Related gene-specific medical variations for Gene (Select 408263) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3279434	NM_001001343.4(FNDC9):c.179C>T (p.Ser60Phe)	CYFIP2, FNDC9 (S60F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279433	NM_001001343.4(FNDC9):c.178T>A (p.Ser60Thr)	CYFIP2, FNDC9 (S60T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279432	NM_001001343.4(FNDC9):c.553C>T (p.Arg185Cys)	CYFIP2, FNDC9 (R185C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096118	NM_001001343.4(FNDC9):c.64C>T (p.Pro22Ser)	CYFIP2, FNDC9 (P22S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2655995	NM_001001343.4(FNDC9):c.150C>T (p.His50=)	CYFIP2, FNDC9	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655994	NM_001037333.3(CYFIP2):c.2673+1988A>G	CYFIP2, FNDC9 (I131T)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2604659	NM_001001343.4(FNDC9):c.632G>T (p.Gly211Val)	CYFIP2, FNDC9 (G211V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543399	NM_001001343.4(FNDC9):c.288T>A (p.Asp96Glu)	CYFIP2, FNDC9 (D96E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463686	NM_001001343.4(FNDC9):c.260A>G (p.His87Arg)	FNDC9, CYFIP2 (H87R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398347	NM_001001343.4(FNDC9):c.428C>T (p.Pro143Leu)	CYFIP2, FNDC9 (P143L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395764	NM_001001343.4(FNDC9):c.287A>G (p.Asp96Gly)	CYFIP2, FNDC9 (D96G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381292	NM_001001343.4(FNDC9):c.134G>A (p.Arg45His)	CYFIP2, FNDC9 (R45H)	Single nucleotide variant (intron variant +1 more)	not specified	GUncertain significance
Select item 2366028	NM_001001343.4(FNDC9):c.630G>T (p.Arg210Ser)	CYFIP2, FNDC9 (R210S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353553	NM_001001343.4(FNDC9):c.325C>T (p.Pro109Ser)	CYFIP2, FNDC9 (P109S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336393	NM_001001343.4(FNDC9):c.581T>C (p.Leu194Pro)	CYFIP2, FNDC9 (L194P)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2315183	NM_001001343.4(FNDC9):c.629G>A (p.Arg210Lys)	CYFIP2, FNDC9 (R210K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2268286	NM_001001343.4(FNDC9):c.539T>A (p.Leu180Gln)	CYFIP2, FNDC9 (L180Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1335608	NM_001001343.4(FNDC9):c.576T>G (p.Ala192=)	CYFIP2, FNDC9	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign