List of variants reported as uncertain significance for vascular neoplasm by Fulgent Genetics, Fulgent Genetics

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.460G>A (p.Gly154Ser)	rs137852789	0.00004
NM_000546.6(TP53):c.214C>G (p.Pro72Ala)	rs587782769	0.00003
NM_000546.6(TP53):c.467G>A (p.Arg156His)	rs371524413	0.00003
NM_000546.6(TP53):c.466C>T (p.Arg156Cys)	rs563378859	0.00002
NM_033360.4(KRAS):c.389C>T (p.Ala130Val)	rs730880473	0.00002
NM_000546.6(TP53):c.1000G>C (p.Gly334Arg)	rs730882028	0.00001
NM_000546.6(TP53):c.461G>A (p.Gly154Asp)	rs762846821	0.00001
NM_000546.6(TP53):c.587G>A (p.Arg196Gln)	rs483352697	0.00001
NM_000546.6(TP53):c.604C>T (p.Arg202Cys)	rs587780072	0.00001
NM_000546.6(TP53):c.649G>A (p.Val217Met)	rs35163653	0.00001
NM_000546.6(TP53):c.760A>G (p.Ile254Val)	rs746601313	0.00001
NM_004985.5(KRAS):c.407G>A (p.Ser136Asn)	rs757816355	0.00001
NM_004985.5(KRAS):c.487A>G (p.Ile163Val)	rs1470495974	0.00001
NM_000546.6(TP53):c.1080G>T (p.Gly360=)	rs2150994011
NM_000546.6(TP53):c.110C>T (p.Ser37Phe)	rs1567557177
NM_000546.6(TP53):c.11C>G (p.Pro4Arg)	rs878854064
NM_000546.6(TP53):c.256G>A (p.Ala86Thr)	rs587782148
NM_000546.6(TP53):c.412G>A (p.Ala138Thr)	rs28934875
NM_000546.6(TP53):c.528C>G (p.Cys176Trp)	rs1057519980
NM_000546.6(TP53):c.587G>T (p.Arg196Leu)	rs483352697
NM_000546.6(TP53):c.677G>C (p.Gly226Ala)	rs970212462
NM_000546.6(TP53):c.875A>C (p.Lys292Thr)	rs121912663
NM_004985.5(KRAS):c.168C>T (p.Leu56=)
NM_004985.5(KRAS):c.184GAG[1] (p.Glu63del)	rs730880469
NM_004985.5(KRAS):c.331A>G (p.Met111Val)
NM_004985.5(KRAS):c.352T>C (p.Cys118Arg)	rs1951384485
NM_004985.5(KRAS):c.365C>G (p.Ser122Cys)
NM_004985.5(KRAS):c.388_389delinsAT (p.Ala130Ile)	rs1951383854
NM_004985.5(KRAS):c.450+5G>A
NM_004985.5(KRAS):c.451-6T>C
NM_033360.4(KRAS):c.101_106del	rs1339924833
NM_182925.5(FLT4):c.1109A>G (p.Lys370Arg)
NM_182925.5(FLT4):c.3712G>A (p.Gly1238Arg)

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