"Ambry Genetics"[submitter] AND "TMEM26"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3179352	NM_178505.8(TMEM26):c.1084G>T (p.Asp362Tyr)	LOC126860941, TMEM26 (D362Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179351	NM_178505.8(TMEM26):c.1084G>A (p.Asp362Asn)	LOC126860941, TMEM26 (D362N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179350	NM_178505.8(TMEM26):c.1076T>A (p.Val359Asp)	LOC126860941, TMEM26 (V359D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471399	NM_178505.8(TMEM26):c.985C>T (p.Arg329Trp)	LOC126860941, TMEM26 (R329W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179358	NM_178505.8(TMEM26):c.977A>G (p.His326Arg)	LOC126860941, TMEM26 (H326R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179357	NM_178505.8(TMEM26):c.941C>T (p.Ser314Leu)	LOC126860941, TMEM26 (S314L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179356	NM_178505.8(TMEM26):c.934C>T (p.Arg312Cys)	LOC126860941, TMEM26 (R312C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2259273	NM_178505.8(TMEM26):c.859G>T (p.Val287Leu)	LOC126860941, TMEM26 (V287L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286169	NM_178505.8(TMEM26):c.833A>G (p.Tyr278Cys)	LOC126860941, TMEM26 (Y278C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2280134	NM_178505.8(TMEM26):c.772G>A (p.Gly258Arg)	LOC126860941, TMEM26 (G258R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383625	NM_178505.8(TMEM26):c.740T>G (p.Phe247Cys)	LOC126860941, TMEM26 (F247C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242176	NM_178505.8(TMEM26):c.643T>C (p.Trp215Arg)	TMEM26 (W215R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317373	NM_178505.8(TMEM26):c.622G>C (p.Val208Leu)	TMEM26 (V208L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318789	NM_178505.8(TMEM26):c.595C>G (p.Gln199Glu)	TMEM26 (Q199E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2477653	NM_178505.8(TMEM26):c.564A>G (p.Ile188Met)	TMEM26 (I188M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179355	NM_178505.8(TMEM26):c.535C>G (p.Leu179Val)	TMEM26 (L179V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179354	NM_178505.8(TMEM26):c.532C>T (p.Leu178Phe)	TMEM26 (L178F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596630	NM_178505.8(TMEM26):c.503G>A (p.Gly168Glu)	TMEM26 (G168E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179353	NM_178505.8(TMEM26):c.494T>C (p.Ile165Thr)	TMEM26 (I165T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224917	NM_178505.8(TMEM26):c.383C>T (p.Thr128Met)	TMEM26 (T128M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461518	NM_178505.8(TMEM26):c.326T>C (p.Phe109Ser)	TMEM26 (F109S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336060	NM_178505.8(TMEM26):c.296C>A (p.Thr99Lys)	TMEM26 (T99K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297052	NM_178505.8(TMEM26):c.262G>A (p.Glu88Lys)	TMEM26 (E88K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300291	NM_178505.8(TMEM26):c.256C>T (p.His86Tyr)	TMEM26 (H86Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219719	NM_178505.8(TMEM26):c.245T>A (p.Leu82His)	TMEM26 (L82H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1330988	NM_178505.8(TMEM26):c.229G>A (p.Val77Ile)	TMEM26 (V77I)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance

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Items: 26