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

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2329964	NM_016205.3(PDGFC):c.943A>G (p.Thr315Ala)	PDGFC (T315A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210831	NM_016205.3(PDGFC):c.841G>A (p.Gly281Ser)	PDGFC (G281S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461076	NM_016205.3(PDGFC):c.532C>G (p.Pro178Ala)	PDGFC (P178A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210828	NM_016205.3(PDGFC):c.493C>A (p.Pro165Thr)	PDGFC (P165T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322358	NM_016205.3(PDGFC):c.409G>A (p.Gly137Arg)	PDGFC (G137R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402152	NM_016205.3(PDGFC):c.138T>A (p.His46Gln)	PDGFC (H46Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210827	NM_016205.3(PDGFC):c.127G>T (p.Asp43Tyr)	PDGFC (D43Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454339	NM_016205.3(PDGFC):c.65C>T (p.Ala22Val)	PDGFC (A22V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210829	NM_016205.3(PDGFC):c.59C>T (p.Thr20Ile)	PDGFC (T20I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559445	NM_016205.3(PDGFC):c.41C>G (p.Ala14Gly)	PDGFC (A14G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance