CD226[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140456	NM_001303618.2(CD226):c.910A>G (p.Ile304Val)	CD226 (I149V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140455	NM_001303618.2(CD226):c.893A>G (p.Asn298Ser)	CD226 (N143S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544875	NM_001303618.2(CD226):c.848G>A (p.Arg283Lys)	CD226 (R128K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2516408	NM_001303618.2(CD226):c.748A>T (p.Thr250Ser)	CD226 (T250S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264779	NM_001303618.2(CD226):c.736G>A (p.Asp246Asn)	CD226 (D246N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140454	NM_001303618.2(CD226):c.676G>A (p.Ala226Thr)	CD226 (A71T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229540	NM_001303618.2(CD226):c.638C>G (p.Thr213Arg)	CD226 (T213R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382906	NM_001303618.2(CD226):c.631G>A (p.Asp211Asn)	CD226 (D56N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2570361	NM_001303618.2(CD226):c.616G>A (p.Val206Ile)	CD226 (V206I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140453	NM_001303618.2(CD226):c.509C>T (p.Pro170Leu)	CD226 (P15L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328449	NM_001303618.2(CD226):c.437A>G (p.Lys146Arg)	CD226 (K146R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624110	NM_001303618.2(CD226):c.350C>T (p.Thr117Ile)	CD226 (T117I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298605	NM_001303618.2(CD226):c.343C>A (p.Gln115Lys)	CD226 (Q115K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454755	NM_001303618.2(CD226):c.257T>C (p.Met86Thr)	CD226 (M86T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484925	NM_001303618.2(CD226):c.148T>A (p.Trp50Arg)	CD226 (W50R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363641	NM_001303618.2(CD226):c.91G>A (p.Glu31Lys)	CD226 (E31K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2372331	NM_001303618.2(CD226):c.25G>C (p.Ala9Pro)	CD226 (A9P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance