ClinVar Miner

List of variants in gene MYO15A reported by Eurofins NTD LLC (GA)

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Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_016239.4(MYO15A):c.5929T>C (p.Cys1977Arg) rs854777 0.79149
NM_016239.4(MYO15A):c.7857G>A (p.Gly2619=) rs854772 0.55976
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.2152T>G (p.Trp718Gly) rs2955367 0.34123
NM_016239.4(MYO15A):c.9486C>T (p.Asp3162=) rs8077577 0.19129
NM_016239.4(MYO15A):c.2462A>C (p.Gln821Pro) rs372125621 0.02081
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.6796G>A (p.Val2266Met) rs114274755 0.00791
NM_016239.4(MYO15A):c.2680C>T (p.Pro894Ser) rs76707172 0.00765
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.1941A>C (p.Pro647=) rs537016494 0.00437
NM_016239.4(MYO15A):c.1385G>A (p.Gly462Asp) rs145292219 0.00326
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.4033A>T (p.Ile1345Leu) rs201234482 0.00191
NM_016239.4(MYO15A):c.9754A>G (p.Asn3252Asp) rs147458358 0.00177
NM_016239.4(MYO15A):c.6785G>A (p.Arg2262His) rs200623501 0.00168
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.54G>A (p.Lys18=) rs144909486 0.00142
NM_016239.4(MYO15A):c.2194C>T (p.Pro732Ser) rs376451611 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.1552G>A (p.Glu518Lys) rs189255177 0.00105
NM_016239.4(MYO15A):c.9181G>A (p.Glu3061Lys) rs116833707 0.00089
NM_016239.4(MYO15A):c.2418C>T (p.Phe806=) rs564053026 0.00087
NM_016239.4(MYO15A):c.5060C>T (p.Pro1687Leu) rs58625281 0.00087
NM_016239.4(MYO15A):c.1454T>C (p.Val485Ala) rs200532919 0.00079
NM_016239.4(MYO15A):c.269T>C (p.Met90Thr) rs373294263 0.00076
NM_016239.4(MYO15A):c.8157C>T (p.His2719=) rs373955726 0.00067
NM_016239.4(MYO15A):c.7984C>G (p.Leu2662Val) rs200930743 0.00058
NM_016239.4(MYO15A):c.877G>A (p.Asp293Asn) rs201415651 0.00051
NM_016239.4(MYO15A):c.9322G>A (p.Val3108Ile) rs201734915 0.00049
NM_016239.4(MYO15A):c.858C>G (p.Pro286=) rs200424851 0.00045
NM_016239.4(MYO15A):c.3999C>T (p.Ala1333=) rs192570479 0.00040
NM_016239.4(MYO15A):c.3659G>A (p.Gly1220Glu) rs201689819 0.00036
NM_016239.4(MYO15A):c.7069G>A (p.Gly2357Ser) rs201540919 0.00034
NM_016239.4(MYO15A):c.1196A>G (p.Tyr399Cys) rs368682932 0.00033
NM_016239.4(MYO15A):c.730G>A (p.Asp244Asn) rs199899548 0.00032
NM_016239.4(MYO15A):c.2225G>T (p.Arg742Leu) rs772776336 0.00028
NM_016239.4(MYO15A):c.5866C>T (p.Arg1956Trp) rs185873402 0.00016
NM_016239.4(MYO15A):c.7533C>T (p.Pro2511=) rs369717113 0.00010
NM_016239.4(MYO15A):c.6764+2T>A rs763975867 0.00009
NM_016239.4(MYO15A):c.6357G>A (p.Ala2119=) rs374951514 0.00006
NM_016239.4(MYO15A):c.9539A>G (p.Gln3180Arg) rs771508906 0.00006
NM_016239.4(MYO15A):c.5193C>T (p.Phe1731=) rs767426819 0.00004
NM_016239.4(MYO15A):c.6623C>T (p.Pro2208Leu) rs376939609 0.00004
NM_016239.4(MYO15A):c.6729G>A (p.Thr2243=) rs531965733 0.00004
NM_016239.4(MYO15A):c.9518-10G>A rs570587230 0.00004
NM_016239.4(MYO15A):c.2629G>T (p.Glu877Ter) rs771720649 0.00003
NM_016239.4(MYO15A):c.3989G>A (p.Arg1330His) rs199511042 0.00003
NM_016239.4(MYO15A):c.8134C>A (p.Leu2712Ile) rs760123012 0.00003
NM_016239.4(MYO15A):c.1414T>A (p.Ser472Thr) rs886042317 0.00002
NM_016239.4(MYO15A):c.4642G>A (p.Ala1548Thr) rs201067821 0.00002
NM_016239.4(MYO15A):c.7838C>A (p.Ala2613Asp) rs886043362 0.00002
NM_016239.4(MYO15A):c.3183C>T (p.Leu1061=) rs200093968 0.00001
NM_016239.4(MYO15A):c.3505C>T (p.Arg1169Ter) rs781546107 0.00001
NM_016239.4(MYO15A):c.3646C>T (p.Arg1216Cys) rs547573001 0.00001
NM_016239.4(MYO15A):c.3841G>A (p.Gly1281Arg) rs576515898 0.00001
NM_016239.4(MYO15A):c.3866+1G>A rs374742590 0.00001
NM_016239.4(MYO15A):c.4990C>A (p.Gln1664Lys) rs374989174 0.00001
NM_016239.4(MYO15A):c.5651T>A (p.Leu1884Gln) rs767235021 0.00001
NM_016239.4(MYO15A):c.6634G>A (p.Glu2212Lys) rs371352836 0.00001
NM_016239.4(MYO15A):c.7544G>A (p.Arg2515His) rs754267428 0.00001
NM_016239.4(MYO15A):c.10312A>G (p.Asn3438Asp) rs1567666999
NM_016239.4(MYO15A):c.1137del (p.Tyr380fs) rs769260536
NM_016239.4(MYO15A):c.1323G>A (p.Ala441=) rs376905344
NM_016239.4(MYO15A):c.2258_2259del (p.Ala753fs) rs1555539322
NM_016239.4(MYO15A):c.32_40del (p.Ala11_Lys13del) rs1567617546
NM_016239.4(MYO15A):c.394A>G (p.Thr132Ala) rs762617660
NM_016239.4(MYO15A):c.4198G>C (p.Val1400Leu) rs749136456
NM_016239.4(MYO15A):c.5315C>T (p.Ala1772Val) rs199723446
NM_016239.4(MYO15A):c.534C>T (p.Ala178=) rs749146534
NM_016239.4(MYO15A):c.6178-1G>A rs886044338
NM_016239.4(MYO15A):c.6253G>A (p.Ala2085Thr) rs1555545009
NM_016239.4(MYO15A):c.8789G>T (p.Gly2930Val) rs765432573
NM_016239.4(MYO15A):c.932A>C (p.Asp311Ala) rs759576870

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