ARMCX6[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2661066	NM_019007.4(ARMCX6):c.651C>T (p.Ala217=)	ARMCX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3129707	NM_019007.4(ARMCX6):c.476G>C (p.Ser159Thr)	ARMCX6 (S159T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402516	NM_019007.4(ARMCX6):c.421G>A (p.Glu141Lys)	ARMCX6 (E141K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405163	NM_019007.4(ARMCX6):c.359A>G (p.Asn120Ser)	ARMCX6 (N120S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129706	NM_019007.4(ARMCX6):c.338G>C (p.Trp113Ser)	ARMCX6 (W113S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298939	NM_019007.4(ARMCX6):c.269G>A (p.Gly90Glu)	ARMCX6 (G90E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410334	NM_019007.4(ARMCX6):c.225G>C (p.Trp75Cys)	ARMCX6 (W75C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315873	NM_019007.4(ARMCX6):c.133T>G (p.Trp45Gly)	ARMCX6 (W45G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2661067	NM_019007.4(ARMCX6):c.53C>T (p.Ala18Val)	ARMCX6 (A18V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3315875	NM_019007.4(ARMCX6):c.31G>T (p.Ala11Ser)	ARMCX6 (A11S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance