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

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2407748	NM_001042371.3(PGP):c.923A>G (p.Tyr308Cys)	PGP (Y308C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386211	NM_001042371.3(PGP):c.902A>C (p.Lys301Thr)	PGP (K301T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211878	NM_001042371.3(PGP):c.877C>G (p.Gln293Glu)	LOC130058218, PGP (Q293E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557134	NM_001042371.3(PGP):c.868A>C (p.Lys290Gln)	LOC130058218, PGP (K290Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282308	NM_001042371.3(PGP):c.718A>G (p.Ile240Val)	PGP (I240V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303002	NM_001042371.3(PGP):c.683G>A (p.Arg228His)	PGP (R228H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393976	NM_001042371.3(PGP):c.575G>A (p.Gly192Asp)	PGP (G192D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211875	NM_001042371.3(PGP):c.352G>A (p.Ala118Thr)	PGP (A118T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211874	NM_001042371.3(PGP):c.206A>G (p.Asn69Ser)	PGP (N69S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3306025	NM_001042371.3(PGP):c.140C>G (p.Pro47Arg)	PGP (P47R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3306024	NM_001042371.3(PGP):c.41T>C (p.Val14Ala)	PGP (V14A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3306023	NM_001042371.3(PGP):c.34C>T (p.Arg12Cys)	PGP (R12C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605846	NM_001042371.3(PGP):c.31G>A (p.Ala11Thr)	PGP (A11T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378834	NM_001042371.3(PGP):c.26A>G (p.Asp9Gly)	PGP (D9G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211877	NM_001042371.3(PGP):c.5C>T (p.Ala2Val)	LOC112340387, PGP (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance