ClinVar Miner

Variants in gene MYO15A with conflicting interpretations

See also:
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 per condition Variants with at least 2 submissions on the same condition 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 conflict
615 83 0 46 29 0 7 73

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 2 4 1 2
likely pathogenic 2 0 3 0 0
uncertain significance 4 3 0 25 10
likely benign 1 0 25 0 44
benign 2 0 10 44 0

All variants with conflicting interpretations #

Total variants: 73
Download table as spreadsheet
HGVS dbSNP
NM_016239.3(MYO15A):c.419dup (p.Phe141Valfs) rs750130520
NM_016239.4(MYO15A):c.10121G>A (p.Arg3374His) rs201794696
NM_016239.4(MYO15A):c.10182G>A (p.Ala3394=) rs79230542
NM_016239.4(MYO15A):c.10242C>T (p.Phe3414=) rs188485743
NM_016239.4(MYO15A):c.10393C>T (p.Arg3465Trp) rs201028204
NM_016239.4(MYO15A):c.10394G>A (p.Arg3465Gln) rs199783506
NM_016239.4(MYO15A):c.10443G>A (p.Ala3481=) rs190486507
NM_016239.4(MYO15A):c.1185dup (p.Glu396fs) rs772536599
NM_016239.4(MYO15A):c.1385G>A (p.Gly462Asp) rs145292219
NM_016239.4(MYO15A):c.1454T>C (p.Val485Ala) rs200532919
NM_016239.4(MYO15A):c.1552G>A (p.Glu518Lys) rs189255177
NM_016239.4(MYO15A):c.1634C>T (p.Ala545Val) rs199740747
NM_016239.4(MYO15A):c.1941A>C (p.Pro647=) rs537016494
NM_016239.4(MYO15A):c.2020C>T (p.Pro674Ser) rs557225435
NM_016239.4(MYO15A):c.2028C>A (p.Pro676=) rs577023485
NM_016239.4(MYO15A):c.2194C>T (p.Pro732Ser) rs376451611
NM_016239.4(MYO15A):c.2238G>T (p.Arg746Ser) rs79760961
NM_016239.4(MYO15A):c.2418C>T (p.Phe806=) rs564053026
NM_016239.4(MYO15A):c.2680C>T (p.Pro894Ser) rs76707172
NM_016239.4(MYO15A):c.3026C>A (p.Pro1009His) rs117612144
NM_016239.4(MYO15A):c.3130_3147dup (p.Ile1044_Asp1049dup) rs377177611
NM_016239.4(MYO15A):c.3140C>G (p.Pro1047Arg) rs77565048
NM_016239.4(MYO15A):c.3196G>C (p.Ala1066Pro) rs199537186
NM_016239.4(MYO15A):c.3201G>A (p.Ala1067=) rs148356427
NM_016239.4(MYO15A):c.3591G>A (p.Pro1197=) rs200222411
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.3659G>A (p.Gly1220Glu) rs201689819
NM_016239.4(MYO15A):c.3756C>T (p.Tyr1252=) rs59933498
NM_016239.4(MYO15A):c.3774C>T (p.Ile1258=) rs148723625
NM_016239.4(MYO15A):c.3979C>T (p.Leu1327=) rs146245515
NM_016239.4(MYO15A):c.3999C>T (p.Ala1333=) rs192570479
NM_016239.4(MYO15A):c.4033A>T (p.Ile1345Leu) rs201234482
NM_016239.4(MYO15A):c.4623G>A (p.Thr1541=) rs926074
NM_016239.4(MYO15A):c.4779+9G>A rs183256997
NM_016239.4(MYO15A):c.4888C>T (p.Arg1630Cys) rs138861831
NM_016239.4(MYO15A):c.5193C>T (p.Phe1731=) rs767426819
NM_016239.4(MYO15A):c.5287C>T (p.Arg1763Trp) rs200146361
NM_016239.4(MYO15A):c.549T>C (p.Pro183=) rs200088596
NM_016239.4(MYO15A):c.54G>A (p.Lys18=) rs144909486
NM_016239.4(MYO15A):c.5809C>T (p.Arg1937Cys) rs749465098
NM_016239.4(MYO15A):c.5880C>T (p.His1960=) rs201487604
NM_016239.4(MYO15A):c.5894G>A (p.Arg1965His) rs139347804
NM_016239.4(MYO15A):c.5925G>A (p.Trp1975Ter) rs375290498
NM_016239.4(MYO15A):c.6186C>A (p.Ala2062=) rs141475629
NM_016239.4(MYO15A):c.6192G>A (p.Gly2064=) rs55688805
NM_016239.4(MYO15A):c.6336C>T (p.Tyr2112=) rs76886140
NM_016239.4(MYO15A):c.6589C>T (p.Gln2197Ter) rs779445819
NM_016239.4(MYO15A):c.6614C>T (p.Thr2205Ile) rs121908970
NM_016239.4(MYO15A):c.6764+2T>A rs763975867
NM_016239.4(MYO15A):c.6785G>A (p.Arg2262His) rs200623501
NM_016239.4(MYO15A):c.6796G>A (p.Val2266Met) rs114274755
NM_016239.4(MYO15A):c.7069G>A (p.Gly2357Ser) rs201540919
NM_016239.4(MYO15A):c.730G>A (p.Asp244Asn) rs199899548
NM_016239.4(MYO15A):c.7367C>G (p.Ala2456Gly) rs199953758
NM_016239.4(MYO15A):c.7396-8C>G rs370351502
NM_016239.4(MYO15A):c.7655-7C>G rs191171943
NM_016239.4(MYO15A):c.8050T>C (p.Tyr2684His) rs376351191
NM_016239.4(MYO15A):c.8269G>A (p.Val2757Met) rs140140417
NM_016239.4(MYO15A):c.858C>G (p.Pro286=) rs200424851
NM_016239.4(MYO15A):c.876C>T (p.Pro292=) rs368755362
NM_016239.4(MYO15A):c.8811C>T (p.His2937=) rs200583193
NM_016239.4(MYO15A):c.8841G>A (p.Leu2947=) rs201809145
NM_016239.4(MYO15A):c.915C>T (p.Tyr305=) rs200695102
NM_016239.4(MYO15A):c.9181G>A (p.Glu3061Lys) rs116833707
NM_016239.4(MYO15A):c.9322G>A (p.Val3108Ile) rs201734915
NM_016239.4(MYO15A):c.9478C>T (p.Leu3160Phe) rs140029076
NM_016239.4(MYO15A):c.9518-10G>A rs570587230
NM_016239.4(MYO15A):c.9691-3C>A rs142996507
NM_016239.4(MYO15A):c.9754A>G (p.Asn3252Asp) rs147458358
NM_016239.4(MYO15A):c.9792G>A (p.Gln3264=) rs149189607
NM_016239.4(MYO15A):c.9861C>T (p.Gly3287=) rs372466080
NM_016239.4(MYO15A):c.9873C>T (p.Leu3291=) rs146865523

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