LCN8[gene] and "single gene"[properties] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290302	NM_178469.4(LCN8):c.398G>A (p.Gly133Asp)	LCN8 (G133D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459420	NM_178469.4(LCN8):c.377G>A (p.Arg126Gln)	LCN8 (R126Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250378	NM_178469.4(LCN8):c.356G>A (p.Arg119Gln)	LCN8 (R119Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2508742	NM_178469.4(LCN8):c.355C>T (p.Arg119Trp)	LCN8 (R119W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508497	NM_178469.4(LCN8):c.299G>A (p.Arg100Gln)	LCN8 (R123Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2411885	NM_178469.4(LCN8):c.283G>A (p.Val95Met)	LCN8 (V118M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456039	NM_178469.4(LCN8):c.281G>A (p.Arg94Gln)	LCN8 (R94Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118135	NM_178469.4(LCN8):c.262G>C (p.Glu88Gln)	LCN8 (E88Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279698	NM_178469.4(LCN8):c.237G>C (p.Glu79Asp)	LCN8 (E102D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538052	NM_178469.4(LCN8):c.171G>T (p.Glu57Asp)	LCN8 (E80D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118134	NM_178469.4(LCN8):c.165C>G (p.Ser55Arg)	LCN8 (S55R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224848	NM_178469.4(LCN8):c.161G>A (p.Gly54Glu)	LCN8 (G77E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288986	NM_178469.4(LCN8):c.148T>A (p.Tyr50Asn)	LCN8 (Y50N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356020	NM_178469.4(LCN8):c.136G>A (p.Val46Met)	LCN8 (V69M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224454	NM_178469.4(LCN8):c.121G>A (p.Gly41Arg)	LCN8 (G41R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118132	NM_178469.4(LCN8):c.104T>C (p.Leu35Ser)	LCN8 (L58S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118136	NM_178469.4(LCN8):c.86C>T (p.Pro29Leu)	LCN8 (P29L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290301	NM_178469.4(LCN8):c.50G>A (p.Gly17Asp)	LCN8 (G17D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290304	NM_178469.4(LCN8):c.35T>C (p.Phe12Ser)	LCN8 (F12S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290303	NM_178469.4(LCN8):c.17G>T (p.Arg6Leu)	LCN8 (R6L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2362175	NM_178469.4(LCN8):c.17G>A (p.Arg6Gln)	LCN8 (R6Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 21