Related gene-specific medical variations for Gene (Select 51012) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2601236	NM_016045.3(PRELID3B):c.298T>C (p.Phe100Leu)	PRELID3B, SLMO2-ATP5E (F70L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2594862	NM_016045.3(PRELID3B):c.85A>G (p.Met29Val)	PRELID3B, SLMO2-ATP5E (M29V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2494194	NM_016045.3(PRELID3B):c.20A>G (p.Glu7Gly)	LOC130066279, PRELID3B +1 more (E7G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2461911	NM_016045.3(PRELID3B):c.320A>G (p.Asp107Gly)	PRELID3B, SLMO2-ATP5E (D107G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2335728	NM_016045.3(PRELID3B):c.470G>A (p.Arg157Gln)	PRELID3B, SLMO2-ATP5E (R157Q +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2332724	NM_016045.3(PRELID3B):c.539G>A (p.Gly180Glu)	PRELID3B, SLMO2-ATP5E (G150E +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2270105	NM_016045.3(PRELID3B):c.332T>C (p.Ile111Thr)	PRELID3B, SLMO2-ATP5E (I111T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

ClinVar