ClinVar Miner

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

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Total variants: 67
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HGVS dbSNP
NC_000016.10:g.15708831G>C
NM_002474.2(MYH11):c.5786+6_5786+8delGAG rs1064794454
NM_002474.3(MYH11):c.*19G>A rs187644296
NM_002474.3(MYH11):c.3891C>T (p.Asn1297=) rs541280738
NM_002474.3(MYH11):c.3927C>T (p.Asp1309=) rs150712107
NM_002474.3(MYH11):c.3928G>A (p.Val1310Met) rs7196804
NM_002474.3(MYH11):c.3933G>A (p.Ala1311=) rs78857360
NM_002474.3(MYH11):c.4068G>A (p.Met1356Ile) rs794728663
NM_002474.3(MYH11):c.4117-14C>T rs374648974
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.4236G>A (p.Ala1412=) rs771460474
NM_002474.3(MYH11):c.4242T>A (p.Ala1414=) rs2075511
NM_002474.3(MYH11):c.4293C>T (p.Asp1431=) rs143588920
NM_002474.3(MYH11):c.4296G>A (p.Leu1432=)
NM_002474.3(MYH11):c.4366-131T>C
NM_002474.3(MYH11):c.4374C>T (p.Ala1458=) rs767066866
NM_002474.3(MYH11):c.4579-140T>C
NM_002474.3(MYH11):c.4579-29T>C
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.4674G>A (p.Thr1558=) rs778499852
NM_002474.3(MYH11):c.4680C>T (p.Asp1560=) rs142613263
NM_002474.3(MYH11):c.4774A>C (p.Arg1592=) rs114556043
NM_002474.3(MYH11):c.4792-6G>C rs766965358
NM_002474.3(MYH11):c.4809G>A (p.Thr1603=) rs140577744
NM_002474.3(MYH11):c.4872G>A (p.Gly1624=) rs764800035
NM_002474.3(MYH11):c.4884C>T (p.Asp1628=) rs780786328
NM_002474.3(MYH11):c.4899C>T (p.Ala1633=) rs760584464
NM_002474.3(MYH11):c.4953+15G>A rs767255396
NM_002474.3(MYH11):c.4954-14G>C rs375979600
NM_002474.3(MYH11):c.5053T>C (p.Leu1685=) rs1057522597
NM_002474.3(MYH11):c.5082+20G>A rs527381094
NM_002474.3(MYH11):c.5094C>T (p.Ala1698=) rs771742318
NM_002474.3(MYH11):c.5157T>C (p.Ser1719=) rs771625605
NM_002474.3(MYH11):c.5171+86T>G
NM_002474.3(MYH11):c.5172-255G>A
NM_002474.3(MYH11):c.5172-286C>G
NM_002474.3(MYH11):c.5214C>T (p.Ile1738=) rs1439627120
NM_002474.3(MYH11):c.5226G>C (p.Glu1742Asp) rs144421849
NM_002474.3(MYH11):c.5247G>A (p.Gln1749=) rs757501817
NM_002474.3(MYH11):c.5277C>T (p.Val1759=) rs112564682
NM_002474.3(MYH11):c.5328G>A (p.Glu1776=) rs773366562
NM_002474.3(MYH11):c.5336C>T (p.Thr1779Met) rs201960644
NM_002474.3(MYH11):c.5451G>A (p.Ala1817=) rs774717188
NM_002474.3(MYH11):c.5454G>A (p.Ala1818=) rs374486989
NM_002474.3(MYH11):c.5490C>A (p.Val1830=)
NM_002474.3(MYH11):c.5504+268C>G
NM_002474.3(MYH11):c.5504+6C>A rs371348553
NM_002474.3(MYH11):c.5528C>T (p.Ser1843Leu) rs148621523
NM_002474.3(MYH11):c.5586C>G (p.Arg1862=) rs542765381
NM_002474.3(MYH11):c.5614-18del rs1555550026
NM_002474.3(MYH11):c.5760G>A (p.Glu1920=) rs199997929
NM_002474.3(MYH11):c.5786+12G>A rs748529228
NM_002474.3(MYH11):c.5786+18C>T rs769309834
NM_002474.3(MYH11):c.5786+220C>A
NM_002474.3(MYH11):c.5787-4661C>T rs373484327
NM_002474.3(MYH11):c.5787-4672G>A
NM_002474.3(MYH11):c.5787-4707C>G rs111588143
NM_002474.3(MYH11):c.5787-4709C>A rs1057524493
NM_002474.3(MYH11):c.5787-4714dup rs747392139
NM_002474.3(MYH11):c.5787-4737G>A rs769187225
NM_002474.3(MYH11):c.5787-4998A>G
NM_002474.3(MYH11):c.5800A>T (p.Thr1934Ser) rs113667224
NM_002474.3(MYH11):c.5829A>G (p.Gly1943=) rs199752132
NM_002474.3(MYH11):c.5873C>T (p.Thr1958Met) rs149701021

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