ClinVar Miner

Variants in gene MYO15A with conflicting interpretations

Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission Variants with at least 2 submissions and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any kind of conflict
418 45 0 45 46 0 9 89

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 0 4 4 1 1
likely pathogenic 4 0 5 0 0
uncertain significance 4 5 0 31 24
likely benign 1 0 31 0 41
benign 1 0 24 41 0

All variants with conflicting interpretations #

Total variants: 89
Download table as spreadsheet
HGVS dbSNP
NM_016239.3(MYO15A):c.10182G>A (p.Ala3394=) rs79230542
NM_016239.3(MYO15A):c.10242C>T (p.Phe3414=) rs188485743
NM_016239.3(MYO15A):c.10403G>A (p.Arg3468Gln) rs200456053
NM_016239.3(MYO15A):c.10431T>C (p.Tyr3477=) rs854800
NM_016239.3(MYO15A):c.10443G>A (p.Ala3481=) rs190486507
NM_016239.3(MYO15A):c.1137delC (p.Tyr380Metfs) rs769260536
NM_016239.3(MYO15A):c.1385G>A (p.Gly462Asp) rs145292219
NM_016239.3(MYO15A):c.1454T>C (p.Val485Ala) rs200532919
NM_016239.3(MYO15A):c.1783G>A (p.Ala595Thr) rs2955365
NM_016239.3(MYO15A):c.1791G>A (p.Ala597=) rs114552047
NM_016239.3(MYO15A):c.1899A>G (p.Pro633=) rs2955366
NM_016239.3(MYO15A):c.2152T>G (p.Trp718Gly) rs2955367
NM_016239.3(MYO15A):c.2238G>T (p.Arg746Ser) rs79760961
NM_016239.3(MYO15A):c.2418C>T (p.Phe806=) rs564053026
NM_016239.3(MYO15A):c.2462A>C (p.Gln821Pro) rs372125621
NM_016239.3(MYO15A):c.2562C>T (p.Cys854=) rs182293382
NM_016239.3(MYO15A):c.2680C>T (p.Pro894Ser) rs76707172
NM_016239.3(MYO15A):c.2790C>T (p.Asp930=) rs185688918
NM_016239.3(MYO15A):c.3012A>G (p.Ser1004=) rs376387472
NM_016239.3(MYO15A):c.3023C>G (p.Thr1008Ser) rs143316414
NM_016239.3(MYO15A):c.3130_3147dup (p.Asp1049_Val1050insIleThrProProLysAsp) rs377177611
NM_016239.3(MYO15A):c.3658G>A (p.Gly1220Arg) rs146754758
NM_016239.3(MYO15A):c.3659G>A (p.Gly1220Glu) rs201689819
NM_016239.3(MYO15A):c.3756C>T (p.Tyr1252=) rs59933498
NM_016239.3(MYO15A):c.3774C>T (p.Ile1258=) rs148723625
NM_016239.3(MYO15A):c.3979C>T (p.Leu1327=) rs146245515
NM_016239.3(MYO15A):c.3999C>T (p.Ala1333=) rs192570479
NM_016239.3(MYO15A):c.4033A>T (p.Ile1345Leu) rs201234482
NM_016239.3(MYO15A):c.419dup (p.Phe141Valfs) rs750130520
NM_016239.3(MYO15A):c.4206+13C>G rs141183007
NM_016239.3(MYO15A):c.4533C>T (p.Ala1511=) rs114328138
NM_016239.3(MYO15A):c.4719G>A (p.Ala1573=) rs186426892
NM_016239.3(MYO15A):c.4779+9G>A rs183256997
NM_016239.3(MYO15A):c.4888C>T (p.Arg1630Cys) rs138861831
NM_016239.3(MYO15A):c.4954C>T (p.Leu1652=) rs2280777
NM_016239.3(MYO15A):c.5212-14C>T rs2072652
NM_016239.3(MYO15A):c.5287C>T (p.Arg1763Trp) rs200146361
NM_016239.3(MYO15A):c.54G>A (p.Lys18=) rs144909486
NM_016239.3(MYO15A):c.5526C>T (p.Ile1842=) rs370047914
NM_016239.3(MYO15A):c.5649+14G>A rs2072653
NM_016239.3(MYO15A):c.5754T>G (p.Ile1918Met) rs150403702
NM_016239.3(MYO15A):c.5826-12A>C rs854778
NM_016239.3(MYO15A):c.5880C>T (p.His1960=) rs201487604
NM_016239.3(MYO15A):c.5894G>A (p.Arg1965His) rs139347804
NM_016239.3(MYO15A):c.5925G>A (p.Trp1975Ter) rs375290498
NM_016239.3(MYO15A):c.5929T>C (p.Cys1977Arg) rs854777
NM_016239.3(MYO15A):c.5978G>A (p.Arg1993Gln) rs117071200
NM_016239.3(MYO15A):c.6052G>A (p.Gly2018Arg) rs2272571
NM_016239.3(MYO15A):c.6186C>A (p.Ala2062=) rs141475629
NM_016239.3(MYO15A):c.6192G>A (p.Gly2064=) rs55688805
NM_016239.3(MYO15A):c.6274-10C>T rs201459354
NM_016239.3(MYO15A):c.6589C>T (p.Gln2197Ter) rs779445819
NM_016239.3(MYO15A):c.6614C>T (p.Thr2205Ile) rs121908970
NM_016239.3(MYO15A):c.6669G>A (p.Ala2223=) rs558947304
NM_016239.3(MYO15A):c.6764+2T>A rs763975867
NM_016239.3(MYO15A):c.6785G>A (p.Arg2262His) rs200623501
NM_016239.3(MYO15A):c.6796G>A (p.Val2266Met) rs114274755
NM_016239.3(MYO15A):c.6863C>T (p.Ser2288Leu) rs886052676
NM_016239.3(MYO15A):c.7069G>A (p.Gly2357Ser) rs201540919
NM_016239.3(MYO15A):c.7396-8C>G rs370351502
NM_016239.3(MYO15A):c.7468G>A (p.Ala2490Thr) rs16960959
NM_016239.3(MYO15A):c.7473+10G>T rs181355572
NM_016239.3(MYO15A):c.7503G>A (p.Thr2501=) rs16960961
NM_016239.3(MYO15A):c.7655-7C>G rs191171943
NM_016239.3(MYO15A):c.7857G>A (p.Gly2619=) rs854772
NM_016239.3(MYO15A):c.7961C>G (p.Thr2654Ser) rs200355614
NM_016239.3(MYO15A):c.8005dup (p.Thr2669Asnfs) rs1221876133
NM_016239.3(MYO15A):c.8045A>T (p.Tyr2682Phe) rs712270
NM_016239.3(MYO15A):c.8050T>C (p.Tyr2684His) rs376351191
NM_016239.3(MYO15A):c.8088+5C>G rs9916193
NM_016239.3(MYO15A):c.8262G>A (p.Thr2754=) rs1006770
NM_016239.3(MYO15A):c.8269G>A (p.Val2757Met) rs140140417
NM_016239.3(MYO15A):c.8322C>T (p.Ser2774=) rs712272
NM_016239.3(MYO15A):c.8460-15C>T rs861278
NM_016239.3(MYO15A):c.858C>G (p.Pro286=) rs200424851
NM_016239.3(MYO15A):c.876C>T (p.Pro292=) rs368755362
NM_016239.3(MYO15A):c.8811C>T (p.His2937=) rs200583193
NM_016239.3(MYO15A):c.8816G>A (p.Arg2939His) rs377389290
NM_016239.3(MYO15A):c.915C>T (p.Tyr305=) rs200695102
NM_016239.3(MYO15A):c.9322G>A (p.Val3108Ile) rs201734915
NM_016239.3(MYO15A):c.9478C>T (p.Leu3160Phe) rs140029076
NM_016239.3(MYO15A):c.9486C>T (p.Asp3162=) rs8077577
NM_016239.3(MYO15A):c.9518-10G>A rs570587230
NM_016239.3(MYO15A):c.9518-11T>C rs62073604
NM_016239.3(MYO15A):c.9620G>A (p.Arg3207His) rs199621031
NM_016239.3(MYO15A):c.9708G>A (p.Val3236=) rs115393178
NM_016239.3(MYO15A):c.9754A>G (p.Asn3252Asp) rs147458358
NM_016239.3(MYO15A):c.9792G>A (p.Gln3264=) rs149189607
NM_016239.3(MYO15A):c.9861C>T (p.Gly3287=) rs372466080

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