"Ambry Genetics"[submitter] AND "FBXL16"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2532371	NM_153350.4(FBXL16):c.1123G>C (p.Glu375Gln)	FBXL16 (E375Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093494	NM_153350.4(FBXL16):c.1060T>G (p.Ser354Ala)	FBXL16 (S354A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093497	NM_153350.4(FBXL16):c.947T>G (p.Val316Gly)	FBXL16, LOC130058125 (V316G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093496	NM_153350.4(FBXL16):c.725C>T (p.Ala242Val)	FBXL16 (A242V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093495	NM_153350.4(FBXL16):c.374G>A (p.Arg125Gln)	FBXL16 (R125Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484930	NM_153350.4(FBXL16):c.373C>T (p.Arg125Trp)	FBXL16 (R125W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226113	NM_153350.4(FBXL16):c.269C>T (p.Ala90Val)	FBXL16 (A90V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2459091	NM_153350.4(FBXL16):c.241G>C (p.Ala81Pro)	FBXL16 (A81P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254019	NM_153350.4(FBXL16):c.73G>A (p.Gly25Ser)	FBXL16 (G25S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521218	NM_153350.4(FBXL16):c.22G>A (p.Gly8Ser)	FBXL16 (G8S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384998	NM_153350.4(FBXL16):c.19G>A (p.Asp7Asn)	FBXL16 (D7N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance