"Ambry Genetics"[submitter] AND "RDM1"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2588101	NM_145654.4(RDM1):c.828A>C (p.Glu276Asp)	RDM1 (E253D +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477214	NM_145654.4(RDM1):c.800A>T (p.Tyr267Phe)	RDM1 (Y149F +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344144	NM_145654.4(RDM1):c.742G>A (p.Gly248Ser)	RDM1 (G215S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3313470	NM_145654.4(RDM1):c.661G>A (p.Val221Ile)	RDM1 (V221I +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2320405	NM_145654.4(RDM1):c.433A>G (p.Asn145Asp)	RDM1 (N145D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3313469	NM_145654.4(RDM1):c.346G>C (p.Glu116Gln)	RDM1 (E116Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3313471	NM_145654.4(RDM1):c.233A>T (p.Lys78Met)	RDM1 (K55M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261470	NM_145654.4(RDM1):c.226G>C (p.Ala76Pro)	RDM1 (A53P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314016	NM_145654.4(RDM1):c.164C>T (p.Ala55Val)	RDM1 (A55V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251678	NM_145654.4(RDM1):c.139T>G (p.Ser47Ala)	RDM1 (S24A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622426	NM_145654.4(RDM1):c.17C>T (p.Pro6Leu)	RDM1 (P6L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance