TMEM134[gene] and "single gene"[properties] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3178792	NM_025124.4(TMEM134):c.579C>G (p.Phe193Leu)	TMEM134 (F184L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514425	NM_025124.4(TMEM134):c.561C>A (p.Phe187Leu)	TMEM134 (F172L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258162	NM_025124.4(TMEM134):c.555C>A (p.Phe185Leu)	TMEM134 (F170L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509921	NM_025124.4(TMEM134):c.539A>G (p.Lys180Arg)	TMEM134 (K171R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178791	NM_025124.4(TMEM134):c.524T>G (p.Ile175Ser)	TMEM134 (I160S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327188	NM_025124.4(TMEM134):c.499C>T (p.Pro167Ser)	TMEM134 (P167S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390735	NM_025124.4(TMEM134):c.479C>T (p.Pro160Leu)	TMEM134 (P145L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216956	NM_025124.4(TMEM134):c.457T>G (p.Ser153Ala)	TMEM134 (S138A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178789	NM_025124.4(TMEM134):c.416T>C (p.Leu139Pro)	TMEM134 (L130P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3326788	NM_025124.4(TMEM134):c.383T>C (p.Phe128Ser)	TMEM134 (F119S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3326787	NM_025124.4(TMEM134):c.379T>G (p.Ser127Ala)	TMEM134 (S127A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353036	NM_025124.4(TMEM134):c.307C>T (p.Arg103Cys)	TMEM134 (R94C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488077	NM_025124.4(TMEM134):c.272A>C (p.Gln91Pro)	TMEM134 (Q82P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327628	NM_025124.4(TMEM134):c.268T>C (p.Ser90Pro)	TMEM134 (S81P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3326785	NM_025124.4(TMEM134):c.264C>T (p.Arg88=)	TMEM134	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 2522911	NM_025124.4(TMEM134):c.262C>T (p.Arg88Cys)	TMEM134 (R88C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2642020	NM_025124.4(TMEM134):c.250C>T (p.Arg84Ter)	TMEM134 (R84*)	Single nucleotide variant (nonsense +2 more)	not provided	GLikely benign
Select item 3178788	NM_025124.4(TMEM134):c.197G>A (p.Gly66Glu)	TMEM134 (G66E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178787	NM_025124.4(TMEM134):c.173A>C (p.Gln58Pro)	TMEM134 (Q58P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407325	NM_025124.4(TMEM134):c.169T>C (p.Tyr57His)	TMEM134 (Y57H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3178786	NM_025124.4(TMEM134):c.155A>G (p.Gln52Arg)	TMEM134 (Q52R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2554781	NM_025124.4(TMEM134):c.77A>T (p.Glu26Val)	TMEM134 (E26V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314076	NM_025124.4(TMEM134):c.61G>C (p.Gly21Arg)	TMEM134 (G21R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615711	NM_025124.4(TMEM134):c.7G>T (p.Ala3Ser)	TMEM134 (A3S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24