ClinVar Miner

List of variants in gene MYBPC3 reported as uncertain significance for Left ventricular noncompaction cardiomyopathy

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_000256.3(MYBPC3):c.471C>T (p.Phe157=) rs150291001 0.00034
NM_000256.3(MYBPC3):c.74G>A (p.Ser25Asn) rs371140684 0.00019
NM_000256.3(MYBPC3):c.3415G>A (p.Val1139Ile) rs373519667 0.00018
NM_000256.3(MYBPC3):c.1553T>C (p.Met518Thr) rs886048378 0.00006
NC_000011.10:g.47333340G>A rs373012629 0.00003
NC_000011.10:g.47346380G>A rs201078659 0.00003
NM_000256.3(MYBPC3):c.1056C>G (p.Leu352=) rs375007425 0.00003
NM_000256.3(MYBPC3):c.1812C>T (p.Asp604=) rs397515929 0.00002
NM_000256.3(MYBPC3):c.332C>T (p.Ala111Val) rs730880530 0.00001
NM_000256.3(MYBPC3):c.*163C>A rs886048366
NM_000256.3(MYBPC3):c.*26+3A>G rs886048369
NM_000256.3(MYBPC3):c.*327C>A rs886048364
NM_000256.3(MYBPC3):c.*95G>T rs886048368
NM_000256.3(MYBPC3):c.1458-9C>T rs886048379
NM_000256.3(MYBPC3):c.2603-4C>A rs886048377
NM_000256.3(MYBPC3):c.2603G>T (p.Gly868Val) rs886048376
NM_000256.3(MYBPC3):c.2622C>A (p.Thr874=) rs886048375
NM_000256.3(MYBPC3):c.2639A>C (p.Asp880Ala) rs886048374
NM_000256.3(MYBPC3):c.2892G>T (p.Val964=) rs886048372
NM_000256.3(MYBPC3):c.2905+7G>C rs886048371
NM_000256.3(MYBPC3):c.3627+6G>T rs886048370
NM_000256.3(MYBPC3):c.927-7G>T rs886048381

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