"Ambry Genetics"[submitter] AND "OGN"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3204162	NM_014057.5(OGN):c.790C>T (p.Arg264Trp)	CENPP, OGN (R264W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624186	NM_014057.5(OGN):c.665A>G (p.His222Arg)	CENPP, OGN (H222R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302233	NM_014057.5(OGN):c.547C>T (p.Pro183Ser)	CENPP, OGN (P241S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302235	NM_014057.5(OGN):c.481G>A (p.Gly161Ser)	CENPP, OGN (G161S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302234	NM_014057.5(OGN):c.471T>A (p.Asp157Glu)	CENPP, OGN (D157E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204161	NM_014057.5(OGN):c.397A>C (p.Lys133Gln)	CENPP, OGN (K133Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278949	NM_014057.5(OGN):c.364G>A (p.Ala122Thr)	CENPP, OGN (A180T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204160	NM_014057.5(OGN):c.352C>G (p.Pro118Ala)	CENPP, OGN (P176A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304444	NM_014057.5(OGN):c.242C>T (p.Pro81Leu)	CENPP, OGN (P139L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204159	NM_014057.5(OGN):c.233C>T (p.Ala78Val)	CENPP, OGN (A136V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3204158	NM_014057.5(OGN):c.201T>A (p.Asn67Lys)	CENPP, OGN (N125K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2280955	NM_014057.5(OGN):c.83G>A (p.Arg28His)	CENPP, OGN (R28H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367684	NM_014057.5(OGN):c.79T>A (p.Ser27Thr)	CENPP, OGN (S27T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance