ARHGEF11[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312966	NM_198236.3(ARHGEF11):c.3511G>A (p.Gly1171Arg)	ARHGEF11 (G1161R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548689	NM_198236.3(ARHGEF11):c.3436G>A (p.Gly1146Ser)	ARHGEF11 (G1136S +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3313018	NM_198236.3(ARHGEF11):c.3427G>A (p.Ala1143Thr)	ARHGEF11 (A1103T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543198	NM_198236.3(ARHGEF11):c.3382G>A (p.Ala1128Thr)	ARHGEF11 (A1088T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356064	NM_198236.3(ARHGEF11):c.3380C>A (p.Ala1127Asp)	ARHGEF11 (A1087D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204552	NM_198236.3(ARHGEF11):c.3356G>A (p.Arg1119Gln)	ARHGEF11 (R1079Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312998	NM_198236.3(ARHGEF11):c.3290A>G (p.Tyr1097Cys)	ARHGEF11 (Y1057C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129049	NM_198236.3(ARHGEF11):c.3269A>G (p.Lys1090Arg)	ARHGEF11 (K1087R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313017	NM_198236.3(ARHGEF11):c.3253A>G (p.Ile1085Val)	ARHGEF11 (I1075V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129048	NM_198236.3(ARHGEF11):c.3163T>C (p.Ser1055Pro)	ARHGEF11 (S1015P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129047	NM_198236.3(ARHGEF11):c.2869C>G (p.Leu957Val)	ARHGEF11 (L917V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129046	NM_198236.3(ARHGEF11):c.2848C>T (p.Arg950Trp)	ARHGEF11 (R940W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588533	NM_198236.3(ARHGEF11):c.2567G>A (p.Arg856Gln)	ARHGEF11 (R846Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129045	NM_198236.3(ARHGEF11):c.2459C>T (p.Pro820Leu)	ARHGEF11 (P817L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260408	NM_198236.3(ARHGEF11):c.2450G>A (p.Arg817Gln)	ARHGEF11 (R814Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495877	NM_198236.3(ARHGEF11):c.2408G>A (p.Arg803Gln)	ARHGEF11 (R800Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2639471	NM_198236.3(ARHGEF11):c.2295G>A (p.Val765=)	ARHGEF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2492660	NM_198236.3(ARHGEF11):c.2194C>T (p.Leu732Phe)	ARHGEF11 (L722F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488294	NM_198236.3(ARHGEF11):c.2186C>T (p.Thr729Ile)	ARHGEF11 (T719I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588068	NM_198236.3(ARHGEF11):c.2157C>A (p.Ser719Arg)	ARHGEF11 (S719R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381490	NM_198236.3(ARHGEF11):c.2146G>A (p.Gly716Ser)	ARHGEF11 (G706S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244805	NM_198236.3(ARHGEF11):c.2093G>A (p.Ser698Asn)	ARHGEF11 (S688N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312947	NM_198236.3(ARHGEF11):c.1940T>C (p.Ile647Thr)	ARHGEF11 (I637T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609692	NM_198236.3(ARHGEF11):c.1921G>A (p.Asp641Asn)	ARHGEF11 (D601N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327761	NM_198236.3(ARHGEF11):c.1811A>G (p.Asn604Ser)	ARHGEF11 (N594S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402155	NM_198236.3(ARHGEF11):c.1789C>A (p.Pro597Thr)	ARHGEF11 (P557T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611999	NM_198236.3(ARHGEF11):c.1787C>T (p.Ser596Phe)	ARHGEF11 (S556F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3313008	NM_198236.3(ARHGEF11):c.1660A>G (p.Lys554Glu)	ARHGEF11 (K550E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246882	NM_198236.3(ARHGEF11):c.1615G>A (p.Ala539Thr)	ARHGEF11 (A535T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539120	NM_198236.3(ARHGEF11):c.1454G>A (p.Arg485Gln)	ARHGEF11 (R445Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239824	NM_198236.3(ARHGEF11):c.1347G>T (p.Met449Ile)	ARHGEF11 (M445I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309870	NM_198236.3(ARHGEF11):c.1303G>A (p.Glu435Lys)	ARHGEF11 (E431K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409868	NM_198236.3(ARHGEF11):c.1289G>A (p.Arg430His)	ARHGEF11 (R390H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129044	NM_198236.3(ARHGEF11):c.1231A>G (p.Lys411Glu)	ARHGEF11 (K411E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339863	NM_198236.3(ARHGEF11):c.1132A>G (p.Ser378Gly)	ARHGEF11 (S374G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344082	NM_198236.3(ARHGEF11):c.1116C>G (p.Phe372Leu)	ARHGEF11 (F368L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129059	NM_198236.3(ARHGEF11):c.1111A>G (p.Ile371Val)	ARHGEF11 (I367V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537292	NM_198236.3(ARHGEF11):c.1019C>T (p.Pro340Leu)	ARHGEF11 (P340L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129058	NM_198236.3(ARHGEF11):c.983A>C (p.Lys328Thr)	ARHGEF11 (K288T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542927	NM_198236.3(ARHGEF11):c.965G>A (p.Gly322Asp)	ARHGEF11 (G282D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547112	NM_198236.3(ARHGEF11):c.955G>A (p.Gly319Ser)	ARHGEF11 (G315S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3312955	NM_198236.3(ARHGEF11):c.923G>A (p.Arg308Gln)	ARHGEF11 (R304Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268784	NM_198236.3(ARHGEF11):c.826T>A (p.Ser276Thr)	ARHGEF11 (S272T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254125	NM_198236.3(ARHGEF11):c.784G>T (p.Gly262Cys)	ARHGEF11 (G258C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279289	NM_198236.3(ARHGEF11):c.424C>T (p.Pro142Ser)	ARHGEF11 (P142S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385400	NM_198236.3(ARHGEF11):c.406C>A (p.Pro136Thr)	ARHGEF11 (P132T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312988	NM_198236.3(ARHGEF11):c.338C>T (p.Ala113Val)	ARHGEF11 (A113V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313016	NM_198236.3(ARHGEF11):c.329A>G (p.Lys110Arg)	ARHGEF11 (K106R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3025358	NM_198236.3(ARHGEF11):c.138C>G (p.Arg46=)	ARHGEF11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 771314	NM_198236.3(ARHGEF11):c.135A>G (p.Gln45=)	ARHGEF11	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 50