly214=)
n.641G=
c.2879G= (p.Gly960=)
c.2867G= (p.Gly956=)
c.2840G= (p.Gly947=)
n.3418G=
n.3420G=
c.3188G= (p.Gly1063=)
c.2957G= (p.Gly986=)
n.3203G=
11g.77182144G>TCA381944353MYO7Ac.3098G>T (p.Gly1033Val)
c.1163G>T (p.Gly388Val)
c.939G>T
c.3065G>T (p.Gly1022Val)
c.641G>T (p.Gly214Val)
n.641G>T
c.2879G>T (p.Gly960Val)
c.2867G>T (p.Gly956Val)
c.2840G>T (p.Gly947Val)
n.3418G>T
n.3420G>T
c.3188G>T (p.Gly1063Val)
c.2957G>T (p.Gly986Val)
n.3203G>T
11g.77182145T>GCA2499221321MYO7Ac.3099T>G (p.Gly1033=)
c.1164T>G (p.Gly388=)
c.940T>G
c.3066T>G (p.Gly1022=)
c.642T>G (p.Gly214=)
n.642T>G
c.2880T>G (p.Gly960=)
c.2868T>G (p.Gly956=)
c.2841T>G (p.Gly947=)
n.3419T>G
n.3421T>G
c.3189T>G (p.Gly1063=)
c.2958T>G (p.Gly986=)
n.3204T>G
ClinVar dbSNP gnomAD v4
11g.77182146G>ACA381944355MYO7Ac.3100G>A (p.Asp1034Asn)
c.1165G>A (p.Asp389Asn)
c.941G>A
c.3067G>A (p.Asp1023Asn)
c.643G>A (p.Asp215Asn)
n.643G>A
c.2881G>A (p.Asp961Asn)
c.2869G>A (p.Asp957Asn)
c.2842G>A (p.Asp948Asn)
n.3420G>A
n.3422G>A
c.3190G>A (p.Asp1064Asn)
c.2959G>A (p.Asp987Asn)
n.3205G>A
11g.77182146G>CCA381944358MYO7Ac.3100G>C (p.Asp1034His)
c.1165G>C (p.Asp389His)
c.941G>C
c.3067G>C (p.Asp1023His)
c.643G>C (p.Asp215His)
n.643G>C
c.2881G>C (p.Asp961His)
c.2869G>C (p.Asp957His)
c.2842G>C (p.Asp948His)
n.3420G>C
n.3422G>C
c.3190G>C (p.Asp1064His)
c.2959G>C (p.Asp987His)
n.3205G>C
11g.77182146G>TCA381944356MYO7Ac.3100G>T (p.Asp1034Tyr)
c.1165G>T (p.Asp389Tyr)
c.941G>T
c.3067G>T (p.Asp1023Tyr)
c.643G>T (p.Asp215Tyr)
n.643G>T
c.2881G>T (p.Asp961Tyr)
c.2869G>T (p.Asp957Tyr)
c.2842G>T (p.Asp948Tyr)
n.3420G>T
n.3422G>T
c.3190G>T (p.Asp1064Tyr)
c.2959G>T (p.Asp987Tyr)
n.3205G>T
11g.77182147A>CCA381944360MYO7Ac.3101A>C (p.Asp1034Ala)
c.1166A>C (p.Asp389Ala)
c.942A>C
c.3068A>C (p.Asp1023Ala)
c.644A>C (p.Asp215Ala)
n.644A>C
c.2882A>C (p.Asp961Ala)
c.2870A>C (p.Asp957Ala)
c.2843A>C (p.Asp948Ala)
n.3421A>C
n.3423A>C
c.3191A>C (p.Asp1064Ala)
c.2960A>C (p.Asp987Ala)
n.3206A>C
11g.77182147A>GCA381944363MYO7Ac.3101A>G (p.Asp1034Gly)
c.1166A>G (p.Asp389Gly)
c.942A>G
c.3068A>G (p.Asp1023Gly)
c.644A>G (p.Asp215Gly)
n.644A>G
c.2882A>G (p.Asp961Gly)
c.2870A>G (p.Asp957Gly)
c.2843A>G (p.Asp948Gly)
n.3421A>G
n.3423A>G
c.3191A>G (p.Asp1064Gly)
c.2960A>G (p.Asp987Gly)
n.3206A>G
11g.77182147A>TCA381944362MYO7Ac.3101A>T (p.Asp1034Val)
c.1166A>T (p.Asp389Val)
c.942A>T
c.3068A>T (p.Asp1023Val)
c.644A>T (p.Asp215Val)
n.644A>T
c.2882A>T (p.Asp961Val)
c.2870A>T (p.Asp957Val)
c.2843A>T (p.Asp948Val)
n.3421A>T
n.3423A>T
c.3191A>T (p.Asp1064Val)
c.2960A>T (p.Asp987Val)
n.3206A>T
11g.77182148C>ACA381944364MYO7Ac.3102C>A (p.Asp1034Glu)
c.1167C>A (p.Asp389Glu)
c.943C>A
c.3069C>A (p.Asp1023Glu)
c.645C>A (p.Asp215Glu)
n.645C>A
c.2883C>A (p.Asp961Glu)
c.2871C>A (p.Asp957Glu)
c.2844C>A (p.Asp948Glu)
n.3422C>A
n.3424C>A
c.3192C>A (p.Asp1064Glu)
c.2961C>A (p.Asp987Glu)
n.3207C>A
11g.77182148C>GCA381944366MYO7Ac.3102C>G (p.Asp1034Glu)
c.1167C>G (p.Asp389Glu)
c.943C>G
c.3069C>G (p.Asp1023Glu)
c.645C>G (p.Asp215Glu)
n.645C>G
c.2883C>G (p.Asp961Glu)
c.2871C>G (p.Asp957Glu)
c.2844C>G (p.Asp948Glu)
n.3422C>G
n.3424C>G
c.3192C>G (p.Asp1064Glu)
c.2961C>G (p.Asp987Glu)
n.3207C>G
11g.77182149C>ACA381944368MYO7Ac.3103C>A (p.Gln1035Lys)
c.1168C>A (p.Gln390Lys)
c.944C>A
c.3070C>A (p.Gln1024Lys)
c.646C>A (p.Gln216Lys)
n.646C>A
c.2884C>A (p.Gln962Lys)
c.2872C>A (p.Gln958Lys)
c.2845C>A (p.Gln949Lys)
n.3423C>A
n.3425C>A
c.3193C>A (p.Gln1065Lys)
c.2962C>A (p.Gln988Lys)
n.3208C>A
11g.77182149C>GCA381944370MYO7Ac.3103C>G (p.Gln1035Glu)
c.1168C>G (p.Gln390Glu)
c.944C>G
c.3070C>G (p.Gln1024Glu)
c.646C>G (p.Gln216Glu)
n.646C>G
c.2884C>G (p.Gln962Glu)
c.2872C>G (p.Gln958Glu)
c.2845C>G (p.Gln949Glu)
n.3423C>G
n.3425C>G
c.3193C>G (p.Gln1065Glu)
c.2962C>G (p.Gln988Glu)
n.3208C>G
11g.77182149C>TCA381944372MYO7Ac.3103C>T (p.Gln1035Ter)
c.1168C>T (p.Gln390Ter)
c.944C>T
c.3070C>T (p.Gln1024Ter)
c.646C>T (p.Gln216Ter)
n.646C>T
c.2884C>T (p.Gln962Ter)
c.2872C>T (p.Gln958Ter)
c.2845C>T (p.Gln949Ter)
n.3423C>T
n.3425C>T
c.3193C>T (p.Gln1065Ter)
c.2962C>T (p.Gln988Ter)
n.3208C>T
gnomAD v4
11g.77182150A>CCA381944374MYO7Ac.3104A>C (p.Gln1035Pro)
c.1169A>C (p.Gln390Pro)
c.945A>C
c.3071A>C (p.Gln1024Pro)
c.647A>C (p.Gln216Pro)
n.647A>C
c.2885A>C (p.Gln962Pro)
c.2873A>C (p.Gln958Pro)
c.2846A>C (p.Gln949Pro)
n.3424A>C
n.3426A>C
c.3194A>C (p.Gln1065Pro)
c.2963A>C (p.Gln988Pro)
n.3209A>C
11g.77182150A>GCA381944376MYO7Ac.3104A>G (p.Gln1035Arg)
c.1169A>G (p.Gln390Arg)
c.945A>G
c.3071A>G (p.Gln1024Arg)
c.647A>G (p.Gln216Arg)
n.647A>G
c.2885A>G (p.Gln962Arg)
c.2873A>G (p.Gln958Arg)
c.2846A>G (p.Gln949Arg)
n.3424A>G
n.3426A>G
c.3194A>G (p.Gln1065Arg)
c.2963A>G (p.Gln988Arg)
n.3209A>G
11g.77182150A>TCA381944378MYO7Ac.3104A>T (p.Gln1035Leu)
c.1169A>T (p.Gln390Leu)
c.945A>T
c.3071A>T (p.Gln1024Leu)
c.647A>T (p.Gln216Leu)
n.647A>T
c.2885A>T (p.Gln962Leu)
c.2873A>T (p.Gln958Leu)
c.2846A>T (p.Gln949Leu)
n.3424A>T
n.3426A>T
c.3194A>T (p.Gln1065Leu)
c.2963A>T (p.Gln988Leu)
n.3209A>T
11g.77182151G>CCA381944380MYO7Ac.3105G>C (p.Gln1035His)
c.1170G>C (p.Gln390His)
c.946G>C
c.3072G>C (p.Gln1024His)
c.648G>C (p.Gln216His)
n.648G>C
c.2886G>C (p.Gln962His)
c.2874G>C (p.Gln958His)
c.2847G>C (p.Gln949His)
n.3425G>C
n.3427G>C
c.3195G>C (p.Gln1065His)
c.2964G>C (p.Gln988His)
n.3210G>C
11g.77182151G>TCA381944381MYO7Ac.3105G>T (p.Gln1035His)
c.1170G>T (p.Gln390His)
c.946G>T
c.3072G>T (p.Gln1024His)
c.648G>T (p.Gln216His)
n.648G>T
c.2886G>T (p.Gln962His)
c.2874G>T (p.Gln958His)
c.2847G>T (p.Gln949His)
n.3425G>T
n.3427G>T
c.3195G>T (p.Gln1065His)
c.2964G>T (p.Gln988His)
n.3210G>T
11g.77182152C>ACA381944383MYO7Ac.3106C>A (p.Leu1036Met)
c.1171C>A (p.Leu391Met)
c.947C>A
c.3073C>A (p.Leu1025Met)
c.649C>A (p.Leu217Met)
n.649C>A
c.2887C>A (p.Leu963Met)
c.2875C>A (p.Leu959Met)
c.2848C>A (p.Leu950Met)
n.3426C>A
n.3428C>A
c.3196C>A (p.Leu1066Met)
c.2965C>A (p.Leu989Met)
n.3211C>A
11g.77182152C>GCA381944385MYO7Ac.3106C>G (p.Leu1036Val)
c.1171C>G (p.Leu391Val)
c.947C>G
c.3073C>G (p.Leu1025Val)
c.649C>G (p.Leu217Val)
n.649C>G
c.2887C>G (p.Leu963Val)
c.2875C>G (p.Leu959Val)
c.2848C>G (p.Leu950Val)
n.3426C>G
n.3428C>G
c.3196C>G (p.Leu1066Val)
c.2965C>G (p.Leu989Val)
n.3211C>G
11g.77182152C>TCA2697548828MYO7Ac.3106C>T (p.Leu1036=)
c.1171C>T (p.Leu391=)
c.947C>T
c.3073C>T (p.Leu1025=)
c.649C>T (p.Leu217=)
n.649C>T
c.2887C>T (p.Leu963=)
c.2875C>T (p.Leu959=)
c.2848C>T (p.Leu950=)
n.3426C>T
n.3428C>T
c.3196C>T (p.Leu1066=)
c.2965C>T (p.Leu989=)
n.3211C>T
ClinVar
11g.77182153T>ACA381944387MYO7Ac.3107T>A (p.Leu1036Gln)
c.1172T>A (p.Leu391Gln)
c.948T>A
c.3074T>A (p.Leu1025Gln)
c.650T>A (p.Leu217Gln)
n.650T>A
c.2888T>A (p.Leu963Gln)
c.2876T>A (p.Leu959Gln)
c.2849T>A (p.Leu950Gln)
n.3427T>A
n.3429T>A
c.3197T>A (p.Leu1066Gln)
c.2966T>A (p.Leu989Gln)
n.3212T>A
11g.77182153T>CCA381944389MYO7Ac.3107T>C (p.Leu1036Pro)
c.1172T>C (p.Leu391Pro)
c.948T>C
c.3074T>C (p.Leu1025Pro)
c.650T>C (p.Leu217Pro)
n.650T>C
c.2888T>C (p.Leu963Pro)
c.2876T>C (p.Leu959Pro)
c.2849T>C (p.Leu950Pro)
n.3427T>C
n.3429T>C
c.3197T>C (p.Leu1066Pro)
c.2966T>C (p.Leu989Pro)
n.3212T>C
11g.77182153T>GCA381944390MYO7Ac.3107T>G (p.Leu1036Arg)
c.1172T>G (p.Leu391Arg)
c.948T>G
c.3074T>G (p.Leu1025Arg)
c.650T>G (p.Leu217Arg)
n.650T>G
c.2888T>G (p.Leu963Arg)
c.2876T>G (p.Leu959Arg)
c.2849T>G (p.Leu950Arg)
n.3427T>G
n.3429T>G
c.3197T>G (p.Leu1066Arg)
c.2966T>G (p.Leu989Arg)
n.3212T>G
11g.77182154G>CCA2573147754MYO7Ac.3108G>C (p.Leu1036=)
c.1173G>C (p.Leu391=)
c.949G>C
c.3075G>C (p.Leu1025=)
c.651G>C (p.Leu217=)
n.651G>C
c.2889G>C (p.Leu963=)
c.2877G>C (p.Leu959=)
c.2850G>C (p.Leu950=)
n.3428G>C
n.3430G>C
c.3198G>C (p.Leu1066=)
c.2967G>C (p.Leu989=)
n.3213G>C
ClinVar dbSNP

Number of alleles fetched