ClinVar Miner

List of variants in gene MYO15A reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 100
Download table as spreadsheet
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.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.4206+13C>G rs141183007 0.00838
NM_016239.4(MYO15A):c.10182G>A (p.Ala3394=) rs79230542 0.00665
NM_016239.4(MYO15A):c.6192G>A (p.Gly2064=) rs55688805 0.00470
NM_016239.4(MYO15A):c.2562C>T (p.Cys854=) rs182293382 0.00413
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.4779+9G>A rs183256997 0.00264
NM_016239.4(MYO15A):c.5287C>T (p.Arg1763Trp) rs200146361 0.00205
NM_016239.4(MYO15A):c.5754T>G (p.Ile1918Met) rs150403702 0.00197
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.823G>C (p.Gly275Arg) rs183969516 0.00158
NM_016239.4(MYO15A):c.1111C>A (p.Pro371Thr) rs200382813 0.00153
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.2194C>T (p.Pro732Ser) rs376451611 0.00132
NM_016239.4(MYO15A):c.6186C>A (p.Ala2062=) rs141475629 0.00123
NM_016239.4(MYO15A):c.2150G>C (p.Ser717Thr) rs546018470 0.00113
NM_016239.4(MYO15A):c.2163C>T (p.Phe721=) rs572234398 0.00113
NM_016239.4(MYO15A):c.2354G>T (p.Gly785Val) rs368667118 0.00112
NM_016239.4(MYO15A):c.1582G>A (p.Gly528Ser) rs199695398 0.00111
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.709G>A (p.Asp237Asn) rs201737186 0.00099
NM_016239.4(MYO15A):c.1387A>G (p.Met463Val) rs201794569 0.00096
NM_016239.4(MYO15A):c.1454T>C (p.Val485Ala) rs200532919 0.00079
NM_016239.4(MYO15A):c.10393C>T (p.Arg3465Trp) rs201028204 0.00073
NM_016239.4(MYO15A):c.3363G>A (p.Val1121=) rs201197589 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.9322G>A (p.Val3108Ile) rs201734915 0.00049
NM_016239.4(MYO15A):c.858C>G (p.Pro286=) rs200424851 0.00045
NM_016239.4(MYO15A):c.915C>T (p.Tyr305=) rs200695102 0.00045
NM_016239.4(MYO15A):c.10403G>A (p.Arg3468Gln) rs200456053 0.00036
NM_016239.4(MYO15A):c.3659G>A (p.Gly1220Glu) rs201689819 0.00036
NM_016239.4(MYO15A):c.3647G>A (p.Arg1216His) rs202148411 0.00032
NM_016239.4(MYO15A):c.9998G>A (p.Arg3333Gln) rs200605472 0.00027
NM_016239.4(MYO15A):c.250T>A (p.Ser84Thr) rs188609046 0.00024
NM_016239.4(MYO15A):c.4142+6T>C rs368090576 0.00024
NM_016239.4(MYO15A):c.3591G>A (p.Pro1197=) rs200222411 0.00023
NM_016239.4(MYO15A):c.8652G>A (p.Ala2884=) rs373922407 0.00023
NM_016239.4(MYO15A):c.4407T>C (p.Ser1469=) rs202180744 0.00018
NM_016239.4(MYO15A):c.4482+10C>T rs200857668 0.00016
NM_016239.4(MYO15A):c.5100C>T (p.Thr1700=) rs529758445 0.00016
NM_016239.4(MYO15A):c.7367C>G (p.Ala2456Gly) rs199953758 0.00015
NM_016239.4(MYO15A):c.4461C>T (p.Asn1487=) rs201076604 0.00011
NM_016239.4(MYO15A):c.9861C>T (p.Gly3287=) rs372466080 0.00011
NM_016239.4(MYO15A):c.5803C>G (p.Arg1935Gly) rs200041829 0.00009
NM_016239.4(MYO15A):c.10227C>T (p.Ser3409=) rs199520412 0.00006
NM_016239.4(MYO15A):c.4848C>G (p.Phe1616Leu) rs368430972 0.00006
NM_016239.4(MYO15A):c.6657G>A (p.Lys2219=) rs727504708 0.00002
NM_016239.4(MYO15A):c.3505C>T (p.Arg1169Ter) rs781546107 0.00001
NM_016239.4(MYO15A):c.7893+10G>A rs373557101 0.00001
NM_016239.4(MYO15A):c.10006G>A (p.Glu3336Lys)
NM_016239.4(MYO15A):c.10192C>T (p.His3398Tyr)
NM_016239.4(MYO15A):c.10389G>A (p.Ser3463=)
NM_016239.4(MYO15A):c.1318del (p.Asp440fs)
NM_016239.4(MYO15A):c.1323G>C (p.Ala441=)
NM_016239.4(MYO15A):c.1432C>T (p.Arg478Cys)
NM_016239.4(MYO15A):c.1854C>T (p.Asp618=) rs886038623
NM_016239.4(MYO15A):c.2302C>A (p.Arg768=) rs373561242
NM_016239.4(MYO15A):c.2470C>G (p.Pro824Ala)
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.4146C>T (p.Gly1382=)
NM_016239.4(MYO15A):c.484_488delinsACTT (p.Arg162fs)
NM_016239.4(MYO15A):c.6046+18G>A rs369719467
NM_016239.4(MYO15A):c.6638G>A (p.Trp2213Ter) rs1567649945
NM_016239.4(MYO15A):c.6711G>A (p.Pro2237=)
NM_016239.4(MYO15A):c.765G>A (p.Glu255=)
NM_016239.4(MYO15A):c.7720C>T (p.Gln2574Ter)
NM_016239.4(MYO15A):c.8088+5C>G rs9916193
NM_016239.4(MYO15A):c.8883G>A (p.Thr2961=)
NM_016239.4(MYO15A):c.9107A>G (p.Lys3036Arg)
NM_016239.4(MYO15A):c.92del (p.Lys31fs)
NM_016239.4(MYO15A):c.9612+1G>A
NM_016239.4(MYO15A):c.9949-10C>T

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.