"Fulgent Genetics, Fulgent Genetics"[submitter] AND "FN1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1368582	NM_212482.4(FN1):c.7402G>A (p.Val2468Ile)	ATIC, FN1 (V2321I +16 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GUncertain significance
Select item 1587702	NM_212482.4(FN1):c.7363-20del	ATIC, FN1	Deletion (intron variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GBenign/Likely benign
Select item 1035792	NM_212482.4(FN1):c.7310C>T (p.Thr2437Ile)	ATIC, FN1 (T2136I +16 more)	Single nucleotide variant (missense variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GUncertain significance
Select item 1484159	NM_212482.4(FN1):c.7160ATG[2] (p.Asp2389del)	ATIC, FN1 (D2088del +16 more)	Microsatellite (inframe_deletion)	not provided +2 more	GUncertain significance
Select item 1555984	NM_212482.4(FN1):c.7116C>T (p.Asn2372=)	ATIC, FN1	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1487177	NM_212482.4(FN1):c.7069C>T (p.Arg2357Cys)	ATIC, FN1 (R2056C +16 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +3 more	GUncertain significance
Select item 1165708	NM_212482.4(FN1):c.6923T>C (p.Val2308Ala)	ATIC, FN1 (V2007A +16 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GBenign/Likely benign
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 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 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 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 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 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 1590368	NM_212482.4(FN1):c.6158-7C>T	FN1	Single nucleotide variant (intron variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GLikely benign
Select item 1374587	NM_212482.4(FN1):c.6157+4T>C	FN1	Single nucleotide variant (intron variant)	not provided +2 more	GUncertain significance
Select item 1041916	NM_212482.4(FN1):c.6121C>T (p.Arg2041Trp)	FN1 (R1860W +3 more)	Single nucleotide variant (missense variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GUncertain significance
Select item 1552592	NM_212482.4(FN1):c.6066C>T (p.Thr2022=)	FN1	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1509406	NM_212482.4(FN1):c.6052C>T (p.Arg2018Cys)	FN1 (R1837C +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1392753	NM_212482.4(FN1):c.6002G>A (p.Arg2001His)	FN1, LOC126806496 (R1820H +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1055248	NM_212482.4(FN1):c.5983G>A (p.Asp1995Asn)	FN1, LOC126806496 (D1814N +3 more)	Single nucleotide variant (missense variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GConflicting classifications of pathogenicity
Select item 1594663	NM_212482.4(FN1):c.5977+7A>G	FN1, LOC126806496	Single nucleotide variant (intron variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GLikely benign
Select item 1166950	NM_212482.4(FN1):c.5964C>T (p.Ile1988=)	FN1, LOC126806496	Single nucleotide variant (synonymous variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GBenign/Likely benign
Select item 1582669	NM_212482.4(FN1):c.5943T>C (p.Ala1981=)	FN1, LOC126806496	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1504652	NM_212482.4(FN1):c.5903C>G (p.Thr1968Ser)	FN1, LOC126806496 (T1877S +3 more)	Single nucleotide variant (missense variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GUncertain significance
Select item 1302813	NM_212482.4(FN1):c.5761A>T (p.Ile1921Phe)	FN1 (I1740F +3 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GBenign/Likely benign
Select item 1004186	NM_212482.4(FN1):c.5741C>A (p.Thr1914Lys)	FN1 (T1733K +3 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 1007901	NM_212482.4(FN1):c.5735G>A (p.Arg1912His)	FN1 (R1731H +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1493939	NM_212482.4(FN1):c.5659A>G (p.Lys1887Glu)	FN1 (K1796E +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1598621	NM_212482.4(FN1):c.5623-13C>G	FN1	Single nucleotide variant (intron variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GBenign/Likely benign
Select item 1063626	NM_212482.4(FN1):c.5608G>T (p.Val1870Leu)	FN1 (V1689L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 1051358	NM_212482.4(FN1):c.5602G>A (p.Val1868Met)	FN1 (V1687M +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 725308	NM_212482.4(FN1):c.5532A>C (p.Arg1844=)	FN1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1614324	NM_212482.4(FN1):c.5511T>C (p.Asn1837=)	FN1	Single nucleotide variant (synonymous variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GLikely benign
Select item 1404305	NM_212482.4(FN1):c.5482A>G (p.Ser1828Gly)	FN1 (S1647G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 1367879	NM_212482.4(FN1):c.5369_5370del (p.Thr1790fs)	FN1 (T1699fs +1 more)	Microsatellite (frameshift variant +1 more)	Glomerulopathy with fibronectin deposits 2 +2 more	GUncertain significance
Select item 1646003	NM_212482.4(FN1):c.5164+14G>T	FN1	Single nucleotide variant (intron variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GBenign/Likely benign
Select item 1408898	NM_212482.4(FN1):c.5164+3A>G	FN1	Single nucleotide variant (intron variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GUncertain significance
Select item 1534344	NM_212482.4(FN1):c.5051-9C>A	FN1	Single nucleotide variant (intron variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1470533	NM_212482.4(FN1):c.4879A>G (p.Ile1627Val)	FN1 (I1536V +1 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GUncertain significance
Select item 1365477	NM_212482.4(FN1):c.4858G>A (p.Ala1620Thr)	FN1 (A1529T +1 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GUncertain significance
Select item 1359662	NM_212482.4(FN1):c.4801C>T (p.Pro1601Ser)	FN1 (P1601S +1 more)	Single nucleotide variant (missense variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GConflicting classifications of pathogenicity
Select item 775185	NM_212482.4(FN1):c.4791C>T (p.Ser1597=)	FN1	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GBenign/Likely benign
Select item 1149136	NM_212482.4(FN1):c.4719C>T (p.Tyr1573=)	FN1	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1364561	NM_212482.4(FN1):c.4649C>A (p.Ala1550Glu)	FN1 (A1459E +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 752810	NM_212482.4(FN1):c.4626G>A (p.Pro1542=)	FN1	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1450581	NM_212482.4(FN1):c.4586C>G (p.Pro1529Arg)	FN1 (P1438R +1 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +3 more	GUncertain significance
Select item 795049	NM_212482.4(FN1):c.4559T>G (p.Val1520Gly)	FN1 (V1429G +1 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +3 more	GConflicting classifications of pathogenicity
Select item 1406898	NM_212482.4(FN1):c.4558G>A (p.Val1520Ile)	FN1 (V1429I +1 more)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GUncertain significance
Select item 1042834	NM_212482.4(FN1):c.4262C>G (p.Pro1421Arg)	FN1 (P1330R +1 more)	Single nucleotide variant (missense variant)	Spondylometaphyseal dysplasia - Sutcliffe type +3 more	GConflicting classifications of pathogenicity
Select item 1432363	NM_212482.4(FN1):c.4217C>T (p.Ser1406Leu)	FN1, LOC126806497 (S1315L +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1122008	NM_212482.4(FN1):c.4161C>A (p.Thr1387=)	FN1, LOC126806497	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 767851	NM_212482.4(FN1):c.4146A>G (p.Pro1382=)	FN1, LOC126806497	Single nucleotide variant (synonymous variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GBenign/Likely benign
Select item 1562366	NM_212482.4(FN1):c.4143C>T (p.Pro1381=)	FN1, LOC126806497	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1439843	NM_212482.4(FN1):c.3968A>G (p.Tyr1323Cys)	FN1 (Y1323C)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 1010389	NM_212482.4(FN1):c.3959T>C (p.Val1320Ala)	FN1 (V1320A)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 1638177	NM_212482.4(FN1):c.3909T>G (p.Val1303=)	FN1	Single nucleotide variant (synonymous variant +1 more)	Glomerulopathy with fibronectin deposits 2 +2 more	GLikely benign
Select item 1367318	NM_212482.4(FN1):c.3866C>T (p.Pro1289Leu)	FN1 (P1289L)	Single nucleotide variant (missense variant +1 more)	Glomerulopathy with fibronectin deposits 2 +2 more	GUncertain significance
Select item 1093293	NM_212482.4(FN1):c.3492G>A (p.Ala1164=)	FN1	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1369716	NM_212482.4(FN1):c.3415G>A (p.Val1139Ile)	FN1 (V1139I)	Single nucleotide variant (missense variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GUncertain significance
Select item 1049911	NM_212482.4(FN1):c.3289G>A (p.Glu1097Lys)	FN1 (E1097K)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1141083	NM_212482.4(FN1):c.3288C>T (p.Thr1096=)	FN1	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1021256	NM_212482.4(FN1):c.3271A>G (p.Ile1091Val)	FN1 (I1091V)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GUncertain significance
Select item 1436151	NM_212482.4(FN1):c.3199G>A (p.Val1067Met)	FN1 (V1067M)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 787007	NM_212482.4(FN1):c.3189C>T (p.Thr1063=)	FN1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1619606	NM_212482.4(FN1):c.3187A>G (p.Thr1063Ala)	FN1 (T1063A)	Single nucleotide variant (missense variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1499265	NM_212482.4(FN1):c.3149A>C (p.Lys1050Thr)	FN1 (K1050T)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 915850	NM_212482.4(FN1):c.3130G>A (p.Val1044Met)	FN1 (V1044M)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +3 more	GConflicting classifications of pathogenicity
Select item 1051103	NM_212482.4(FN1):c.3061C>T (p.Arg1021Trp)	FN1 (R1021W)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1047503	NM_212482.4(FN1):c.3020A>G (p.Asn1007Ser)	FN1 (N1007S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 732642	NM_212482.4(FN1):c.3012G>A (p.Gln1004=)	FN1	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1562789	NM_212482.4(FN1):c.2967G>C (p.Leu989=)	FN1	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 16325	NM_212482.4(FN1):c.2918A>G (p.Tyr973Cys)	FN1 (Y973C)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +1 more	GPathogenic
Select item 1414102	NM_212482.4(FN1):c.2879C>G (p.Thr960Ser)	FN1 (T960S)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 729122	NM_212482.4(FN1):c.2829C>T (p.Pro943=)	FN1	Single nucleotide variant (synonymous variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GBenign/Likely benign
Select item 1498737	NM_212482.4(FN1):c.2717C>T (p.Thr906Ile)	FN1 (T906I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 1165709	NM_212482.4(FN1):c.2714-11_2714-10del	FN1	Deletion (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1560524	NM_212482.4(FN1):c.2713+20A>G	FN1	Single nucleotide variant (intron variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 738109	NM_212482.4(FN1):c.2538G>A (p.Ser846=)	FN1	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1174898	NM_212482.4(FN1):c.2518+12G>C	FN1	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1010246	NM_212482.4(FN1):c.2429C>T (p.Ala810Val)	FN1 (A810V)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GUncertain significance
Select item 1582337	NM_212482.4(FN1):c.2413A>G (p.Thr805Ala)	FN1 (T805A)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1641876	NM_212482.4(FN1):c.2299+16C>T	FN1	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign
Select item 1010526	NM_212482.4(FN1):c.2299+3A>T	FN1	Single nucleotide variant (intron variant)	not provided +2 more	GUncertain significance
Select item 1470698	NM_212482.4(FN1):c.2150C>G (p.Pro717Arg)	FN1 (P717R)	Single nucleotide variant (missense variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GConflicting classifications of pathogenicity
Select item 735841	NM_212482.4(FN1):c.2130C>T (p.Thr710=)	FN1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1647003	NM_212482.4(FN1):c.1942-38GT[14]	FN1	Microsatellite (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1268952	NM_212482.4(FN1):c.1942-38GT[13]	FN1	Microsatellite (intron variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GBenign/Likely benign
Select item 1252598	NM_212482.4(FN1):c.1942-38GT[12]	FN1	Microsatellite (intron variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GBenign
Select item 1408608	NM_212482.4(FN1):c.1871A>G (p.Asn624Ser)	FN1 (N624S)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 720420	NM_212482.4(FN1):c.1860G>A (p.Pro620=)	FN1	Single nucleotide variant (synonymous variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GLikely benign
Select item 1621270	NM_212482.4(FN1):c.1820-16A>G	FN1	Single nucleotide variant (intron variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GLikely benign
Select item 816643	NM_212482.4(FN1):c.1757A>G (p.Gln586Arg)	FN1 (Q586R)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1634653	NM_212482.4(FN1):c.1676-9G>A	FN1	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 758619	NM_212482.4(FN1):c.1638C>T (p.Phe546=)	FN1, LOC122861289	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 752916	NM_212482.4(FN1):c.1626C>T (p.Asn542=)	FN1, LOC122861289	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 717899	NM_212482.4(FN1):c.1547-6A>G	FN1, LOC122861289	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1474447	NM_212482.4(FN1):c.1544G>A (p.Arg515Gln)	FN1 (R515Q)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1388073	NM_212482.4(FN1):c.1481T>C (p.Met494Thr)	FN1 (M494T)	Single nucleotide variant (missense variant)	Spondylometaphyseal dysplasia - Sutcliffe type +2 more	GUncertain significance
Select item 736976	NM_212482.4(FN1):c.1449G>A (p.Gln483=)	FN1	Single nucleotide variant (synonymous variant)	Glomerulopathy with fibronectin deposits 2 +2 more	GLikely benign

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