Related gene-specific medical variations for Gene (Select 51531) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329044	NM_016481.5(TRMO):c.43C>G (p.Pro15Ala)	LOC130002191, TRMO (P15A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3329042	NM_016481.5(TRMO):c.7G>T (p.Gly3Cys)	LOC130002191, TRMO (G3C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3182967	NM_016481.5(TRMO):c.55G>T (p.Val19Phe)	LOC130002191, TRMO (V19F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2376229	NM_016481.5(TRMO):c.41C>T (p.Thr14Ile)	LOC130002191, TRMO (T14I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2373199	NM_016481.5(TRMO):c.25C>T (p.Pro9Ser)	LOC130002191, TRMO (P9S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2280890	NM_016481.5(TRMO):c.52T>C (p.Cys18Arg)	LOC130002191, TRMO (C18R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

ClinVar