ClinVar Miner

List of variants in gene combination LOC114827851, MYH6 reported by Ambry Genetics

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Gene type:
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Total variants: 98
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.411G>A (p.Glu137=) rs2277474 0.22054
NM_002471.4(MYH6):c.393G>A (p.Leu131=) rs17277970 0.06973
NM_002471.4(MYH6):c.166G>A (p.Gly56Arg) rs28711516 0.06950
NM_002471.4(MYH6):c.399G>A (p.Val133=) rs78891557 0.01343
NM_002471.4(MYH6):c.330G>A (p.Ala110=) rs77679218 0.00490
NM_002471.4(MYH6):c.36G>A (p.Ala12=) rs141014719 0.00487
NM_002471.4(MYH6):c.86G>A (p.Arg29Gln) rs150574114 0.00455
NM_002471.4(MYH6):c.-5C>A rs183611755 0.00438
NM_002471.4(MYH6):c.622G>A (p.Asp208Asn) rs142027794 0.00415
NM_002471.4(MYH6):c.210T>C (p.Thr70=) rs147397431 0.00041
NM_002471.4(MYH6):c.492C>T (p.Tyr164=) rs201380776 0.00041
NM_002471.4(MYH6):c.292G>A (p.Glu98Lys) rs140596256 0.00030
NM_002471.4(MYH6):c.408C>T (p.Ala136=) rs140732380 0.00024
NM_002471.4(MYH6):c.346-2A>G rs141187241 0.00014
NM_002471.4(MYH6):c.115G>A (p.Val39Met) rs142850511 0.00012
NM_002471.4(MYH6):c.7G>A (p.Asp3Asn) rs371667049 0.00011
NM_002471.4(MYH6):c.161G>A (p.Arg54Gln) rs727503239 0.00010
NM_002471.4(MYH6):c.420C>T (p.Ala140=) rs145023897 0.00010
NM_002471.4(MYH6):c.203C>T (p.Thr68Met) rs751285148 0.00009
NM_002471.4(MYH6):c.421G>A (p.Ala141Thr) rs776853139 0.00009
NM_002471.4(MYH6):c.642+4C>T rs369858520 0.00007
NM_002471.4(MYH6):c.100C>T (p.Arg34Cys) rs765792077 0.00006
NM_002471.4(MYH6):c.226G>A (p.Val76Met) rs977234074 0.00006
NM_002471.4(MYH6):c.190G>A (p.Glu64Lys) rs750818212 0.00005
NM_002471.4(MYH6):c.611G>A (p.Arg204His) rs200623022 0.00005
NM_002471.4(MYH6):c.268A>G (p.Met90Val) rs778199745 0.00004
NM_002471.4(MYH6):c.291C>T (p.His97=) rs144535842 0.00004
NM_002471.4(MYH6):c.297C>T (p.Pro99=) rs751088892 0.00004
NM_002471.4(MYH6):c.233A>G (p.Gln78Arg) rs772216708 0.00003
NM_002471.4(MYH6):c.329C>T (p.Ala110Val) rs149454728 0.00003
NM_002471.4(MYH6):c.467C>G (p.Ser156Cys) rs372298082 0.00003
NM_002471.4(MYH6):c.502+5G>A rs764301017 0.00003
NM_002471.4(MYH6):c.635C>T (p.Ala212Val) rs780456381 0.00003
NM_002471.4(MYH6):c.636G>A (p.Ala212=) rs111265123 0.00003
NM_002471.4(MYH6):c.121G>A (p.Asp41Asn) rs201161721 0.00002
NM_002471.4(MYH6):c.160C>T (p.Arg54Trp) rs369366244 0.00002
NM_002471.4(MYH6):c.189C>T (p.Thr63=) rs758633104 0.00002
NM_002471.4(MYH6):c.244C>T (p.Pro82Ser) rs754260713 0.00002
NM_002471.4(MYH6):c.354G>A (p.Ser118=) rs373427673 0.00002
NM_002471.4(MYH6):c.409G>A (p.Glu137Lys) rs752658033 0.00002
NM_002471.4(MYH6):c.453G>A (p.Pro151=) rs777360238 0.00002
NM_002471.4(MYH6):c.480C>T (p.Asn160=) rs780910329 0.00002
NM_002471.4(MYH6):c.85C>T (p.Arg29Trp) rs752885646 0.00002
NM_002471.4(MYH6):c.114C>T (p.Phe38=) rs777057620 0.00001
NM_002471.4(MYH6):c.182C>T (p.Ala61Val) rs730880148 0.00001
NM_002471.4(MYH6):c.253G>A (p.Asp85Asn) rs397516758 0.00001
NM_002471.4(MYH6):c.269T>C (p.Met90Thr) rs919307122 0.00001
NM_002471.4(MYH6):c.333C>A (p.Ala111=) rs774402902 0.00001
NM_002471.4(MYH6):c.369C>T (p.Val123=) rs780659186 0.00001
NM_002471.4(MYH6):c.396G>A (p.Pro132=) rs369139462 0.00001
NM_002471.4(MYH6):c.493A>T (p.Met165Leu) rs972242173 0.00001
NM_002471.4(MYH6):c.540C>T (p.Ser180=) rs766589542 0.00001
NM_002471.4(MYH6):c.568C>T (p.Arg190Cys) rs397516777 0.00001
NM_002471.4(MYH6):c.627T>C (p.Asn209=) rs751659257 0.00001
NM_002471.4(MYH6):c.71T>C (p.Leu24Pro) rs1320990570 0.00001
NM_002471.4(MYH6):c.77C>G (p.Ala26Gly) rs559973480 0.00001
NM_002471.4(MYH6):c.-4C>G
NM_002471.4(MYH6):c.145G>A (p.Ala49Thr)
NM_002471.4(MYH6):c.147C>T (p.Ala49=)
NM_002471.4(MYH6):c.165G>A (p.Glu55=)
NM_002471.4(MYH6):c.168A>C (p.Gly56=)
NM_002471.4(MYH6):c.174G>C (p.Lys58Asn)
NM_002471.4(MYH6):c.175del (p.Val59fs)
NM_002471.4(MYH6):c.189C>A (p.Thr63=)
NM_002471.4(MYH6):c.204G>A (p.Thr68=)
NM_002471.4(MYH6):c.206T>A (p.Val69Glu)
NM_002471.4(MYH6):c.234G>C (p.Gln78His)
NM_002471.4(MYH6):c.245C>T (p.Pro82Leu) rs529427223
NM_002471.4(MYH6):c.252C>A (p.Phe84Leu)
NM_002471.4(MYH6):c.275T>C (p.Met92Thr)
NM_002471.4(MYH6):c.288G>A (p.Leu96=)
NM_002471.4(MYH6):c.300G>A (p.Ala100=) rs200520512
NM_002471.4(MYH6):c.304C>A (p.Leu102Ile)
NM_002471.4(MYH6):c.341T>C (p.Ile114Thr)
NM_002471.4(MYH6):c.342A>G (p.Ile114Met)
NM_002471.4(MYH6):c.345+3G>C
NM_002471.4(MYH6):c.358C>G (p.Leu120Val)
NM_002471.4(MYH6):c.375C>T (p.Val125=)
NM_002471.4(MYH6):c.404A>G (p.Asn135Ser)
NM_002471.4(MYH6):c.416T>C (p.Val139Ala)
NM_002471.4(MYH6):c.427C>A (p.Arg143=) rs2277473
NM_002471.4(MYH6):c.427C>G (p.Arg143Gly)
NM_002471.4(MYH6):c.437A>G (p.Lys146Arg) rs1555335081
NM_002471.4(MYH6):c.444T>C (p.Ser148=)
NM_002471.4(MYH6):c.449C>T (p.Ala150Val)
NM_002471.4(MYH6):c.502+3G>A
NM_002471.4(MYH6):c.544G>A (p.Ala182Thr)
NM_002471.4(MYH6):c.546G>A (p.Ala182=) rs150015506
NM_002471.4(MYH6):c.569G>A (p.Arg190His) rs1891729151
NM_002471.4(MYH6):c.616AAG[1] (p.Lys207del) rs1404018896
NM_002471.4(MYH6):c.631A>T (p.Asn211Tyr)
NM_002471.4(MYH6):c.633T>A (p.Asn211Lys) rs886039039
NM_002471.4(MYH6):c.642+3G>A rs374013248
NM_002471.4(MYH6):c.70C>A (p.Leu24Ile) rs573489857
NM_002471.4(MYH6):c.86G>T (p.Arg29Leu) rs150574114
NM_002471.4(MYH6):c.87G>T (p.Arg29=)
NM_002471.4(MYH6):c.92T>C (p.Phe31Ser)
NM_002471.4(MYH6):c.94G>C (p.Asp32His)

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