Related gene-specific medical variations for Gene (Select 158800) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314248	NM_139282.3(RHOXF1):c.416A>C (p.Asn139Thr)	RHOXF1, RHOXF1-AS1 (N139T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154122	NM_139282.3(RHOXF1):c.544G>A (p.Val182Ile)	RHOXF1, RHOXF1-AS1 (V182I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3154121	NM_139282.3(RHOXF1):c.528C>A (p.Asp176Glu)	RHOXF1, RHOXF1-AS1 (D176E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154120	NM_139282.3(RHOXF1):c.479G>A (p.Arg160Gln)	RHOXF1, RHOXF1-AS1 (R160Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154119	NM_139282.3(RHOXF1):c.395C>A (p.Thr132Lys)	RHOXF1, RHOXF1-AS1 (T132K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154118	NM_139282.3(RHOXF1):c.196A>G (p.Met66Val)	RHOXF1, RHOXF1-AS1 (M66V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2483935	NM_139282.3(RHOXF1):c.283G>A (p.Gly95Ser)	RHOXF1, RHOXF1-AS1 (G95S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352813	NM_139282.3(RHOXF1):c.29T>C (p.Val10Ala)	RHOXF1, RHOXF1-AS1 (V10A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311725	NM_139282.3(RHOXF1):c.472T>C (p.Cys158Arg)	RHOXF1, RHOXF1-AS1 (C158R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207467	NM_139282.3(RHOXF1):c.134T>C (p.Met45Thr)	RHOXF1, RHOXF1-AS1 (M45T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777826	NM_139282.3(RHOXF1):c.228G>A (p.Glu76=)	RHOXF1, RHOXF1-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 715990	NM_139282.3(RHOXF1):c.515G>A (p.Arg172His)	RHOXF1, RHOXF1-AS1 (R172H)	Single nucleotide variant (missense variant)	not provided	GBenign