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

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2557443	NM_001172223.3(MOB2):c.772G>A (p.Gly258Ser)	MOB2 (G227S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471441	NM_001172223.3(MOB2):c.761C>T (p.Ala254Val)	MOB2 (A223V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2607543	NM_001172223.3(MOB2):c.584A>G (p.Lys195Arg)	MOB2 (K164R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593843	NM_001172223.3(MOB2):c.462G>A (p.Thr154=)	MOB2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 2220388	NM_001172223.3(MOB2):c.359G>A (p.Cys120Tyr)	MOB2 (C89Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2522301	NM_001172223.3(MOB2):c.150G>A (p.Ala50=)	MOB2	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 2364387	NM_001172223.3(MOB2):c.109A>G (p.Arg37Gly)	MOB2 (R37G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2336582	NM_001172223.3(MOB2):c.47G>C (p.Gly16Ala)	MOB2 (G16A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271915	NM_001172223.3(MOB2):c.46G>A (p.Gly16Ser)	MOB2 (G16S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign