ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

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Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP
NM_000257.4(MYH7):c.1272T>A (p.Thr424=) rs1555338337
NM_000257.4(MYH7):c.1311C>A (p.Asn437Lys) rs1595086845
NM_000257.4(MYH7):c.1783C>A (p.Gln595Lys) rs1595085351
NM_000257.4(MYH7):c.1784A>G (p.Gln595Arg) rs1381638438
NM_000257.4(MYH7):c.2573G>T (p.Arg858Leu) rs2856897
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu) rs45496496
NM_000257.4(MYH7):c.3067G>A (p.Ala1023Thr) rs1595081240
NM_000257.4(MYH7):c.3267T>G (p.Ala1089=) rs1456297955
NM_000257.4(MYH7):c.3286G>T (p.Asp1096Tyr) rs45478699
NM_000257.4(MYH7):c.3301G>A (p.Gly1101Ser) rs367546859
NM_000257.4(MYH7):c.3563C>G (p.Thr1188Ser) rs1566527771
NM_000257.4(MYH7):c.363C>G (p.Phe121Leu) rs777462283
NM_000257.4(MYH7):c.3844A>G (p.Thr1282Ala) rs1595077544
NM_000257.4(MYH7):c.3927C>A (p.Thr1309=) rs1430666956
NM_000257.4(MYH7):c.4200T>C (p.Ala1400=) rs760638048
NM_000257.4(MYH7):c.4210G>A (p.Val1404Met) rs371552806
NM_000257.4(MYH7):c.482C>T (p.Ala161Val) rs1555338763
NM_000257.4(MYH7):c.50G>A (p.Arg17His) rs727503280
NM_000257.4(MYH7):c.5243G>A (p.Cys1748Tyr) rs200303340
NM_000257.4(MYH7):c.5328C>T (p.Ser1776=) rs765263589
NM_000257.4(MYH7):c.5400C>G (p.Ala1800=) rs556490774
NM_000257.4(MYH7):c.5453G>A (p.Arg1818Gln) rs730880819
NM_000257.4(MYH7):c.5507C>T (p.Ser1836Leu) rs727503242
NM_000257.4(MYH7):c.5561C>T (p.Thr1854Met) rs372381770
NM_000257.4(MYH7):c.5690G>A (p.Arg1897His) rs727503240
NM_000257.4(MYH7):c.5735T>A (p.Ile1912Asn) rs1595070419
NM_000257.4(MYH7):c.610C>T (p.Arg204Cys) rs397516259

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