"Ambry Genetics"[submitter] AND "RASGRF1"[gene] - ClinVar

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Items: 47

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2356247	NM_001145648.3(RASGRF1):c.3749G>A (p.Arg1250Gln)	RASGRF1 (R482Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151831	NM_001145648.3(RASGRF1):c.3746T>A (p.Leu1249His)	RASGRF1 (L1265H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336548	NM_001145648.3(RASGRF1):c.3737A>G (p.Glu1246Gly)	RASGRF1 (E1246G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312924	NM_001145648.3(RASGRF1):c.3655G>A (p.Ala1219Thr)	RASGRF1 (A451T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300715	NM_001145648.3(RASGRF1):c.3422C>T (p.Ala1141Val)	LOC100129540, RASGRF1 (A1141V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454609	NM_001145648.3(RASGRF1):c.3307A>G (p.Ile1103Val)	LOC100129540, RASGRF1 (I335V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3312919	NM_001145648.3(RASGRF1):c.3245T>C (p.Ile1082Thr)	LOC100129540, RASGRF1 (I314T +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3151830	NM_001145648.3(RASGRF1):c.3185A>G (p.Tyr1062Cys)	RASGRF1 (Y1062C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258667	NM_001145648.3(RASGRF1):c.3062A>T (p.His1021Leu)	RASGRF1 (H1037L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312920	NM_001145648.3(RASGRF1):c.3020C>T (p.Thr1007Met)	RASGRF1 (T239M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337899	NM_001145648.3(RASGRF1):c.2962A>G (p.Ile988Val)	RASGRF1 (I220V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616233	NM_001145648.3(RASGRF1):c.2917G>A (p.Asp973Asn)	RASGRF1 (D205N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151829	NM_001145648.3(RASGRF1):c.2827C>T (p.Arg943Cys)	RASGRF1 (R175C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151828	NM_001145648.3(RASGRF1):c.2717A>C (p.Lys906Thr)	RASGRF1 (K138T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464468	NM_001145648.3(RASGRF1):c.2659G>A (p.Ala887Thr)	RASGRF1 (A887T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151827	NM_001145648.3(RASGRF1):c.2654C>T (p.Ser885Leu)	RASGRF1 (S117L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604334	NM_001145648.3(RASGRF1):c.2615C>G (p.Thr872Ser)	RASGRF1 (T872S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312922	NM_001145648.3(RASGRF1):c.2428C>A (p.Pro810Thr)	LOC126862187, RASGRF1 (P42T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592773	NM_001145648.3(RASGRF1):c.2422G>A (p.Glu808Lys)	LOC126862187, RASGRF1 (E824K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509340	NM_001145648.3(RASGRF1):c.2398G>A (p.Gly800Ser)	LOC126862187, RASGRF1 (G32S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151825	NM_001145648.3(RASGRF1):c.2378C>T (p.Thr793Ile)	LOC126862187, RASGRF1 (T809I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332823	NM_001145648.3(RASGRF1):c.2312C>T (p.Ser771Leu)	LOC126862187, RASGRF1 (S771L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151823	NM_001145648.3(RASGRF1):c.2305A>G (p.Met769Val)	LOC126862187, RASGRF1 (M769V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312926	NM_001145648.3(RASGRF1):c.2272G>A (p.Ala758Thr)	LOC126862187, RASGRF1 (A774T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397962	NM_001145648.3(RASGRF1):c.2198C>T (p.Ser733Leu)	LOC126862187, RASGRF1 (S733L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333709	NM_001145648.3(RASGRF1):c.2193G>C (p.Lys731Asn)	LOC126862187, RASGRF1 (K731N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521204	NM_001145648.3(RASGRF1):c.2144C>T (p.Pro715Leu)	LOC126862187, RASGRF1 (P731L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151822	NM_001145648.3(RASGRF1):c.2134C>T (p.Pro712Ser)	LOC126862187, RASGRF1 (P712S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598433	NM_001145648.3(RASGRF1):c.2131C>G (p.Pro711Ala)	LOC126862187, RASGRF1 (P711A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151821	NM_001145648.3(RASGRF1):c.2102G>A (p.Gly701Asp)	LOC126862187, RASGRF1 (G717D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151820	NM_001145648.3(RASGRF1):c.2017G>A (p.Val673Met)	RASGRF1 (V686M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224243	NM_001145648.3(RASGRF1):c.1783G>A (p.Ala595Thr)	RASGRF1 (A595T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260944	NM_001145648.3(RASGRF1):c.1760G>A (p.Arg587Gln)	RASGRF1 (R587Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248476	NM_001145648.3(RASGRF1):c.1730G>A (p.Ser577Asn)	RASGRF1 (S577N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151819	NM_001145648.3(RASGRF1):c.1616C>T (p.Ser539Phe)	RASGRF1 (S539F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240459	NM_001145648.3(RASGRF1):c.1450C>G (p.Leu484Val)	RASGRF1 (L484V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374434	NM_001145648.3(RASGRF1):c.1061G>A (p.Arg354His)	RASGRF1 (R354H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151833	NM_001145648.3(RASGRF1):c.856G>A (p.Val286Ile)	RASGRF1 (V286I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151832	NM_001145648.3(RASGRF1):c.812G>A (p.Arg271Gln)	RASGRF1 (R271Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312921	NM_001145648.3(RASGRF1):c.729G>C (p.Gln243His)	RASGRF1 (Q243H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335124	NM_001145648.3(RASGRF1):c.589A>G (p.Asn197Asp)	RASGRF1 (N197D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312925	NM_001145648.3(RASGRF1):c.571A>T (p.Thr191Ser)	RASGRF1 (T191S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151826	NM_001145648.3(RASGRF1):c.251C>G (p.Ser84Trp)	RASGRF1 (S84W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312923	NM_001145648.3(RASGRF1):c.239A>G (p.Lys80Arg)	RASGRF1 (K80R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468400	NM_001145648.3(RASGRF1):c.236C>A (p.Pro79His)	RASGRF1 (P79H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151818	NM_001145648.3(RASGRF1):c.133G>A (p.Ala45Thr)	RASGRF1 (A45T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618071	NM_001145648.3(RASGRF1):c.31C>A (p.His11Asn)	RASGRF1 (H11N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 47