"Ambry Genetics"[submitter] AND "MSRB2"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3212289	NM_012228.4(MSRB2):c.7C>T (p.Arg3Trp)	LOC130003509, MSRB2 (R3W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287808	NM_012228.4(MSRB2):c.14T>G (p.Leu5Arg)	LOC130003509, MSRB2 (L5R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3212274	NM_012228.4(MSRB2):c.44C>T (p.Thr15Ile)	LOC130003509, MSRB2 (T15I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278568	NM_012228.4(MSRB2):c.55C>T (p.Arg19Trp)	LOC130003509, MSRB2 (R19W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520747	NM_012228.4(MSRB2):c.61G>A (p.Val21Met)	LOC130003509, MSRB2 (V21M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508657	NM_012228.4(MSRB2):c.74C>A (p.Ala25Glu)	LOC130003509, MSRB2 (A25E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233150	NM_012228.4(MSRB2):c.92G>C (p.Gly31Ala)	LOC130003509, MSRB2 (G31A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363940	NM_012228.4(MSRB2):c.94A>C (p.Thr32Pro)	LOC130003509, MSRB2 (T32P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226806	NM_012228.4(MSRB2):c.113A>G (p.Glu38Gly)	LOC130003509, MSRB2 (E38G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207086	NM_012228.4(MSRB2):c.151A>G (p.Lys51Glu)	MSRB2 (K51E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278064	NM_012228.4(MSRB2):c.193G>A (p.Val65Ile)	MSRB2 (V65I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350255	NM_012228.4(MSRB2):c.196A>G (p.Thr66Ala)	MSRB2 (T66A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296461	NM_012228.4(MSRB2):c.212C>T (p.Thr71Met)	MSRB2 (T71M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363541	NM_012228.4(MSRB2):c.243T>A (p.Asn81Lys)	MSRB2 (N81K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3212262	NM_012228.4(MSRB2):c.271G>A (p.Val91Met)	MSRB2 (V91M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3212265	NM_012228.4(MSRB2):c.292T>C (p.Phe98Leu)	MSRB2 (F98L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3212269	NM_012228.4(MSRB2):c.421C>T (p.Arg141Cys)	MSRB2 (R141C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486423	NM_012228.4(MSRB2):c.422G>A (p.Arg141His)	MSRB2 (R141H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272984	NM_012228.4(MSRB2):c.472C>T (p.Pro158Ser)	MSRB2 (P158S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526545	NM_012228.4(MSRB2):c.526A>G (p.Lys176Glu)	MSRB2 (K176E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 20