FOXN2[gene] and "single gene"[properties] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3096514	NM_002158.4(FOXN2):c.28G>C (p.Asp10His)	FOXN2 (D10H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096518	NM_002158.4(FOXN2):c.61A>T (p.Ile21Phe)	FOXN2 (I21F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279631	NM_002158.4(FOXN2):c.65C>T (p.Ala22Val)	FOXN2 (A22V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211543	NM_002158.4(FOXN2):c.125C>G (p.Pro42Arg)	FOXN2 (P42R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096513	NM_002158.4(FOXN2):c.241A>G (p.Ile81Val)	FOXN2 (I81V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533283	NM_002158.4(FOXN2):c.247A>C (p.Ser83Arg)	FOXN2 (S83R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308498	NM_002158.4(FOXN2):c.254T>G (p.Leu85Trp)	FOXN2 (L85W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617740	NM_002158.4(FOXN2):c.359T>C (p.Leu120Pro)	FOXN2 (L120P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096516	NM_002158.4(FOXN2):c.388A>G (p.Asn130Asp)	FOXN2 (N130D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 770869	NM_002158.4(FOXN2):c.522A>G (p.Glu174=)	FOXN2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3096517	NM_002158.4(FOXN2):c.542A>C (p.Asn181Thr)	FOXN2 (N181T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2259523	NM_002158.4(FOXN2):c.572C>T (p.Pro191Leu)	FOXN2 (P191L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213997	NM_002158.4(FOXN2):c.587A>G (p.Asn196Ser)	FOXN2 (N196S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096519	NM_002158.4(FOXN2):c.686A>G (p.Gln229Arg)	FOXN2 (Q229R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510454	NM_002158.4(FOXN2):c.692G>A (p.Arg231Gln)	FOXN2 (R231Q)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3096520	NM_002158.4(FOXN2):c.732G>C (p.Met244Ile)	FOXN2 (M244I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2241527	NM_002158.4(FOXN2):c.735G>A (p.Met245Ile)	FOXN2 (M245I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2485441	NM_002158.4(FOXN2):c.748T>A (p.Ser250Thr)	FOXN2 (S250T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2614607	NM_002158.4(FOXN2):c.799G>A (p.Ala267Thr)	FOXN2 (A267T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2462533	NM_002158.4(FOXN2):c.803T>C (p.Leu268Ser)	FOXN2 (L268S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2613157	NM_002158.4(FOXN2):c.836A>G (p.His279Arg)	FOXN2 (H279R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2368708	NM_002158.4(FOXN2):c.857T>C (p.Leu286Ser)	FOXN2 (L286S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2525564	NM_002158.4(FOXN2):c.890A>G (p.Asp297Gly)	FOXN2 (D297G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 786762	NM_002158.4(FOXN2):c.945A>T (p.Ala315=)	FOXN2	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2325279	NM_002158.4(FOXN2):c.967C>G (p.Leu323Val)	FOXN2 (L323V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3096510	NM_002158.4(FOXN2):c.1001C>G (p.Pro334Arg)	FOXN2 (P334R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2620965	NM_002158.4(FOXN2):c.1015G>A (p.Val339Met)	FOXN2 (V339M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3279629	NM_002158.4(FOXN2):c.1093A>G (p.Ser365Gly)	FOXN2 (S365G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3096512	NM_002158.4(FOXN2):c.1109A>T (p.Gln370Leu)	FOXN2 (Q370L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3279630	NM_002158.4(FOXN2):c.1193A>G (p.Lys398Arg)	FOXN2 (K398R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2243498	NM_002158.4(FOXN2):c.1231C>T (p.Arg411Cys)	FOXN2 (R411C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2411581	NM_002158.4(FOXN2):c.1286G>A (p.Arg429Gln)	FOXN2 (R429Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 979344	GRCh37/hg19 2p16.3(chr2:48509668-48619172)x1	FOXN2	Copy number loss	not provided	GUncertain significance

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Items: 33