ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as benign by GeneDx

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Gene type:
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Total variants: 43
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HGVS dbSNP
NM_001040113.1(MYH11):c.3721G>A (p.Ala1241Thr) rs16967494
NM_001040113.1(MYH11):c.3988C>T (p.Leu1330=) rs12907
NM_001040113.1(MYH11):c.4137+11delC rs543763112
NM_001040113.1(MYH11):c.4422C>T (p.Tyr1474=) rs8046180
NM_001040113.1(MYH11):c.4812+16G>T rs189463893
NM_001040113.1(MYH11):c.5317-4C>T rs183176702
NM_001040113.1(MYH11):c.5819C>A (p.Pro1940Gln) rs111588143
NM_001143979.1(NDE1):c.948-6917G>A rs35295469
NM_001143979.1(NDE1):c.948-6986C>T rs1050162
NM_001143979.1(NDE1):c.948-7025C>T rs1050163
NM_002474.2(MYH11):c.*13A>G rs191562149
NM_002474.2(MYH11):c.*5C>G rs1875184
NM_002474.2(MYH11):c.3866T>C (p.Val1289Ala) rs16967510
NM_002474.2(MYH11):c.3949C>A (p.Leu1317Ile) rs141159831
NM_002474.2(MYH11):c.4095C>T (p.His1365=) rs374454281
NM_002474.2(MYH11):c.4116+12G>A rs193005461
NM_002474.2(MYH11):c.4158C>T (p.Thr1386=) rs112377790
NM_002474.2(MYH11):c.4242T>G (p.Ala1414=) rs2075511
NM_002474.2(MYH11):c.4506C>T (p.Leu1502=) rs76890940
NM_002474.2(MYH11):c.4522A>G (p.Met1508Val) rs35176378
NM_002474.2(MYH11):c.4578+19T>C rs118072250
NM_002474.2(MYH11):c.4578+3A>G rs143288748
NM_002474.2(MYH11):c.4579-13G>A rs181115969
NM_002474.2(MYH11):c.4579-14C>T rs377410503
NM_002474.2(MYH11):c.4579-6C>T rs200223639
NM_002474.2(MYH11):c.4770G>A (p.Lys1590=) rs11648119
NM_002474.2(MYH11):c.4791+4C>T rs142108062
NM_002474.2(MYH11):c.4953+18C>T rs371462392
NM_002474.2(MYH11):c.5160C>T (p.Ser1720=) rs199564260
NM_002474.2(MYH11):c.5172-13G>A rs373378619
NM_002474.2(MYH11):c.5172-14C>T rs34839877
NM_002474.2(MYH11):c.5172-5C>T rs574893374
NM_002474.2(MYH11):c.5313C>T (p.Asn1771=) rs190675029
NM_002474.2(MYH11):c.5379G>A (p.Gln1793=) rs375230260
NM_002474.2(MYH11):c.5504+8G>C rs148691719
NM_002474.2(MYH11):c.5517G>A (p.Ala1839=) rs28505375
NM_002474.2(MYH11):c.5566C>T (p.Leu1856=) rs142639688
NM_002474.2(MYH11):c.5595C>T (p.Ala1865=) rs760286479
NM_002474.2(MYH11):c.5676G>C (p.Glu1892Asp) rs113964173
NM_002474.2(MYH11):c.5691C>T (p.Asn1897=) rs149566621
NM_002474.2(MYH11):c.5757C>T (p.Arg1919=) rs138168272
NM_002474.2(MYH11):c.5796C>T (p.Asn1932=) rs149529195
NM_022844.2(MYH11):c.5787-11_5787-8delCTCT rs747642850

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