Related gene-specific medical variations for Gene (Select 2913) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282870	NM_000840.3(GRM3):c.650C>A (p.Ala217Asp)	GRM3, GRM3-AS1 (A217D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102657	NM_000840.3(GRM3):c.887C>G (p.Thr296Ser)	GRM3, GRM3-AS1 (T296S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102656	NM_000840.3(GRM3):c.799C>T (p.Pro267Ser)	GRM3, GRM3-AS1 (P267S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102655	NM_000840.3(GRM3):c.791T>C (p.Leu264Ser)	GRM3, GRM3-AS1 (L264S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102654	NM_000840.3(GRM3):c.612C>G (p.Ile204Met)	GRM3, GRM3-AS1 (I204M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102649	NM_000840.3(GRM3):c.1261G>A (p.Ala421Thr)	GRM3, GRM3-AS1 (A421T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2681307	NM_000840.3(GRM3):c.699A>C (p.Glu233Asp)	GRM3, GRM3-AS1 (E233D)	Single nucleotide variant (missense variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2532701	NM_000840.3(GRM3):c.1153G>A (p.Glu385Lys)	GRM3, GRM3-AS1 (E385K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468929	NM_000840.3(GRM3):c.616C>T (p.Arg206Cys)	GRM3, GRM3-AS1 (R206C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781037	NM_000840.3(GRM3):c.738G>A (p.Lys246=)	GRM3, GRM3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 737837	NM_000840.3(GRM3):c.816G>C (p.Val272=)	GRM3, GRM3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign