"Ambry Genetics"[submitter] AND "NRF1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2552376	NM_005011.5(NRF1):c.55G>T (p.Ala19Ser)	NRF1 (A19S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3301023	NM_005011.5(NRF1):c.115A>G (p.Ser39Gly)	NRF1 (S39G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325091	NM_005011.5(NRF1):c.1074A>C (p.Gln358His)	NRF1 (Q358H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554260	NM_005011.5(NRF1):c.1207A>G (p.Thr403Ala)	NRF1 (T242A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333744	NM_005011.5(NRF1):c.1306G>A (p.Ala436Thr)	NRF1 (A436T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223072	NM_005011.5(NRF1):c.1318G>A (p.Gly440Arg)	NRF1 (G279R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar