ClinVar Miner

List of variants in gene MYO15A reported as likely benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_016239.4(MYO15A):c.*628C>G rs55973639
NM_016239.4(MYO15A):c.10573A>G (p.Ser3525Gly) rs182332665
NM_016239.4(MYO15A):c.1385G>A (p.Gly462Asp) rs145292219
NM_016239.4(MYO15A):c.1791G>A (p.Ala597=) rs114552047
NM_016239.4(MYO15A):c.2028C>A (p.Pro676=) rs577023485
NM_016239.4(MYO15A):c.3026C>A (p.Pro1009His) rs117612144
NM_016239.4(MYO15A):c.3203G>T (p.Cys1068Phe) rs189061214
NM_016239.4(MYO15A):c.3413A>G (p.Gln1138Arg) rs76468019
NM_016239.4(MYO15A):c.4533C>T (p.Ala1511=) rs114328138
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.7503G>A (p.Thr2501=) rs16960961
NM_016239.4(MYO15A):c.7908C>T (p.Ala2636=) rs201535856
NM_016239.4(MYO15A):c.9478C>T (p.Leu3160Phe) rs140029076
NM_016239.4(MYO15A):c.9708G>A (p.Val3236=) rs115393178
NM_016239.4(MYO15A):c.9754A>G (p.Asn3252Asp) rs147458358

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