"Ambry Genetics"[submitter] AND "PRMT3"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2469070	NM_005788.4(PRMT3):c.38G>A (p.Gly13Asp)	PRMT3 (G13D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371006	NM_005788.4(PRMT3):c.81C>A (p.Ser27Arg)	PRMT3 (S27R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218925	NM_005788.4(PRMT3):c.326T>C (p.Ile109Thr)	PRMT3 (I47T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310244	NM_005788.4(PRMT3):c.408A>T (p.Glu136Asp)	PRMT3 (E136D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214238	NM_005788.4(PRMT3):c.449A>G (p.Asn150Ser)	PRMT3 (N150S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218926	NM_005788.4(PRMT3):c.493A>G (p.Met165Val)	PRMT3 (M103V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568784	NM_005788.4(PRMT3):c.538C>T (p.Arg180Cys)	PRMT3 (R103C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516183	NM_005788.4(PRMT3):c.539G>A (p.Arg180His)	PRMT3 (R118H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257010	NM_005788.4(PRMT3):c.589A>C (p.Thr197Pro)	PRMT3 (T120P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268548	NM_005788.4(PRMT3):c.685A>T (p.Ile229Leu)	PRMT3 (I152L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276273	NM_005788.4(PRMT3):c.731G>A (p.Arg244Gln)	PRMT3 (R167Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534978	NM_005788.4(PRMT3):c.755A>G (p.His252Arg)	PRMT3 (H252R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352420	NM_005788.4(PRMT3):c.760T>C (p.Phe254Leu)	PRMT3 (F177L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218927	NM_005788.4(PRMT3):c.782A>T (p.Asp261Val)	PRMT3 (D184V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242620	NM_005788.4(PRMT3):c.901A>G (p.Lys301Glu)	PRMT3 (K224E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218928	NM_005788.4(PRMT3):c.995G>A (p.Gly332Asp)	PRMT3 (G270D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298191	NM_005788.4(PRMT3):c.1020G>A (p.Met340Ile)	PRMT3 (M278I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623545	NM_005788.4(PRMT3):c.1028C>T (p.Ser343Phe)	PRMT3 (S281F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481725	NM_005788.4(PRMT3):c.1132G>A (p.Asp378Asn)	PRMT3 (D301N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218922	NM_005788.4(PRMT3):c.1168A>G (p.Lys390Glu)	PRMT3 (K313E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310242	NM_005788.4(PRMT3):c.1196T>C (p.Ile399Thr)	PRMT3 (I399T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310246	NM_005788.4(PRMT3):c.1323A>T (p.Lys441Asn)	PRMT3 (K379N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218923	NM_005788.4(PRMT3):c.1369A>G (p.Ile457Val)	PRMT3 (I380V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482771	NM_005788.4(PRMT3):c.1373A>G (p.Tyr458Cys)	PRMT3 (Y458C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229106	NM_005788.4(PRMT3):c.1405T>C (p.Phe469Leu)	PRMT3 (F392L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218924	NM_005788.4(PRMT3):c.1412C>T (p.Thr471Met)	PRMT3 (T394M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550385	NM_005788.4(PRMT3):c.1450G>C (p.Val484Leu)	PRMT3 (V484L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568773	NM_005788.4(PRMT3):c.1468C>A (p.Pro490Thr)	PRMT3 (P490T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473861	NM_005788.4(PRMT3):c.1474T>G (p.Ser492Ala)	PRMT3 (S415A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310243	NM_005788.4(PRMT3):c.1534C>T (p.Pro512Ser)	PRMT3 (P435S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 30