ARHGEF19[gene] and "single gene"[properties] - ClinVar

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Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2351809	NM_153213.5(ARHGEF19):c.2361T>A (p.Asn787Lys)	ARHGEF19 (N787K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340205	NM_153213.5(ARHGEF19):c.2195A>G (p.Asp732Gly)	ARHGEF19 (D732G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494371	NM_153213.5(ARHGEF19):c.2150G>A (p.Cys717Tyr)	ARHGEF19 (C717Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129188	NM_153213.5(ARHGEF19):c.2129T>C (p.Val710Ala)	ARHGEF19 (V710A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523598	NM_153213.5(ARHGEF19):c.2081G>A (p.Arg694Gln)	ARHGEF19 (R694Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521201	NM_153213.5(ARHGEF19):c.2059C>T (p.Arg687Trp)	ARHGEF19 (R687W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129186	NM_153213.5(ARHGEF19):c.2053C>T (p.Arg685Trp)	ARHGEF19 (R685W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543511	NM_153213.5(ARHGEF19):c.2038C>T (p.His680Tyr)	ARHGEF19 (H680Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523573	NM_153213.5(ARHGEF19):c.2023G>A (p.Gly675Arg)	ARHGEF19 (G675R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313467	NM_153213.5(ARHGEF19):c.1930G>A (p.Val644Ile)	ARHGEF19 (V644I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348337	NM_153213.5(ARHGEF19):c.1900C>T (p.Arg634Trp)	ARHGEF19 (R634W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786848	NM_153213.5(ARHGEF19):c.1898G>A (p.Arg633Gln)	ARHGEF19 (R633Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2340724	NM_153213.5(ARHGEF19):c.1862A>G (p.Tyr621Cys)	ARHGEF19 (Y621C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129183	NM_153213.5(ARHGEF19):c.1790G>C (p.Gly597Ala)	ARHGEF19 (G597A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129182	NM_153213.5(ARHGEF19):c.1733A>G (p.His578Arg)	ARHGEF19 (H578R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292140	NM_153213.5(ARHGEF19):c.1554G>C (p.Arg518Ser)	ARHGEF19 (R518S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469354	NM_153213.5(ARHGEF19):c.1486C>T (p.Arg496Cys)	ARHGEF19 (R496C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313476	NM_153213.5(ARHGEF19):c.1467G>T (p.Arg489Ser)	ARHGEF19 (R489S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222230	NM_153213.5(ARHGEF19):c.1443G>T (p.Gln481His)	ARHGEF19 (Q481H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372896	NM_153213.5(ARHGEF19):c.1382C>T (p.Ala461Val)	ARHGEF19 (A461V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233575	NM_153213.5(ARHGEF19):c.1328A>T (p.Glu443Val)	ARHGEF19 (E443V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353418	NM_153213.5(ARHGEF19):c.1289C>T (p.Thr430Ile)	ARHGEF19 (T430I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129179	NM_153213.5(ARHGEF19):c.1150C>G (p.Leu384Val)	ARHGEF19 (L384V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129195	NM_153213.5(ARHGEF19):c.845A>T (p.Glu282Val)	ARHGEF19 (E282V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129194	NM_153213.5(ARHGEF19):c.836G>T (p.Ser279Ile)	ARHGEF19 (S279I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253355	NM_153213.5(ARHGEF19):c.731T>C (p.Met244Thr)	ARHGEF19 (M244T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2249697	NM_153213.5(ARHGEF19):c.719G>T (p.Arg240Leu)	ARHGEF19 (R240L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260069	NM_153213.5(ARHGEF19):c.698A>G (p.Lys233Arg)	ARHGEF19 (K233R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377082	NM_153213.5(ARHGEF19):c.629G>A (p.Arg210His)	ARHGEF19 (R210H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3234202	NM_153213.5(ARHGEF19):c.610C>T (p.Arg204Trp)	ARHGEF19 (R204W)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2485213	NM_153213.5(ARHGEF19):c.581G>A (p.Arg194Lys)	ARHGEF19 (R194K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549484	NM_153213.5(ARHGEF19):c.571C>T (p.Pro191Ser)	ARHGEF19 (P191S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227138	NM_153213.5(ARHGEF19):c.526C>A (p.Pro176Thr)	ARHGEF19 (P176T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129192	NM_153213.5(ARHGEF19):c.469G>T (p.Ala157Ser)	ARHGEF19 (A157S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303999	NM_153213.5(ARHGEF19):c.462G>T (p.Glu154Asp)	ARHGEF19 (E154D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611684	NM_153213.5(ARHGEF19):c.451G>C (p.Gly151Arg)	ARHGEF19 (G151R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129191	NM_153213.5(ARHGEF19):c.409G>C (p.Ala137Pro)	ARHGEF19 (A137P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129190	NM_153213.5(ARHGEF19):c.391G>A (p.Gly131Ser)	ARHGEF19 (G131S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233794	NM_153213.5(ARHGEF19):c.388C>T (p.His130Tyr)	ARHGEF19 (H130Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382391	NM_153213.5(ARHGEF19):c.377G>A (p.Arg126His)	ARHGEF19 (R126H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343073	NM_153213.5(ARHGEF19):c.307C>G (p.Pro103Ala)	ARHGEF19 (P103A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129189	NM_153213.5(ARHGEF19):c.262G>A (p.Glu88Lys)	ARHGEF19 (E88K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129187	NM_153213.5(ARHGEF19):c.206C>T (p.Thr69Ile)	ARHGEF19 (T69I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618890	NM_153213.5(ARHGEF19):c.191G>A (p.Arg64His)	ARHGEF19 (R64H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129184	NM_153213.5(ARHGEF19):c.190C>T (p.Arg64Cys)	ARHGEF19 (R64C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129181	NM_153213.5(ARHGEF19):c.160G>A (p.Ala54Thr)	ARHGEF19 (A54T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2340796	NM_153213.5(ARHGEF19):c.145G>C (p.Asp49His)	ARHGEF19 (D49H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489108	NM_153213.5(ARHGEF19):c.137T>C (p.Val46Ala)	ARHGEF19 (V46A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405927	NM_153213.5(ARHGEF19):c.115G>A (p.Ala39Thr)	ARHGEF19 (A39T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3313491	NM_153213.5(ARHGEF19):c.108G>C (p.Glu36Asp)	ARHGEF19 (E36D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313481	NM_153213.5(ARHGEF19):c.90G>C (p.Glu30Asp)	ARHGEF19 (E30D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 51