List of variants in gene MUTYH reported as uncertain significance for carcinoma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.1347G>C (p.Thr449=)	rs74318065	0.00596
NM_001048174.2(MUTYH):c.1192C>T (p.Arg398Cys)	rs150792276	0.00081
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp)	rs75321043	0.00044
NM_001128425.2(MUTYH):c.42C>T (p.Ile14=)	rs202240122	0.00017
NM_001048174.2(MUTYH):c.566G>A (p.Arg189His)	rs147754007	0.00010
NM_001048174.2(MUTYH):c.583A>G (p.Ile195Val)	rs200872702	0.00009
NM_001048174.2(MUTYH):c.1400G>A (p.Arg467His)	rs144111588	0.00008
NM_001048174.2(MUTYH):c.262C>T (p.Arg88Trp)	rs373766973	0.00007
NM_001048174.2(MUTYH):c.1309C>G (p.Pro437Ala)	rs375597447	0.00004
NM_001048174.2(MUTYH):c.1336C>T (p.Arg446Cys)	rs200229669	0.00004
NM_001048174.2(MUTYH):c.1006C>T (p.Arg336Cys)	rs151316420	0.00001
NM_001048174.2(MUTYH):c.170A>G (p.His57Arg)	rs558707786	0.00001
NM_001048174.2(MUTYH):c.206G>A (p.Arg69Gln)	rs755653922	0.00001
NM_001048174.2(MUTYH):c.469C>T (p.Arg157Trp)	rs750592289	0.00001
NM_001048174.2(MUTYH):c.572C>T (p.Thr191Ile)	rs2149150096
NM_001048174.2(MUTYH):c.806G>T (p.Cys269Phe)	rs879254257
NM_001128425.2(MUTYH):c.37G>A (p.Ala13Thr)	rs375349172

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