IGFL2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2603539	NM_001135113.2(IGFL2):c.55T>A (p.Cys19Ser)	IGFL2 (C19S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232795	NM_001135113.2(IGFL2):c.61A>G (p.Arg21Gly)	IGFL2 (R21G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508223	NM_001135113.2(IGFL2):c.80C>T (p.Ala27Val)	IGFL2 (A38V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3285547	NM_001135113.2(IGFL2):c.83G>A (p.Gly28Asp)	IGFL2 (G28D +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3285546	NM_001135113.2(IGFL2):c.161A>G (p.Asn54Ser)	IGFL2 (N54S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604844	NM_001135113.2(IGFL2):c.166G>A (p.Ala56Thr)	IGFL2 (A67T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213762	NM_001135113.2(IGFL2):c.223T>C (p.Cys75Arg)	IGFL2 (C75R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108640	NM_001135113.2(IGFL2):c.266A>G (p.Asp89Gly)	IGFL2 (D100G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108641	NM_001135113.2(IGFL2):c.350G>A (p.Arg117His)	IGFL2 (R128H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance