"Ambry Genetics"[submitter] AND "FRYL"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2289181	NM_015030.2(FRYL):c.8971C>T (p.Arg2991Cys)	FRYL (R2991C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097112	NM_015030.2(FRYL):c.8920G>A (p.Glu2974Lys)	FRYL (E2974K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279987	NM_015030.2(FRYL):c.8702T>G (p.Ile2901Arg)	FRYL (I2901R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097111	NM_015030.2(FRYL):c.8653G>A (p.Ala2885Thr)	FRYL (A2885T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347068	NM_015030.2(FRYL):c.8629A>G (p.Ser2877Gly)	FRYL (S2877G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097110	NM_015030.2(FRYL):c.8581A>T (p.Asn2861Tyr)	FRYL (N2861Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243396	NM_015030.2(FRYL):c.8501G>T (p.Arg2834Ile)	FRYL (R2834I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254021	NM_015030.2(FRYL):c.8446A>G (p.Ile2816Val)	FRYL (I2816V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279981	NM_015030.2(FRYL):c.8420T>C (p.Phe2807Ser)	FRYL (F2807S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097109	NM_015030.2(FRYL):c.8407T>G (p.Cys2803Gly)	FRYL (C2803G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204434	NM_015030.2(FRYL):c.8301G>T (p.Met2767Ile)	FRYL (M2767I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321077	NM_015030.2(FRYL):c.8287G>T (p.Ala2763Ser)	FRYL (A2763S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359013	NM_015030.2(FRYL):c.8181G>T (p.Glu2727Asp)	FRYL (E2727D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097108	NM_015030.2(FRYL):c.8062C>T (p.Arg2688Cys)	FRYL (R2688C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097107	NM_015030.2(FRYL):c.8032G>A (p.Val2678Met)	FRYL (V2678M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386970	NM_015030.2(FRYL):c.7991C>T (p.Pro2664Leu)	FRYL (P2664L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097106	NM_015030.2(FRYL):c.7975C>G (p.Gln2659Glu)	FRYL (Q2659E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279978	NM_015030.2(FRYL):c.7940A>G (p.Gln2647Arg)	FRYL (Q2647R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279975	NM_015030.2(FRYL):c.7927G>A (p.Gly2643Arg)	FRYL (G2643R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492160	NM_015030.2(FRYL):c.7913A>C (p.Glu2638Ala)	FRYL (E2638A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097105	NM_015030.2(FRYL):c.7828G>A (p.Ala2610Thr)	FRYL (A2610T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286283	NM_015030.2(FRYL):c.7726A>G (p.Thr2576Ala)	FRYL (T2576A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2263802	NM_015030.2(FRYL):c.7679G>A (p.Arg2560Gln)	FRYL (R2560Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3097103	NM_015030.2(FRYL):c.7540A>G (p.Thr2514Ala)	FRYL (T2514A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2344893	NM_015030.2(FRYL):c.7520T>A (p.Met2507Lys)	FRYL (M2507K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556159	NM_015030.2(FRYL):c.7511G>A (p.Arg2504His)	FRYL (R2504H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590967	NM_015030.2(FRYL):c.7352G>A (p.Arg2451His)	FRYL (R2451H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279990	NM_015030.2(FRYL):c.7321G>C (p.Glu2441Gln)	FRYL (E2441Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555058	NM_015030.2(FRYL):c.7262A>C (p.Gln2421Pro)	FRYL (Q2421P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097101	NM_015030.2(FRYL):c.7067G>A (p.Arg2356Gln)	FRYL (R2356Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598251	NM_015030.2(FRYL):c.6880G>A (p.Asp2294Asn)	FRYL (D2294N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469276	NM_015030.2(FRYL):c.6815C>A (p.Ser2272Tyr)	FRYL (S2272Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097100	NM_015030.2(FRYL):c.6707G>A (p.Ser2236Asn)	FRYL (S2236N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279982	NM_015030.2(FRYL):c.6627G>C (p.Leu2209Phe)	FRYL (L2209F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387749	NM_015030.2(FRYL):c.6559G>A (p.Ala2187Thr)	FRYL (A2187T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393502	NM_015030.2(FRYL):c.6529G>T (p.Asp2177Tyr)	FRYL (D2177Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359045	NM_015030.2(FRYL):c.6515A>G (p.His2172Arg)	FRYL (H2172R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368781	NM_015030.2(FRYL):c.6385A>G (p.Ile2129Val)	FRYL (I2129V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494442	NM_015030.2(FRYL):c.6364T>A (p.Cys2122Ser)	FRYL (C2122S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279980	NM_015030.2(FRYL):c.6208G>A (p.Ala2070Thr)	FRYL (A2070T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229923	NM_015030.2(FRYL):c.6107A>G (p.Asp2036Gly)	FRYL (D2036G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247107	NM_015030.2(FRYL):c.5963A>G (p.Tyr1988Cys)	FRYL (Y1988C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495583	NM_015030.2(FRYL):c.5866C>T (p.Arg1956Trp)	FRYL (R1956W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359870	NM_015030.2(FRYL):c.5864G>A (p.Arg1955Gln)	FRYL (R1955Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097099	NM_015030.2(FRYL):c.5849G>A (p.Arg1950Gln)	FRYL (R1950Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097098	NM_015030.2(FRYL):c.5804G>A (p.Ser1935Asn)	FRYL (S1935N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255953	NM_015030.2(FRYL):c.5722T>C (p.Tyr1908His)	FRYL (Y1908H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279988	NM_015030.2(FRYL):c.5542G>A (p.Val1848Ile)	FRYL (V1848I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279989	NM_015030.2(FRYL):c.5458T>C (p.Cys1820Arg)	FRYL (C1820R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097097	NM_015030.2(FRYL):c.5280A>G (p.Arg1760=)	FRYL	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2623073	NM_015030.2(FRYL):c.5038G>T (p.Val1680Phe)	FRYL (V1680F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222456	NM_015030.2(FRYL):c.4973A>G (p.Asn1658Ser)	FRYL (N1658S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477817	NM_015030.2(FRYL):c.4966A>C (p.Asn1656His)	FRYL (N1656H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097096	NM_015030.2(FRYL):c.4930C>T (p.Arg1644Cys)	FRYL (R1644C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097095	NM_015030.2(FRYL):c.4840G>T (p.Val1614Leu)	FRYL (V1614L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496450	NM_015030.2(FRYL):c.4757C>G (p.Thr1586Arg)	FRYL (T1586R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097094	NM_015030.2(FRYL):c.4730C>T (p.Ser1577Leu)	FRYL (S1577L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097093	NM_015030.2(FRYL):c.4680G>T (p.Glu1560Asp)	FRYL (E1560D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254161	NM_015030.2(FRYL):c.4592G>T (p.Arg1531Leu)	FRYL (R1531L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507726	NM_015030.2(FRYL):c.4567C>T (p.Arg1523Trp)	FRYL (R1523W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297623	NM_015030.2(FRYL):c.4510A>G (p.Ile1504Val)	FRYL (I1504V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273894	NM_015030.2(FRYL):c.4499T>C (p.Ile1500Thr)	FRYL (I1500T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283175	NM_015030.2(FRYL):c.4495C>T (p.Pro1499Ser)	FRYL (P1499S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279979	NM_015030.2(FRYL):c.4489A>C (p.Asn1497His)	FRYL (N1497H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279976	NM_015030.2(FRYL):c.4426G>A (p.Val1476Ile)	FRYL (V1476I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214590	NM_015030.2(FRYL):c.4397G>A (p.Arg1466His)	FRYL (R1466H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290717	NM_015030.2(FRYL):c.4318G>C (p.Glu1440Gln)	FRYL (E1440Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097092	NM_015030.2(FRYL):c.4306A>G (p.Met1436Val)	FRYL (M1436V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470574	NM_015030.2(FRYL):c.4255C>T (p.Leu1419Phe)	FRYL (L1419F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097091	NM_015030.2(FRYL):c.4235G>A (p.Gly1412Glu)	FRYL (G1412E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097090	NM_015030.2(FRYL):c.4153G>T (p.Val1385Leu)	FRYL (V1385L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228591	NM_015030.2(FRYL):c.4148C>T (p.Ser1383Leu)	FRYL (S1383L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549075	NM_015030.2(FRYL):c.4094T>C (p.Val1365Ala)	FRYL (V1365A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278558	NM_015030.2(FRYL):c.3988C>T (p.His1330Tyr)	FRYL (H1330Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279984	NM_015030.2(FRYL):c.3959A>G (p.Asp1320Gly)	FRYL (D1320G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290812	NM_015030.2(FRYL):c.3700C>G (p.Leu1234Val)	FRYL (L1234V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097089	NM_015030.2(FRYL):c.3621G>A (p.Met1207Ile)	FRYL (M1207I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279983	NM_015030.2(FRYL):c.3101C>G (p.Ser1034Cys)	FRYL (S1034C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318437	NM_015030.2(FRYL):c.2855T>C (p.Ile952Thr)	FRYL (I952T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097087	NM_015030.2(FRYL):c.2794A>G (p.Ile932Val)	FRYL (I932V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535944	NM_015030.2(FRYL):c.2752T>G (p.Phe918Val)	FRYL (F918V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601180	NM_015030.2(FRYL):c.2705A>G (p.Tyr902Cys)	FRYL (Y902C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097086	NM_015030.2(FRYL):c.2701G>A (p.Gly901Ser)	FRYL (G901S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333074	NM_015030.2(FRYL):c.2698A>G (p.Ser900Gly)	FRYL (S900G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269014	NM_015030.2(FRYL):c.2684C>T (p.Ala895Val)	FRYL (A895V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359012	NM_015030.2(FRYL):c.2678C>T (p.Thr893Met)	FRYL (T893M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265066	NM_015030.2(FRYL):c.2669C>T (p.Pro890Leu)	FRYL (P890L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403512	NM_015030.2(FRYL):c.2665T>G (p.Ser889Ala)	FRYL (S889A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492846	NM_015030.2(FRYL):c.2471A>G (p.Tyr824Cys)	FRYL (Y824C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097084	NM_015030.2(FRYL):c.2285C>T (p.Ser762Leu)	FRYL (S762L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508734	NM_015030.2(FRYL):c.2229G>T (p.Glu743Asp)	FRYL (E743D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209889	NM_015030.2(FRYL):c.2221A>G (p.Ile741Val)	FRYL (I741V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097083	NM_015030.2(FRYL):c.2141G>A (p.Arg714Gln)	FRYL (R714Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346660	NM_015030.2(FRYL):c.2096G>A (p.Arg699Gln)	FRYL (R699Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607019	NM_015030.2(FRYL):c.2042C>G (p.Ser681Cys)	FRYL (S681C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2692419	NM_015030.2(FRYL):c.1987-1G>A	FRYL	Single nucleotide variant (splice acceptor variant)	not specified +1 more	GUncertain significance
Select item 3097082	NM_015030.2(FRYL):c.1935A>G (p.Ile645Met)	FRYL (I645M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279985	NM_015030.2(FRYL):c.1879A>T (p.Thr627Ser)	FRYL (T627S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464399	NM_015030.2(FRYL):c.1870C>T (p.Arg624Cys)	FRYL (R624C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259286	NM_015030.2(FRYL):c.1832G>A (p.Arg611Gln)	FRYL (R611Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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