Related gene-specific medical variations for Gene (Select 3215) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3106641	NM_002147.4(HOXB5):c.556A>C (p.Ser186Arg)	HOXB-AS3, HOXB5 (S186R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106640	NM_002147.4(HOXB5):c.424C>G (p.Pro142Ala)	HOXB-AS3, HOXB5 (P142A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106639	NM_002147.4(HOXB5):c.213G>C (p.Glu71Asp)	HOXB-AS3, HOXB5 (E71D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400321	NM_002147.4(HOXB5):c.34C>A (p.Arg12Ser)	HOXB-AS3, HOXB5 (R12S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389869	NM_002147.4(HOXB5):c.242A>G (p.Gln81Arg)	HOXB-AS3, HOXB5 +1 more (Q81R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347729	NM_002147.4(HOXB5):c.79G>A (p.Gly27Ser)	HOXB-AS3, HOXB5 (G27S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231991	NM_002147.4(HOXB5):c.355G>T (p.Asp119Tyr)	HOXB-AS3, HOXB5 (D119Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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