Related gene-specific medical variations for Gene (Select 55170) - ClinVar - NCBI

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Links from Gene

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060084	NM_018137.3(PRMT6):c.581C>T (p.Ala194Val)	LOC129931066, PRMT6 (A194V)	Single nucleotide variant (missense variant)	PRMT6-related condition	GBenign
Select item 2384238	NM_018137.3(PRMT6):c.730G>A (p.Glu244Lys)	LOC129931066, PRMT6 (E244K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2357279	NM_018137.3(PRMT6):c.574T>C (p.Phe192Leu)	LOC129931066, PRMT6 (F192L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351143	NM_018137.3(PRMT6):c.316C>T (p.Arg106Trp)	LOC129931064, PRMT6 (R106W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2333926	NM_018137.3(PRMT6):c.503G>A (p.Ser168Asn)	LOC129931065, PRMT6 (S168N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2323839	NM_018137.3(PRMT6):c.597G>C (p.Gln199His)	LOC129931066, PRMT6 (Q199H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2300464	NM_018137.3(PRMT6):c.450T>A (p.Asp150Glu)	LOC129931065, PRMT6 (D150E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2289461	NM_018137.3(PRMT6):c.349T>A (p.Trp117Arg)	LOC129931064, PRMT6 (W117R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2225889	NM_018137.3(PRMT6):c.688C>T (p.Leu230Phe)	LOC129931066, PRMT6 (L230F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance