TMEM176B[gene] and "single gene"[properties] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3326862	NM_001101312.2(TMEM176B):c.699T>G (p.Cys233Trp)	TMEM176B (C249W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526582	NM_001101312.2(TMEM176B):c.650A>G (p.Lys217Arg)	TMEM176B (K180R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546189	NM_001101312.2(TMEM176B):c.620G>T (p.Arg207Leu)	TMEM176B (R207L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178986	NM_001101312.2(TMEM176B):c.619C>T (p.Arg207Cys)	TMEM176B (R170C +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2279542	NM_001101312.2(TMEM176B):c.619C>A (p.Arg207Ser)	TMEM176B (R170S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256403	NM_001101312.2(TMEM176B):c.617T>C (p.Ile206Thr)	TMEM176B (I169T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488608	NM_001101312.2(TMEM176B):c.593T>C (p.Met198Thr)	TMEM176B (M198T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277237	NM_001101312.2(TMEM176B):c.586A>T (p.Met196Leu)	TMEM176B (M196L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178985	NM_001101312.2(TMEM176B):c.563A>C (p.Gln188Pro)	TMEM176B (Q188P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484858	NM_001101312.2(TMEM176B):c.542G>A (p.Arg181Gln)	TMEM176B (R197Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3178984	NM_001101312.2(TMEM176B):c.520A>G (p.Thr174Ala)	TMEM176B (T137A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220181	NM_001101312.2(TMEM176B):c.431T>C (p.Val144Ala)	TMEM176B (V107A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337916	NM_001101312.2(TMEM176B):c.281G>A (p.Ser94Asn)	TMEM176B (S110N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279394	NM_001101312.2(TMEM176B):c.224G>A (p.Gly75Glu)	TMEM176B (G91E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392883	NM_001101312.2(TMEM176B):c.157A>G (p.Thr53Ala)	TMEM176B (T69A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369661	NM_001101312.2(TMEM176B):c.155A>T (p.Asp52Val)	TMEM176B (D52V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315489	NM_001101312.2(TMEM176B):c.152G>A (p.Gly51Glu)	TMEM176B (G67E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261096	NM_001101312.2(TMEM176B):c.134A>G (p.Lys45Arg)	TMEM176B (K45R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556294	NM_001101312.2(TMEM176B):c.71A>C (p.Asn24Thr)	TMEM176B (N24T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359586	NM_001101312.2(TMEM176B):c.35C>T (p.Ala12Val)	TMEM176B (A12V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315799	NM_001101312.2(TMEM176B):c.28G>A (p.Gly10Arg)	TMEM176B (G10R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 21