FREM3[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3096854	NM_001168235.2(FREM3):c.6323C>T (p.Pro2108Leu)	FREM3 (P2108L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310090	NM_001168235.2(FREM3):c.6258C>G (p.Ile2086Met)	FREM3 (I2086M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519045	NM_001168235.2(FREM3):c.6239A>G (p.Gln2080Arg)	FREM3 (Q2080R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096853	NM_001168235.2(FREM3):c.6233G>T (p.Arg2078Leu)	FREM3 (R2078L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2564113	NM_001168235.2(FREM3):c.6233G>A (p.Arg2078His)	FREM3 (R2078H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2376316	NM_001168235.2(FREM3):c.6157T>G (p.Ser2053Ala)	FREM3 (S2053A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593546	NM_001168235.2(FREM3):c.6146G>A (p.Arg2049His)	FREM3 (R2049H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 780493	NM_001168235.2(FREM3):c.6142G>A (p.Val2048Met)	FREM3 (V2048M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2570297	NM_001168235.2(FREM3):c.6139G>A (p.Ala2047Thr)	FREM3 (A2047T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3096852	NM_001168235.2(FREM3):c.6080G>A (p.Arg2027His)	FREM3 (R2027H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096851	NM_001168235.2(FREM3):c.6019C>T (p.Arg2007Cys)	FREM3 (R2007C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655103	NM_001168235.2(FREM3):c.5994C>T (p.Thr1998=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2509538	NM_001168235.2(FREM3):c.5987T>A (p.Phe1996Tyr)	FREM3 (F1996Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096850	NM_001168235.2(FREM3):c.5923G>A (p.Glu1975Lys)	FREM3 (E1975K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096849	NM_001168235.2(FREM3):c.5873A>G (p.Asn1958Ser)	FREM3 (N1958S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568400	NM_001168235.2(FREM3):c.5800T>G (p.Ser1934Ala)	FREM3 (S1934A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548771	NM_001168235.2(FREM3):c.5773C>T (p.Arg1925Cys)	FREM3 (R1925C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 285891	NM_001168235.2(FREM3):c.5728C>T (p.Arg1910Ter)	FREM3 (R1910*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 3096848	NM_001168235.2(FREM3):c.5525G>T (p.Arg1842Met)	FREM3 (R1842M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358853	NM_001168235.2(FREM3):c.5492A>G (p.Gln1831Arg)	FREM3 (Q1831R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614721	NM_001168235.2(FREM3):c.5401C>T (p.Leu1801Phe)	FREM3 (L1801F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462813	NM_001168235.2(FREM3):c.5242A>G (p.Lys1748Glu)	FREM3 (K1748E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378830	NM_001168235.2(FREM3):c.5171G>A (p.Arg1724Gln)	FREM3 (R1724Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539044	NM_001168235.2(FREM3):c.5125G>C (p.Glu1709Gln)	FREM3 (E1709Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096847	NM_001168235.2(FREM3):c.5090A>C (p.His1697Pro)	FREM3 (H1697P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472322	NM_001168235.2(FREM3):c.5080G>C (p.Asp1694His)	FREM3 (D1694H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391106	NM_001168235.2(FREM3):c.5074G>C (p.Asp1692His)	FREM3 (D1692H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614608	NM_001168235.2(FREM3):c.4964T>C (p.Leu1655Ser)	FREM3 (L1655S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299413	NM_001168235.2(FREM3):c.4837A>T (p.Ser1613Cys)	FREM3 (S1613C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487602	NM_001168235.2(FREM3):c.4834G>A (p.Gly1612Ser)	FREM3 (G1612S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377457	NM_001168235.2(FREM3):c.4801C>G (p.Leu1601Val)	FREM3 (L1601V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096846	NM_001168235.2(FREM3):c.4772G>A (p.Arg1591His)	FREM3 (R1591H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2389045	NM_001168235.2(FREM3):c.4618T>A (p.Leu1540Met)	FREM3 (L1540M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619874	NM_001168235.2(FREM3):c.4582A>T (p.Ile1528Phe)	FREM3 (I1528F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348214	NM_001168235.2(FREM3):c.4552G>A (p.Glu1518Lys)	FREM3 (E1518K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231989	NM_001168235.2(FREM3):c.4549G>A (p.Gly1517Ser)	FREM3 (G1517S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2512031	NM_001168235.2(FREM3):c.4510G>A (p.Asp1504Asn)	FREM3 (D1504N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210032	NM_001168235.2(FREM3):c.4416C>G (p.His1472Gln)	FREM3 (H1472Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616998	NM_001168235.2(FREM3):c.4414C>T (p.His1472Tyr)	FREM3 (H1472Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300897	NM_001168235.2(FREM3):c.4406G>A (p.Ser1469Asn)	FREM3 (S1469N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221399	NM_001168235.2(FREM3):c.4399G>A (p.Ala1467Thr)	FREM3 (A1467T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247914	NM_001168235.2(FREM3):c.4298G>T (p.Arg1433Met)	FREM3 (R1433M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290551	NM_001168235.2(FREM3):c.4258G>A (p.Gly1420Ser)	FREM3 (G1420S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369857	NM_001168235.2(FREM3):c.4256T>C (p.Ile1419Thr)	FREM3 (I1419T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321220	NM_001168235.2(FREM3):c.4180G>A (p.Gly1394Arg)	FREM3 (G1394R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096845	NM_001168235.2(FREM3):c.4165C>G (p.His1389Asp)	FREM3 (H1389D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096844	NM_001168235.2(FREM3):c.4027A>C (p.Ser1343Arg)	FREM3 (S1343R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1239413	NM_001168235.2(FREM3):c.3987C>A (p.Ile1329=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2594734	NM_001168235.2(FREM3):c.3946A>C (p.Lys1316Gln)	FREM3 (K1316Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360652	NM_001168235.2(FREM3):c.3920C>T (p.Pro1307Leu)	FREM3 (P1307L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347657	NM_001168235.2(FREM3):c.3814G>T (p.Asp1272Tyr)	FREM3 (D1272Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461740	NM_001168235.2(FREM3):c.3805G>A (p.Glu1269Lys)	FREM3 (E1269K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374743	NM_001168235.2(FREM3):c.3785A>G (p.Glu1262Gly)	FREM3 (E1262G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366789	NM_001168235.2(FREM3):c.3761G>C (p.Ser1254Thr)	FREM3 (S1254T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258463	NM_001168235.2(FREM3):c.3759C>A (p.His1253Gln)	FREM3 (H1253Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594733	NM_001168235.2(FREM3):c.3757C>G (p.His1253Asp)	FREM3 (H1253D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096842	NM_001168235.2(FREM3):c.3676A>G (p.Asn1226Asp)	FREM3 (N1226D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340485	NM_001168235.2(FREM3):c.3632T>C (p.Ile1211Thr)	FREM3 (I1211T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379973	NM_001168235.2(FREM3):c.3621G>A (p.Met1207Ile)	FREM3 (M1207I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210367	NM_001168235.2(FREM3):c.3607G>T (p.Val1203Leu)	FREM3 (V1203L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2564037	NM_001168235.2(FREM3):c.3605A>G (p.Lys1202Arg)	FREM3 (K1202R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554603	NM_001168235.2(FREM3):c.3589T>G (p.Phe1197Val)	FREM3 (F1197V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489319	NM_001168235.2(FREM3):c.3457C>G (p.Gln1153Glu)	FREM3 (Q1153E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096841	NM_001168235.2(FREM3):c.3302A>G (p.His1101Arg)	FREM3 (H1101R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538390	NM_001168235.2(FREM3):c.3221T>C (p.Val1074Ala)	FREM3 (V1074A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592520	NM_001168235.2(FREM3):c.3107G>T (p.Ser1036Ile)	FREM3 (S1036I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293119	NM_001168235.2(FREM3):c.3099T>A (p.Asp1033Glu)	FREM3 (D1033E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370072	NM_001168235.2(FREM3):c.3097G>A (p.Asp1033Asn)	FREM3 (D1033N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343029	NM_001168235.2(FREM3):c.3047G>T (p.Arg1016Ile)	FREM3 (R1016I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318051	NM_001168235.2(FREM3):c.2912T>C (p.Val971Ala)	FREM3 (V971A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557627	NM_001168235.2(FREM3):c.2875G>A (p.Val959Ile)	FREM3 (V959I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205428	NM_001168235.2(FREM3):c.2870T>C (p.Ile957Thr)	FREM3 (I957T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096839	NM_001168235.2(FREM3):c.2867C>T (p.Ser956Phe)	FREM3 (S956F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655104	NM_001168235.2(FREM3):c.2847T>C (p.Ser949=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2527840	NM_001168235.2(FREM3):c.2824A>T (p.Ser942Cys)	FREM3 (S942C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096838	NM_001168235.2(FREM3):c.2819A>C (p.Asn940Thr)	FREM3 (N940T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267723	NM_001168235.2(FREM3):c.2771A>G (p.His924Arg)	FREM3 (H924R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096837	NM_001168235.2(FREM3):c.2698G>A (p.Val900Ile)	FREM3 (V900I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512882	NM_001168235.2(FREM3):c.2692G>A (p.Gly898Arg)	FREM3 (G898R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521280	NM_001168235.2(FREM3):c.2676A>T (p.Gln892His)	FREM3 (Q892H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281030	NM_001168235.2(FREM3):c.2489C>T (p.Pro830Leu)	FREM3 (P830L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096835	NM_001168235.2(FREM3):c.2455A>T (p.Thr819Ser)	FREM3 (T819S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551636	NM_001168235.2(FREM3):c.2440G>A (p.Val814Met)	FREM3 (V814M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096834	NM_001168235.2(FREM3):c.2395G>A (p.Val799Ile)	FREM3 (V799I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096833	NM_001168235.2(FREM3):c.2381G>A (p.Gly794Asp)	FREM3 (G794D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264054	NM_001168235.2(FREM3):c.2352A>C (p.Lys784Asn)	FREM3 (K784N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536287	NM_001168235.2(FREM3):c.2287G>A (p.Val763Met)	FREM3 (V763M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527015	NM_001168235.2(FREM3):c.2287G>C (p.Val763Leu)	FREM3 (V763L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238264	NM_001168235.2(FREM3):c.2243C>T (p.Pro748Leu)	FREM3 (P748L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096832	NM_001168235.2(FREM3):c.2156A>T (p.Gln719Leu)	FREM3 (Q719L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275424	NM_001168235.2(FREM3):c.2107C>T (p.Pro703Ser)	FREM3 (P703S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655105	NM_001168235.2(FREM3):c.2067C>T (p.His689=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3096831	NM_001168235.2(FREM3):c.2006T>C (p.Met669Thr)	FREM3 (M669T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544467	NM_001168235.2(FREM3):c.1993C>A (p.Pro665Thr)	FREM3 (P665T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1268668	NM_001168235.2(FREM3):c.1908G>A (p.Gly636=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2569949	NM_001168235.2(FREM3):c.1835A>C (p.Asp612Ala)	FREM3 (D612A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096829	NM_001168235.2(FREM3):c.1832G>A (p.Gly611Glu)	FREM3 (G611E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277854	NM_001168235.2(FREM3):c.1759C>A (p.Pro587Thr)	FREM3 (P587T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655106	NM_001168235.2(FREM3):c.1695T>C (p.Phe565=)	FREM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3096828	NM_001168235.2(FREM3):c.1690C>T (p.Pro564Ser)	FREM3 (P564S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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