ClinVar Miner

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

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Total variants: 28
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HGVS dbSNP
NM_001040113.2(MYH11):c.5813C>A (p.Pro1938His) rs765030635
NM_001040113.2(MYH11):c.5819C>T (p.Pro1940Leu) rs111588143
NM_002474.3(MYH11):c.3874G>A (p.Val1292Ile) rs151058774
NM_002474.3(MYH11):c.4015C>A (p.Arg1339Ser) rs754951425
NM_002474.3(MYH11):c.4117-6T>G rs370252949
NM_002474.3(MYH11):c.4123G>A (p.Asp1375Asn) rs143467011
NM_002474.3(MYH11):c.4303G>A (p.Asp1435Asn) rs794728668
NM_002474.3(MYH11):c.4345A>C (p.Lys1449Gln) rs775809843
NM_002474.3(MYH11):c.4603C>T (p.Arg1535Trp) rs143402648
NM_002474.3(MYH11):c.4663C>G (p.Leu1555Val) rs202231621
NM_002474.3(MYH11):c.4735G>A (p.Asp1579Asn) rs369751362
NM_002474.3(MYH11):c.4756C>G (p.Gln1586Glu) rs794728680
NM_002474.3(MYH11):c.4906G>C (p.Ala1636Pro) rs376331652
NM_002474.3(MYH11):c.4953G>C (p.Gln1651His) rs756832190
NM_002474.3(MYH11):c.5092G>A (p.Ala1698Thr) rs187172581
NM_002474.3(MYH11):c.5120A>G (p.Asp1707Gly) rs1567691518
NM_002474.3(MYH11):c.5248G>A (p.Gly1750Ser) rs749462800
NM_002474.3(MYH11):c.5273G>A (p.Arg1758Gln) rs142546324
NM_002474.3(MYH11):c.5275G>A (p.Val1759Ile) rs138059405
NM_002474.3(MYH11):c.5299G>A (p.Glu1767Lys) rs377663370
NM_002474.3(MYH11):c.5353A>T (p.Ser1785Cys) rs772663756
NM_002474.3(MYH11):c.5453C>T (p.Ala1818Val) rs771343446
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.5596G>A (p.Glu1866Lys) rs148743922
NM_002474.3(MYH11):c.5614G>A (p.Ala1872Thr) rs1355377006
NM_002474.3(MYH11):c.5666C>T (p.Ala1889Val) rs369950711
NM_002474.3(MYH11):c.5713C>T (p.Arg1905Trp) rs749422717

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