Related gene-specific medical variations for Gene (Select 3203) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284644	NM_024014.4(HOXA6):c.668G>T (p.Ser223Ile)	HOXA-AS3, HOXA3 +1 more (S223I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284643	NM_024014.4(HOXA6):c.558C>G (p.Ile186Met)	HOXA-AS3, HOXA3 +1 more (I186M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106595	NM_024014.4(HOXA6):c.616C>G (p.Arg206Gly)	HOXA-AS3, HOXA3 +1 more (R206G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106594	NM_024014.4(HOXA6):c.559G>A (p.Glu187Lys)	HOXA-AS3, HOXA3 +1 more (E187K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106593	NM_024014.4(HOXA6):c.395A>G (p.Tyr132Cys)	HOXA-AS3, HOXA3 +1 more (Y132C)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3106592	NM_024014.4(HOXA6):c.293G>A (p.Gly98Asp)	HOXA-AS3, HOXA3 +1 more (G98D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532101	NM_024014.4(HOXA6):c.652A>G (p.Asn218Asp)	HOXA-AS3, HOXA3 +1 more (N218D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490565	NM_024014.4(HOXA6):c.670G>T (p.Gly224Trp)	HOXA-AS3, HOXA3 +1 more (G224W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392560	NM_024014.4(HOXA6):c.491G>T (p.Arg164Leu)	HOXA-AS3, HOXA3 +1 more (R164L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380150	NM_024014.4(HOXA6):c.676G>A (p.Asp226Asn)	HOXA-AS3, HOXA3 +1 more (D226N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354607	NM_024014.4(HOXA6):c.490C>T (p.Arg164Cys)	HOXA-AS3, HOXA3 +1 more (R164C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335986	NM_024014.4(HOXA6):c.402C>A (p.Ser134Arg)	HOXA-AS3, HOXA3 +1 more (S134R)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2332347	NM_024014.4(HOXA6):c.217G>C (p.Glu73Gln)	HOXA-AS3, HOXA3 +1 more (E73Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323430	NM_024014.4(HOXA6):c.110C>A (p.Pro37His)	HOXA-AS3, HOXA3 +1 more (P37H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309313	NM_024014.4(HOXA6):c.502C>A (p.Leu168Met)	HOXA-AS3, HOXA3 +1 more (L168M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289764	NM_024014.4(HOXA6):c.656C>T (p.Ser219Phe)	HOXA-AS3, HOXA3 +1 more (S219F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250608	NM_024014.4(HOXA6):c.89C>A (p.Ala30Asp)	HOXA-AS3, HOXA3 +1 more (A30D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance