ClinVar Miner

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

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Total variants: 81
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HGVS dbSNP
NC_000016.10:g.15724138G>A
NC_000016.10:g.15724453G>A
NC_000016.10:g.15725198G>A
NM_001040113.1(MYH11):c.4137+11delC rs543763112
NM_002474.3(MYH11):c.*13A>G rs191562149
NM_002474.3(MYH11):c.*5C>G rs1875184
NM_002474.3(MYH11):c.3700G>A (p.Ala1234Thr) rs16967494
NM_002474.3(MYH11):c.3858+874G>A rs73519694
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.3928G>A (p.Val1310Met) rs7196804
NM_002474.3(MYH11):c.3949C>A (p.Leu1317Ile) rs141159831
NM_002474.3(MYH11):c.3967C>T (p.Leu1323=) rs12907
NM_002474.3(MYH11):c.3973C>G (p.Gln1325Glu) rs150033906
NM_002474.3(MYH11):c.4095C>T (p.His1365=) rs374454281
NM_002474.3(MYH11):c.4116+12G>A rs193005461
NM_002474.3(MYH11):c.4117-44C>T rs11130
NM_002474.3(MYH11):c.4158C>T (p.Thr1386=) rs112377790
NM_002474.3(MYH11):c.4197G>A (p.Lys1399=) rs113302393
NM_002474.3(MYH11):c.4203C>T (p.Ile1401=) rs760611400
NM_002474.3(MYH11):c.4239C>T (p.Ala1413=) rs138573101
NM_002474.3(MYH11):c.4242T>G (p.Ala1414=) rs2075511
NM_002474.3(MYH11):c.4365+310A>G
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+19T>C rs118072250
NM_002474.3(MYH11):c.4578+3A>G rs143288748
NM_002474.3(MYH11):c.4579-13G>A rs181115969
NM_002474.3(MYH11):c.4579-14C>T rs377410503
NM_002474.3(MYH11):c.4579-6C>T rs200223639
NM_002474.3(MYH11):c.4673C>T (p.Thr1558Met) rs111854563
NM_002474.3(MYH11):c.4770G>A (p.Lys1590=) rs11648119
NM_002474.3(MYH11):c.4774A>C (p.Arg1592=) rs114556043
NM_002474.3(MYH11):c.4791+16G>T rs189463893
NM_002474.3(MYH11):c.4791+226T>C
NM_002474.3(MYH11):c.4791+4C>T rs142108062
NM_002474.3(MYH11):c.4792-108T>C
NM_002474.3(MYH11):c.4953+18C>T rs371462392
NM_002474.3(MYH11):c.4953+63G>A
NM_002474.3(MYH11):c.4954-196G>T
NM_002474.3(MYH11):c.4954-63C>T
NM_002474.3(MYH11):c.4974A>G (p.Gln1658=) rs762733113
NM_002474.3(MYH11):c.5083-46C>A
NM_002474.3(MYH11):c.5160C>T (p.Ser1720=) rs199564260
NM_002474.3(MYH11):c.5172-13G>A rs373378619
NM_002474.3(MYH11):c.5172-14C>T rs34839877
NM_002474.3(MYH11):c.5172-5C>T rs574893374
NM_002474.3(MYH11):c.5295+76C>T
NM_002474.3(MYH11):c.5296-49C>G
NM_002474.3(MYH11):c.5296-4C>T rs183176702
NM_002474.3(MYH11):c.5313C>T (p.Asn1771=) rs190675029
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.5379G>A (p.Gln1793=) rs375230260
NM_002474.3(MYH11):c.5439G>A (p.Lys1813=) rs1050162
NM_002474.3(MYH11):c.5478G>A (p.Leu1826=) rs1050163
NM_002474.3(MYH11):c.5504+115C>G
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.5566C>T (p.Leu1856=) rs142639688
NM_002474.3(MYH11):c.5585G>A (p.Arg1862His) rs146228576
NM_002474.3(MYH11):c.5586C>G (p.Arg1862=) rs542765381
NM_002474.3(MYH11):c.5595C>T (p.Ala1865=) rs760286479
NM_002474.3(MYH11):c.5614-7G>A rs202120792
NM_002474.3(MYH11):c.5676G>C (p.Glu1892Asp) rs113964173
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.5757C>T (p.Arg1919=) rs138168272
NM_002474.3(MYH11):c.5787-230C>A
NM_002474.3(MYH11):c.5787-4683C>G rs886038393
NM_002474.3(MYH11):c.5787-4707C>A rs111588143
NM_002474.3(MYH11):c.5787-4714dup rs747392139
NM_002474.3(MYH11):c.5787-4733CT[2] rs747642850
NM_002474.3(MYH11):c.5787-4966C>A
NM_002474.3(MYH11):c.5796C>T (p.Asn1932=) rs149529195

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