ClinVar Miner

List of variants in gene MYH14 reported as likely benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_001145809.2(MYH14):c.*301C>T rs529409417
NM_001145809.2(MYH14):c.*368C>G
NM_001145809.2(MYH14):c.*427T>C
NM_001145809.2(MYH14):c.*81A>G rs772326631
NM_001145809.2(MYH14):c.*86G>A
NM_001145809.2(MYH14):c.1115-4C>T rs142696359
NM_001145809.2(MYH14):c.1329+15C>T rs200176028
NM_001145809.2(MYH14):c.1919G>A (p.Arg640Gln) rs199696801
NM_001145809.2(MYH14):c.2334C>A (p.Leu778=) rs190941610
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val) rs201337011
NM_001145809.2(MYH14):c.2544C>T (p.Ile848=)
NM_001145809.2(MYH14):c.263G>A (p.Arg88Gln)
NM_001145809.2(MYH14):c.2645C>T (p.Ala882Val)
NM_001145809.2(MYH14):c.3172-12T>C rs374486787
NM_001145809.2(MYH14):c.3303A>G (p.Leu1101=) rs543799021
NM_001145809.2(MYH14):c.36G>A (p.Lys12=) rs372741317
NM_001145809.2(MYH14):c.3871G>T (p.Val1291Leu) rs202242879
NM_001145809.2(MYH14):c.3974G>A (p.Arg1325Gln)
NM_001145809.2(MYH14):c.4094G>A (p.Ser1365Asn) rs202225655
NM_001145809.2(MYH14):c.4138-13C>T rs183327883
NM_001145809.2(MYH14):c.4417G>A (p.Val1473Met) rs112716976
NM_001145809.2(MYH14):c.4903G>A (p.Glu1635Lys)
NM_001145809.2(MYH14):c.5041G>A (p.Glu1681Lys) rs556548077
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646
NM_001145809.2(MYH14):c.5384G>T (p.Arg1795Leu)
NM_001145809.2(MYH14):c.5447G>A (p.Arg1816His) rs201923258
NM_001145809.2(MYH14):c.5599C>T (p.Arg1867Cys) rs187789045
NM_001145809.2(MYH14):c.565C>T (p.Arg189Cys) rs200818171
NM_001145809.2(MYH14):c.5850G>A (p.Glu1950=)
NM_001145809.2(MYH14):c.820A>G (p.Ile274Val) rs200424400

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