ClinVar Miner

List of variants in gene MYO7A reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_000260.4(MYO7A):c.5324T>C (p.Ile1775Thr) rs115123584 0.00303
NM_000260.4(MYO7A):c.1007G>A (p.Arg336His) rs45629132 0.00164
NM_000260.4(MYO7A):c.*8C>T rs370206645 0.00099
NM_000260.4(MYO7A):c.803A>G (p.Lys268Arg) rs184866544 0.00098
NM_000260.4(MYO7A):c.5259G>A (p.Lys1753=) rs370062187 0.00096
NM_000260.4(MYO7A):c.3503+17G>A rs369969967 0.00073
NM_000260.4(MYO7A):c.2283G>A (p.Arg761=) rs111033229 0.00064
NM_000260.4(MYO7A):c.1343+50T>A rs77568474 0.00061
NM_000260.4(MYO7A):c.2097C>T (p.Gly699=) rs373495082 0.00046
NM_000260.4(MYO7A):c.735+3G>A rs371398512 0.00037
NM_000260.4(MYO7A):c.849+7C>G rs370740228 0.00035
NM_000260.4(MYO7A):c.4757A>G (p.Asn1586Ser) rs201251963 0.00034
NM_000260.4(MYO7A):c.5169-5G>A rs727505232 0.00034
NM_000260.4(MYO7A):c.4281G>A (p.Thr1427=) rs185607254 0.00032
NM_000260.4(MYO7A):c.5108C>T (p.Ala1703Val) rs199561332 0.00032
NM_000260.4(MYO7A):c.5253G>T (p.Pro1751=) rs377388669 0.00032
NM_000260.4(MYO7A):c.448C>A (p.Arg150=) rs121965079 0.00031
NM_000260.4(MYO7A):c.6013A>G (p.Lys2005Glu) rs186644871 0.00031
NM_000260.4(MYO7A):c.6546C>T (p.Cys2182=) rs185748200 0.00022
NM_000260.4(MYO7A):c.5005G>A (p.Val1669Ile) rs374655803 0.00021
NM_000260.4(MYO7A):c.6363G>A (p.Thr2121=) rs367738288 0.00021
NM_000260.4(MYO7A):c.879G>A (p.Val293=) rs185844002 0.00020
NM_000260.4(MYO7A):c.3858G>A (p.Ala1286=) rs372623270 0.00019
NM_000260.4(MYO7A):c.2106C>T (p.Arg702=) rs369787754 0.00017
NM_000260.4(MYO7A):c.3630+7A>G rs373958166 0.00015
NM_000260.4(MYO7A):c.1872G>A (p.Thr624=) rs370110939 0.00011
NM_000260.4(MYO7A):c.4917G>A (p.Thr1639=) rs367670696 0.00011
NM_000260.4(MYO7A):c.2091G>A (p.Lys697=) rs768972429 0.00009
NM_000260.4(MYO7A):c.3954C>T (p.His1318=) rs749218462 0.00009
NM_000260.4(MYO7A):c.4938G>A (p.Ser1646=) rs550479429 0.00009
NM_000260.4(MYO7A):c.519G>A (p.Gln173=) rs369757929 0.00008
NM_000260.4(MYO7A):c.3507C>T (p.Asp1169=) rs782788403 0.00007
NM_000260.4(MYO7A):c.4650G>A (p.Pro1550=) rs751242817 0.00007
NM_000260.4(MYO7A):c.2235C>T (p.Thr745=) rs782065768 0.00005
NM_000260.4(MYO7A):c.2724C>T (p.Asp908=) rs199979876 0.00005
NM_000260.4(MYO7A):c.5079C>T (p.Asp1693=) rs751298357 0.00005
NM_000260.4(MYO7A):c.133-6C>T rs376963984 0.00004
NM_000260.4(MYO7A):c.3109-13C>T rs551521854 0.00004
NM_000260.4(MYO7A):c.4539C>T (p.Phe1513=) rs780198980 0.00004
NM_000260.4(MYO7A):c.5374G>A (p.Val1792Ile) rs369424114 0.00004
NM_000260.4(MYO7A):c.5943C>T (p.Asp1981=) rs773907543 0.00004
NM_000260.4(MYO7A):c.4647C>A (p.Thr1549=) rs757971917 0.00003
NM_000260.4(MYO7A):c.286-4G>A rs782708856 0.00002
NM_000260.4(MYO7A):c.1710A>G (p.Arg570=) rs782763913 0.00001
NM_000260.4(MYO7A):c.1881C>G (p.Ala627=) rs908932600 0.00001
NM_000260.4(MYO7A):c.2142C>G (p.Gly714=) rs1555079508 0.00001
NM_000260.4(MYO7A):c.3702C>G (p.Thr1234=) rs77299211 0.00001
NM_000260.4(MYO7A):c.5029C>T (p.Pro1677Ser) rs535102352 0.00001
NM_000260.4(MYO7A):c.5793C>T (p.Ile1931=) rs550891509 0.00001
NM_000260.4(MYO7A):c.1343+8G>T rs2276278
NM_000260.4(MYO7A):c.19-4A>G
NM_000260.4(MYO7A):c.2523C>T (p.Leu841=) rs988933838
NM_000260.4(MYO7A):c.3042G>A (p.Thr1014=) rs111033507
NM_000260.4(MYO7A):c.3138C>T (p.Leu1046=)
NM_000260.4(MYO7A):c.3631-8G>A
NM_000260.4(MYO7A):c.3822G>A (p.Thr1274=)
NM_000260.4(MYO7A):c.5043+8G>A rs1957072020
NM_000260.4(MYO7A):c.5227C>A (p.Arg1743=) rs111033287
NM_000260.4(MYO7A):c.5227C>T (p.Arg1743Trp) rs111033287
NM_000260.4(MYO7A):c.5589C>T (p.His1863=) rs727504024

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