"Ambry Genetics"[submitter] AND "FN3KRP"[gene] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2603593	NM_024619.4(FN3KRP):c.17G>A (p.Arg6Lys)	FN3KRP (R6K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3095970	NM_024619.4(FN3KRP):c.23A>G (p.Glu8Gly)	FN3KRP (E8G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523574	NM_024619.4(FN3KRP):c.28G>C (p.Gly10Arg)	FN3KRP, LOC130062059 (G10R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398771	NM_024619.4(FN3KRP):c.49A>T (p.Thr17Ser)	FN3KRP, LOC130062059 (T17S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095973	NM_024619.4(FN3KRP):c.61G>C (p.Gly21Arg)	FN3KRP, LOC130062059 (G21R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225145	NM_024619.4(FN3KRP):c.77G>A (p.Ser26Asn)	FN3KRP, LOC130062059 (S26N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244001	NM_024619.4(FN3KRP):c.79C>G (p.Gln27Glu)	FN3KRP, LOC130062059 (Q27E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236414	NM_024619.4(FN3KRP):c.94G>C (p.Asp32His)	FN3KRP, LOC130062059 (D32H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620831	NM_024619.4(FN3KRP):c.101A>G (p.Asp34Gly)	FN3KRP, LOC130062059 (D34G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279382	NM_024619.4(FN3KRP):c.106G>A (p.Gly36Arg)	FN3KRP, LOC130062059 (G36R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279381	NM_024619.4(FN3KRP):c.109C>G (p.Arg37Gly)	FN3KRP (R37G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095968	NM_024619.4(FN3KRP):c.179C>T (p.Thr60Ile)	FN3KRP (T60I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621050	NM_024619.4(FN3KRP):c.304A>C (p.Lys102Gln)	FN3KRP (K102Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279384	NM_024619.4(FN3KRP):c.322G>C (p.Ala108Pro)	FN3KRP (A108P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2253591	NM_024619.4(FN3KRP):c.361C>T (p.Arg121Cys)	FN3KRP (R121C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381074	NM_024619.4(FN3KRP):c.409C>T (p.Arg137Trp)	FN3KRP (R137W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352468	NM_024619.4(FN3KRP):c.410G>A (p.Arg137Gln)	FN3KRP (R137Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350505	NM_024619.4(FN3KRP):c.429T>G (p.Phe143Leu)	FN3KRP (F143L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250457	NM_024619.4(FN3KRP):c.458A>G (p.Tyr153Cys)	FN3KRP (Y153C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279385	NM_024619.4(FN3KRP):c.464C>T (p.Pro155Leu)	FN3KRP (P155L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347805	NM_024619.4(FN3KRP):c.467A>G (p.Gln156Arg)	FN3KRP (Q156R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279386	NM_024619.4(FN3KRP):c.473A>G (p.Asn158Ser)	FN3KRP (N158S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095972	NM_024619.4(FN3KRP):c.509G>A (p.Arg170Gln)	FN3KRP (R170Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2354084	NM_024619.4(FN3KRP):c.559A>G (p.Arg187Gly)	FN3KRP (R187G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536739	NM_024619.4(FN3KRP):c.580T>C (p.Ser194Pro)	FN3KRP (S194P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349824	NM_024619.4(FN3KRP):c.689C>T (p.Pro230Leu)	FN3KRP (P230L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240362	NM_024619.4(FN3KRP):c.696T>G (p.Ile232Met)	FN3KRP (I232M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618173	NM_024619.4(FN3KRP):c.710C>A (p.Ser237Tyr)	FN3KRP (S237Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521580	NM_024619.4(FN3KRP):c.718G>A (p.Gly240Ser)	FN3KRP (G240S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598896	NM_024619.4(FN3KRP):c.725C>T (p.Ser242Leu)	FN3KRP (S242L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556071	NM_024619.4(FN3KRP):c.751A>G (p.Met251Val)	FN3KRP (M251V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614208	NM_024619.4(FN3KRP):c.764T>C (p.Phe255Ser)	FN3KRP (F255S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345354	NM_024619.4(FN3KRP):c.784G>A (p.Ala262Thr)	FN3KRP (A262T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095974	NM_024619.4(FN3KRP):c.811C>A (p.Pro271Thr)	FN3KRP (P271T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240241	NM_024619.4(FN3KRP):c.826C>T (p.Arg276Cys)	FN3KRP (R276C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095975	NM_024619.4(FN3KRP):c.827G>A (p.Arg276His)	FN3KRP (R276H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239451	NM_024619.4(FN3KRP):c.854A>G (p.Tyr285Cys)	FN3KRP (Y285C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095976	NM_024619.4(FN3KRP):c.869A>C (p.Asn290Thr)	FN3KRP (N290T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279383	NM_024619.4(FN3KRP):c.881C>T (p.Ser294Leu)	FN3KRP (S294L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095977	NM_024619.4(FN3KRP):c.895T>A (p.Ser299Thr)	FN3KRP (S299T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 40