List of variants in gene FLT4 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_182925.5(FLT4):c.2860C>T (p.Pro954Ser)	rs34255532	0.00275
NM_182925.5(FLT4):c.2563G>A (p.Ala855Thr)	rs121909657	0.00009
NM_182925.5(FLT4):c.1083C>G (p.Tyr361Ter)
NM_182925.5(FLT4):c.1622dup (p.Gln542fs)	rs1581655293
NM_182925.5(FLT4):c.2569G>A (p.Gly857Arg)	rs267606818
NM_182925.5(FLT4):c.2632G>A (p.Val878Met)	rs121909654
NM_182925.5(FLT4):c.3104A>G (p.His1035Arg)	rs121909653
NM_182925.5(FLT4):c.3122G>C (p.Arg1041Pro)	rs121909650
NM_182925.5(FLT4):c.3131T>C (p.Leu1044Pro)	rs121909651
NM_182925.5(FLT4):c.3257T>C (p.Ile1086Thr)	rs121909655
NM_182925.5(FLT4):c.3316G>A (p.Glu1106Lys)	rs121909656
NM_182925.5(FLT4):c.3320TCT[1] (p.Phe1108del)	rs587776833
NM_182925.5(FLT4):c.3332-356_3894-1373del
NM_182925.5(FLT4):c.3341C>T (p.Pro1114Leu)	rs121909652
NM_182925.5(FLT4):c.3574C>T (p.Gln1192Ter)	rs1581616817
NM_182925.5(FLT4):c.89del (p.Pro30fs)	rs755445139

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