ClinVar Miner

List of variants in gene MYO15A reported as benign for not specified

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Gene type:
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Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_016239.4(MYO15A):c.7185T>C (p.Phe2395=) rs2955379 0.99481
NM_016239.4(MYO15A):c.5929T>C (p.Cys1977Arg) rs854777 0.79149
NM_016239.4(MYO15A):c.10431T>C (p.Tyr3477=) rs854800 0.78890
NM_016239.4(MYO15A):c.5826-12A>C rs854778 0.76256
NM_016239.4(MYO15A):c.7857G>A (p.Gly2619=) rs854772 0.55976
NM_016239.4(MYO15A):c.4954C>T (p.Leu1652=) rs2280777 0.52028
NM_016239.4(MYO15A):c.1899A>G (p.Pro633=) rs2955366 0.41355
NM_016239.4(MYO15A):c.1783G>A (p.Ala595Thr) rs2955365 0.39950
NM_016239.4(MYO15A):c.8322C>T (p.Ser2774=) rs712272 0.34416
NM_016239.4(MYO15A):c.8045A>T (p.Tyr2682Phe) rs712270 0.34278
NM_016239.4(MYO15A):c.8460-15C>T rs861278 0.34259
NM_016239.4(MYO15A):c.2152T>G (p.Trp718Gly) rs2955367 0.34123
NM_016239.4(MYO15A):c.9518-11T>C rs62073604 0.19159
NM_016239.4(MYO15A):c.9486C>T (p.Asp3162=) rs8077577 0.19129
NM_016239.4(MYO15A):c.5212-14C>T rs2072652 0.16745
NM_016239.4(MYO15A):c.6052G>A (p.Gly2018Arg) rs2272571 0.16711
NM_016239.4(MYO15A):c.7655-17G>A rs2056841 0.15514
NM_016239.4(MYO15A):c.5649+14G>A rs2072653 0.15358
NM_016239.4(MYO15A):c.7468G>A (p.Ala2490Thr) rs16960959 0.03924
NM_016239.4(MYO15A):c.7503G>A (p.Thr2501=) rs16960961 0.02872
NM_016239.4(MYO15A):c.2462A>C (p.Gln821Pro) rs372125621 0.02081
NM_016239.4(MYO15A):c.4533C>T (p.Ala1511=) rs114328138 0.01906
NM_016239.4(MYO15A):c.3413A>G (p.Gln1138Arg) rs76468019 0.01903
NM_016239.4(MYO15A):c.9708G>A (p.Val3236=) rs115393178 0.01622
NM_016239.4(MYO15A):c.2238G>T (p.Arg746Ser) rs79760961 0.01604
NM_016239.4(MYO15A):c.3023C>G (p.Thr1008Ser) rs143316414 0.01192
NM_016239.4(MYO15A):c.8262G>A (p.Thr2754=) rs1006770 0.01178
NM_016239.4(MYO15A):c.1791G>A (p.Ala597=) rs114552047 0.01041
NM_016239.4(MYO15A):c.4206+13C>G rs141183007 0.00838
NM_016239.4(MYO15A):c.6796G>A (p.Val2266Met) rs114274755 0.00791
NM_016239.4(MYO15A):c.2680C>T (p.Pro894Ser) rs76707172 0.00765
NM_016239.4(MYO15A):c.6336C>T (p.Tyr2112=) rs76886140 0.00725
NM_016239.4(MYO15A):c.3140C>G (p.Pro1047Arg) rs77565048 0.00686
NM_016239.4(MYO15A):c.10182G>A (p.Ala3394=) rs79230542 0.00665
NM_016239.4(MYO15A):c.9478C>T (p.Leu3160Phe) rs140029076 0.00658
NM_016239.4(MYO15A):c.6614C>T (p.Thr2205Ile) rs121908970 0.00599
NM_016239.4(MYO15A):c.2790C>T (p.Asp930=) rs185688918 0.00559
NM_016239.4(MYO15A):c.6192G>A (p.Gly2064=) rs55688805 0.00470
NM_016239.4(MYO15A):c.3756C>T (p.Tyr1252=) rs59933498 0.00463
NM_016239.4(MYO15A):c.5894G>A (p.Arg1965His) rs139347804 0.00451
NM_016239.4(MYO15A):c.8339C>T (p.Thr2780Met) rs143826293 0.00394
NM_016239.4(MYO15A):c.3026C>A (p.Pro1009His) rs117612144 0.00347
NM_016239.4(MYO15A):c.5880C>T (p.His1960=) rs201487604 0.00331
NM_016239.4(MYO15A):c.1385G>A (p.Gly462Asp) rs145292219 0.00326
NM_016239.4(MYO15A):c.1158C>T (p.Gly386=) rs186829587 0.00324
NM_016239.4(MYO15A):c.4888C>T (p.Arg1630Cys) rs138861831 0.00280
NM_016239.4(MYO15A):c.10242C>T (p.Phe3414=) rs188485743 0.00264
NM_016239.4(MYO15A):c.4779+9G>A rs183256997 0.00264
NM_016239.4(MYO15A):c.3774C>T (p.Ile1258=) rs148723625 0.00241
NM_016239.4(MYO15A):c.5133+15A>G rs150128469 0.00214
NM_016239.4(MYO15A):c.7655-7C>G rs191171943 0.00211
NM_016239.4(MYO15A):c.10443G>A (p.Ala3481=) rs190486507 0.00208
NM_016239.4(MYO15A):c.4033A>T (p.Ile1345Leu) rs201234482 0.00191
NM_016239.4(MYO15A):c.8811C>T (p.His2937=) rs200583193 0.00190
NM_016239.4(MYO15A):c.9754A>G (p.Asn3252Asp) rs147458358 0.00177
NM_016239.4(MYO15A):c.10573A>G (p.Ser3525Gly) rs182332665 0.00151
NM_016239.4(MYO15A):c.4719G>A (p.Ala1573=) rs186426892 0.00146
NM_016239.4(MYO15A):c.8269G>A (p.Val2757Met) rs140140417 0.00139
NM_016239.4(MYO15A):c.4655+11G>A rs117021471 0.00132
NM_016239.4(MYO15A):c.6186C>A (p.Ala2062=) rs141475629 0.00123
NM_016239.4(MYO15A):c.3979C>T (p.Leu1327=) rs146245515 0.00063
NM_016239.4(MYO15A):c.915C>T (p.Tyr305=) rs200695102 0.00045
NM_016239.4(MYO15A):c.9792G>A (p.Gln3264=) rs149189607 0.00042
NM_016239.4(MYO15A):c.3999C>T (p.Ala1333=) rs192570479 0.00040
NM_016239.4(MYO15A):c.876C>T (p.Pro292=) rs368755362 0.00039
NM_016239.4(MYO15A):c.6743C>T (p.Ala2248Val) rs199831544 0.00036
NM_016239.4(MYO15A):c.9873C>T (p.Leu3291=) rs146865523 0.00026
NM_016239.4(MYO15A):c.6274-10C>T rs201459354 0.00022
NM_016239.4(MYO15A):c.9436C>T (p.His3146Tyr) rs201230033 0.00006
NM_016239.4(MYO15A):c.3130_3147dup (p.Ile1044_Asp1049dup) rs377177611
NM_016239.4(MYO15A):c.3658G>A (p.Gly1220Arg) rs146754758
NM_016239.4(MYO15A):c.3658G>C (p.Gly1220Arg) rs146754758
NM_016239.4(MYO15A):c.8088+5C>G rs9916193

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