Related gene-specific medical variations for Gene (Select 3212) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284654	NM_002145.4(HOXB2):c.275C>T (p.Ala92Val)	HOXB-AS1, HOXB2 (A92V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106617	NM_002145.4(HOXB2):c.365C>T (p.Pro122Leu)	HOXB-AS1, HOXB2 (P122L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106616	NM_002145.4(HOXB2):c.221A>C (p.Asp74Ala)	HOXB-AS1, HOXB2 (D74A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540810	NM_002145.4(HOXB2):c.181T>C (p.Ser61Pro)	HOXB-AS1, HOXB2 (S61P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364443	NM_002145.4(HOXB2):c.155C>A (p.Thr52Asn)	HOXB-AS1, HOXB2 (T52N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350893	NM_002145.4(HOXB2):c.46C>T (p.Pro16Ser)	HOXB-AS1, HOXB2 (P16S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273752	NM_002145.4(HOXB2):c.263C>T (p.Ala88Val)	HOXB-AS1, HOXB2 (A88V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248996	NM_002145.4(HOXB2):c.335C>T (p.Thr112Met)	HOXB-AS1, HOXB2 (T112M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231213	NM_002145.4(HOXB2):c.178G>A (p.Ala60Thr)	HOXB-AS1, HOXB2 (A60T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance