Related gene-specific medical variations for Gene (Select 387082) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3172109	NM_001002255.2(SUMO4):c.206G>C (p.Gly69Ala)	SUMO4, TAB2 (G69A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3172108	NM_001002255.2(SUMO4):c.102T>G (p.Ile34Met)	SUMO4, TAB2 (I34M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3067497	NM_001002255.2(SUMO4):c.168G>A (p.Lys56=)	SUMO4, TAB2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2656989	NM_001002255.2(SUMO4):c.2T>C (p.Met1Thr)	SUMO4, TAB2 (M1T)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2512211	NM_001002255.2(SUMO4):c.99G>T (p.Lys33Asn)	SUMO4, TAB2 (K33N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467850	NM_001002255.2(SUMO4):c.27A>C (p.Glu9Asp)	SUMO4, TAB2 (E9D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373964	NM_001002255.2(SUMO4):c.199A>G (p.Ile67Val)	SUMO4, TAB2 (I67V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2287941	NM_001002255.2(SUMO4):c.214A>G (p.Lys72Glu)	SUMO4, TAB2 (K72E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1700889	NM_001292034.3(TAB2):c.1939+1208A>G	SUMO4, TAB2 (M1V)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 776170	NM_001002255.2(SUMO4):c.272C>T (p.Thr91Met)	SUMO4, TAB2 (T91M)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 776169	NM_001002255.2(SUMO4):c.152G>A (p.Arg51Gln)	SUMO4, TAB2 (R51Q)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2062	NM_001002255.2(SUMO4):c.163G>A (p.Val55Met)	SUMO4, TAB2 (V55M)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GBenign