Related gene-specific medical variations for Gene (Select 3202) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3106590	NM_019102.4(HOXA5):c.340A>T (p.Ser114Cys)	HOXA-AS3, HOXA3 +1 more (S114C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106589	NM_019102.4(HOXA5):c.160C>G (p.Leu54Val)	HOXA-AS3, HOXA3 +1 more (L54V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619775	NM_019102.4(HOXA5):c.31G>C (p.Gly11Arg)	HOXA-AS3, HOXA3 +1 more (G11R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618771	NM_019102.4(HOXA5):c.6C>G (p.Ser2Arg)	HOXA-AS3, HOXA3 +1 more (S2R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515896	NM_019102.4(HOXA5):c.244G>C (p.Ala82Pro)	HOXA-AS3, HOXA3 +1 more (A82P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402826	NM_019102.4(HOXA5):c.590G>C (p.Arg197Thr)	HOXA-AS3, HOXA3 +1 more (R197T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379689	NM_019102.4(HOXA5):c.478G>A (p.Ala160Thr)	HOXA-AS3, HOXA3 +1 more (A160T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378532	NM_019102.4(HOXA5):c.788C>T (p.Ala263Val)	HOXA-AS3, HOXA3 +1 more (A263V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 774314	NM_019102.4(HOXA5):c.81T>C (p.His27=)	HOXA-AS3, HOXA3 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign