Related gene-specific medical variations for Gene (Select 51110) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3117331	NM_016027.3(LACTB2):c.859C>T (p.His287Tyr)	LACTB2, LACTB2-AS1 (H287Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117330	NM_016027.3(LACTB2):c.686G>A (p.Arg229His)	LACTB2, LACTB2-AS1 (R229H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3117328	NM_016027.3(LACTB2):c.635A>T (p.Gln212Leu)	LACTB2, LACTB2-AS1 (Q212L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117327	NM_016027.3(LACTB2):c.210C>G (p.Ile70Met)	LACTB2, LACTB2-AS1 (I70M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2394250	NM_016027.3(LACTB2):c.659G>A (p.Arg220Gln)	LACTB2, LACTB2-AS1 (R220Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390938	NM_016027.3(LACTB2):c.571A>C (p.Lys191Gln)	LACTB2, LACTB2-AS1 (K191Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379620	NM_016027.3(LACTB2):c.430G>A (p.Gly144Ser)	LACTB2, LACTB2-AS1 (G144S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364222	NM_016027.3(LACTB2):c.296A>G (p.Tyr99Cys)	LACTB2, LACTB2-AS1 (Y99C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316292	NM_016027.3(LACTB2):c.170G>T (p.Ser57Ile)	LACTB2, LACTB2-AS1 (S57I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2219362	NM_016027.3(LACTB2):c.656T>C (p.Ile219Thr)	LACTB2, LACTB2-AS1 (I219T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209741	NM_016027.3(LACTB2):c.340A>G (p.Ile114Val)	LACTB2, LACTB2-AS1 (I114V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance