C4748924[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 885932	NM_177438.3(DICER1):c.5604-12G>A	DICER1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +6 more	GBenign/Likely benign
Select item 690455	NM_177438.3(DICER1):c.5171C>T (p.Pro1724Leu)	DICER1 (P1724L)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 133973	NM_177438.3(DICER1):c.4923T>G (p.Cys1641Trp)	DICER1 (C1641W)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 221072	NM_177438.3(DICER1):c.4891T>G (p.Ser1631Ala)	DICER1 (S1631A)	Single nucleotide variant (missense variant)	Rhabdomyosarcoma, embryonal, 2 +8 more	GBenign/Likely benign
Select item 1087123	NM_177438.3(DICER1):c.4608T>C (p.Gly1536=)	DICER1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +5 more	GLikely benign
Select item 483407	NM_177438.3(DICER1):c.4475T>C (p.Met1492Thr)	DICER1 (M1492T)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GLikely benign FDA Recognized database
Select item 577152	NM_177438.3(DICER1):c.4449G>A (p.Met1483Ile)	DICER1 (M1483I)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GUncertain significance FDA Recognized database
Select item 1596046	NM_177438.3(DICER1):c.3269+12C>T	DICER1	Single nucleotide variant (intron variant)	DICER1-related tumor predisposition +5 more	GLikely benign
Select item 242080	NM_177438.3(DICER1):c.3213A>G (p.Arg1071=)	DICER1	Single nucleotide variant (synonymous variant)	not provided +6 more	GBenign/Likely benign
Select item 477106	NM_177438.3(DICER1):c.2536A>G (p.Ile846Val)	DICER1 (I846V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 412093	NM_177438.3(DICER1):c.2494A>G (p.Lys832Glu)	DICER1 (K832E)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition +4 more	GUncertain significance
Select item 221128	NM_177438.3(DICER1):c.2370G>A (p.Arg790=)	DICER1	Single nucleotide variant (synonymous variant)	Rhabdomyosarcoma, embryonal, 2 +7 more	GBenign
Select item 644692	NM_177438.3(DICER1):c.2210C>T (p.Pro737Leu)	DICER1 (P737L)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +5 more	GUncertain significance
Select item 254301	NM_177438.3(DICER1):c.1966C>T (p.Arg656Ter)	DICER1 (R656*)	Single nucleotide variant (nonsense)	not provided +6 more	GPathogenic
Select item 242053	NM_177438.3(DICER1):c.1908-4A>G	DICER1	Single nucleotide variant (intron variant)	not provided +6 more	GBenign/Likely benign
Select item 417112	NM_177438.3(DICER1):c.1770T>C (p.Cys590=)	DICER1	Single nucleotide variant (synonymous variant)	DICER1-related tumor predisposition +5 more	GLikely benign
Select item 242044	NM_177438.3(DICER1):c.1510-4del	DICER1	Deletion (intron variant)	Pleuropulmonary blastoma +7 more	GBenign/Likely benign
Select item 220838	NM_177438.3(DICER1):c.1377-4T>G	DICER1	Single nucleotide variant (intron variant)	Rhabdomyosarcoma, embryonal, 2 +7 more	GBenign/Likely benign
Select item 1407132	NM_177438.3(DICER1):c.1377-18T>A	DICER1	Single nucleotide variant (intron variant)	Pleuropulmonary blastoma +4 more	GConflicting classifications of pathogenicity
Select item 242153	NM_177438.3(DICER1):c.920G>A (p.Arg307His)	DICER1 (R307H)	Single nucleotide variant (missense variant)	Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome +6 more	GConflicting classifications of pathogenicity

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Items: 20