List of variants in gene FLT4 reported as likely pathogenic for not provided

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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_182925.5(FLT4):c.2554G>T (p.Gly852Cys)
NM_182925.5(FLT4):c.298_304del (p.Glu100fs)
NM_182925.5(FLT4):c.3170G>A (p.Gly1057Asp)
NM_182925.5(FLT4):c.3172C>G (p.Leu1058Val)	rs2127802292
NM_182925.5(FLT4):c.3242T>G (p.Met1081Arg)
NM_182925.5(FLT4):c.3287A>G (p.Asp1096Gly)
NM_182925.5(FLT4):c.3295T>C (p.Ser1099Pro)
NM_182925.5(FLT4):c.3296C>T (p.Ser1099Phe)
NM_182925.5(FLT4):c.3320TCT[1] (p.Phe1108del)	rs587776833
NM_182925.5(FLT4):c.3341C>T (p.Pro1114Leu)	rs121909652
NM_182925.5(FLT4):c.3391G>C (p.Gly1131Arg)	rs1554109707
NM_182925.5(FLT4):c.3410C>T (p.Pro1137Leu)	rs1762335528
NM_182925.5(FLT4):c.3486C>A (p.Phe1162Leu)
NM_182925.5(FLT4):c.3823A>G (p.Ser1275Gly)
NM_182925.5(FLT4):c.3999C>A (p.Tyr1333Ter)	rs2127781697
NM_182925.5(FLT4):c.474T>A (p.Cys158Ter)	rs1302178938
NM_182925.5(FLT4):c.513G>A (p.Ser171=)

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