ClinVar Miner

Variants in gene MYO15A with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 77
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HGVS dbSNP gnomAD frequency
NM_016239.4(MYO15A):c.4533C>T (p.Ala1511=) rs114328138 0.01906
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.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.2028C>A (p.Pro676=) rs577023485 0.00762
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.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.1941A>C (p.Pro647=) rs537016494 0.00437
NM_016239.4(MYO15A):c.3201G>A (p.Ala1067=) rs148356427 0.00415
NM_016239.4(MYO15A):c.2562C>T (p.Cys854=) rs182293382 0.00413
NM_016239.4(MYO15A):c.3866+18G>A rs73979300 0.00413
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.5910+17A>C rs58914384 0.00235
NM_016239.4(MYO15A):c.2020C>T (p.Pro674Ser) rs557225435 0.00223
NM_016239.4(MYO15A):c.5133+15A>G rs150128469 0.00214
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.8841G>A (p.Leu2947=) rs201809145 0.00166
NM_016239.4(MYO15A):c.823G>C (p.Gly275Arg) rs183969516 0.00158
NM_016239.4(MYO15A):c.4623G>A (p.Thr1541=) rs926074 0.00155
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.54G>A (p.Lys18=) rs144909486 0.00142
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.9691-3C>A rs142996507 0.00110
NM_016239.4(MYO15A):c.709G>A (p.Asp237Asn) rs201737186 0.00099
NM_016239.4(MYO15A):c.7655-16C>T rs376816545 0.00093
NM_016239.4(MYO15A):c.10393C>T (p.Arg3465Trp) rs201028204 0.00073
NM_016239.4(MYO15A):c.8157C>T (p.His2719=) rs373955726 0.00067
NM_016239.4(MYO15A):c.8224+8G>C rs115647199 0.00067
NM_016239.4(MYO15A):c.1634C>T (p.Ala545Val) rs199740747 0.00063
NM_016239.4(MYO15A):c.3979C>T (p.Leu1327=) rs146245515 0.00063
NM_016239.4(MYO15A):c.4497G>T (p.Glu1499Asp) rs149813580 0.00049
NM_016239.4(MYO15A):c.7665C>T (p.Ser2555=) rs183834387 0.00045
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.2517G>A (p.Pro839=) rs911527113 0.00040
NM_016239.4(MYO15A):c.10403G>A (p.Arg3468Gln) rs200456053 0.00036
NM_016239.4(MYO15A):c.6743C>T (p.Ala2248Val) rs199831544 0.00036
NM_016239.4(MYO15A):c.3647G>A (p.Arg1216His) rs202148411 0.00032
NM_016239.4(MYO15A):c.3591G>A (p.Pro1197=) rs200222411 0.00023
NM_016239.4(MYO15A):c.7367C>G (p.Ala2456Gly) rs199953758 0.00015
NM_016239.4(MYO15A):c.1602C>T (p.Phe534=) rs547305039 0.00013
NM_016239.4(MYO15A):c.10420A>G (p.Ser3474Gly) rs150181830 0.00012
NM_016239.4(MYO15A):c.549T>C (p.Pro183=) rs200088596 0.00011
NM_016239.4(MYO15A):c.5803C>G (p.Arg1935Gly) rs200041829 0.00009
NM_016239.4(MYO15A):c.6795C>T (p.Thr2265=) rs78015149 0.00008
NM_016239.4(MYO15A):c.10227C>T (p.Ser3409=) rs199520412 0.00006
NM_016239.4(MYO15A):c.9436C>T (p.His3146Tyr) rs201230033 0.00006
NM_016239.4(MYO15A):c.5925G>A (p.Trp1975Ter) rs375290498 0.00005
NM_016239.4(MYO15A):c.2159C>T (p.Ala720Val) rs746972322 0.00004
NM_016239.4(MYO15A):c.9518-10G>A rs570587230 0.00004
NM_016239.4(MYO15A):c.6669G>A (p.Ala2223=) rs558947304 0.00001
NM_016239.4(MYO15A):c.10006G>A (p.Glu3336Lys)
NM_016239.4(MYO15A):c.2470C>G (p.Pro824Ala)
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.4038+8GT[25] rs59214589
NM_016239.4(MYO15A):c.4038+8GT[26] rs59214589
NM_016239.4(MYO15A):c.4038+8GT[31] rs59214589

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