RXFP3[gene] and "single gene"[properties] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2290876	NM_016568.3(RXFP3):c.58A>C (p.Lys20Gln)	RXFP3 (K20Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157292	NM_016568.3(RXFP3):c.95T>C (p.Leu32Pro)	RXFP3 (L32P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157289	NM_016568.3(RXFP3):c.277G>A (p.Ala93Thr)	RXFP3 (A93T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617799	NM_016568.3(RXFP3):c.301C>G (p.Leu101Val)	RXFP3 (L101V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234556	NM_016568.3(RXFP3):c.314T>C (p.Leu105Pro)	RXFP3 (L105P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253409	NM_016568.3(RXFP3):c.326T>G (p.Met109Arg)	RXFP3 (M109R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309734	NM_016568.3(RXFP3):c.346T>C (p.Ser116Pro)	RXFP3 (S116P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230434	NM_016568.3(RXFP3):c.349A>G (p.Ile117Val)	RXFP3 (I117V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 773190	NM_016568.3(RXFP3):c.370C>T (p.Leu124=)	RXFP3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2589213	NM_016568.3(RXFP3):c.406C>A (p.Pro136Thr)	RXFP3 (P136T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308571	NM_016568.3(RXFP3):c.427G>T (p.Ala143Ser)	RXFP3 (A143S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618301	NM_016568.3(RXFP3):c.560C>A (p.Ala187Asp)	RXFP3 (A187D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507983	NM_016568.3(RXFP3):c.617T>C (p.Leu206Pro)	RXFP3 (L206P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265575	NM_016568.3(RXFP3):c.668C>G (p.Ala223Gly)	RXFP3 (A223G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157291	NM_016568.3(RXFP3):c.836C>T (p.Pro279Leu)	RXFP3 (P279L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518983	NM_016568.3(RXFP3):c.850A>G (p.Ile284Val)	RXFP3 (I284V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250514	NM_016568.3(RXFP3):c.888C>G (p.Asp296Glu)	RXFP3 (D296E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287077	NM_016568.3(RXFP3):c.896C>G (p.Ala299Gly)	RXFP3 (A299G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599131	NM_016568.3(RXFP3):c.947C>T (p.Ala316Val)	RXFP3 (A316V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292769	NM_016568.3(RXFP3):c.1026C>A (p.Asn342Lys)	RXFP3 (N342K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488979	NM_016568.3(RXFP3):c.1058A>G (p.Lys353Arg)	RXFP3 (K353R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157286	NM_016568.3(RXFP3):c.1145G>A (p.Ser382Asn)	RXFP3 (S382N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157287	NM_016568.3(RXFP3):c.1189C>G (p.Arg397Gly)	RXFP3 (R397G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488650	NM_016568.3(RXFP3):c.1216C>G (p.Arg406Gly)	RXFP3 (R406G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261136	NM_016568.3(RXFP3):c.1223C>A (p.Ala408Glu)	RXFP3 (A408E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476597	NM_016568.3(RXFP3):c.1287G>C (p.Gln429His)	RXFP3 (Q429H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336735	NM_016568.3(RXFP3):c.1296G>C (p.Gln432His)	RXFP3 (Q432H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157288	NM_016568.3(RXFP3):c.1301C>G (p.Pro434Arg)	RXFP3 (P434R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488482	NM_016568.3(RXFP3):c.1309C>A (p.Pro437Thr)	RXFP3 (P437T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 29