"Ambry Genetics"[submitter] AND "POLD3"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3216313	NM_006591.3(POLD3):c.83A>G (p.Tyr28Cys)	POLD3 (Y28C)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2268764	NM_006591.3(POLD3):c.371G>A (p.Ser124Asn)	POLD3 (S85N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273676	NM_006591.3(POLD3):c.449C>G (p.Ser150Trp)	POLD3 (S111W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369286	NM_006591.3(POLD3):c.524A>G (p.Asn175Ser)	POLD3 (N136S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3216312	NM_006591.3(POLD3):c.629A>C (p.Glu210Ala)	POLD3 (E210A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515631	NM_006591.3(POLD3):c.890A>C (p.Glu297Ala)	POLD3 (E258A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272499	NM_006591.3(POLD3):c.901G>C (p.Gly301Arg)	POLD3 (G262R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211350	NM_006591.3(POLD3):c.938A>G (p.Glu313Gly)	POLD3 (E313G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474636	NM_006591.3(POLD3):c.1041G>T (p.Glu347Asp)	POLD3 (E308D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239949	NM_006591.3(POLD3):c.1060C>T (p.Pro354Ser)	POLD3 (P315S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609031	NM_006591.3(POLD3):c.1094C>G (p.Thr365Ser)	POLD3 (T365S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306462	NM_006591.3(POLD3):c.1099C>T (p.Pro367Ser)	POLD3 (P328S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282708	NM_006591.3(POLD3):c.1153C>T (p.Arg385Cys)	POLD3 (R385C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262545	NM_006591.3(POLD3):c.1216G>A (p.Glu406Lys)	POLD3 (E367K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3216311	NM_006591.3(POLD3):c.1289T>G (p.Met430Arg)	POLD3 (M391R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance