"Revvity Omics, Revvity"[submitter] AND "DICER1"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 133970	NM_177438.3(DICER1):c.3553G>A (p.Ala1185Thr)	DICER1 (A1185T)	Single nucleotide variant (missense variant)	DICER1-related tumor predisposition	GBenign FDA Recognized database
Select item 2440787	NM_177438.3(DICER1):c.3377C>G (p.Thr1126Arg)	DICER1 (T1032R +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1093026	NM_177438.3(DICER1):c.2637A>G (p.Leu879=)	DICER1	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 477094	NM_177438.3(DICER1):c.2246A>T (p.Tyr749Phe)	DICER1 (Y749F)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 412156	NM_177438.3(DICER1):c.2201C>G (p.Thr734Ser)	DICER1 (T734S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 242037	NM_177438.3(DICER1):c.1381A>G (p.Ile461Val)	DICER1 (I461V)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 477286	NM_177438.3(DICER1):c.776C>T (p.Pro259Leu)	DICER1 (P259L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 819961	NM_177438.3(DICER1):c.173A>G (p.His58Arg)	DICER1 (H58R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance