RPUSD1[gene] and "single gene"[properties] - ClinVar

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Items: 47

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3156337	NM_058192.3(RPUSD1):c.929C>T (p.Pro310Leu)	RPUSD1 (P184L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386808	NM_058192.3(RPUSD1):c.916T>C (p.Trp306Arg)	RPUSD1 (W180R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315364	NM_058192.3(RPUSD1):c.899T>C (p.Leu300Pro)	RPUSD1 (L174P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3156336	NM_058192.3(RPUSD1):c.860C>T (p.Thr287Ile)	RPUSD1 (T158I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517485	NM_058192.3(RPUSD1):c.859A>G (p.Thr287Ala)	RPUSD1 (T271A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274548	NM_058192.3(RPUSD1):c.842G>A (p.Arg281Gln)	RPUSD1 (R152Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329605	NM_058192.3(RPUSD1):c.838G>T (p.Gly280Cys)	RPUSD1 (G264C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315365	NM_058192.3(RPUSD1):c.787G>A (p.Glu263Lys)	RPUSD1 (E247K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521271	NM_058192.3(RPUSD1):c.773C>T (p.Pro258Leu)	RPUSD1 (P132L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372205	NM_058192.3(RPUSD1):c.770C>A (p.Thr257Asn)	RPUSD1 (T257N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606679	NM_058192.3(RPUSD1):c.769A>T (p.Thr257Ser)	RPUSD1 (T257S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2645863	NM_058192.3(RPUSD1):c.750C>G (p.Leu250=)	RPUSD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3156333	NM_058192.3(RPUSD1):c.737C>T (p.Ser246Leu)	RPUSD1 (S117L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409836	NM_058192.3(RPUSD1):c.736T>C (p.Ser246Pro)	RPUSD1 (S120P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3156332	NM_058192.3(RPUSD1):c.694C>T (p.Pro232Ser)	RPUSD1 (P106S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316050	NM_058192.3(RPUSD1):c.685C>T (p.Pro229Ser)	RPUSD1 (P232S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543393	NM_058192.3(RPUSD1):c.677C>T (p.Thr226Met)	RPUSD1 (T229M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3156331	NM_058192.3(RPUSD1):c.658G>A (p.Glu220Lys)	RPUSD1 (E220K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315363	NM_058192.3(RPUSD1):c.628G>T (p.Ala210Ser)	RPUSD1 (A194S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534164	NM_058192.3(RPUSD1):c.626A>G (p.His209Arg)	RPUSD1 (H83R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3156330	NM_058192.3(RPUSD1):c.617T>C (p.Met206Thr)	RPUSD1 (M80T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3156329	NM_058192.3(RPUSD1):c.596G>A (p.Arg199Gln)	RPUSD1 (R183Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2377486	NM_058192.3(RPUSD1):c.580G>A (p.Gly194Arg)	RPUSD1 (G197R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354978	NM_058192.3(RPUSD1):c.548T>C (p.Leu183Pro)	RPUSD1 (L57P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297339	NM_058192.3(RPUSD1):c.530G>A (p.Arg177His)	RPUSD1 (R180H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161795	NM_058192.3(RPUSD1):c.521A>G (p.His174Arg)	RPUSD1 (H174R +4 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 2624017	NM_058192.3(RPUSD1):c.488A>G (p.Lys163Arg)	RPUSD1 (K166R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474950	NM_058192.3(RPUSD1):c.433C>G (p.Leu145Val)	RPUSD1 (L148V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262962	NM_058192.3(RPUSD1):c.428C>T (p.Pro143Leu)	RPUSD1 (Q109* +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207762	NM_058192.3(RPUSD1):c.373G>A (p.Gly125Ser)	RPUSD1 (G109S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3315367	NM_058192.3(RPUSD1):c.368C>T (p.Thr123Met)	RPUSD1 (T107M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156326	NM_058192.3(RPUSD1):c.364A>G (p.Ser122Gly)	RPUSD1 (S122G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2616501	NM_058192.3(RPUSD1):c.344G>C (p.Ser115Thr)	RPUSD1 (S99T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2357620	NM_058192.3(RPUSD1):c.316C>T (p.His106Tyr)	RPUSD1 (H106Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2206764	NM_058192.3(RPUSD1):c.308T>C (p.Leu103Pro)	RPUSD1 (L103P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2393065	NM_058192.3(RPUSD1):c.284T>C (p.Val95Ala)	RPUSD1 (V95A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156324	NM_058192.3(RPUSD1):c.278G>A (p.Arg93Gln)	RPUSD1 (R77Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156323	NM_058192.3(RPUSD1):c.247G>A (p.Ala83Thr)	RPUSD1 (A67T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3156322	NM_058192.3(RPUSD1):c.175G>C (p.Gly59Arg)	RPUSD1 (G59R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156321	NM_058192.3(RPUSD1):c.134G>A (p.Arg45Gln)	RPUSD1 (R45Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2211502	NM_058192.3(RPUSD1):c.110C>G (p.Thr37Ser)	RPUSD1 (T37S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156320	NM_058192.3(RPUSD1):c.103C>T (p.Arg35Trp)	RPUSD1 (R35W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3315368	NM_058192.3(RPUSD1):c.88G>A (p.Asp30Asn)	RPUSD1 (D30N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156334	NM_058192.3(RPUSD1):c.83G>A (p.Arg28His)	RPUSD1 (R28H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2382301	NM_058192.3(RPUSD1):c.65A>G (p.Asn22Ser)	RPUSD1 (N22S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3156327	NM_058192.3(RPUSD1):c.41G>A (p.Arg14Gln)	RPUSD1 (R14Q)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3315366	NM_058192.3(RPUSD1):c.14G>A (p.Ser5Asn)	RPUSD1 (S5N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 47