List of variants reported as uncertain significance for familial papillary or follicular thyroid carcinoma by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000314.8(PTEN):c.892C>G (p.Gln298Glu)	rs371387815	0.00009
NM_005343.4(HRAS):c.506G>A (p.Arg169Gln)	rs142218590	0.00007
NM_005343.4(HRAS):c.508A>T (p.Lys170Ter)	rs372936166	0.00005
NM_005343.4(HRAS):c.412G>A (p.Gly138Ser)	rs397517142	0.00003
NM_005343.4(HRAS):c.505C>T (p.Arg169Trp)	rs151229168	0.00003
NM_005343.4(HRAS):c.367C>T (p.Arg123Cys)	rs369106578	0.00002
NM_005343.4(HRAS):c.11A>G (p.Tyr4Cys)	rs764622691	0.00001
NM_005343.4(HRAS):c.391C>T (p.Gln131Ter)	rs376688893	0.00001
NM_005343.4(HRAS):c.410A>C (p.Tyr137Ser)	rs1180561549	0.00001
NM_005343.4(HRAS):c.546G>A (p.Met182Ile)	rs748639813	0.00001
NM_002524.5(NRAS):c.25G>A (p.Val9Ile)	rs1553244682
NM_004473.4(FOXE1):c.608C>G (p.Pro203Arg)
NM_005343.4(HRAS):c.481C>T (p.Arg161Cys)	rs758956556
NM_005343.4(HRAS):c.491G>C (p.Arg164Pro)	rs753977266
NM_005343.4(HRAS):c.550T>G (p.Cys184Gly)

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