GALR2[gene] and "single gene"[properties] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3098269	NM_003857.4(GALR2):c.7G>A (p.Val3Ile)	GALR2 (V3I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237872	NM_003857.4(GALR2):c.10T>C (p.Ser4Pro)	GALR2 (S4P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098263	NM_003857.4(GALR2):c.11C>T (p.Ser4Leu)	GALR2 (S4L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098264	NM_003857.4(GALR2):c.149T>G (p.Leu50Arg)	GALR2 (L50R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489375	NM_003857.4(GALR2):c.214C>A (p.Leu72Met)	GALR2 (L72M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547240	NM_003857.4(GALR2):c.239C>T (p.Pro80Leu)	GALR2 (P80L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241817	NM_003857.4(GALR2):c.328C>A (p.His110Asn)	GALR2 (H110N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391609	NM_003857.4(GALR2):c.330C>G (p.His110Gln)	GALR2 (H110Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 739873	NM_003857.4(GALR2):c.351C>A (p.Ala117=)	GALR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2601546	NM_003857.4(GALR2):c.418C>G (p.Arg140Gly)	GALR2 (R140G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552202	NM_003857.4(GALR2):c.513C>A (p.Asn171Lys)	GALR2 (N171K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352619	NM_003857.4(GALR2):c.548G>A (p.Arg183His)	GALR2 (R183H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485636	NM_003857.4(GALR2):c.592C>A (p.Leu198Ile)	GALR2 (L198I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098266	NM_003857.4(GALR2):c.632T>C (p.Leu211Ser)	GALR2 (L211S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494257	NM_003857.4(GALR2):c.634C>A (p.Arg212Ser)	GALR2 (R212S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775336	NM_003857.4(GALR2):c.676G>A (p.Gly226Ser)	GALR2 (G226S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3098267	NM_003857.4(GALR2):c.685C>T (p.Arg229Cys)	GALR2 (R229C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338466	NM_003857.4(GALR2):c.719T>C (p.Ile240Thr)	GALR2 (I240T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098268	NM_003857.4(GALR2):c.721G>C (p.Val241Leu)	GALR2 (V241L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 788155	NM_003857.4(GALR2):c.746G>T (p.Trp249Leu)	GALR2 (W249L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2326168	NM_003857.4(GALR2):c.792C>G (p.Phe264Leu)	GALR2 (F264L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098270	NM_003857.4(GALR2):c.821G>A (p.Arg274His)	GALR2 (R274H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287236	NM_003857.4(GALR2):c.842C>T (p.Ser281Phe)	GALR2 (S281F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489801	NM_003857.4(GALR2):c.913A>G (p.Thr305Ala)	GALR2 (T305A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098271	NM_003857.4(GALR2):c.937C>G (p.Arg313Gly)	GALR2 (R313G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361043	NM_003857.4(GALR2):c.971C>T (p.Ala324Val)	GALR2 (A324V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2512577	NM_003857.4(GALR2):c.993T>A (p.Ser331Arg)	GALR2 (S331R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 710117	NM_003857.4(GALR2):c.1007A>C (p.Glu336Ala)	GALR2 (E336A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3098261	NM_003857.4(GALR2):c.1014G>T (p.Glu338Asp)	GALR2 (E338D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325381	NM_003857.4(GALR2):c.1057C>T (p.Arg353Cys)	GALR2 (R353C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2350703	NM_003857.4(GALR2):c.1072G>C (p.Ala358Pro)	GALR2 (A358P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098262	NM_003857.4(GALR2):c.1139G>C (p.Ser380Thr)	GALR2 (S380T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 32