ClinVar Miner

List of variants in gene combination LOC126861898, MYH7 reported as likely benign for Cardiomyopathy

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.2349C>T (p.Arg783=) rs139882431 0.00036
NM_000257.4(MYH7):c.2334C>T (p.Asp778=) rs2069544 0.00035
NM_000257.4(MYH7):c.2526T>C (p.Ser842=) rs554560162 0.00013
NM_000257.4(MYH7):c.2679+7C>T rs368653983 0.00009
NM_000257.4(MYH7):c.2360G>A (p.Arg787His) rs376754645 0.00008
NM_000257.4(MYH7):c.2637C>T (p.Ser879=) rs199915408 0.00004
NM_000257.4(MYH7):c.2295C>T (p.Phe765=) rs1490366072 0.00003
NM_000257.4(MYH7):c.2643G>T (p.Leu881=) rs754470231 0.00003
NM_000257.4(MYH7):c.2658C>T (p.Asp886=) rs765948561 0.00003
NM_000257.4(MYH7):c.2391C>G (p.Ala797=) rs1323525268 0.00002
NM_000257.4(MYH7):c.2640G>C (p.Leu880=) rs753565218 0.00002
NM_000257.4(MYH7):c.2641C>T (p.Leu881=) rs907992794 0.00002
NM_000257.4(MYH7):c.2287-4G>A rs1231476855 0.00001
NM_000257.4(MYH7):c.2352C>T (p.Ile784=) rs397516143 0.00001
NM_000257.4(MYH7):c.2355C>T (p.Ile785=) rs1892652131 0.00001
NM_000257.4(MYH7):c.2410C>T (p.Leu804=) rs1169056407 0.00001
NM_000257.4(MYH7):c.2472C>T (p.Val824=) rs397516150 0.00001
NM_000257.4(MYH7):c.2484C>G (p.Pro828=) rs1555337746 0.00001
NM_000257.4(MYH7):c.2499C>T (p.Tyr833=) rs397516151 0.00001
NM_000257.4(MYH7):c.2586G>A (p.Ala862=) rs112677962 0.00001
NM_000257.4(MYH7):c.2598C>T (p.Ser866=) rs1202278618 0.00001
NM_000257.4(MYH7):c.2604T>C (p.Ala868=) rs769628768 0.00001
NM_000257.4(MYH7):c.2607C>T (p.Arg869=) rs1365184293 0.00001
NM_000257.4(MYH7):c.2638C>T (p.Leu880=) rs748621952 0.00001
NM_000257.4(MYH7):c.2679+3G>A rs553486562 0.00001
NM_000257.4(MYH7):c.2289G>A (p.Val763=) rs2502286358
NM_000257.4(MYH7):c.2301C>T (p.Ala767=) rs768380939
NM_000257.4(MYH7):c.2307G>T (p.Leu769=) rs2502286230
NM_000257.4(MYH7):c.2308C>T (p.Leu770=) rs2502286222
NM_000257.4(MYH7):c.2313G>A (p.Gly771=) rs2138667275
NM_000257.4(MYH7):c.2388C>T (p.Leu796=) rs397516144
NM_000257.4(MYH7):c.2403C>T (p.Tyr801=) rs775113608
NM_000257.4(MYH7):c.2409G>A (p.Lys803=)
NM_000257.4(MYH7):c.2412G>T (p.Leu804=) rs2138666900
NM_000257.4(MYH7):c.2424-15A>G rs2502284538
NM_000257.4(MYH7):c.2424-7C>T rs759141144
NM_000257.4(MYH7):c.2442C>A (p.Ile814=) rs1892638805
NM_000257.4(MYH7):c.2460C>T (p.Ala820=) rs2502284206
NM_000257.4(MYH7):c.2472C>G (p.Val824=) rs397516150
NM_000257.4(MYH7):c.2502C>T (p.Phe834=) rs397516152
NM_000257.4(MYH7):c.2523G>A (p.Lys841=) rs1892634440
NM_000257.4(MYH7):c.2538G>A (p.Glu846=) rs2502283812
NM_000257.4(MYH7):c.2553C>T (p.Ser851=) rs144291282
NM_000257.4(MYH7):c.2619G>A (p.Leu873=) rs771118861
NM_000257.4(MYH7):c.2640G>A (p.Leu880=) rs753565218
NM_000257.4(MYH7):c.2646G>A (p.Gln882=) rs1566531295
NM_000257.4(MYH7):c.2679+6G>A rs2502282838

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