TMEM71[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2623891	NM_001382403.1(TMEM71):c.794C>T (p.Ser265Leu)	TMEM71 (S260L +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270993	NM_001382403.1(TMEM71):c.762G>A (p.Met254Ile)	TMEM71 (M253I +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536123	NM_001382403.1(TMEM71):c.742G>T (p.Ala248Ser)	TMEM71 (A185S +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179631	NM_001382403.1(TMEM71):c.683G>T (p.Arg228Met)	TMEM71 (R229M +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327177	NM_001382403.1(TMEM71):c.560C>T (p.Thr187Ile)	TMEM71 (T188I +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242736	NM_001382403.1(TMEM71):c.537G>T (p.Lys179Asn)	TMEM71 (K160N +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376041	NM_001382403.1(TMEM71):c.519T>A (p.Asp173Glu)	TMEM71 (D154E +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312114	NM_001382403.1(TMEM71):c.296A>G (p.Tyr99Cys)	TMEM71 (Y99C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363320	NM_001382403.1(TMEM71):c.274C>A (p.Pro92Thr)	TMEM71 (P92T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179630	NM_001382403.1(TMEM71):c.236G>A (p.Ser79Asn)	TMEM71 (S74N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179629	NM_001382403.1(TMEM71):c.214T>C (p.Tyr72His)	TMEM71 (Y67H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411796	NM_001382403.1(TMEM71):c.174C>G (p.His58Gln)	TMEM71 (H53Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462595	NM_001382403.1(TMEM71):c.110G>T (p.Cys37Phe)	TMEM71 (C37F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327178	NM_001382403.1(TMEM71):c.88T>C (p.Cys30Arg)	TMEM71 (C30R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance