"Ambry Genetics"[submitter] AND "PRMT6"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2401635	NM_018137.3(PRMT6):c.14A>G (p.Lys5Arg)	PRMT6 (K5R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218937	NM_018137.3(PRMT6):c.34G>T (p.Gly12Trp)	PRMT6 (G12W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287943	NM_018137.3(PRMT6):c.34G>C (p.Gly12Arg)	PRMT6 (G12R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218935	NM_018137.3(PRMT6):c.109C>G (p.Arg37Gly)	PRMT6 (R37G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218936	NM_018137.3(PRMT6):c.160G>T (p.Val54Phe)	PRMT6 (V54F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351143	NM_018137.3(PRMT6):c.316C>T (p.Arg106Trp)	LOC129931064, PRMT6 (R106W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289461	NM_018137.3(PRMT6):c.349T>A (p.Trp117Arg)	LOC129931064, PRMT6 (W117R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218938	NM_018137.3(PRMT6):c.395G>A (p.Arg132Gln)	LOC129931064, PRMT6 (R132Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218939	NM_018137.3(PRMT6):c.410C>T (p.Pro137Leu)	PRMT6 (P137L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300464	NM_018137.3(PRMT6):c.450T>A (p.Asp150Glu)	LOC129931065, PRMT6 (D150E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333926	NM_018137.3(PRMT6):c.503G>A (p.Ser168Asn)	LOC129931065, PRMT6 (S168N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310249	NM_018137.3(PRMT6):c.536A>G (p.Lys179Arg)	LOC129931065, PRMT6 (K179R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357279	NM_018137.3(PRMT6):c.574T>C (p.Phe192Leu)	LOC129931066, PRMT6 (F192L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323839	NM_018137.3(PRMT6):c.597G>C (p.Gln199His)	LOC129931066, PRMT6 (Q199H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218940	NM_018137.3(PRMT6):c.631G>C (p.Val211Leu)	LOC129931066, PRMT6 (V211L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225889	NM_018137.3(PRMT6):c.688C>T (p.Leu230Phe)	LOC129931066, PRMT6 (L230F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384238	NM_018137.3(PRMT6):c.730G>A (p.Glu244Lys)	LOC129931066, PRMT6 (E244K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218941	NM_018137.3(PRMT6):c.761C>G (p.Ala254Gly)	PRMT6 (A254G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218942	NM_018137.3(PRMT6):c.781G>C (p.Ala261Pro)	PRMT6 (A261P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458536	NM_018137.3(PRMT6):c.788T>C (p.Leu263Ser)	PRMT6 (L263S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309080	NM_018137.3(PRMT6):c.818G>T (p.Gly273Val)	PRMT6 (G273V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218943	NM_018137.3(PRMT6):c.853A>C (p.Met285Leu)	PRMT6 (M285L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2528418	NM_018137.3(PRMT6):c.853A>G (p.Met285Val)	PRMT6 (M285V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218944	NM_018137.3(PRMT6):c.858T>G (p.His286Gln)	PRMT6 (H286Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559599	NM_018137.3(PRMT6):c.892G>A (p.Gly298Arg)	PRMT6 (G298R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220912	NM_018137.3(PRMT6):c.892G>C (p.Gly298Arg)	PRMT6 (G298R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218945	NM_018137.3(PRMT6):c.893G>A (p.Gly298Glu)	PRMT6 (G298E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218946	NM_018137.3(PRMT6):c.943G>T (p.Ala315Ser)	PRMT6 (A315S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594730	NM_018137.3(PRMT6):c.979G>A (p.Glu327Lys)	PRMT6 (E327K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218934	NM_018137.3(PRMT6):c.1039C>T (p.Arg347Trp)	PRMT6 (R347W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218933	NM_018137.3(PRMT6):c.1039C>G (p.Arg347Gly)	PRMT6 (R347G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31