Related gene-specific medical variations for Gene (Select 10875) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278704	NM_006682.3(FGL2):c.743G>C (p.Gly248Ala)	CCDC146, FGL2 (G248A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278703	NM_006682.3(FGL2):c.379G>T (p.Asp127Tyr)	CCDC146, FGL2 +1 more (D127Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094861	NM_006682.3(FGL2):c.652G>A (p.Ala218Thr)	CCDC146, FGL2 (A218T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3094859	NM_006682.3(FGL2):c.265G>A (p.Val89Ile)	CCDC146, FGL2 (V89I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3065177	NM_006682.3(FGL2):c.614_617del (p.Val205fs)	CCDC146, FGL2 (V205fs)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2560198	NM_006682.3(FGL2):c.292G>C (p.Asp98His)	CCDC146, FGL2 +1 more (D98H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2496411	NM_006682.3(FGL2):c.818C>G (p.Ala273Gly)	CCDC146, FGL2 (A273G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376089	NM_006682.3(FGL2):c.610C>G (p.Pro204Ala)	CCDC146, FGL2 (P204A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317833	NM_006682.3(FGL2):c.595C>G (p.Gln199Glu)	CCDC146, FGL2 (Q199E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314661	NM_006682.3(FGL2):c.1090G>T (p.Asp364Tyr)	CCDC146, FGL2 (D364Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244867	NM_006682.3(FGL2):c.517G>T (p.Val173Phe)	CCDC146, FGL2 (V173F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance