ClinVar Miner

List of variants in gene MYO15A reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Total variants: 25
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HGVS dbSNP gnomAD frequency
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.10394G>A (p.Arg3465Gln) rs199783506 0.00026
NM_016239.4(MYO15A):c.7396-8C>G rs370351502 0.00025
NM_016239.4(MYO15A):c.10181C>T (p.Ala3394Val) rs200249886 0.00024
NM_016239.4(MYO15A):c.2116G>A (p.Ala706Thr) rs932191004 0.00017
NM_016239.4(MYO15A):c.10166G>A (p.Arg3389Gln) rs373536607 0.00006
NM_016239.4(MYO15A):c.3623G>A (p.Arg1208His) rs778112788 0.00003
NM_016239.4(MYO15A):c.526T>C (p.Ser176Pro) rs933766276 0.00003
NM_016239.4(MYO15A):c.773A>C (p.Glu258Ala) rs368814566 0.00003
NM_016239.4(MYO15A):c.3317G>A (p.Arg1106Gln) rs199952218 0.00002
NM_016239.4(MYO15A):c.2834G>A (p.Gly945Glu) rs377573336 0.00001
NM_016239.4(MYO15A):c.3751A>C (p.Ile1251Leu) rs755138984 0.00001
NM_016239.4(MYO15A):c.1529C>A (p.Ala510Glu)
NM_016239.4(MYO15A):c.2947G>T (p.Ala983Ser) rs1367828749
NM_016239.4(MYO15A):c.349_357del (p.Tyr117_Arg119del) rs876657898
NM_016239.4(MYO15A):c.374G>A (p.Arg125Gln)
NM_016239.4(MYO15A):c.4235T>A (p.Phe1412Tyr) rs1597779977
NM_016239.4(MYO15A):c.4964A>G (p.Tyr1655Cys)
NM_016239.4(MYO15A):c.5197C>T (p.Arg1733Trp) rs369755064
NM_016239.4(MYO15A):c.5831G>A (p.Arg1944His)
NM_016239.4(MYO15A):c.6554A>T (p.Gln2185Leu) rs2046510604
NM_016239.4(MYO15A):c.7385C>A (p.Ala2462Asp)
NM_016239.4(MYO15A):c.9223T>C (p.Phe3075Leu) rs2142393377
NM_016239.4(MYO15A):c.9371A>G (p.Asn3124Ser) rs760618055

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