"PreventionGenetics, part of Exact Sciences"[submitter] AND "HOXA4"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052573	NM_002141.5(HOXA4):c.559C>G (p.Leu187Val)	HOXA4, HOXA3 (L187V)	Single nucleotide variant (missense variant +1 more)	HOXA4-related condition	GLikely benign
Select item 3053757	NM_002141.5(HOXA4):c.524G>A (p.Cys175Tyr)	HOXA3, HOXA4 (C175Y)	Single nucleotide variant (missense variant +1 more)	HOXA4-related condition	GLikely benign
Select item 3052841	NM_002141.5(HOXA4):c.414C>G (p.Pro138=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	HOXA4-related condition	GLikely benign
Select item 3032651	NM_002141.5(HOXA4):c.285C>T (p.Ala95=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	HOXA4-related condition	GLikely benign
Select item 3034411	NM_002141.5(HOXA4):c.243G>C (p.Glu81Asp)	HOXA3, HOXA4 (E81D)	Single nucleotide variant (missense variant +1 more)	HOXA4-related condition	GLikely benign
Select item 1269767	NM_002141.5(HOXA4):c.208A>C (p.Thr70Pro)	HOXA3, HOXA4 (T70P)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3054235	NM_002141.5(HOXA4):c.162G>A (p.Pro54=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	HOXA4-related condition	GLikely benign

ClinVar