"Ambry Genetics"[submitter] AND "GRM7"[gene] - ClinVar

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Items: 49

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2028389	NM_000844.4(GRM7):c.26G>A (p.Arg9His)	GRM7 (R9H)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2353574	NM_000844.4(GRM7):c.196C>T (p.Pro66Ser)	GRM7 (P66S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493572	NM_000844.4(GRM7):c.211A>G (p.Lys71Glu)	GRM7 (K71E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2284107	NM_000844.4(GRM7):c.223G>A (p.Gly75Arg)	GRM7 (G75R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2323022	NM_000844.4(GRM7):c.294C>A (p.Asn98Lys)	GRM7 (N98K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2513825	NM_000844.4(GRM7):c.311G>A (p.Arg104Gln)	GRM7 (R104Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2485442	NM_000844.4(GRM7):c.349G>A (p.Glu117Lys)	GRM7 (E117K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102699	NM_000844.4(GRM7):c.364T>A (p.Phe122Ile)	GRM7 (F122I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102700	NM_000844.4(GRM7):c.415G>A (p.Gly139Ser)	GRM7 (G139S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102701	NM_000844.4(GRM7):c.433G>C (p.Val145Leu)	GRM7 (V145L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3282905	NM_000844.4(GRM7):c.568C>T (p.Arg190Trp)	GRM7 (R190W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1590868	NM_000844.4(GRM7):c.569G>A (p.Arg190Gln)	GRM7 (R190Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2261540	NM_000844.4(GRM7):c.631G>A (p.Asp211Asn)	GRM7 (D211N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2222990	NM_000844.4(GRM7):c.853A>G (p.Ile285Val)	GRM7 (I285V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2225490	NM_000844.4(GRM7):c.878+4A>G	GRM7	Single nucleotide variant (intron variant)	Inborn genetic diseases	GUncertain significance
Select item 2330435	NM_000844.4(GRM7):c.883A>G (p.Ile295Val)	GRM7 (I295V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2213916	NM_000844.4(GRM7):c.895G>A (p.Ala299Thr)	GRM7 (A299T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102702	NM_000844.4(GRM7):c.931G>A (p.Val311Met)	GRM7 (V311M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102703	NM_000844.4(GRM7):c.985A>G (p.Ile329Val)	GRM7 (I329V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2511527	NM_000844.4(GRM7):c.988G>A (p.Ala330Thr)	GRM7 (A330T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102693	NM_000844.4(GRM7):c.1013C>T (p.Pro338Leu)	GRM7 (P338L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3282900	NM_000844.4(GRM7):c.1034G>A (p.Gly345Glu)	GRM7 (G345E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102694	NM_000844.4(GRM7):c.1093G>A (p.Ala365Thr)	GRM7 (A365T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2230854	NM_000844.4(GRM7):c.1111A>G (p.Asn371Asp)	GRM7 (N371D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2618260	NM_000844.4(GRM7):c.1156A>G (p.Thr386Ala)	GRM7 (T386A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3282899	NM_000844.4(GRM7):c.1300C>T (p.Arg434Trp)	GRM7 (R434W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2243859	NM_000844.4(GRM7):c.1304G>A (p.Gly435Asp)	GRM7 (G435D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102695	NM_000844.4(GRM7):c.1312C>G (p.Pro438Ala)	GRM7 (P438A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3282903	NM_000844.4(GRM7):c.1372A>G (p.Asn458Asp)	GRM7 (N458D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3282904	NM_000844.4(GRM7):c.1435A>G (p.Ile479Val)	GRM7 (I479V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2622396	NM_000844.4(GRM7):c.1451C>A (p.Thr484Asn)	GRM7 (T484N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1334746	NM_000844.4(GRM7):c.1478G>A (p.Arg493His)	GRM7 (R493H)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1522125	NM_000844.4(GRM7):c.1501G>A (p.Glu501Lys)	GRM7 (E501K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2188142	NM_000844.4(GRM7):c.1583A>G (p.Lys528Arg)	GRM7 (K528R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2043539	NM_000844.4(GRM7):c.1665T>G (p.Phe555Leu)	GRM7 (F555L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2385857	NM_000844.4(GRM7):c.1684C>A (p.His562Asn)	GRM7 (H562N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3282901	NM_000844.4(GRM7):c.1765C>T (p.Pro589Ser)	GRM7 (P589S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2529934	NM_000844.4(GRM7):c.1802G>A (p.Gly601Glu)	GRM7 (G601E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1409830	NM_000844.4(GRM7):c.1840C>T (p.Arg614Cys)	GRM7 (R614C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3102696	NM_000844.4(GRM7):c.1901C>T (p.Thr634Met)	GRM7 (T634M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3282902	NM_000844.4(GRM7):c.2099C>A (p.Thr700Lys)	GRM7 (T700K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1401282	NM_000844.4(GRM7):c.2308T>A (p.Cys770Ser)	GRM7 (C770S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1936002	NM_000844.4(GRM7):c.2460A>G (p.Ile820Met)	GRM7 (I820M)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2617902	NM_000844.4(GRM7):c.2471C>T (p.Thr824Met)	GRM7 (T824M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102697	NM_000844.4(GRM7):c.2479A>G (p.Ile827Val)	GRM7 (I827V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2968578	NM_000844.4(GRM7):c.2621C>T (p.Ser874Leu)	GRM7 (S874L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2280055	NM_000844.4(GRM7):c.2644G>A (p.Asp882Asn)	GRM7 (D882N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3102698	NM_000844.4(GRM7):c.2713A>C (p.Lys905Gln)	GRM7 (K905Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1904733	NM_000844.4(GRM7):c.2729A>G (p.Tyr910Cys)	GRM7 (Y910C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance

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Items: 49