RHOXF2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2661315	NM_032498.3(RHOXF2):c.186G>A (p.Ser62=)	RHOXF2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1206410	NM_032498.3(RHOXF2):c.206A>C (p.Glu69Ala)	RHOXF2 (E69A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217743	NM_032498.3(RHOXF2):c.223G>A (p.Gly75Arg)	RHOXF2 (G75R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348523	NM_032498.3(RHOXF2):c.250G>A (p.Gly84Arg)	RHOXF2 (G84R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2661316	NM_032498.3(RHOXF2):c.282C>T (p.Leu94=)	RHOXF2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2224034	NM_032498.3(RHOXF2):c.295G>A (p.Gly99Ser)	RHOXF2 (G99S)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2535413	NM_032498.3(RHOXF2):c.333G>T (p.Glu111Asp)	RHOXF2 (E111D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284797	NM_032498.3(RHOXF2):c.367G>A (p.Gly123Ser)	RHOXF2 (G123S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358782	NM_032498.3(RHOXF2):c.370G>A (p.Ala124Thr)	RHOXF2 (A124T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204827	NM_032498.3(RHOXF2):c.373G>A (p.Val125Ile)	RHOXF2 (V125I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154123	NM_032498.3(RHOXF2):c.391G>A (p.Gly131Ser)	RHOXF2 (G131S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310897	NM_032498.3(RHOXF2):c.397G>A (p.Ala133Thr)	RHOXF2 (A133T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314249	NM_032498.3(RHOXF2):c.410A>G (p.Asn137Ser)	RHOXF2 (N137S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2661317	NM_032498.3(RHOXF2):c.411C>T (p.Asn137=)	RHOXF2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1205942	NM_032498.3(RHOXF2):c.415C>T (p.His139Tyr)	RHOXF2 (H139Y)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3154124	NM_032498.3(RHOXF2):c.436C>G (p.Leu146Val)	RHOXF2 (L146V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154125	NM_032498.3(RHOXF2):c.490C>G (p.Arg164Gly)	RHOXF2 (R164G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247580	NM_032498.3(RHOXF2):c.704A>G (p.Asp235Gly)	RHOXF2 (D235G)	Single nucleotide variant (missense variant)	not specified	GLikely benign