"GRM8-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044373	NM_000845.3(GRM8):c.2431-10dup	GRM8	Duplication (intron variant)	GRM8-related disorder	GBenign
Select item 3033409	NM_000845.3(GRM8):c.2157C>G (p.Pro719=)	GRM8	Single nucleotide variant (synonymous variant +1 more)	GRM8-related disorder	GLikely benign
Select item 3044864	NM_000845.3(GRM8):c.1878A>T (p.Leu626=)	GRM8	Single nucleotide variant (synonymous variant +1 more)	GRM8-related disorder	GLikely benign
Select item 3042719	NM_000845.3(GRM8):c.1584G>A (p.Thr528=)	GRM8	Single nucleotide variant (synonymous variant +1 more)	GRM8-related disorder	GLikely benign
Select item 726532	NM_000845.3(GRM8):c.1538C>T (p.Ala513Val)	GRM8 (A308V +1 more)	Single nucleotide variant (missense variant +1 more)	GRM8-related disorder +1 more	GLikely benign
Select item 768199	NM_000845.3(GRM8):c.1534C>G (p.Pro512Ala)	GRM8 (P307A +1 more)	Single nucleotide variant (missense variant +1 more)	GRM8-related disorder +1 more	GBenign
Select item 3038215	NM_000845.3(GRM8):c.1157-3C>A	GRM8	Single nucleotide variant (intron variant)	GRM8-related disorder	GBenign
Select item 776257	NM_000845.3(GRM8):c.693T>C (p.Gly231=)	GRM8	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 785232	NM_000845.3(GRM8):c.357C>T (p.Phe119=)	GRM8	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GBenign
Select item 712684	NM_000845.3(GRM8):c.96C>G (p.His32Gln)	GRM8 (H32Q)	Single nucleotide variant (missense variant +2 more)	GRM8-related disorder +1 more	GBenign
Select item 769731	NM_000845.3(GRM8):c.62T>G (p.Phe21Cys)	GRM8 (F21C)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GBenign
Select item 769732	NM_000845.3(GRM8):c.29C>G (p.Ser10Cys)	GRM8 (S10C)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GBenign