ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as uncertain significance by Ambry Genetics

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Total variants: 38
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HGVS dbSNP
NM_002474.3(MYH11):c.3910A>C (p.Ile1304Leu) rs200737737
NM_002474.3(MYH11):c.3973C>G (p.Gln1325Glu) rs150033906
NM_002474.3(MYH11):c.4000G>C (p.Val1334Leu) rs139377348
NM_002474.3(MYH11):c.4007C>T (p.Thr1336Met) rs771330136
NM_002474.3(MYH11):c.4015C>A (p.Arg1339Ser) rs754951425
NM_002474.3(MYH11):c.4069G>A (p.Glu1357Lys) rs141184241
NM_002474.3(MYH11):c.4135A>C (p.Lys1379Gln) rs753312858
NM_002474.3(MYH11):c.4177G>C (p.Gly1393Arg) rs143620567
NM_002474.3(MYH11):c.4240_4242delinsACG (p.Ala1414Thr) rs794728676
NM_002474.3(MYH11):c.4262C>T (p.Thr1421Ile) rs146817436
NM_002474.3(MYH11):c.4327G>A (p.Val1443Met) rs141262029
NM_002474.3(MYH11):c.4372G>A (p.Ala1458Thr) rs775154820
NM_002474.3(MYH11):c.4396A>C (p.Lys1466Gln) rs749181134
NM_002474.3(MYH11):c.4403C>T (p.Ala1468Val) rs370240337
NM_002474.3(MYH11):c.4433C>G (p.Ala1478Gly) rs886039156
NM_002474.3(MYH11):c.4543G>A (p.Asp1515Asn) rs200909802
NM_002474.3(MYH11):c.4681G>A (p.Ala1561Thr) rs138863103
NM_002474.3(MYH11):c.4706T>C (p.Met1569Thr) rs145074004
NM_002474.3(MYH11):c.4728C>G (p.Phe1576Leu) rs765435868
NM_002474.3(MYH11):c.4747C>T (p.Arg1583Trp) rs777170587
NM_002474.3(MYH11):c.4861A>C (p.Lys1621Gln) rs34321232
NM_002474.3(MYH11):c.5122C>G (p.Leu1708Val) rs1353911032
NM_002474.3(MYH11):c.5275G>A (p.Val1759Ile) rs138059405
NM_002474.3(MYH11):c.5275G>T (p.Val1759Phe) rs138059405
NM_002474.3(MYH11):c.5296-3C>G rs370866058
NM_002474.3(MYH11):c.5336C>A (p.Thr1779Lys) rs201960644
NM_002474.3(MYH11):c.5338G>T (p.Ala1780Ser) rs1041344233
NM_002474.3(MYH11):c.5360G>A (p.Arg1787Gln) rs759000207
NM_002474.3(MYH11):c.5393G>A (p.Arg1798Gln) rs148938946
NM_002474.3(MYH11):c.5450C>T (p.Ala1817Val) rs142654744
NM_002474.3(MYH11):c.5470G>A (p.Ala1824Thr) rs147710374
NM_002474.3(MYH11):c.5499G>C (p.Glu1833Asp) rs145252402
NM_002474.3(MYH11):c.5516C>T (p.Ala1839Val) rs112948385
NM_002474.3(MYH11):c.5528C>T (p.Ser1843Leu) rs148621523
NM_002474.3(MYH11):c.5585G>A (p.Arg1862His) rs146228576
NM_002474.3(MYH11):c.5596G>A (p.Glu1866Lys) rs148743922
NM_002474.3(MYH11):c.5666C>T (p.Ala1889Val) rs369950711
NM_002474.3(MYH11):c.5684G>A (p.Arg1895His) rs375148396

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