ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as likely benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 39
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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.*899C>A rs79015533 0.11286
NM_002474.3(MYH11):c.5517G>A (p.Ala1839=) rs28505375 0.07791
NM_002474.3(MYH11):c.3866T>C (p.Val1289Ala) rs16967510 0.03954
NM_017668.3(NDE1):c.947+6711G>C rs12932063 0.03681
NM_017668.3(NDE1):c.948-5739G>A rs34839877 0.03595
NM_002474.3(MYH11):c.5370C>T (p.Leu1790=) rs35295469 0.03116
NM_017668.3(NDE1):c.947+7126G>C rs1875184 0.02929
NM_017668.3(NDE1):c.947+6587C>T rs116721094 0.01717
NM_017668.3(NDE1):c.*1784A>G rs113405225 0.01698
NM_002474.3(MYH11):c.4770G>A (p.Lys1590=) rs11648119 0.01341
NM_002474.3(MYH11):c.4401C>T (p.Tyr1467=) rs8046180 0.01019
NM_017668.3(NDE1):c.*2090T>C rs140519946 0.00926
NM_017668.3(NDE1):c.*384C>T rs193005461 0.00847
NM_002474.3(MYH11):c.4158C>T (p.Thr1386=) rs112377790 0.00746
NM_017668.3(NDE1):c.948-3356G>A rs142108062 0.00664
NM_017668.3(NDE1):c.947+6500G>A rs112926446 0.00650
NM_017668.3(NDE1):c.948-6839G>A rs183176702 0.00636
NM_002474.3(MYH11):c.3949C>A (p.Leu1317Ile) rs141159831 0.00600
NM_017668.3(NDE1):c.948-7059C>G rs148691719 0.00511
NM_002474.3(MYH11):c.5676G>C (p.Glu1892Asp) rs113964173 0.00462
NM_017668.3(NDE1):c.*238C>G rs7196012 0.00411
NM_002474.3(MYH11):c.5757C>T (p.Arg1919=) rs138168272 0.00312
NM_002474.3(MYH11):c.5691C>T (p.Asn1897=) rs149566621 0.00257
NM_017668.3(NDE1):c.*863C>G rs12927605 0.00231
NM_017668.3(NDE1):c.*1509A>G rs140080894 0.00221
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_002474.3(MYH11):c.4506C>T (p.Leu1502=) rs76890940 0.00116
NM_017668.3(NDE1):c.947+7094G>T rs182768107 0.00041
NM_017668.3(NDE1):c.*943C>T rs149894916 0.00022
NM_017668.3(NDE1):c.948-3127C>T rs181115969 0.00022
NM_017668.3(NDE1):c.947+6521C>T rs189033300 0.00019
NM_002474.3(MYH11):c.5226G>C (p.Glu1742Asp) rs144421849 0.00009
NM_002474.3(MYH11):c.5696A>G (p.Asn1899Ser) rs79129097 0.00003
NM_017668.3(NDE1):c.948-5748G>A rs574893374 0.00001
NM_017668.3(NDE1):c.*367T>C rs138543179
NM_017668.3(NDE1):c.947+7069_947+7073del rs5815842

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