Related gene-specific medical variations for Gene (Select 391192) - ClinVar

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Links from Gene

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3302722	NM_001004687.2(OR2L3):c.280A>G (p.Thr94Ala)	OR2L13, OR2L3 (T94A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302721	NM_001004687.2(OR2L3):c.401G>A (p.Arg134His)	OR2L13, OR2L3 (R134H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205181	NM_001004687.2(OR2L3):c.883G>A (p.Glu295Lys)	OR2L13, OR2L3 (E295K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205180	NM_001004687.2(OR2L3):c.847A>G (p.Met283Val)	OR2L13, OR2L3 (M283V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205179	NM_001004687.2(OR2L3):c.653G>T (p.Gly218Val)	OR2L13, OR2L3 (G218V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606671	NM_001004687.2(OR2L3):c.322G>A (p.Gly108Ser)	OR2L13, OR2L3 (G108S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2594505	NM_001004687.2(OR2L3):c.262A>G (p.Asn88Asp)	OR2L13, OR2L3 (N88D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588126	NM_001004687.2(OR2L3):c.929G>T (p.Gly310Val)	OR2L13, OR2L3 (G310V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2570370	NM_001004687.2(OR2L3):c.655C>T (p.Arg219Trp)	OR2L13, OR2L3 (R219W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2562510	NM_001004687.2(OR2L3):c.359A>G (p.Asp120Gly)	OR2L13, OR2L3 (D120G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520854	NM_001004687.2(OR2L3):c.887T>A (p.Val296Glu)	OR2L13, OR2L3 (V296E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515221	NM_001004687.2(OR2L3):c.836C>T (p.Thr279Ile)	OR2L13, OR2L3 (T279I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2396929	NM_001004687.2(OR2L3):c.754G>A (p.Ala252Thr)	OR2L13, OR2L3 (A252T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343160	NM_001004687.2(OR2L3):c.455C>T (p.Ser152Leu)	OR2L13, OR2L3 (S152L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339433	NM_001004687.2(OR2L3):c.662T>C (p.Leu221Pro)	OR2L13, OR2L3 (L221P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320539	NM_001004687.2(OR2L3):c.593T>A (p.Val198Glu)	OR2L13, OR2L3 (V198E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312171	NM_001004687.2(OR2L3):c.349A>G (p.Met117Val)	OR2L13, OR2L3 (M117V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295316	NM_001004687.2(OR2L3):c.807G>C (p.Glu269Asp)	OR2L13, OR2L3 (E269D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279563	NM_001004687.2(OR2L3):c.337C>T (p.Leu113Phe)	OR2L13, OR2L3 (L113F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249714	NM_001004687.2(OR2L3):c.82A>G (p.Ile28Val)	OR2L13, OR2L3 (I28V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221679	NM_001004687.2(OR2L3):c.778C>T (p.Arg260Cys)	OR2L13, OR2L3 (R260C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 21