ClinVar Miner

List of variants in gene MYO15A studied for Rare genetic deafness

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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_016239.4(MYO15A):c.9620G>A (p.Arg3207His) rs199621031 0.00026
NM_016239.4(MYO15A):c.8090T>C (p.Val2697Ala) rs200451098 0.00013
NM_016239.4(MYO15A):c.8183G>A (p.Arg2728His) rs184435771 0.00011
NM_016239.4(MYO15A):c.9861C>T (p.Gly3287=) rs372466080 0.00011
NM_016239.4(MYO15A):c.6764+2T>A rs763975867 0.00009
NM_016239.4(MYO15A):c.4198G>A (p.Val1400Met) rs749136456 0.00006
NM_016239.4(MYO15A):c.8714-1G>A rs377015931 0.00006
NM_016239.4(MYO15A):c.5925G>A (p.Trp1975Ter) rs375290498 0.00005
NM_016239.4(MYO15A):c.6046+1G>A rs201978571 0.00005
NM_016239.4(MYO15A):c.8767C>T (p.Arg2923Ter) rs373462792 0.00005
NM_016239.4(MYO15A):c.6863C>T (p.Ser2288Leu) rs886052676 0.00004
NM_016239.4(MYO15A):c.9517+2T>C rs1322423998 0.00004
NM_016239.4(MYO15A):c.2311del (p.Ser771fs) rs754865266 0.00002
NM_016239.4(MYO15A):c.3385C>T (p.Arg1129Ter) rs748868741 0.00002
NM_016239.4(MYO15A):c.8341-2A>C rs778404517 0.00002
NM_016239.4(MYO15A):c.10045C>T (p.Gln3349Ter) rs1345580310 0.00001
NM_016239.4(MYO15A):c.4252G>A (p.Gly1418Arg) rs753790346 0.00001
NM_016239.4(MYO15A):c.5896C>T (p.Arg1966Ter) rs765468034 0.00001
NM_016239.4(MYO15A):c.6437G>A (p.Arg2146Gln) rs760980785 0.00001
NM_016239.4(MYO15A):c.6610C>T (p.Arg2204Cys) rs727503312 0.00001
NM_016239.4(MYO15A):c.7893+1G>A rs727503316 0.00001
NM_016239.4(MYO15A):c.996C>G (p.Tyr332Ter) rs759523751 0.00001
NM_016239.4(MYO15A):c.10136C>A (p.Ser3379Ter) rs546575046
NM_016239.4(MYO15A):c.10247CCT[1] (p.Ser3417del) rs760069953
NM_016239.4(MYO15A):c.1137del (p.Tyr380fs) rs769260536
NM_016239.4(MYO15A):c.1171_1177dup (p.Tyr393fs) rs1567620939
NM_016239.4(MYO15A):c.1185dup (p.Glu396fs) rs772536599
NM_016239.4(MYO15A):c.2570del (p.Pro857fs)
NM_016239.4(MYO15A):c.2704del (p.Ala902fs)
NM_016239.4(MYO15A):c.3006del (p.Lys1003fs) rs1162296750
NM_016239.4(MYO15A):c.3026del (p.Pro1009fs) rs1555539827
NM_016239.4(MYO15A):c.352G>A (p.Gly118Ser)
NM_016239.4(MYO15A):c.3795C>A (p.Tyr1265Ter) rs1597768378
NM_016239.4(MYO15A):c.5531+1G>A rs727503309
NM_016239.4(MYO15A):c.5891_5900del (p.Ser1964fs)
NM_016239.4(MYO15A):c.6479del (p.Pro2160fs)
NM_016239.4(MYO15A):c.6491dup (p.Asn2165fs)
NM_016239.4(MYO15A):c.6788G>A (p.Gly2263Asp) rs397517285
NM_016239.4(MYO15A):c.6892C>T (p.Arg2298Ter)
NM_016239.4(MYO15A):c.7006dup (p.Gln2336fs) rs397517286
NM_016239.4(MYO15A):c.7124_7127del (p.Asp2375fs) rs780170125
NM_016239.4(MYO15A):c.7184_7185del (p.Leu2394_Phe2395insTer) rs1415858976
NM_016239.4(MYO15A):c.7226del (p.Pro2409fs) rs727503315
NM_016239.4(MYO15A):c.750_753del (p.Leu251fs)
NM_016239.4(MYO15A):c.8100del (p.Lys2701fs) rs397517287
NM_016239.4(MYO15A):c.9303+1G>T rs876657708
NM_016239.4(MYO15A):c.9612+9_10082del
NM_016239.4(MYO15A):c.9942C>A (p.Tyr3314Ter)
NM_016239.4(MYO15A):c.997G>T (p.Glu333Ter)

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