ClinVar Miner

List of variants in gene MYO6 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP gnomAD frequency
NM_004999.4(MYO6):c.2534C>T (p.Thr845Ile) rs55662069 0.00322
NM_004999.4(MYO6):c.1025C>T (p.Ala342Val) rs145564837 0.00128
NM_004999.4(MYO6):c.92T>C (p.Ile31Thr) rs148735953 0.00093
NM_004999.4(MYO6):c.3529C>T (p.Arg1177Cys) rs146419641 0.00069
NM_004999.4(MYO6):c.875T>C (p.Leu292Ser) rs144038082 0.00056
NM_004999.4(MYO6):c.1546+6T>C rs199999513 0.00052
NM_004999.4(MYO6):c.2836C>T (p.Arg946Cys) rs141845119 0.00039
NM_004999.4(MYO6):c.18C>T (p.Pro6=) rs138024490 0.00035
NM_004999.4(MYO6):c.262-12T>G rs368072756 0.00017
NM_004999.4(MYO6):c.1224-15A>G rs376927352 0.00016
NM_004999.4(MYO6):c.553+13T>A rs369806112 0.00013
NM_004999.4(MYO6):c.441C>T (p.Ile147=) rs565770950 0.00012
NM_004999.4(MYO6):c.600C>T (p.Asn200=) rs145665265 0.00011
NM_004999.4(MYO6):c.3537C>T (p.Ala1179=) rs371212410 0.00006
NM_004999.4(MYO6):c.966G>A (p.Thr322=) rs375754710 0.00005
NM_004999.4(MYO6):c.1926C>T (p.Ser642=) rs184784079 0.00004
NM_004999.4(MYO6):c.3107+11C>T rs201968938 0.00004
NM_004999.4(MYO6):c.1945-16T>C rs373824667 0.00002
NM_004999.4(MYO6):c.27G>A (p.Ala9=) rs767670766 0.00002
NM_004999.4(MYO6):c.297A>G (p.Pro99=) rs375790985 0.00002
NM_004999.4(MYO6):c.3659-10A>G rs765929647 0.00002
NM_004999.4(MYO6):c.2286+8T>C rs780274416 0.00001
NM_004999.4(MYO6):c.2337G>A (p.Glu779=) rs762207024 0.00001
NM_004999.4(MYO6):c.498-11A>G rs749261743 0.00001
NM_004999.4(MYO6):c.564C>T (p.Leu188=) rs750374337 0.00001
NM_004999.4(MYO6):c.1078+12A>G
NM_004999.4(MYO6):c.1095G>A (p.Lys365=)
NM_004999.4(MYO6):c.1128T>C (p.Ala376=) rs1583282758
NM_004999.4(MYO6):c.117+11C>T
NM_004999.4(MYO6):c.1223+16A>T rs974546034
NM_004999.4(MYO6):c.1474-12T>C
NM_004999.4(MYO6):c.1675-18A>G
NM_004999.4(MYO6):c.1749G>A (p.Ala583=)
NM_004999.4(MYO6):c.1749G>T (p.Ala583=)
NM_004999.4(MYO6):c.1866A>G (p.Glu622=)
NM_004999.4(MYO6):c.188-19T>G
NM_004999.4(MYO6):c.1944+18T>G
NM_004999.4(MYO6):c.1944+7G>A
NM_004999.4(MYO6):c.1944+7G>T rs1265157032
NM_004999.4(MYO6):c.1984-5C>T
NM_004999.4(MYO6):c.1992C>T (p.Ser664=)
NM_004999.4(MYO6):c.2078-20G>T
NM_004999.4(MYO6):c.222C>G (p.Leu74=)
NM_004999.4(MYO6):c.222C>T (p.Leu74=) rs1395892527
NM_004999.4(MYO6):c.2287-9A>G
NM_004999.4(MYO6):c.2417-7C>T
NM_004999.4(MYO6):c.2507+12A>G rs1214613190
NM_004999.4(MYO6):c.2507+19A>G
NM_004999.4(MYO6):c.2508-19T>C
NM_004999.4(MYO6):c.264A>G (p.Thr88=)
NM_004999.4(MYO6):c.2898AGA[3] (p.Glu970del) rs727504743
NM_004999.4(MYO6):c.2946+16G>T
NM_004999.4(MYO6):c.2972G>T (p.Arg991Leu) rs529167250
NM_004999.4(MYO6):c.3099G>T (p.Ala1033=)
NM_004999.4(MYO6):c.3103C>A (p.Arg1035=) rs551471138
NM_004999.4(MYO6):c.3107+19G>A rs538399704
NM_004999.4(MYO6):c.3107+19G>T
NM_004999.4(MYO6):c.3138-4G>A
NM_004999.4(MYO6):c.3176+14A>C
NM_004999.4(MYO6):c.3177-15G>A
NM_004999.4(MYO6):c.3281-18G>A
NM_004999.4(MYO6):c.3281-18G>T rs75371739
NM_004999.4(MYO6):c.3288G>A (p.Glu1096=)
NM_004999.4(MYO6):c.3321G>A (p.Arg1107=)
NM_004999.4(MYO6):c.3412+8G>C
NM_004999.4(MYO6):c.3413-20C>T
NM_004999.4(MYO6):c.3439+14T>G
NM_004999.4(MYO6):c.3531C>T (p.Arg1177=)
NM_004999.4(MYO6):c.3659-5T>C
NM_004999.4(MYO6):c.3723T>C (p.Gly1241=)
NM_004999.4(MYO6):c.3762A>G (p.Glu1254=)
NM_004999.4(MYO6):c.3822C>A (p.Thr1274=)
NM_004999.4(MYO6):c.3840G>A (p.Leu1280=) rs1257266201
NM_004999.4(MYO6):c.522A>G (p.Thr174=)
NM_004999.4(MYO6):c.553+17A>G
NM_004999.4(MYO6):c.652-9G>T
NM_004999.4(MYO6):c.897+19C>G
NM_004999.4(MYO6):c.933A>G (p.Leu311=)

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