Related gene-specific medical variations for Gene (Select 284339) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3178844	NM_173633.3(TMEM145):c.74C>G (p.Pro25Arg)	LOC130064575, TMEM145 (P25R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178840	NM_173633.3(TMEM145):c.41C>T (p.Pro14Leu)	LOC130064575, TMEM145 (P14L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178839	NM_173633.3(TMEM145):c.16G>T (p.Ala6Ser)	LOC130064575, TMEM145 (A6S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555206	NM_173633.3(TMEM145):c.100G>A (p.Gly34Ser)	LOC130064575, TMEM145 (G34S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539992	NM_173633.3(TMEM145):c.4G>A (p.Glu2Lys)	LOC130064575, TMEM145 (E2K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327323	NM_173633.3(TMEM145):c.116A>T (p.Lys39Met)	LOC130064575, TMEM145 (K39M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar