"Ambry Genetics"[submitter] AND "LIAT1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2258275	NM_001013672.5(LIAT1):c.64C>G (p.Pro22Ala)	LIAT1, LOC105371430 +1 more (P22A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366412	NM_001013672.5(LIAT1):c.381G>C (p.Glu127Asp)	LIAT1, LOC105371430 (E127D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2216780	NM_001013672.5(LIAT1):c.381G>T (p.Glu127Asp)	LIAT1, LOC105371430 (E127D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2342489	NM_001013672.5(LIAT1):c.688G>A (p.Glu230Lys)	LIAT1, LOC105371430 (E230K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2351331	NM_001013672.5(LIAT1):c.709C>A (p.Pro237Thr)	LIAT1, LOC105371430 (P237T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358686	NM_001013672.5(LIAT1):c.1240C>T (p.His414Tyr)	LIAT1 (H414Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar