"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "HOXB3"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3026547	NM_001384749.1(HOXB3):c.962A>T (p.Tyr321Phe)	HOXB-AS1, HOXB3 (Y189F +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3067467	NM_001384749.1(HOXB3):c.471C>T (p.Gly157=)	HOXB-AS1, HOXB3	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 444852	GRCh37/hg19 17q21.32-22(chr17:46481089-51396368)x1	HOXB3, HOXB4 +67 more	Copy number loss	not provided	GLikely pathogenic

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