Related gene-specific medical variations for Gene (Select 124790) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284164	NM_001303441.2(HEXIM2):c.782C>A (p.Thr261Asn)	HEXIM2, LOC105371795 (T283N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3284163	NM_001303441.2(HEXIM2):c.836G>A (p.Arg279His)	HEXIM2, LOC105371795 (R279H +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3284162	NM_001303441.2(HEXIM2):c.79C>T (p.Pro27Ser)	HEXIM2, LOC105371795 (P49S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3105589	NM_001303441.2(HEXIM2):c.842A>T (p.Asp281Val)	HEXIM2, LOC105371795 (D281V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3105588	NM_001303441.2(HEXIM2):c.779G>A (p.Arg260Gln)	HEXIM2, LOC105371795 (R260Q +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3105587	NM_001303441.2(HEXIM2):c.653T>G (p.Leu218Arg)	HEXIM2, LOC105371795 (L218R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3105586	NM_001303441.2(HEXIM2):c.632A>G (p.Gln211Arg)	HEXIM2, LOC105371795 (Q211R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3105585	NM_001303441.2(HEXIM2):c.526G>A (p.Gly176Arg)	HEXIM2, LOC105371795 (G176R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3105584	NM_001303441.2(HEXIM2):c.478G>A (p.Val160Met)	HEXIM2, LOC105371795 (V182M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2592552	NM_001303441.2(HEXIM2):c.836G>T (p.Arg279Leu)	HEXIM2, LOC105371795 (R301L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2568546	NM_001303441.2(HEXIM2):c.752A>G (p.Glu251Gly)	HEXIM2, LOC105371795 (E251G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2508746	NM_001303441.2(HEXIM2):c.592G>C (p.Glu198Gln)	HEXIM2, LOC105371795 (E198Q +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2482870	NM_001303441.2(HEXIM2):c.793C>T (p.Arg265Trp)	HEXIM2, LOC105371795 (R265W +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2363294	NM_001303441.2(HEXIM2):c.498C>G (p.His166Gln)	HEXIM2, LOC105371795 (H166Q +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2322045	NM_001303441.2(HEXIM2):c.757G>T (p.Ala253Ser)	HEXIM2, LOC105371795 (A275S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2293304	NM_001303441.2(HEXIM2):c.281G>T (p.Arg94Leu)	HEXIM2, LOC105371795 (R116L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2255574	NM_001303441.2(HEXIM2):c.169G>C (p.Asp57His)	HEXIM2, LOC105371795 (D79H +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 994226	NM_001303441.2(HEXIM2):c.80C>G (p.Pro27Arg)	LOC105371795, HEXIM2 (P27R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance