Related gene-specific medical variations for Gene (Select 100874107) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3296810	NM_001033602.4(MTUS2):c.3253G>A (p.Glu1085Lys)	MTUS2, MTUS2-AS1 (E64K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2643709	NM_001033602.4(MTUS2):c.3246C>T (p.Phe1082=)	MTUS2, MTUS2-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2598709	NM_001033602.4(MTUS2):c.3205G>A (p.Glu1069Lys)	MTUS2, MTUS2-AS1 (E1069K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592453	NM_001033602.4(MTUS2):c.3215A>G (p.Gln1072Arg)	MTUS2, MTUS2-AS1 (Q1071R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403263	NM_001033602.4(MTUS2):c.3242G>T (p.Arg1081Leu)	MTUS2, MTUS2-AS1 (R1015L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259301	NM_001033602.4(MTUS2):c.3341G>A (p.Arg1114His)	MTUS2, MTUS2-AS1 (R1048H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225543	NM_001033602.4(MTUS2):c.3380G>A (p.Arg1127Gln)	MTUS2, MTUS2-AS1 (R1061Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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