"Ambry Genetics"[submitter] AND "LXN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2304393	NM_020169.4(LXN):c.560T>C (p.Ile187Thr)	GFM1, LXN (I187T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237417	NM_020169.4(LXN):c.391C>G (p.Pro131Ala)	GFM1, LXN (P131A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3292345	NM_020169.4(LXN):c.322C>G (p.Gln108Glu)	GFM1, LXN (Q108E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3292342	NM_020169.4(LXN):c.208T>C (p.Cys70Arg)	GFM1, LXN (C70R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463612	NM_020169.4(LXN):c.80C>T (p.Thr27Ile)	GFM1, LXN (T27I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3292344	NM_020169.4(LXN):c.65A>G (p.Asn22Ser)	GFM1, LXN (N22S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324480	NM_020169.4(LXN):c.52C>G (p.Gln18Glu)	GFM1, LXN (Q18E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

ClinVar