RGS20[gene] and "single gene"[properties] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2412475	NM_170587.4(RGS20):c.100T>C (p.Tyr34His)	RGS20 (Y34H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597669	NM_170587.4(RGS20):c.172C>A (p.Pro58Thr)	RGS20 (P58T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314102	NM_170587.4(RGS20):c.203C>T (p.Ala68Val)	RGS20 (A68V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314103	NM_170587.4(RGS20):c.243C>A (p.Ser81Arg)	RGS20 (S81R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470578	NM_170587.4(RGS20):c.289G>A (p.Ala97Thr)	RGS20 (A97T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470579	NM_170587.4(RGS20):c.290C>A (p.Ala97Asp)	RGS20 (A97D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 778397	NM_170587.4(RGS20):c.336G>A (p.Pro112=)	RGS20	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2350996	NM_170587.4(RGS20):c.394G>C (p.Gly132Arg)	RGS20 (G132R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2658601	NM_003702.5(RGS20):c.9G>C (p.Thr3=)	RGS20	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2514247	NM_003702.5(RGS20):c.104G>A (p.Arg35Gln)	RGS20 (R35Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383582	NM_003702.5(RGS20):c.119C>T (p.Ala40Val)	RGS20 (A187V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286650	NM_003702.5(RGS20):c.122A>G (p.Gln41Arg)	RGS20 (Q73R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227786	NM_003702.5(RGS20):c.133G>A (p.Gly45Ser)	RGS20 (G192S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514343	NM_003702.5(RGS20):c.154G>A (p.Gly52Arg)	RGS20 (G84R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 754436	NM_003702.5(RGS20):c.161G>A (p.Gly54Glu)	RGS20 (G86E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2344699	NM_003702.5(RGS20):c.166C>T (p.Arg56Cys)	RGS20 (R88C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153863	NM_003702.5(RGS20):c.175A>C (p.Asn59His)	RGS20 (N59H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297486	NM_003702.5(RGS20):c.231A>C (p.Arg77Ser)	RGS20 (R16S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 776334	NM_003702.5(RGS20):c.324A>G (p.Glu108=)	RGS20	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3153864	NM_003702.5(RGS20):c.446A>G (p.Glu149Gly)	RGS20 (E181G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223120	NM_003702.5(RGS20):c.553C>T (p.Arg185Trp)	RGS20 (R124W +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597610	NM_003702.5(RGS20):c.554G>A (p.Arg185Gln)	RGS20 (R124Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306483	NM_003702.5(RGS20):c.662T>G (p.Phe221Cys)	RGS20 (F253C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524140	NM_003702.5(RGS20):c.722C>T (p.Ala241Val)	RGS20 (A180V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24