ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys) rs3729823 0.00861
NM_000257.4(MYH7):c.4566T>C (p.Thr1522=) rs2754155 0.00831
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101 0.00024
NM_000257.4(MYH7):c.4513C>T (p.Leu1505=) rs139928934 0.00014
NM_000257.4(MYH7):c.4423C>T (p.Arg1475Cys) rs139646545 0.00009
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242 0.00008
NM_000257.4(MYH7):c.4618C>T (p.Leu1540=) rs368734580 0.00007
NM_000257.4(MYH7):c.4283T>C (p.Leu1428Ser) rs727503244 0.00006
NM_000257.4(MYH7):c.4353+5G>A rs200436876 0.00006
NM_000257.4(MYH7):c.4363G>A (p.Glu1455Lys) rs876661373 0.00006
NM_000257.4(MYH7):c.4290G>T (p.Val1430=) rs372476972 0.00005
NM_000257.4(MYH7):c.4294G>A (p.Val1432Ile) rs144200285 0.00005
NM_000257.4(MYH7):c.4347C>T (p.Phe1449=) rs182311329 0.00005
NM_000257.4(MYH7):c.4348G>A (p.Asp1450Asn) rs397516211 0.00004
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=) rs578166720 0.00004
NM_000257.4(MYH7):c.4458C>T (p.Asn1486=) rs571704020 0.00004
NM_000257.4(MYH7):c.4605C>T (p.Ala1535=) rs746261895 0.00004
NM_000257.4(MYH7):c.4389G>A (p.Ser1463=) rs781203524 0.00002
NM_000257.4(MYH7):c.4499G>A (p.Arg1500Gln) rs121913647 0.00002
NM_000257.4(MYH7):c.4500G>A (p.Arg1500=) rs199995198 0.00002
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=) rs150552664 0.00002
NM_000257.4(MYH7):c.4641C>T (p.Ala1547=) rs376854724 0.00002
NM_000257.4(MYH7):c.4341G>A (p.Arg1447=) rs778233579 0.00001
NM_000257.4(MYH7):c.4343A>T (p.Asn1448Ile) rs753484341 0.00001
NM_000257.4(MYH7):c.4390C>T (p.Gln1464Ter) rs754829218 0.00001
NM_000257.4(MYH7):c.4440G>T (p.Glu1480Asp) rs1351661186 0.00001
NM_000257.4(MYH7):c.4450C>A (p.Leu1484Ile) rs1555336651 0.00001
NM_000257.4(MYH7):c.4459G>A (p.Ala1487Thr) rs766909770 0.00001
NM_000257.4(MYH7):c.4487A>C (p.Glu1496Ala) rs397516218 0.00001
NM_000257.4(MYH7):c.4572T>C (p.His1524=) rs1246893810 0.00001
NM_000257.4(MYH7):c.4584G>A (p.Lys1528=) rs1892237100 0.00001
NM_000257.4(MYH7):c.4588C>T (p.Arg1530Ter) rs397516225 0.00001
NM_000257.4(MYH7):c.4606G>A (p.Glu1536Lys) rs779315151 0.00001
NM_000257.3(MYH7):c.4522_4524del rs397516220
NM_000257.4(MYH7):c.4275C>A (p.Ile1425=) rs57680382
NM_000257.4(MYH7):c.4276G>A (p.Glu1426Lys) rs397516208
NM_000257.4(MYH7):c.4279G>A (p.Asp1427Asn)
NM_000257.4(MYH7):c.4285_4287dup (p.Met1429dup) rs1892274161
NM_000257.4(MYH7):c.4371G>C (p.Lys1457Asn) rs1555336697
NM_000257.4(MYH7):c.4377G>A (p.Lys1459=) rs201307101
NM_000257.4(MYH7):c.4382A>G (p.Glu1461Gly) rs995126992
NM_000257.4(MYH7):c.4395G>A (p.Ser1465=) rs397516213
NM_000257.4(MYH7):c.4395G>T (p.Ser1465=) rs397516213
NM_000257.4(MYH7):c.4399C>G (p.Leu1467Val) rs397516214
NM_000257.4(MYH7):c.4402G>A (p.Glu1468Lys) rs876657884
NM_000257.4(MYH7):c.4411C>T (p.Gln1471Ter) rs397516216
NM_000257.4(MYH7):c.4414_4416del (p.Lys1472del) rs1555336672
NM_000257.4(MYH7):c.4440G>A (p.Glu1480=)
NM_000257.4(MYH7):c.4457A>G (p.Asn1486Ser) rs2138645374
NM_000257.4(MYH7):c.4460C>T (p.Ala1487Val) rs1595074732
NM_000257.4(MYH7):c.4464T>C (p.Tyr1488=)
NM_000257.4(MYH7):c.4469A>G (p.Glu1490Gly)
NM_000257.4(MYH7):c.4493_4494delinsAT (p.Phe1498Tyr) rs2138645175
NM_000257.4(MYH7):c.4496A>G (p.Lys1499Arg)
NM_000257.4(MYH7):c.4498C>T (p.Arg1500Trp) rs45544633
NM_000257.4(MYH7):c.4515G>T (p.Leu1505=) rs397516219
NM_000257.4(MYH7):c.4519+1G>A
NM_000257.4(MYH7):c.4532A>G (p.Asp1511Gly)
NM_000257.4(MYH7):c.4551T>C (p.Gly1517=) rs1892238660
NM_000257.4(MYH7):c.4571A>C (p.His1524Pro) rs767148171
NM_000257.4(MYH7):c.4585G>T (p.Val1529Phe)
NM_000257.4(MYH7):c.4588C>A (p.Arg1530=)
NM_000257.4(MYH7):c.4589G>A (p.Arg1530Gln) rs730880803
NM_000257.4(MYH7):c.4642G>A (p.Glu1548Lys)
NM_000257.4(MYH7):c.4644+5G>C rs730880797

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