"PreventionGenetics, part of Exact Sciences"[submitter] AND "FAT4"[gen - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1562488	NM_001291303.3(FAT4):c.91C>T (p.Leu31=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GLikely benign
Select item 679813	NM_001291303.3(FAT4):c.185G>C (p.Gly62Ala)	FAT4 (G62A)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1421199	NM_001291303.3(FAT4):c.188C>T (p.Thr63Ile)	FAT4 (T63I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2180158	NM_001291303.3(FAT4):c.235G>T (p.Ala79Ser)	FAT4 (A79S)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 1500387	NM_001291303.3(FAT4):c.247A>G (p.Ile83Val)	FAT4 (I83V)	Single nucleotide variant (missense variant)	FAT4-related disorder +1 more	GUncertain significance
Select item 1606074	NM_001291303.3(FAT4):c.390C>T (p.Asp130=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 380918	NM_001291303.3(FAT4):c.739C>A (p.Pro247Thr)	FAT4 (P247T)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 1105289	NM_001291303.3(FAT4):c.829G>A (p.Ala277Thr)	FAT4 (A277T)	Single nucleotide variant (missense variant)	FAT4-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 1199864	NM_001291303.3(FAT4):c.842C>T (p.Thr281Ile)	FAT4 (T281I)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
Select item 2632238	NM_001291303.3(FAT4):c.980del (p.Asp327fs)	FAT4 (D327fs)	Deletion (frameshift variant)	FAT4-related disorder	GLikely pathogenic
Select item 993351	NM_001291303.3(FAT4):c.1099G>A (p.Val367Ile)	FAT4 (V367I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 669336	NM_001291303.3(FAT4):c.1299C>G (p.Ser433=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2628976	NM_001291303.3(FAT4):c.1358A>C (p.Gln453Pro)	FAT4 (Q453P)	Single nucleotide variant (missense variant)	FAT4-related disorder	GUncertain significance
Select item 391916	NM_001291303.3(FAT4):c.1698C>T (p.Ala566=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +2 more	GLikely benign
Select item 1595173	NM_001291303.3(FAT4):c.1802A>G (p.Glu601Gly)	FAT4 (E601G)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 1924876	NM_001291303.3(FAT4):c.1817G>C (p.Arg606Thr)	FAT4 (R606T)	Single nucleotide variant (missense variant)	FAT4-related disorder +1 more	GUncertain significance
Select item 746912	NM_001291303.3(FAT4):c.1845C>T (p.Asn615=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 708713	NM_001291303.3(FAT4):c.1855C>T (p.Arg619Cys)	FAT4 (R619C)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2629649	NM_001291303.3(FAT4):c.2006A>C (p.Gln669Pro)	FAT4 (Q669P)	Single nucleotide variant (missense variant)	FAT4-related disorder	GUncertain significance
Select item 1198187	NM_001291303.3(FAT4):c.2057G>A (p.Ser686Asn)	FAT4 (S686N)	Single nucleotide variant (missense variant)	FAT4-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 1943538	NM_001291303.3(FAT4):c.2214C>A (p.Val738=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 506698	NM_001291303.3(FAT4):c.2316A>G (p.Gln772=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1459826	NM_001291303.3(FAT4):c.2376A>G (p.Val792=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1165156	NM_001291303.3(FAT4):c.2450C>T (p.Ala817Val)	FAT4 (A817V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 1986317	NM_001291303.3(FAT4):c.2574G>A (p.Glu858=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1628749	NM_001291303.3(FAT4):c.2646A>T (p.Thr882=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1365451	NM_001291303.3(FAT4):c.2689A>G (p.Ile897Val)	FAT4 (I897V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 419204	NM_001291303.3(FAT4):c.2705TGG[1] (p.Val903del)	FAT4 (V903del)	Microsatellite (inframe_deletion)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1365452	NM_001291303.3(FAT4):c.2824A>G (p.Ile942Val)	FAT4 (I942V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 945556	NM_001291303.3(FAT4):c.2917G>A (p.Val973Ile)	FAT4 (V973I)	Single nucleotide variant (missense variant)	FAT4-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 3038297	NM_001291303.3(FAT4):c.2994A>G (p.Gln998=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder	GLikely benign
Select item 2168666	NM_001291303.3(FAT4):c.3012C>A (p.Thr1004=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 509829	NM_001291303.3(FAT4):c.3294T>A (p.Pro1098=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2189137	NM_001291303.3(FAT4):c.3327C>T (p.Phe1109=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 385548	NM_001291303.3(FAT4):c.3402A>T (p.Glu1134Asp)	FAT4 (E1134D)	Single nucleotide variant (missense variant)	FAT4-related disorder +1 more	GBenign/Likely benign
Select item 449266	NM_001291303.3(FAT4):c.3424G>A (p.Val1142Met)	FAT4 (V1142M)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 2636903	NM_001291303.3(FAT4):c.3598A>G (p.Met1200Val)	FAT4 (M1200V)	Single nucleotide variant (missense variant)	FAT4-related disorder	GUncertain significance
Select item 748114	NM_001291303.3(FAT4):c.3658T>A (p.Ser1220Thr)	FAT4 (S1220T)	Single nucleotide variant (missense variant)	FAT4-related disorder +1 more	GBenign/Likely benign
Select item 384880	NM_001291303.3(FAT4):c.3768A>G (p.Arg1256=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +2 more	GLikely benign
Select item 3000736	NM_001291303.3(FAT4):c.3999C>T (p.Leu1333=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GLikely benign
Select item 384625	NM_001291303.3(FAT4):c.4154T>C (p.Leu1385Ser)	FAT4 (L1385S)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 377854	NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val)	FAT4 (I1435V)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign
Select item 1620754	NM_001291303.3(FAT4):c.4365A>G (p.Leu1455=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GLikely benign
Select item 3031671	NM_001291303.3(FAT4):c.4425A>G (p.Lys1475=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder	GLikely benign
Select item 1621188	NM_001291303.3(FAT4):c.4797C>A (p.Leu1599=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 682361	NM_001291303.3(FAT4):c.4941C>T (p.Asn1647=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 376888	NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val)	FAT4 (I1759V)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 792824	NM_001291303.3(FAT4):c.5308-9T>C	FAT4	Single nucleotide variant (intron variant)	FAT4-related disorder +1 more	GLikely benign
Select item 1603806	NM_001291303.3(FAT4):c.5308-5T>C	FAT4	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1666585	NM_001291303.3(FAT4):c.5404T>C (p.Leu1802=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1622460	NM_001291303.3(FAT4):c.5532C>T (p.Pro1844=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 729522	NM_001291303.3(FAT4):c.5883T>C (p.Ser1961=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GBenign
Select item 1617689	NM_001291303.3(FAT4):c.5924T>C (p.Ile1975Thr)	FAT4 (I1975T)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1562105	NM_001291303.3(FAT4):c.5943T>C (p.Tyr1981=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 435175	NM_001291303.3(FAT4):c.5987A>G (p.Lys1996Arg)	FAT4 (K1996R)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 384835	NM_001291303.3(FAT4):c.6219A>G (p.Gln2073=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +2 more	GBenign/Likely benign
Select item 1666586	NM_001291303.3(FAT4):c.6324C>G (p.Leu2108=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1564922	NM_001291303.3(FAT4):c.6444T>C (p.Asn2148=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GLikely benign
Select item 386576	NM_001291303.3(FAT4):c.6478A>G (p.Lys2160Glu)	FAT4 (K2160E)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1559390	NM_001291303.3(FAT4):c.6531C>T (p.Phe2177=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GLikely benign
Select item 1617797	NM_001291303.3(FAT4):c.6618T>C (p.Ser2206=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1577530	NM_001291303.3(FAT4):c.6729C>T (p.Ser2243=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 445560	NM_001291303.3(FAT4):c.6733G>A (p.Val2245Ile)	FAT4 (V2245I)	Single nucleotide variant (missense variant)	FAT4-related disorder +1 more	GBenign/Likely benign
Select item 1302209	NM_001291303.3(FAT4):c.7052A>G (p.Asn2351Ser)	FAT4 (N2351S)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 424428	NM_001291303.3(FAT4):c.7103C>A (p.Ala2368Glu)	FAT4 (A2368E)	Single nucleotide variant (missense variant)	FAT4-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 498556	NM_001291303.3(FAT4):c.7231A>T (p.Thr2411Ser)	FAT4 (T2409S +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 725748	NM_001291303.3(FAT4):c.7266C>T (p.Ser2422=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GLikely benign
Select item 435176	NM_001291303.3(FAT4):c.7358G>T (p.Ser2453Ile)	FAT4 (S2451I +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder +3 more	GBenign/Likely benign
Select item 1167471	NM_001291303.3(FAT4):c.7452T>C (p.Gly2484=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GBenign/Likely benign
Select item 1167898	NM_001291303.3(FAT4):c.7466C>T (p.Ala2489Val)	FAT4 (A2487V +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder +2 more	GBenign/Likely benign
Select item 3051232	NM_001291303.3(FAT4):c.7725G>T (p.Thr2575=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder	GLikely benign
Select item 380796	NM_001291303.3(FAT4):c.7787T>C (p.Leu2596Ser)	FAT4 (L2594S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 517910	NM_001291303.3(FAT4):c.7813A>G (p.Ile2605Val)	FAT4 (I2603V +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 1605758	NM_001291303.3(FAT4):c.7815C>T (p.Ile2605=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2629144	NM_001291303.3(FAT4):c.7816G>A (p.Ala2606Thr)	FAT4 (A2604T +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder	GUncertain significance
Select item 1395528	NM_001291303.3(FAT4):c.7876A>C (p.Ser2626Arg)	FAT4 (S2626R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 435173	NM_001291303.3(FAT4):c.7935C>T (p.Asp2645=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +2 more	GBenign/Likely benign
Select item 1567941	NM_001291303.3(FAT4):c.7962C>T (p.Tyr2654=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GLikely benign
Select item 420323	NM_001291303.3(FAT4):c.8021A>T (p.Asp2674Val)	FAT4 (D2672V +1 more)	Single nucleotide variant (missense variant)	Van Maldergem syndrome 2 +2 more	GConflicting classifications of pathogenicity
Select item 722056	NM_001291303.3(FAT4):c.8055C>T (p.Ser2685=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1032176	NM_001291303.3(FAT4):c.8313T>C (p.Asn2771=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 383607	NM_001291303.3(FAT4):c.8544C>T (p.Ser2848=)	FAT4	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1597623	NM_001291303.3(FAT4):c.8580C>T (p.Val2860=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1569442	NM_001291303.3(FAT4):c.8854A>C (p.Ser2952Arg)	FAT4 (S2950R +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder +2 more	GLikely benign
Select item 1594158	NM_001291303.3(FAT4):c.9006G>A (p.Thr3002=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1631060	NM_001291303.3(FAT4):c.9057A>G (p.Ser3019=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2171315	NM_001291303.3(FAT4):c.9222A>G (p.Gln3074=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2633004	NM_001291303.3(FAT4):c.9260A>G (p.His3087Arg)	FAT4 (H3085R +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder	GUncertain significance
Select item 1620860	NM_001291303.3(FAT4):c.9282C>T (p.Ser3094=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +1 more	GLikely benign
Select item 2630526	NM_001291303.3(FAT4):c.9295A>G (p.Thr3099Ala)	FAT4 (T3097A +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder	GUncertain significance
Select item 3029232	NM_001291303.3(FAT4):c.9306G>A (p.Glu3102=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder	GLikely benign
Select item 3032727	NM_001291303.3(FAT4):c.9474A>G (p.Leu3158=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder	GLikely benign
Select item 1651150	NM_001291303.3(FAT4):c.9981T>C (p.Arg3327=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3029625	NM_001291303.3(FAT4):c.10116T>G (p.Ser3372=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder	GLikely benign
Select item 506585	NM_001291303.3(FAT4):c.10158A>G (p.Ala3386=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 3031275	NM_001291303.3(FAT4):c.10188C>T (p.Thr3396=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder	GLikely benign
Select item 1402100	NM_001291303.3(FAT4):c.10357G>A (p.Gly3453Ser)	FAT4 (G3453S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 679019	NM_001291303.3(FAT4):c.10390A>G (p.Ile3464Val)	FAT4 (I3464V +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder +1 more	GLikely benign
Select item 737184	NM_001291303.3(FAT4):c.10392C>A (p.Ile3464=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3002176	NM_001291303.3(FAT4):c.10407A>G (p.Glu3469=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign

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