"Ambry Genetics"[submitter] AND "MOB2"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3185950	NM_001172223.3(MOB2):c.806G>A (p.Ter269=)	MOB2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3185928	NM_001172223.3(MOB2):c.786G>T (p.Gln262His)	MOB2 (Q231H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557443	NM_001172223.3(MOB2):c.772G>A (p.Gly258Ser)	MOB2 (G227S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185879	NM_001172223.3(MOB2):c.763G>A (p.Gly255Ser)	MOB2 (G255S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2471441	NM_001172223.3(MOB2):c.761C>T (p.Ala254Val)	MOB2 (A223V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185825	NM_001172223.3(MOB2):c.743G>C (p.Gly248Ala)	MOB2 (G217A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295485	NM_001172223.3(MOB2):c.661A>G (p.Asn221Asp)	MOB2 (N190D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185754	NM_001172223.3(MOB2):c.595G>A (p.Ala199Thr)	MOB2 (A168T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607543	NM_001172223.3(MOB2):c.584A>G (p.Lys195Arg)	MOB2 (K164R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185702	NM_001172223.3(MOB2):c.553G>A (p.Val185Met)	MOB2 (V154M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185667	NM_001172223.3(MOB2):c.484A>G (p.Lys162Glu)	MOB2 (K131E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593843	NM_001172223.3(MOB2):c.462G>A (p.Thr154=)	MOB2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3185546	NM_001172223.3(MOB2):c.396G>A (p.Lys132=)	MOB2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2220388	NM_001172223.3(MOB2):c.359G>A (p.Cys120Tyr)	MOB2 (C89Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185487	NM_001172223.3(MOB2):c.335A>C (p.Glu112Ala)	MOB2 (E112A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295484	NM_001172223.3(MOB2):c.175C>T (p.Pro59Ser)	MOB2 (P28S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522301	NM_001172223.3(MOB2):c.150G>A (p.Ala50=)	MOB2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3295482	NM_001172223.3(MOB2):c.145G>A (p.Ala49Thr)	MOB2 (A18T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364387	NM_001172223.3(MOB2):c.109A>G (p.Arg37Gly)	MOB2 (R37G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185789	NM_001172223.3(MOB2):c.67C>T (p.Leu23Phe)	MOB2 (L23F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336582	NM_001172223.3(MOB2):c.47G>C (p.Gly16Ala)	MOB2 (G16A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271915	NM_001172223.3(MOB2):c.46G>A (p.Gly16Ser)	MOB2 (G16S)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Items: 22