FN1[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1237164	NM_212482.4(FN1):c.6853+298C>G	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290476	NM_212482.4(FN1):c.6853+126C>T	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1214080	NM_212482.4(FN1):c.6853+36C>G	FN1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1216796	NM_212482.4(FN1):c.6853+29G>A	FN1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1620001	NM_212482.4(FN1):c.6853+13G>A	FN1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1048808	NM_212482.4(FN1):c.6853+12C>G	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 722284	NM_212482.4(FN1):c.6841G>A (p.Val2281Met)	FN1 (V2075M +16 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 747227	NM_212482.4(FN1):c.6840C>T (p.Thr2280=)	FN1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2322469	NM_212482.4(FN1):c.6839C>A (p.Thr2280Asn)	FN1 (T2068N +16 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2965429	NM_212482.4(FN1):c.6832GTT[1] (p.Val2279del)	FN1 (V2157del +16 more)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 1169960	NM_212482.4(FN1):c.6824G>A (p.Arg2275Gln)	FN1 (R1974Q +16 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1965919	NM_212482.4(FN1):c.6820G>A (p.Val2274Ile)	FN1 (V2068I +16 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1495022	NM_212482.4(FN1):c.6815A>G (p.His2272Arg)	FN1 (H1971R +16 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2748831	NM_212482.4(FN1):c.6811A>T (p.Arg2271Trp)	FN1 (R2149W +16 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1500911	NM_212482.4(FN1):c.6784A>G (p.Ile2262Val)	FN1 (I2050V +16 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2854450	NM_212482.4(FN1):c.6781= (p.Val2261=)	FN1	Variation (no sequence alteration)	not provided	GUncertain significance
Select item 1169961	NM_212482.4(FN1):c.6781G>A (p.Val2261Ile)	FN1 (V1960I +16 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 830028	NM_212482.4(FN1):c.6779_6781del (p.Asn2260_Val2261delinsIle)	FN1	Deletion (inframe_indel)	Glomerulopathy with fibronectin deposits 2	GUncertain significance
Select item 999976	NM_212482.4(FN1):c.6769G>C (p.Ala2257Pro)	FN1 (A1956P +16 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2860313	NM_212482.4(FN1):c.6767G>A (p.Gly2256Asp)	FN1 (G2166D +16 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2096160	NM_212482.4(FN1):c.6767G>T (p.Gly2256Val)	FN1 (G1955V +16 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 977101	NM_212482.4(FN1):c.6746C>A (p.Thr2249Asn)	FN1 (T1948N +16 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2	GUncertain significance
Select item 3351362	NM_212482.4(FN1):c.6721G>A (p.Val2241Ile)	FN1 (V1940I +16 more)	Single nucleotide variant (missense variant)	FN1-related disorder	GUncertain significance
Select item 1988365	NM_212482.4(FN1):c.6715-11G>A	FN1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961835	NM_212482.4(FN1):c.6715-12C>T	FN1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1654203	NM_212482.4(FN1):c.6715-12C>G	FN1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1244623	NM_212482.4(FN1):c.6715-87A>C	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1216276	NM_212482.4(FN1):c.6715-104T>G	FN1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1243192	NM_212482.4(FN1):c.6715-115G>T	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263081	NM_212482.4(FN1):c.6715-122_6715-117del	FN1	Deletion (intron variant)	not provided	GBenign
Select item 1291666	NM_212482.4(FN1):c.6715-122G>T	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273069	NM_212482.4(FN1):c.6715-233T>C	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274637	NM_212482.4(FN1):c.6714+285dup	FN1	Duplication (intron variant)	not provided	GBenign
Select item 1273687	NM_212482.4(FN1):c.6714+298del	FN1	Deletion (intron variant)	not provided	GBenign
Select item 1277934	NM_212482.4(FN1):c.6714+233_6714+235del	FN1	Deletion (intron variant)	not provided	GBenign
Select item 1239744	NM_212482.4(FN1):c.6714+235del	FN1	Deletion (intron variant)	not provided	GBenign
Select item 1182560	NM_212482.4(FN1):c.6714+234_6714+235del	FN1	Deletion (intron variant)	not provided	GBenign
Select item 1222426	NM_212482.4(FN1):c.6714+221A>G	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221313	NM_212482.4(FN1):c.6714+150A>G	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278880	NM_212482.4(FN1):c.6714+100C>T	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1302822	NM_212482.4(FN1):c.6714+31G>A	FN1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1576768	NM_212482.4(FN1):c.6714+7_6714+10del	FN1	Microsatellite (splice donor variant)	not provided	GLikely benign
Select item 2977467	NM_212482.4(FN1):c.6714+9T>C	FN1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2897086	NM_212482.4(FN1):c.6707C>A (p.Pro2236His)	FN1 (P2024H +16 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2632791	NM_212482.4(FN1):c.6686C>T (p.Pro2229Leu)	FN1 (P1928L +16 more)	Single nucleotide variant (missense variant)	FN1-related disorder +1 more	GUncertain significance
Select item 1442785	NM_212482.4(FN1):c.6655G>A (p.Asp2219Asn)	FN1 (D1982N +16 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1638040	NM_212482.4(FN1):c.6639A>G (p.Ser2213=)	FN1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 738031	NM_212482.4(FN1):c.6639A>C (p.Ser2213=)	FN1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1168742	NM_212482.4(FN1):c.6634A>G (p.Ile2212Val)	FN1 (I1911V +16 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GBenign/Likely benign
Select item 2958716	NM_212482.4(FN1):c.6631A>G (p.Thr2211Ala)	FN1 (T2064A +16 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2307717	NM_212482.4(FN1):c.6619C>G (p.Leu2207Val)	FN1 (L1995V +16 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2042885	NM_212482.4(FN1):c.6615A>G (p.Glu2205=)	FN1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2890592	NM_212482.4(FN1):c.6610C>A (p.Gln2204Lys)	FN1 (Q1994K +16 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2806456	NM_212482.4(FN1):c.6604A>G (p.Thr2202Ala)	FN1 (T1996A +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 740646	NM_212482.4(FN1):c.6600C>T (p.Ala2200=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2060373	NM_212482.4(FN1):c.6584G>A (p.Gly2195Glu)	FN1 (G2014E +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1549893	NM_212482.4(FN1):c.6582G>A (p.Pro2194=)	FN1	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 2605782	NM_212482.4(FN1):c.6581C>T (p.Pro2194Leu)	FN1 (P2078L +6 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1916520	NM_212482.4(FN1):c.6577G>A (p.Gly2193Ser)	FN1 (G2078S +6 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1583618	NM_212482.4(FN1):c.6576C>T (p.His2192=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3016852	NM_212482.4(FN1):c.6568T>A (p.Tyr2190Asn)	FN1 (Y2075N +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1499022	NM_212482.4(FN1):c.6566T>C (p.Leu2189Pro)	FN1 (L2073P +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2176356	NM_212482.4(FN1):c.6564C>T (p.His2188=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2918125	NM_212482.4(FN1):c.6563A>T (p.His2188Leu)	FN1 (H2073L +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1951334	NM_212482.4(FN1):c.6558C>T (p.Asp2186=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1695003	NM_212482.4(FN1):c.6547G>T (p.Glu2183Ter)	FN1 (E1977* +6 more)	Single nucleotide variant (nonsense +1 more)	not provided +2 more	GUncertain significance
Select item 2040328	NM_212482.4(FN1):c.6546G>C (p.Arg2182Ser)	FN1 (R2067S +6 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 739930	NM_212482.4(FN1):c.6537C>T (p.His2179=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2980649	NM_212482.4(FN1):c.6511G>C (p.Val2171Leu)	FN1 (V2080L +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1581108	NM_212482.4(FN1):c.6507G>A (p.Pro2169=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GLikely benign
Select item 1025513	NM_212482.4(FN1):c.6506C>T (p.Pro2169Leu)	FN1 (P1963L +6 more)	Single nucleotide variant (missense variant +1 more)	Glomerulopathy with fibronectin deposits 2 +2 more	GConflicting classifications of pathogenicity
Select item 1424412	NM_212482.4(FN1):c.6503C>T (p.Pro2168Leu)	FN1 (P1962L +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2906380	NM_212482.4(FN1):c.6479T>C (p.Ile2160Thr)	FN1 (I1979T +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2887649	NM_212482.4(FN1):c.6468G>A (p.Thr2156=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1480826	NM_212482.4(FN1):c.6467C>T (p.Thr2156Met)	FN1 (T2040M +6 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1990994	NM_212482.4(FN1):c.6466A>G (p.Thr2156Ala)	FN1 (T1950A +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1577428	NM_212482.4(FN1):c.6459G>A (p.Pro2153=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GLikely benign
Select item 2754001	NM_212482.4(FN1):c.6456_6458delinsTTATGCCTAAAGTGGTTTTAG (p.Pro2153delinsTyrAlaTer)	FN1	Indel (nonsense +1 more)	not provided	GUncertain significance
Select item 2419209	NM_212482.4(FN1):c.6458C>T (p.Pro2153Leu)	FN1 (P1947L +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3095960	NM_212482.4(FN1):c.6457C>T (p.Pro2153Ser)	FN1 (P2038S +6 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2072924	NM_212482.4(FN1):c.6448C>T (p.Arg2150Trp)	FN1 (R2035W +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3095959	NM_212482.4(FN1):c.6433G>A (p.Glu2145Lys)	FN1 (E2145K +6 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3022094	NM_212482.4(FN1):c.6432G>A (p.Glu2144=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1481137	NM_212482.4(FN1):c.6431A>G (p.Glu2144Gly)	FN1 (E1938G +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1719573	NM_212482.4(FN1):c.6430G>A (p.Glu2144Lys)	FN1 (E1938K +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2240025	NM_212482.4(FN1):c.6371G>A (p.Gly2124Asp)	FN1 (G2034D +6 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1704374	NM_212482.4(FN1):c.6348C>A (p.His2116Gln)	FN1 (H2000Q +6 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 2711888	NM_212482.4(FN1):c.6346C>T (p.His2116Tyr)	FN1 (H1910Y +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1634972	NM_212482.4(FN1):c.6340G>A (p.Val2114Ile)	FN1 (V1908I +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1600682	NM_212482.4(FN1):c.6336T>C (p.Pro2112=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 3016578	NM_212482.4(FN1):c.6330G>C (p.Lys2110Asn)	FN1 (K1995N +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3045898	NM_212482.4(FN1):c.6321A>C (p.Thr2107=)	FN1	Single nucleotide variant (synonymous variant +2 more)	FN1-related disorder	GLikely benign
Select item 1058724	NM_212482.4(FN1):c.6308A>G (p.Asp2103Gly)	FN1 (D1922G +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1373068	NM_212482.4(FN1):c.6305T>C (p.Leu2102Ser)	FN1 (L2011S +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1403637	NM_212482.4(FN1):c.6284A>G (p.Asn2095Ser)	FN1 (N1914S +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3058212	NM_212482.4(FN1):c.6282C>T (p.Pro2094=)	FN1	Single nucleotide variant (synonymous variant +1 more)	FN1-related disorder	GLikely benign
Select item 1700693	NM_212482.4(FN1):c.6281C>T (p.Pro2094Leu)	FN1 (P1913L +3 more)	Single nucleotide variant (missense variant +1 more)	See cases	GLikely pathogenic
Select item 1019790	NM_212482.4(FN1):c.6280C>G (p.Pro2094Ala)	FN1 (P1913A +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2166348	NM_212482.4(FN1):c.6261A>C (p.Gln2087His)	FN1 (Q2087H +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1561814	NM_212482.4(FN1):c.6261A>G (p.Gln2087=)	FN1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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