"Ambry Genetics"[submitter] AND "ARHGEF4"[gene] - ClinVar

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

Search results

Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2223630	NM_001367493.1(ARHGEF4):c.3568G>A (p.Glu1190Lys)	ARHGEF4 (E1190K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523781	NM_001367493.1(ARHGEF4):c.3620A>G (p.His1207Arg)	ARHGEF4 (H21R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319233	NM_001367493.1(ARHGEF4):c.3622A>T (p.Met1208Leu)	ARHGEF4 (M22L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464258	NM_001367493.1(ARHGEF4):c.3631G>T (p.Ala1211Ser)	ARHGEF4 (A25S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467807	NM_001367493.1(ARHGEF4):c.3701G>A (p.Arg1234His)	ARHGEF4 (R11H +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2551498	NM_001367493.1(ARHGEF4):c.3709G>T (p.Ala1237Ser)	ARHGEF4 (A1237S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129328	NM_001367493.1(ARHGEF4):c.3722C>T (p.Pro1241Leu)	ARHGEF4 (P70L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374905	NM_001367493.1(ARHGEF4):c.3739C>T (p.Arg1247Cys)	ARHGEF4 (R1247C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525433	NM_001367493.1(ARHGEF4):c.3743C>T (p.Ser1248Leu)	ARHGEF4 (S1248L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212430	NM_001367493.1(ARHGEF4):c.3748G>A (p.Val1250Ile)	ARHGEF4 (V64I +3 more)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 2329851	NM_001367493.1(ARHGEF4):c.3808C>A (p.His1270Asn)	ARHGEF4 (H47N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543462	NM_001367493.1(ARHGEF4):c.3844A>C (p.Lys1282Gln)	ARHGEF4 (K59Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615981	NM_001367493.1(ARHGEF4):c.3915C>G (p.Ser1305Arg)	ARHGEF4 (S1305R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281444	NM_001367493.1(ARHGEF4):c.3940A>G (p.Thr1314Ala)	ARHGEF4 (T143A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615948	NM_001367493.1(ARHGEF4):c.3974C>A (p.Thr1325Lys)	ARHGEF4 (T102K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568891	NM_001367493.1(ARHGEF4):c.3980G>C (p.Gly1327Ala)	ARHGEF4 (G104A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207021	NM_001367493.1(ARHGEF4):c.4039G>A (p.Glu1347Lys)	ARHGEF4 (E38K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224408	NM_001367493.1(ARHGEF4):c.4126C>G (p.Leu1376Val)	ARHGEF4 (L120V +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518419	NM_001367493.1(ARHGEF4):c.4267G>A (p.Ala1423Thr)	ARHGEF4 (A114T +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338643	NM_001367493.1(ARHGEF4):c.4270G>A (p.Asp1424Asn)	ARHGEF4 (D201N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216078	NM_001367493.1(ARHGEF4):c.4300G>A (p.Val1434Ile)	ARHGEF4 (V178I +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272789	NM_001367493.1(ARHGEF4):c.4333G>A (p.Asp1445Asn)	ARHGEF4 (D1445N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612000	NM_001367493.1(ARHGEF4):c.4370A>C (p.Glu1457Ala)	ARHGEF4 (E148A +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536933	NM_001367493.1(ARHGEF4):c.4407G>T (p.Gln1469His)	ARHGEF4 (Q213H +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319234	NM_001367493.1(ARHGEF4):c.4544T>A (p.Ile1515Asn)	ARHGEF4 (I292N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242040	NM_001367493.1(ARHGEF4):c.4620G>C (p.Glu1540Asp)	ARHGEF4 (E1540D +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129327	NM_001367493.1(ARHGEF4):c.4753G>A (p.Val1585Met)	ARHGEF4 (V362M +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476554	NM_001367493.1(ARHGEF4):c.4918G>T (p.Ala1640Ser)	ARHGEF4 (A384S +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512359	NM_001367493.1(ARHGEF4):c.4966C>T (p.Arg1656Trp)	ARHGEF4 (R470W +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388671	NM_001367493.1(ARHGEF4):c.5066C>T (p.Ser1689Leu)	ARHGEF4 (S380L +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337234	NM_001367493.1(ARHGEF4):c.5074C>A (p.Leu1692Met)	ARHGEF4 (L521M +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238965	NM_001367493.1(ARHGEF4):c.5146T>A (p.Tyr1716Asn)	ARHGEF4 (Y323N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520992	NM_001367493.1(ARHGEF4):c.5173G>A (p.Asp1725Asn)	ARHGEF4 (D469N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268884	NM_001367493.1(ARHGEF4):c.5203A>C (p.Met1735Leu)	ARHGEF4 (M512L +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603878	NM_001367493.1(ARHGEF4):c.5209G>A (p.Gly1737Ser)	ARHGEF4 (G551S +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253179	NM_001367493.1(ARHGEF4):c.5288G>A (p.Arg1763His)	ARHGEF4 (R1763H +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354790	NM_001367493.1(ARHGEF4):c.5293G>A (p.Ala1765Thr)	ARHGEF4 (A456T +7 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2495211	NM_001367493.1(ARHGEF4):c.5350C>A (p.Leu1784Ile)	ARHGEF4 (L391I +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279002	NM_001367493.1(ARHGEF4):c.5396A>G (p.Glu1799Gly)	ARHGEF4 (E562G +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470472	NM_001367493.1(ARHGEF4):c.5488C>T (p.Arg1830Trp)	ARHGEF4 (R1830W +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396676	NM_001367493.1(ARHGEF4):c.5504C>T (p.Thr1835Met)	ARHGEF4 (T664M +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129329	NM_001367493.1(ARHGEF4):c.5602A>G (p.Ile1868Val)	ARHGEF4 (I631V +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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: 42