"Ambry Genetics"[submitter] AND "ARMC10"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3129599	NM_031905.5(ARMC10):c.164A>T (p.Glu55Val)	ARMC10 (E55V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312014	NM_031905.5(ARMC10):c.226T>G (p.Ser76Ala)	ARMC10, LOC129999052 (S76A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315328	NM_031905.5(ARMC10):c.323C>T (p.Thr108Met)	ARMC10 (T73M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213170	NM_031905.5(ARMC10):c.331C>T (p.Pro111Ser)	ARMC10 (P76S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287152	NM_031905.5(ARMC10):c.376G>C (p.Ala126Pro)	ARMC10 (A91P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251239	NM_031905.5(ARMC10):c.394G>T (p.Ala132Ser)	ARMC10 (A97S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472610	NM_031905.5(ARMC10):c.431C>G (p.Ala144Gly)	ARMC10 (A144G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2262014	NM_031905.5(ARMC10):c.443A>C (p.Asn148Thr)	ARMC10 (N148T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213608	NM_031905.5(ARMC10):c.448T>A (p.Ser150Thr)	ARMC10 (S115T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315350	NM_031905.5(ARMC10):c.540T>G (p.Ser180Arg)	ARMC10 (S145R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295546	NM_031905.5(ARMC10):c.547T>C (p.Cys183Arg)	ARMC10 (C183R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214291	NM_031905.5(ARMC10):c.592G>A (p.Ala198Thr)	ARMC10 (A198T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129601	NM_031905.5(ARMC10):c.610A>G (p.Thr204Ala)	ARMC10 (T204A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378512	NM_031905.5(ARMC10):c.611C>T (p.Thr204Ile)	ARMC10 (T169I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129602	NM_031905.5(ARMC10):c.616A>G (p.Met206Val)	ARMC10 (M171V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222672	NM_031905.5(ARMC10):c.623T>C (p.Val208Ala)	ARMC10 (V173A +1 more)	Single nucleotide variant (intron variant +1 more)	not specified	GUncertain significance
Select item 3315318	NM_031905.5(ARMC10):c.697A>T (p.Asn233Tyr)	ARMC10 (N233Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248002	NM_031905.5(ARMC10):c.701C>T (p.Thr234Met)	ARMC10 (T199M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2594466	NM_031905.5(ARMC10):c.745C>A (p.Pro249Thr)	ARMC10 (P190T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324512	NM_031905.5(ARMC10):c.752T>C (p.Met251Thr)	ARMC10 (M157T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129603	NM_031905.5(ARMC10):c.783T>A (p.Asp261Glu)	ARMC10 (D143E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315339	NM_031905.5(ARMC10):c.814G>A (p.Val272Ile)	ARMC10 (V272I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129604	NM_031905.5(ARMC10):c.893C>G (p.Ala298Gly)	ARMC10 (A180G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129605	NM_031905.5(ARMC10):c.899A>C (p.Gln300Pro)	ARMC10 (Q241P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360831	NM_031905.5(ARMC10):c.1006G>A (p.Val336Ile)	ARMC10 (V242I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25