"Ambry Genetics"[submitter] AND "LOC130006577"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2530710	NM_001143831.3(GRM5):c.2938G>A (p.Ala980Thr)	GRM5, GRM5-AS1 +1 more (A980T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221664	NM_001143831.3(GRM5):c.2917G>A (p.Gly973Ser)	GRM5, GRM5-AS1 +1 more (G941S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305154	NM_001143831.3(GRM5):c.2899G>A (p.Ala967Thr)	GRM5, GRM5-AS1 +1 more (A935T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316912	NM_001143831.3(GRM5):c.2893G>T (p.Ala965Ser)	GRM5, GRM5-AS1 +1 more (A965S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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