ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as likely benign for Thoracic aortic aneurysm and aortic dissection

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Total variants: 75
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HGVS dbSNP
NM_002474.3(MYH11):c.*37C>A rs182768107
NM_002474.3(MYH11):c.*420C>G rs12932063
NM_002474.3(MYH11):c.*544G>A rs116721094
NM_002474.3(MYH11):c.*5C>G rs1875184
NM_002474.3(MYH11):c.*61_*65del rs5815842
NM_002474.3(MYH11):c.3700G>A (p.Ala1234Thr) rs16967494
NM_002474.3(MYH11):c.3858+507A>G rs140519946
NM_002474.3(MYH11):c.3858+813T>C rs113405225
NM_002474.3(MYH11):c.3858+874G>A rs73519694
NM_002474.3(MYH11):c.3859-122G>C rs12927605
NM_002474.3(MYH11):c.3859-158G>T rs79015533
NM_002474.3(MYH11):c.3859-172T>G rs760024
NM_002474.3(MYH11):c.3859-206C>T rs760023
NM_002474.3(MYH11):c.3859-479C>T rs74009414
NM_002474.3(MYH11):c.3859-558T>C rs16967500
NM_002474.3(MYH11):c.3859-648C>T rs11557090
NM_002474.3(MYH11):c.3866T>C (p.Val1289Ala) rs16967510
NM_002474.3(MYH11):c.3891C>T (p.Asn1297=) rs541280738
NM_002474.3(MYH11):c.3897C>A (p.Ala1299=) rs190546350
NM_002474.3(MYH11):c.3910A>C (p.Ile1304Leu) rs200737737
NM_002474.3(MYH11):c.3928G>A (p.Val1310Met) rs7196804
NM_002474.3(MYH11):c.3967C>T (p.Leu1323=) rs12907
NM_002474.3(MYH11):c.4095C>T (p.His1365=) rs374454281
NM_002474.3(MYH11):c.4096A>G (p.Ile1366Val) rs147127121
NM_002474.3(MYH11):c.4116+12G>A rs193005461
NM_002474.3(MYH11):c.4117-44C>T rs11130
NM_002474.3(MYH11):c.4242T>G (p.Ala1414=) rs2075511
NM_002474.3(MYH11):c.4401C>T (p.Tyr1467=) rs8046180
NM_002474.3(MYH11):c.4506C>T (p.Leu1502=) rs76890940
NM_002474.3(MYH11):c.4522A>G (p.Met1508Val) rs35176378
NM_002474.3(MYH11):c.4578+3A>G rs143288748
NM_002474.3(MYH11):c.4579-13G>A rs181115969
NM_002474.3(MYH11):c.4587G>A (p.Glu1529=) rs1567695324
NM_002474.3(MYH11):c.4604G>A (p.Arg1535Gln) rs137934837
NM_002474.3(MYH11):c.4659C>T (p.Asp1553=) rs141031021
NM_002474.3(MYH11):c.4673C>T (p.Thr1558Met) rs111854563
NM_002474.3(MYH11):c.4681G>A (p.Ala1561Thr) rs138863103
NM_002474.3(MYH11):c.4770G>A (p.Lys1590=) rs11648119
NM_002474.3(MYH11):c.4773G>A (p.Arg1591=) rs747923542
NM_002474.3(MYH11):c.4797C>T (p.His1599=) rs764996278
NM_002474.3(MYH11):c.4809G>A (p.Thr1603=) rs140577744
NM_002474.3(MYH11):c.4920G>A (p.Arg1640=) rs199638486
NM_002474.3(MYH11):c.5052C>T (p.Ser1684=) rs760908992
NM_002474.3(MYH11):c.5160C>T (p.Ser1720=) rs199564260
NM_002474.3(MYH11):c.5172-11C>A rs779166026
NM_002474.3(MYH11):c.5172-14C>T rs34839877
NM_002474.3(MYH11):c.5187C>T (p.Asp1729=) rs145101141
NM_002474.3(MYH11):c.5226G>C (p.Glu1742Asp) rs144421849
NM_002474.3(MYH11):c.5238G>A (p.Glu1746=) rs1567689895
NM_002474.3(MYH11):c.5275G>A (p.Val1759Ile) rs138059405
NM_002474.3(MYH11):c.5277C>T (p.Val1759=) rs112564682
NM_002474.3(MYH11):c.5296-11C>T rs780765461
NM_002474.3(MYH11):c.5296-4C>T rs183176702
NM_002474.3(MYH11):c.5336C>T (p.Thr1779Met) rs201960644
NM_002474.3(MYH11):c.5370C>T (p.Leu1790=) rs35295469
NM_002474.3(MYH11):c.5439G>A (p.Lys1813=) rs1050162
NM_002474.3(MYH11):c.5450C>T (p.Ala1817Val) rs142654744
NM_002474.3(MYH11):c.5478G>A (p.Leu1826=) rs1050163
NM_002474.3(MYH11):c.5499G>C (p.Glu1833Asp) rs145252402
NM_002474.3(MYH11):c.5504+6C>A rs371348553
NM_002474.3(MYH11):c.5504+8G>C rs148691719
NM_002474.3(MYH11):c.5517G>A (p.Ala1839=) rs28505375
NM_002474.3(MYH11):c.5529G>A (p.Ser1843=) rs146024732
NM_002474.3(MYH11):c.5595C>T (p.Ala1865=) rs760286479
NM_002474.3(MYH11):c.5607G>A (p.Lys1869=) rs372546520
NM_002474.3(MYH11):c.5635G>A (p.Val1879Ile) rs138206921
NM_002474.3(MYH11):c.5691C>T (p.Asn1897=) rs149566621
NM_002474.3(MYH11):c.5696A>G (p.Asn1899Ser) rs79129097
NM_002474.3(MYH11):c.5732C>T (p.Thr1911Met) rs748516947
NM_002474.3(MYH11):c.5787-4707C>A rs111588143
NM_002474.3(MYH11):c.5787-4707C>G rs111588143
NM_002474.3(MYH11):c.5787-4727C>T rs745371874
NM_002474.3(MYH11):c.5787-4733CT[2] rs747642850
NM_002474.3(MYH11):c.5787-4733CT[3] rs747642850
NM_002474.3(MYH11):c.5800A>T (p.Thr1934Ser) rs113667224

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