"Ambry Genetics"[submitter] AND "OR2A7"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3302642	NM_001005328.2(OR2A7):c.859C>T (p.Leu287Phe)	ARHGEF35-AS1, OR2A1-AS1 +1 more (L287F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524355	NM_001005328.2(OR2A7):c.809A>G (p.Lys270Arg)	ARHGEF35-AS1, OR2A1-AS1 +1 more (K270R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616128	NM_001005328.2(OR2A7):c.806A>G (p.Gln269Arg)	ARHGEF35-AS1, OR2A1-AS1 +1 more (Q269R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616127	NM_001005328.2(OR2A7):c.805C>A (p.Gln269Lys)	ARHGEF35-AS1, OR2A1-AS1 +1 more (Q269K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3302640	NM_001005328.2(OR2A7):c.751T>C (p.Tyr251His)	ARHGEF35-AS1, OR2A1-AS1 +1 more (Y251H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485702	NM_001005328.2(OR2A7):c.743G>T (p.Gly248Val)	ARHGEF35-AS1, OR2A1-AS1 +1 more (G248V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412511	NM_001005328.2(OR2A7):c.664T>A (p.Cys222Ser)	ARHGEF35-AS1, OR2A1-AS1 +1 more (C222S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3205023	NM_001005328.2(OR2A7):c.582T>G (p.Asn194Lys)	ARHGEF35-AS1, OR2A1-AS1 +1 more (N194K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205022	NM_001005328.2(OR2A7):c.548T>C (p.Val183Ala)	ARHGEF35-AS1, OR2A1-AS1 +1 more (V183A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540681	NM_001005328.2(OR2A7):c.454G>A (p.Val152Ile)	ARHGEF35-AS1, OR2A1-AS1 +1 more (V152I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389525	NM_001005328.2(OR2A7):c.383C>A (p.Pro128His)	ARHGEF35-AS1, OR2A1-AS1 +1 more (P128H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205021	NM_001005328.2(OR2A7):c.293T>C (p.Met98Thr)	ARHGEF35-AS1, OR2A1-AS1 +1 more (M98T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2468588	NM_001005328.2(OR2A7):c.257A>T (p.His86Leu)	ARHGEF35-AS1, OR2A1-AS1 +1 more (H86L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205020	NM_001005328.2(OR2A7):c.238A>C (p.Met80Leu)	ARHGEF35-AS1, OR2A1-AS1 +1 more (M80L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597612	NM_001005328.2(OR2A7):c.236G>A (p.Arg79Gln)	ARHGEF35-AS1, OR2A1-AS1 +1 more (R79Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3302641	NM_001005328.2(OR2A7):c.235C>T (p.Arg79Trp)	ARHGEF35-AS1, OR2A1-AS1 +1 more (R79W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205019	NM_001005328.2(OR2A7):c.215A>G (p.Tyr72Cys)	ARHGEF35-AS1, OR2A1-AS1 +1 more (Y72C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205018	NM_001005328.2(OR2A7):c.155C>G (p.Ser52Cys)	ARHGEF35-AS1, OR2A1-AS1 +1 more (S52C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205017	NM_001005328.2(OR2A7):c.140T>A (p.Leu47His)	ARHGEF35-AS1, OR2A1-AS1 +1 more (L47H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337208	NM_001005328.2(OR2A7):c.14T>C (p.Ile5Thr)	ARHGEF35-AS1, OR2A1-AS1 +1 more (I5T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 20