"Ambry Genetics"[submitter] AND "ARMC1"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2344555	NM_018120.6(ARMC1):c.776G>A (p.Gly259Asp)	ARMC1 (G259D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248299	NM_018120.6(ARMC1):c.772G>C (p.Val258Leu)	ARMC1 (V156L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366585	NM_018120.6(ARMC1):c.464C>T (p.Thr155Met)	ARMC1 (T155M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2326280	NM_018120.6(ARMC1):c.379C>T (p.Arg127Cys)	ARMC1 (R127C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129598	NM_018120.6(ARMC1):c.367G>A (p.Glu123Lys)	ARMC1 (E123K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222564	NM_018120.6(ARMC1):c.166G>A (p.Val56Ile)	ARMC1 (V56I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371095	NM_018120.6(ARMC1):c.133A>G (p.Ile45Val)	ARMC1 (I45V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332489	NM_018120.6(ARMC1):c.104T>G (p.Val35Gly)	ARMC1 (V35G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3129597	NM_018120.6(ARMC1):c.103G>A (p.Val35Ile)	ARMC1 (V35I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2408739	NM_018120.6(ARMC1):c.47C>T (p.Ser16Leu)	ARMC1 (S16L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance