"Ambry Genetics"[submitter] AND "TMEM160"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2464455	NM_017854.2(TMEM160):c.469A>G (p.Met157Val)	TMEM160 (M157V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178903	NM_017854.2(TMEM160):c.461G>A (p.Gly154Asp)	TMEM160 (G154D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569966	NM_017854.2(TMEM160):c.452G>A (p.Cys151Tyr)	TMEM160 (C151Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606639	NM_017854.2(TMEM160):c.431C>T (p.Ala144Val)	TMEM160 (A144V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305371	NM_017854.2(TMEM160):c.371T>C (p.Leu124Pro)	TMEM160 (L124P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288544	NM_017854.2(TMEM160):c.326G>A (p.Cys109Tyr)	TMEM160 (C109Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178901	NM_017854.2(TMEM160):c.145C>G (p.Pro49Ala)	LOC130064789, TMEM160 (P49A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302579	NM_017854.2(TMEM160):c.112G>A (p.Ala38Thr)	LOC130064789, TMEM160 (A38T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547445	NM_017854.2(TMEM160):c.70C>T (p.Pro24Ser)	LOC130064789, TMEM160 (P24S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220880	NM_017854.2(TMEM160):c.49C>T (p.Arg17Cys)	LOC130064789, TMEM160 (R17C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326832	NM_017854.2(TMEM160):c.37C>G (p.Leu13Val)	LOC130064789, TMEM160 (L13V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352557	NM_017854.2(TMEM160):c.35G>T (p.Arg12Leu)	LOC130064789, TMEM160 (R12L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264813	NM_017854.2(TMEM160):c.10G>T (p.Gly4Cys)	TMEM160 (G4C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance