"PreventionGenetics, part of Exact Sciences"[submitter] AND "FN1"[gene - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1618073	NM_212482.4(FN1):c.7295G>C (p.Ser2432Thr)	ATIC, FN1 (S2131T +16 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1169960	NM_212482.4(FN1):c.6824G>A (p.Arg2275Gln)	FN1 (R1974Q +16 more)	Single nucleotide variant (missense variant)	FN1-related condition +1 more	GBenign
Select item 2632791	NM_212482.4(FN1):c.6686C>T (p.Pro2229Leu)	FN1 (P1928L +16 more)	Single nucleotide variant (missense variant)	FN1-related condition	GUncertain significance
Select item 2754001	NM_212482.4(FN1):c.6456_6458delinsTTATGCCTAAAGTGGTTTTAG (p.Pro2153delinsTyrAlaTer)	FN1	Indel (nonsense +1 more)	FN1-related condition +1 more	GUncertain significance
Select item 3045898	NM_212482.4(FN1):c.6321A>C (p.Thr2107=)	FN1	Single nucleotide variant (synonymous variant +2 more)	FN1-related condition	GLikely benign
Select item 3058212	NM_212482.4(FN1):c.6282C>T (p.Pro2094=)	FN1	Single nucleotide variant (synonymous variant +1 more)	FN1-related condition	GLikely benign
Select item 2629157	NM_212482.4(FN1):c.6175G>A (p.Glu2059Lys)	FN1 (E1878K +3 more)	Single nucleotide variant (missense variant)	FN1-related condition	GUncertain significance
Select item 1432814	NM_212482.4(FN1):c.6047C>T (p.Pro2016Leu)	FN1 (P1835L +3 more)	Single nucleotide variant (missense variant)	FN1-related condition +1 more	GConflicting classifications of pathogenicity
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 +3 more	GBenign/Likely benign
Select item 725308	NM_212482.4(FN1):c.5532A>C (p.Arg1844=)	FN1	Single nucleotide variant (synonymous variant)	FN1-related condition +3 more	GBenign/Likely benign
Select item 1165768	NM_212482.4(FN1):c.5274G>T (p.Ser1758=)	FN1	Single nucleotide variant (synonymous variant +1 more)	FN1-related condition +1 more	GBenign/Likely benign
Select item 1093172	NM_212482.4(FN1):c.4857C>T (p.Pro1619=)	FN1	Single nucleotide variant (synonymous variant)	FN1-related condition +1 more	GLikely benign
Select item 3010172	NM_212482.4(FN1):c.4826T>G (p.Val1609Gly)	FN1 (V1518G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2636484	NM_212482.4(FN1):c.4452T>A (p.His1484Gln)	FN1 (H1393Q +1 more)	Single nucleotide variant (missense variant)	FN1-related condition	GUncertain significance
Select item 3053409	NM_212482.4(FN1):c.4449T>C (p.His1483=)	FN1	Single nucleotide variant (synonymous variant)	FN1-related condition	GLikely benign
Select item 2632241	NM_212482.4(FN1):c.4448_4449delinsGC (p.His1483Arg)	FN1 (H1392R +1 more)	Indel (missense variant)	FN1-related condition	GUncertain significance
Select item 1541556	NM_212482.4(FN1):c.4257C>T (p.Leu1419=)	FN1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2192750	NM_212482.4(FN1):c.4175G>A (p.Arg1392His)	FN1, LOC126806497 (R1392H +1 more)	Single nucleotide variant (missense variant)	FN1-related condition +2 more	GUncertain significance
Select item 1586373	NM_212482.4(FN1):c.3804C>T (p.Pro1268=)	FN1	Single nucleotide variant (synonymous variant +1 more)	FN1-related condition +1 more	GLikely benign
Select item 2631872	NM_212482.4(FN1):c.3517+1G>A	FN1	Single nucleotide variant (splice donor variant)	FN1-related condition	GUncertain significance
Select item 721246	NM_212482.4(FN1):c.3307A>C (p.Ile1103Leu)	FN1 (I1103L)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2631222	NM_212482.4(FN1):c.3216C>A (p.Asn1072Lys)	FN1 (N1072K)	Single nucleotide variant (missense variant)	FN1-related condition	GUncertain significance
Select item 1111297	NM_212482.4(FN1):c.3141T>C (p.Ser1047=)	FN1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1008946	NM_212482.4(FN1):c.3062G>A (p.Arg1021Gln)	FN1 (R1021Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1674377	NM_212482.4(FN1):c.2805C>T (p.Thr935=)	FN1	Single nucleotide variant (synonymous variant)	FN1-related condition +1 more	GLikely benign
Select item 1165709	NM_212482.4(FN1):c.2714-11_2714-10del	FN1	Deletion (intron variant)	FN1-related condition +3 more	GBenign/Likely benign
Select item 3052927	NM_212482.4(FN1):c.2451G>A (p.Thr817=)	FN1	Single nucleotide variant (synonymous variant)	FN1-related condition	GLikely 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 +3 more	GUncertain significance
Select item 2633753	NM_212482.4(FN1):c.2235C>A (p.Asp745Glu)	FN1 (D745E)	Single nucleotide variant (missense variant)	FN1-related condition	GUncertain significance
Select item 750263	NM_212482.4(FN1):c.2144C>T (p.Thr715Met)	FN1 (T715M)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 720420	NM_212482.4(FN1):c.1860G>A (p.Pro620=)	FN1	Single nucleotide variant (synonymous variant)	Glomerulopathy with fibronectin deposits 2 +3 more	GLikely benign
Select item 1643496	NM_212482.4(FN1):c.1782T>C (p.Ile594=)	FN1	Single nucleotide variant (synonymous variant)	FN1-related condition +1 more	GBenign/Likely benign
Select item 2633624	NM_212482.4(FN1):c.1503T>G (p.Asn501Lys)	FN1 (N501K)	Single nucleotide variant (missense variant)	FN1-related condition	GUncertain significance
Select item 2635605	NM_212482.4(FN1):c.1261C>T (p.His421Tyr)	FN1, LOC126806498 (H421Y)	Single nucleotide variant (missense variant)	FN1-related condition	GUncertain significance
Select item 1600862	NM_212482.4(FN1):c.1002G>A (p.Thr334=)	FN1	Single nucleotide variant (synonymous variant)	Glomerulopathy with fibronectin deposits 2 +3 more	GBenign/Likely benign
Select item 3045451	NM_212482.4(FN1):c.808T>C (p.Cys270Arg)	FN1 (C270R)	Single nucleotide variant (missense variant)	FN1-related condition	GUncertain significance
Select item 1164619	NM_212482.4(FN1):c.807G>A (p.Lys269=)	FN1	Single nucleotide variant (synonymous variant)	FN1-related condition +1 more	GBenign/Likely benign
Select item 729557	NM_212482.4(FN1):c.751A>T (p.Asn251Tyr)	FN1 (N251Y)	Single nucleotide variant (missense variant)	FN1-related condition +1 more	GBenign/Likely benign
Select item 1099792	NM_212482.4(FN1):c.519A>G (p.Gly173=)	FN1	Single nucleotide variant (synonymous variant)	FN1-related condition +1 more	GLikely benign
Select item 1375582	NM_212482.4(FN1):c.352T>G (p.Ser118Ala)	FN1, LOC126806499 (S118A)	Single nucleotide variant (missense variant)	FN1-related condition +1 more	GUncertain significance
Select item 712430	NM_212482.4(FN1):c.202A>T (p.Thr68Ser)	FN1 (T68S)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign

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Items: 41