"Ambry Genetics"[submitter] AND "UBE2J2"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3185527	NM_058167.3(UBE2J2):c.770C>T (p.Ala257Val)	UBE2J2 (A257V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185526	NM_058167.3(UBE2J2):c.619G>A (p.Gly207Arg)	UBE2J2 (G155R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185525	NM_058167.3(UBE2J2):c.590T>C (p.Leu197Pro)	UBE2J2 (L145P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330558	NM_058167.3(UBE2J2):c.584C>T (p.Thr195Met)	UBE2J2 (T143M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528755	NM_058167.3(UBE2J2):c.577G>C (p.Gly193Arg)	UBE2J2 (G193R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337923	NM_058167.3(UBE2J2):c.565G>C (p.Val189Leu)	UBE2J2 (V137L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185524	NM_058167.3(UBE2J2):c.523G>C (p.Asp175His)	UBE2J2 (D123H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330560	NM_058167.3(UBE2J2):c.506A>G (p.Gln169Arg)	UBE2J2 (Q117R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330559	NM_058167.3(UBE2J2):c.64C>G (p.Leu22Val)	UBE2J2 (L22V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2466292	NM_058167.3(UBE2J2):c.29C>T (p.Pro10Leu)	UBE2J2 (P10L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance