GABRG1[gene] and "single gene"[properties] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2601278	NM_173536.4(GABRG1):c.1378G>A (p.Val460Ile)	GABRG1 (V460I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097848	NM_173536.4(GABRG1):c.1335A>G (p.Ile445Met)	GABRG1 (I445M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097846	NM_173536.4(GABRG1):c.1265G>C (p.Cys422Ser)	GABRG1 (C422S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298754	NM_173536.4(GABRG1):c.1233T>G (p.Asp411Glu)	GABRG1 (D411E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331387	NM_173536.4(GABRG1):c.1225G>T (p.Gly409Cys)	GABRG1 (G409C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310023	NM_173536.4(GABRG1):c.1181T>C (p.Ile394Thr)	GABRG1 (I394T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570504	NM_173536.4(GABRG1):c.1171A>G (p.Met391Val)	GABRG1 (M391V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270969	NM_173536.4(GABRG1):c.1148A>G (p.His383Arg)	GABRG1 (H383R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454335	NM_173536.4(GABRG1):c.1130C>T (p.Ser377Leu)	GABRG1 (S377L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336043	NM_173536.4(GABRG1):c.1099A>G (p.Thr367Ala)	GABRG1 (T367A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474909	NM_173536.4(GABRG1):c.1073C>T (p.Thr358Ile)	GABRG1 (T358I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273229	NM_173536.4(GABRG1):c.642T>G (p.Asn214Lys)	GABRG1 (N214K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489581	NM_173536.4(GABRG1):c.589A>G (p.Met197Val)	GABRG1 (M197V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789997	NM_173536.4(GABRG1):c.387C>T (p.Thr129=)	GABRG1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2316626	NM_173536.4(GABRG1):c.372A>C (p.Leu124Phe)	GABRG1 (L124F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229749	NM_173536.4(GABRG1):c.370T>G (p.Leu124Val)	GABRG1 (L124V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455507	NM_173536.4(GABRG1):c.341T>A (p.Ile114Asn)	GABRG1 (I114N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097850	NM_173536.4(GABRG1):c.328A>G (p.Thr110Ala)	GABRG1 (T110A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518361	NM_173536.4(GABRG1):c.248T>C (p.Ile83Thr)	GABRG1 (I83T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280409	NM_173536.4(GABRG1):c.190A>G (p.Ile64Val)	GABRG1 (I64V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280410	NM_173536.4(GABRG1):c.184G>A (p.Gly62Arg)	GABRG1 (G62R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097849	NM_173536.4(GABRG1):c.172A>G (p.Lys58Glu)	GABRG1 (K58E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097847	NM_173536.4(GABRG1):c.129T>A (p.Asp43Glu)	GABRG1 (D43E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097851	NM_173536.4(GABRG1):c.37C>A (p.Leu13Ile)	GABRG1 (L13I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161829	NM_173536.4(GABRG1):c.32C>T (p.Pro11Leu)	GABRG1 (P11L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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Items: 25