ARMC8[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2234834	NM_001363941.2(ARMC8):c.274A>G (p.Met92Val)	ARMC8 (M78V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129674	NM_001363941.2(ARMC8):c.322C>G (p.Pro108Ala)	ARMC8 (P108A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271757	NM_001363941.2(ARMC8):c.330A>C (p.Leu110Phe)	ARMC8 (L96F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293637	NM_001363941.2(ARMC8):c.356T>C (p.Leu119Pro)	ARMC8 (L77P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318430	NM_001363941.2(ARMC8):c.363T>A (p.Phe121Leu)	ARMC8 (F79L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606509	NM_001363941.2(ARMC8):c.395T>C (p.Ile132Thr)	ARMC8 (I90T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604768	NM_001363941.2(ARMC8):c.482G>A (p.Arg161His)	ARMC8 (R119H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315739	NM_001363941.2(ARMC8):c.593C>T (p.Thr198Ile)	ARMC8 (T167I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490533	NM_001363941.2(ARMC8):c.659C>T (p.Pro220Leu)	ARMC8 (P178L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129675	NM_001363941.2(ARMC8):c.808C>T (p.Arg270Trp)	ARMC8 (R197W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520079	NM_001363941.2(ARMC8):c.809G>A (p.Arg270Gln)	ARMC8 (R228Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314545	NM_001363941.2(ARMC8):c.811A>G (p.Thr271Ala)	ARMC8 (T257A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316379	NM_001363941.2(ARMC8):c.877T>G (p.Leu293Val)	ARMC8 (L220V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343683	NM_001363941.2(ARMC8):c.886G>C (p.Glu296Gln)	ARMC8 (E265Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320057	NM_001363941.2(ARMC8):c.917A>G (p.Tyr306Cys)	ARMC8 (Y264C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129676	NM_001363941.2(ARMC8):c.929C>G (p.Pro310Arg)	ARMC8 (P237R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129671	NM_001363941.2(ARMC8):c.1126C>T (p.Arg376Trp)	ARMC8 (R334W +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance