Related gene-specific medical variations for Gene (Select 100124700) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284672	NM_014212.4(HOXC11):c.98A>G (p.Tyr33Cys)	HOTAIR, HOXC11 (Y33C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106675	NM_014212.4(HOXC11):c.93C>A (p.Asn31Lys)	HOTAIR, HOXC11 (N31K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106673	NM_014212.4(HOXC11):c.70G>C (p.Glu24Gln)	HOTAIR, HOXC11 (E24Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106671	NM_014212.4(HOXC11):c.374A>G (p.His125Arg)	HOTAIR, HOXC11 (H125R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106670	NM_014212.4(HOXC11):c.359C>T (p.Ser120Phe)	HOTAIR, HOXC11 (S120F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106669	NM_014212.4(HOXC11):c.208G>A (p.Val70Ile)	HOTAIR, HOXC11 (V70I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607161	NM_014212.4(HOXC11):c.376C>A (p.His126Asn)	HOTAIR, HOXC11 (H126N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547942	NM_014212.4(HOXC11):c.278A>G (p.Tyr93Cys)	HOTAIR, HOXC11 (Y93C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509196	NM_014212.4(HOXC11):c.191C>T (p.Ser64Leu)	HOTAIR, HOXC11 (S64L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463478	NM_014212.4(HOXC11):c.502G>A (p.Glu168Lys)	HOTAIR, HOXC11 (E168K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405491	NM_014212.4(HOXC11):c.541C>T (p.Pro181Ser)	HOTAIR, HOXC11 (P181S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399350	NM_014212.4(HOXC11):c.404C>G (p.Ala135Gly)	HOTAIR, HOXC11 (A135G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383768	NM_014212.4(HOXC11):c.523G>A (p.Gly175Ser)	HOTAIR, HOXC11 (G175S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374769	NM_014212.4(HOXC11):c.569C>G (p.Ala190Gly)	HOTAIR, HOXC11 +1 more (A190G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2258049	NM_014212.4(HOXC11):c.406G>T (p.Gly136Cys)	HOTAIR, HOXC11 (G136C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228996	NM_014212.4(HOXC11):c.574C>G (p.Arg192Gly)	HOTAIR, HOXC11 +1 more (R192G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207506	NM_014212.4(HOXC11):c.487G>C (p.Gly163Arg)	HOTAIR, HOXC11 (G163R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance