C1970250[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 128038	NM_006361.6(HOXB13):c.832G>T (p.Val278Leu)	HOXB13 (V278L)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 826027	NM_006361.6(HOXB13):c.587del (p.Lys196fs)	HOXB13 (K196fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 9 +2 more	GUncertain significance
Select item 690843	NM_006361.6(HOXB13):c.543G>T (p.Gln181His)	HOXB13 (Q181H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 485694	NM_006361.6(HOXB13):c.526G>C (p.Gly176Arg)	HOXB13 (G176R)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1492546	NM_006361.6(HOXB13):c.327C>A (p.Tyr109Ter)	HOXB13 (Y109*)	Single nucleotide variant (nonsense)	Prostate cancer, hereditary, 9 +1 more	GUncertain significance
Select item 483502	NM_006361.6(HOXB13):c.216G>T (p.Gly72=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 9 +2 more	GConflicting classifications of pathogenicity
Select item 483487	NM_006361.6(HOXB13):c.140A>G (p.Asn47Ser)	HOXB13 (N47S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance

ClinVar