FARP1[gene] and "single gene"[properties] - ClinVar

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Items: 66

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2482866	NM_005766.4(FARP1):c.19A>G (p.Arg7Gly)	FARP1 (R7G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458955	NM_005766.4(FARP1):c.62G>A (p.Gly21Glu)	FARP1 (G21E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277704	NM_005766.4(FARP1):c.122C>G (p.Ser41Cys)	FARP1 (S41C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277705	NM_005766.4(FARP1):c.257C>G (p.Pro86Arg)	FARP1 (P86R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335238	NM_005766.4(FARP1):c.275C>T (p.Thr92Met)	FARP1 (T92M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092877	NM_005766.4(FARP1):c.304G>A (p.Val102Met)	FARP1 (V102M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277711	NM_005766.4(FARP1):c.335T>G (p.Val112Gly)	FARP1 (V112G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381993	NM_005766.4(FARP1):c.364C>T (p.Pro122Ser)	FARP1 (P122S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278660	NM_005766.4(FARP1):c.449C>T (p.Thr150Met)	FARP1 (T150M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2643884	NM_005766.4(FARP1):c.450G>A (p.Thr150=)	FARP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3277709	NM_005766.4(FARP1):c.521C>A (p.Ala174Asp)	FARP1 (A174D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531365	NM_005766.4(FARP1):c.595T>A (p.Phe199Ile)	FARP1 (F199I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345422	NM_005766.4(FARP1):c.610A>G (p.Ile204Val)	FARP1 (I204V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546482	NM_005766.4(FARP1):c.662G>A (p.Arg221Gln)	FARP1 (R221Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546374	NM_005766.4(FARP1):c.672G>A (p.Met224Ile)	FARP1 (M224I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277703	NM_005766.4(FARP1):c.800G>A (p.Arg267Gln)	FARP1 (R267Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277699	NM_005766.4(FARP1):c.841C>T (p.Arg281Trp)	FARP1 (R281W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384850	NM_005766.4(FARP1):c.1046A>C (p.Asp349Ala)	FARP1 (D349A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532055	NM_005766.4(FARP1):c.1091A>G (p.Lys364Arg)	FARP1 (K364R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092865	NM_005766.4(FARP1):c.1105C>G (p.His369Asp)	FARP1 (H369D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279670	NM_005766.4(FARP1):c.1154T>C (p.Val385Ala)	FARP1 (V385A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277706	NM_005766.4(FARP1):c.1186A>G (p.Thr396Ala)	FARP1 (T396A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274837	NM_005766.4(FARP1):c.1197A>T (p.Glu399Asp)	FARP1 (E399D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610075	NM_005766.4(FARP1):c.1255G>A (p.Ala419Thr)	FARP1 (A419T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233994	NM_005766.4(FARP1):c.1264C>G (p.Pro422Ala)	FARP1 (P422A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267179	NM_005766.4(FARP1):c.1289C>G (p.Pro430Arg)	FARP1 (P430R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277701	NM_005766.4(FARP1):c.1330G>C (p.Ala444Pro)	FARP1 (A444P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277707	NM_005766.4(FARP1):c.1337C>T (p.Ala446Val)	FARP1 (A446V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3092866	NM_005766.4(FARP1):c.1460C>T (p.Ser487Leu)	FARP1 (S487L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2681273	NM_005766.4(FARP1):c.1461G>A (p.Ser487=)	FARP1	Single nucleotide variant (synonymous variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2341450	NM_005766.4(FARP1):c.1465G>T (p.Gly489Trp)	FARP1 (G489W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092867	NM_005766.4(FARP1):c.1466G>C (p.Gly489Ala)	FARP1 (G489A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458242	NM_005766.4(FARP1):c.1469G>T (p.Gly490Val)	FARP1 (G490V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215892	NM_005766.4(FARP1):c.1484A>G (p.Asn495Ser)	FARP1 (N495S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277702	NM_005766.4(FARP1):c.1486G>A (p.Val496Met)	FARP1 (V496M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304291	NM_005766.4(FARP1):c.1568C>G (p.Pro523Arg)	FARP1 (P523R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470066	NM_005766.4(FARP1):c.1574C>T (p.Thr525Met)	FARP1 (T525M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508836	NM_005766.4(FARP1):c.1595G>A (p.Arg532Gln)	FARP1 (R532Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289179	NM_005766.4(FARP1):c.1685T>C (p.Ile562Thr)	FARP1 (I562T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481694	NM_005766.4(FARP1):c.1741A>G (p.Lys581Glu)	FARP1 (K581E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395658	NM_005766.4(FARP1):c.1816C>G (p.Leu606Val)	FARP1 (L606V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347912	NM_005766.4(FARP1):c.1831G>A (p.Gly611Ser)	FARP1 (G611S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277713	NM_005766.4(FARP1):c.1933A>G (p.Ser645Gly)	FARP1 (S645G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206567	NM_005766.4(FARP1):c.1976G>A (p.Arg659Gln)	FARP1 (R659Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092868	NM_005766.4(FARP1):c.2060A>C (p.His687Pro)	FARP1 (H687P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277710	NM_005766.4(FARP1):c.2083G>C (p.Val695Leu)	FARP1 (V695L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092869	NM_005766.4(FARP1):c.2093G>C (p.Arg698Pro)	FARP1 (R698P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244521	NM_005766.4(FARP1):c.2122G>A (p.Ala708Thr)	FARP1 (A708T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406724	NM_005766.4(FARP1):c.2284C>T (p.Arg762Cys)	FARP1 (R793C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601921	NM_005766.4(FARP1):c.2285G>A (p.Arg762His)	FARP1 (R762H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092871	NM_005766.4(FARP1):c.2372G>C (p.Arg791Pro)	FARP1 (R791P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384450	NM_005766.4(FARP1):c.2381C>T (p.Thr794Met)	FARP1 (T825M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611570	NM_005766.4(FARP1):c.2402T>G (p.Val801Gly)	FARP1 (V832G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277700	NM_005766.4(FARP1):c.2417C>T (p.Pro806Leu)	FARP1 (P837L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 773275	NM_005766.4(FARP1):c.2424T>C (p.Tyr808=)	FARP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2343586	NM_005766.4(FARP1):c.2483G>A (p.Arg828Gln)	FARP1 (R828Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250087	NM_005766.4(FARP1):c.2522G>C (p.Arg841Pro)	FARP1 (R872P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508765	NM_005766.4(FARP1):c.2557A>G (p.Met853Val)	FARP1 (M884V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 776805	NM_005766.4(FARP1):c.2583C>T (p.Ser861=)	FARP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2381825	NM_005766.4(FARP1):c.2633C>A (p.Ser878Tyr)	FARP1 (S878Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092873	NM_005766.4(FARP1):c.2648C>G (p.Thr883Ser)	FARP1 (T883S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598071	NM_005766.4(FARP1):c.2719C>T (p.Arg907Cys)	FARP1 (R907C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092874	NM_005766.4(FARP1):c.2733G>T (p.Met911Ile)	FARP1 (M942I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092875	NM_005766.4(FARP1):c.2739C>A (p.His913Gln)	FARP1 (H944Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527339	NM_005766.4(FARP1):c.2764G>A (p.Val922Ile)	FARP1 (V953I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277712	NM_005766.4(FARP1):c.2788G>A (p.Ala930Thr)	FARP1 (A961T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 66