ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as likely benign for not specified

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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_002474.3(MYH11):c.5439G>A (p.Lys1813=) rs1050162 0.44262
NM_002474.3(MYH11):c.5478G>A (p.Leu1826=) rs1050163 0.44235
NM_017668.3(NDE1):c.948-53G>A rs7193920 0.07945
NM_002474.3(MYH11):c.5370C>T (p.Leu1790=) rs35295469 0.03116
NM_002474.3(MYH11):c.3928G>A (p.Val1310Met) rs7196804 0.00216
NM_002474.3(MYH11):c.4604G>A (p.Arg1535Gln) rs137934837 0.00216
NM_017668.3(NDE1):c.948-2772T>C rs143288748 0.00138
NM_002474.3(MYH11):c.4774A>C (p.Arg1592=) rs114556043 0.00093
NM_002474.3(MYH11):c.4203C>T (p.Ile1401=) rs760611400 0.00057
NM_002474.3(MYH11):c.5529G>A (p.Ser1843=) rs146024732 0.00039
NM_002474.3(MYH11):c.5273G>A (p.Arg1758Gln) rs142546324 0.00038
NM_002474.3(MYH11):c.5470G>A (p.Ala1824Thr) rs147710374 0.00036
NM_002474.3(MYH11):c.5499G>C (p.Glu1833Asp) rs145252402 0.00036
NM_017668.3(NDE1):c.948-9293G>A rs374454501 0.00034
NM_002474.3(MYH11):c.5275G>A (p.Val1759Ile) rs138059405 0.00033
NM_002474.3(MYH11):c.5635G>A (p.Val1879Ile) rs138206921 0.00032
NM_002474.3(MYH11):c.4197G>A (p.Lys1399=) rs113302393 0.00026
NM_002474.3(MYH11):c.5393G>A (p.Arg1798Gln) rs148938946 0.00025
NM_017668.3(NDE1):c.947+7112C>T rs187644296 0.00020
NM_017668.3(NDE1):c.948-3368C>A rs189463893 0.00019
NM_017668.3(NDE1):c.948-5740C>T rs373378619 0.00019
NM_002474.3(MYH11):c.3932C>T (p.Ala1311Val) rs185720909 0.00016
NM_002474.3(MYH11):c.4659C>T (p.Asp1553=) rs141031021 0.00016
NM_017668.3(NDE1):c.990G>A (p.Arg330=) rs143588920 0.00014
NM_002474.3(MYH11):c.4034G>A (p.Arg1345Gln) rs150883363 0.00013
NM_017668.3(NDE1):c.948-4464C>G rs375979600 0.00013
NM_002474.3(MYH11):c.5226G>C (p.Glu1742Asp) rs144421849 0.00009
NM_002474.3(MYH11):c.4681G>A (p.Ala1561Thr) rs138863103 0.00007
NM_002474.3(MYH11):c.3897C>T (p.Ala1299=) rs190546350 0.00006
NM_002474.3(MYH11):c.5869G>C (p.Glu1957Gln) rs768140376 0.00005
NM_002474.3(MYH11):c.4072G>T (p.Ala1358Ser) rs763280025 0.00004
NM_002474.3(MYH11):c.4236G>A (p.Ala1412=) rs771460474 0.00004
NM_002474.3(MYH11):c.5607G>A (p.Lys1869=) rs372546520 0.00004
NM_002474.3(MYH11):c.5873C>T (p.Thr1958Met) rs149701021 0.00004
NM_017668.3(NDE1):c.948-9300G>A rs769309834 0.00004
NM_002474.3(MYH11):c.5652G>A (p.Arg1884=) rs150860193 0.00003
NM_002474.3(MYH11):c.5696A>G (p.Asn1899Ser) rs79129097 0.00003
NM_017668.3(NDE1):c.*172G>A rs374648974 0.00003
NM_017668.3(NDE1):c.948-4980G>A rs780145425 0.00003
NM_017668.3(NDE1):c.948-7057G>T rs371348553 0.00003
NM_002474.3(MYH11):c.4786A>C (p.Arg1596=) rs754931029 0.00002
NM_002474.3(MYH11):c.5451G>A (p.Ala1817=) rs774717188 0.00002
NM_017668.3(NDE1):c.948-4055C>T rs767255396 0.00002
NM_017668.3(NDE1):c.948-9294C>T rs748529228 0.00002
NM_002474.3(MYH11):c.4069G>A (p.Glu1357Lys) rs141184241 0.00001
NM_002474.3(MYH11):c.4374C>T (p.Ala1458=) rs767066866 0.00001
NM_002474.3(MYH11):c.4648G>A (p.Glu1550Lys) rs751716762 0.00001
NM_002474.3(MYH11):c.4674G>A (p.Thr1558=) rs778499852 0.00001
NM_002474.3(MYH11):c.4872G>A (p.Gly1624=) rs764800035 0.00001
NM_002474.3(MYH11):c.4884C>T (p.Asp1628=) rs780786328 0.00001
NM_002474.3(MYH11):c.5053T>C (p.Leu1685=) rs1057522597 0.00001
NM_002474.3(MYH11):c.5157T>C (p.Ser1719=) rs771625605 0.00001
NM_002474.3(MYH11):c.5422G>A (p.Val1808Ile) rs780870767 0.00001
NM_002474.3(MYH11):c.5586C>G (p.Arg1862=) rs542765381 0.00001
NM_002474.3(MYH11):c.5760G>A (p.Glu1920=) rs199997929 0.00001
NM_002474.3(MYH11):c.5766C>T (p.Asn1922=) rs764020019 0.00001
NM_002474.3(MYH11):c.5829A>G (p.Gly1943=) rs199752132 0.00001
NM_017668.3(NDE1):c.947+12000C>T rs769187225 0.00001
NM_017668.3(NDE1):c.984A>G (p.Thr328=) rs2040630480 0.00001
NM_001040113.2(MYH11):c.5819dup (p.Gln1941fs) rs747392139
NM_002474.3(MYH11):c.3874G>C (p.Val1292Leu) rs151058774
NM_002474.3(MYH11):c.4083C>T (p.Asn1361=) rs769899465
NM_002474.3(MYH11):c.4242T>A (p.Ala1414=) rs2075511
NM_002474.3(MYH11):c.4855AAG[2] (p.Lys1621del) rs755547393
NM_002474.3(MYH11):c.5133G>A (p.Glu1711=)
NM_002474.3(MYH11):c.5336C>T (p.Thr1779Met) rs201960644
NM_002474.3(MYH11):c.5786+19G>A
NM_017668.3(NDE1):c.948-4626C>T rs527381094
NM_017668.3(NDE1):c.948-9092del rs1555550026
NM_017668.3(NDE1):c.948-9287_948-9285del rs1064794454

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