ClinVar (all) for Orgtrack (Select 500161) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 161861	NM_213589.3(RAPH1):c.1123G>T (p.Glu375Ter)	RAPH1 (E375* +1 more)	Single nucleotide variant (nonsense)	Malignant tumor of prostate	GUncertain significance
Select item 161860	NM_207361.6(FREM2):c.3497G>A (p.Arg1166His)	FREM2 (R1166H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161859	NM_207117.4(SLC25A47):c.56C>T (p.Pro19Leu)	SLC25A47 (P19L)	Single nucleotide variant (5 prime UTR variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161858	NM_206933.4(USH2A):c.5837G>T (p.Arg1946Leu)	USH2A, USH2A-AS2 (R1946L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161857	NM_001024845.3(SLC6A9):c.577G>A (p.Glu193Lys)	SLC6A9 (E266K +6 more)	Single nucleotide variant (missense variant +1 more)	Atypical glycine encephalopathy	GUncertain significance
Select item 161856	NM_199340.5(LRRC37A3):c.3859del (p.Ala1287fs)	LRRC37A3 (A405fs +1 more)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 161855	NM_199191.3(BABAM2):c.626A>G (p.Asp209Gly)	BABAM2 (D209G)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161854	NM_152501.5(PYHIN1):c.602G>A (p.Arg201His)	PYHIN1 (R192H +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161853	NM_198512.3(DGAT2L6):c.769C>A (p.Leu257Met)	DGAT2L6 (L257M)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161852	NM_031272.5(TEX14):c.3172-1908C>T	TEX14 (S1088L +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161851	NM_001291867.2(NHS):c.2204G>A (p.Arg735His)	NHS (R714H +3 more)	Single nucleotide variant (missense variant)	Nance-Horan syndrome +1 more	GBenign/Likely benign
Select item 161850	NM_001039372.4(HEPACAM2):c.80-41G>A	HEPACAM2 (M1I)	Single nucleotide variant (missense variant +2 more)	Malignant tumor of prostate	GUncertain significance
Select item 161849	NM_003716.4(CADPS):c.484G>A (p.Ala162Thr)	CADPS (A162T)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161848	NM_016120.4(RLIM):c.260del (p.Asp87fs)	RLIM (D87fs)	Deletion (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 161847	NM_182947.4(ARHGEF25):c.657-7C>A	ARHGEF25	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 161846	NM_181877.4(ZSCAN2):c.1255C>A (p.Gln419Lys)	ZSCAN2 (Q419K)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161845	NM_181808.4(POLN):c.2267G>A (p.Arg756Gln)	POLN (R756Q)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161844	NM_181523.3(PIK3R1):c.1939C>A (p.Leu647Ile)	PIK3R1 (L377I +3 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161843	NM_001530.4(HIF1A):c.700G>A (p.Glu234Lys)	HIF1A, HIF1A-AS3 (E234K +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161842	NM_001378789.1(CERS3):c.609+7G>T	CERS3	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 161841	NM_001366157.1(WDR49):c.2465C>A (p.Ser822Ter)	WDR49 (S470* +2 more)	Single nucleotide variant (nonsense)	Malignant tumor of prostate	GUncertain significance
Select item 161840	NM_001352913.2(PPP2R5C):c.880C>G (p.Leu294Val)	PPP2R5C (L239V +4 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161839	NM_178556.5(TRIML1):c.1188A>T (p.Lys396Asn)	TRIML1 (K396N)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161838	NM_178543.5(ENPP7):c.68C>T (p.Pro23Leu)	ENPP7 (P23L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161837	NM_178468.6(FAM83C):c.863G>A (p.Arg288His)	FAM83C (R288H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161836	NM_018078.4(LARP1B):c.1324G>T (p.Asp442Tyr)	LARP1B (D442Y +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161835	NM_176889.4(TAS2R20):c.254C>G (p.Ser85Cys)	PRH1-PRR4, PRH1-TAS2R14 +2 more (S85C)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161834	NM_175709.5(CBX7):c.227C>G (p.Pro76Arg)	CBX7 (P76R)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161833	NM_173728.4(ARHGEF15):c.1897C>T (p.Arg633Trp)	ARHGEF15 (R633W)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161832	NM_173632.4(ZNF776):c.574A>C (p.Asn192His)	ZNF776 (N192H)	Single nucleotide variant (missense variant +2 more)	Malignant tumor of prostate	GUncertain significance
Select item 161831	NM_173558.4(FGD2):c.882+3A>C	FGD2	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 161830	NM_173550.4(CCDC171):c.2404C>T (p.Arg802Trp)	CCDC171 (R802W +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161829	NM_173536.4(GABRG1):c.32C>T (p.Pro11Leu)	GABRG1 (P11L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161828	NM_173531.4(ZNF100):c.407del (p.Gly136fs)	ZNF100 (G103fs +3 more)	Deletion (frameshift variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161827	NM_173517.6(VKORC1L1):c.493G>T (p.Glu165Ter)	VKORC1L1 (E165* +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161826	NM_138694.4(PKHD1):c.544G>A (p.Ala182Thr)	PKHD1 (A182T)	Single nucleotide variant (missense variant)	Autosomal recessive polycystic kidney disease +1 more	GUncertain significance
Select item 161825	NM_153766.3(KCNJ1):c.1094A>T (p.Asn365Ile)	KCNJ1 (N365I +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161824	NM_001146312.3(MYOCD):c.2678del (p.Lys893fs)	ARHGAP44-AS1, MYOCD (K845fs +2 more)	Deletion (non-coding transcript variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161823	NM_153442.4(GPR26):c.71C>T (p.Ala24Val)	GPR26 (A24V)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161822	NM_153267.5(MAMDC2):c.58G>A (p.Asp20Asn)	MAMDC2 (D20N)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161821	NM_001134658.3(SLC35G1):c.427G>A (p.Ala143Thr)	SLC35G1 (A142T +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161820	NM_153021.5(PLB1):c.3195+7C>A	PLB1	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 161819	NM_152868.3(KCNJ4):c.586C>T (p.Arg196Cys)	KCNJ4 (R196C)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161818	NM_152792.4(ASPRV1):c.-158C>T	LOC122757966, ASPRV1 (P32L)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 161817	NM_152753.4(SCUBE3):c.2462C>T (p.Pro821Leu)	SCUBE3 (P821L +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161816	NM_152744.4(SDK1):c.5214+8C>T	SDK1	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 161815	NM_152476.3(ZNF560):c.1096C>A (p.His366Asn)	ZNF560 (H366N +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161814	NM_152453.4(TMCO5A):c.645G>C (p.Lys215Asn)	TMCO5A (K215N +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161813	NM_194302.4(CFAP65):c.542+58del	CFAP65 (L136fs)	Deletion (frameshift variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161812	NM_007203.5(PALM2AKAP2):c.625G>T (p.Glu209Ter)	PALM2AKAP2 (E209* +1 more)	Single nucleotide variant (nonsense +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161811	NM_004208.4(AIFM1):c.497C>T (p.Pro166Leu)	AIFM1, RAB33A (P162L +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161810	NM_004711.5(SYNGR1):c.483+1398C>T	SYNGR1	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 161809	NM_145263.4(SPATA18):c.991G>A (p.Val331Ile)	SPATA18 (V331I +3 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161808	NM_001286574.2(ARMC12):c.601G>T (p.Asp201Tyr)	ARMC12 (D228Y +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161807	NM_144685.5(HIPK4):c.1279G>A (p.Asp427Asn)	HIPK4 (D427N)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161806	NM_144587.5(BTBD16):c.82C>T (p.Pro28Ser)	BTBD16 (P28S +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161805	NM_138982.4(MAPK10):c.1271G>A (p.Ser424Asn)	MAPK10 (S424N +2 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161804	NM_138778.5(DPH7):c.932A>G (p.Asn311Ser)	DPH7 (N311S +4 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161803	NM_001388308.1(KIF12):c.1698-4C>A	KIF12	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 161802	NM_138391.6(TMEM183A):c.708+1G>A	TMEM183A	Single nucleotide variant (splice donor variant)	Malignant tumor of prostate	GUncertain significance
Select item 161801	NM_133473.4(ZNF431):c.1021G>A (p.Glu341Lys)	ZNF431 (E341K +3 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161800	NM_002839.4(PTPRD):c.5692C>T (p.Arg1898Cys)	PTPRD (R1491C +8 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161799	NM_001290268.2(RIPOR3):c.67G>A (p.Val23Met)	RIPOR3 (V19M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161798	NM_080817.5(GPR82):c.482G>T (p.Gly161Val)	CASK, GPR82 (G161V)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161797	NM_080746.3(RPL10L):c.94C>T (p.Arg32Cys)	RPL10L (R32C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161796	NM_182932.3(SLC8A3):c.1690G>A (p.Val564Ile)	SLC8A3 (V564I)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	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 161794	NM_054106.1(OR5AC2):c.730G>A (p.Gly244Ser)	OR5AC2 (G244S)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161793	NM_053025.4(MYLK):c.1148C>T (p.Pro383Leu)	MYLK (P383L +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161792	NM_052909.5(PLEKHG4B):c.2311C>T (p.Arg771Trp)	PLEKHG4B (R771W)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161791	NM_001281956.2(CSMD2):c.7808G>T (p.Arg2603Leu)	CSMD2 (R2605L +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161790	NM_001102564.3(IFT43):c.21G>T (p.Leu7Phe)	IFT43 (L7F)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161789	NM_033439.4(IL33):c.712G>A (p.Val238Met)	IL33 (V238M +4 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161788	NM_033257.4(DGCR6L):c.608C>T (p.Pro203Leu)	DGCR6L (P203L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161787	NM_033116.6(NEK9):c.1756dup (p.Thr586fs)	NEK9 (T468fs +2 more)	Duplication (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 161786	NM_033004.4(NLRP1):c.2818C>T (p.Arg940Ter)	NLRP1 (R940*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 161785	NM_032932.6(RAB11FIP4):c.1901A>T (p.Glu634Val)	RAB11FIP4 (E634V +4 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161784	NM_178150.3(FBH1):c.2107C>T (p.Arg703Trp)	FBH1 (R754W +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161783	NM_032511.4(FAXC):c.892C>G (p.Gln298Glu)	FAXC (Q298E +2 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161782	NM_032383.5(HPS3):c.1509+6C>G	HPS3	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 161781	NM_032236.8(USP48):c.1243A>G (p.Met415Val)	USP48 (M415V +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161780	NM_031935.3(HMCN1):c.16792C>T (p.Arg5598Ter)	HMCN1 (R5598*)	Single nucleotide variant (nonsense)	Malignant tumor of prostate	GUncertain significance
Select item 161779	NM_031490.5(LONP2):c.471G>T (p.Leu157Phe)	LONP2 (L157F)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161778	NM_031485.4(GRWD1):c.593G>A (p.Arg198Gln)	GRWD1 (R198Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161777	NM_030933.4(SHCBP1L):c.881C>A (p.Thr294Lys)	SHCBP1L (T294K +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161776	NM_030904.2(OR2T1):c.-18G>A	OR2T1 (G46S)	Single nucleotide variant (5 prime UTR variant)	Malignant tumor of prostate	GUncertain significance
Select item 161775	NM_030782.5(CLPTM1L):c.749G>A (p.Arg250His)	CLPTM1L (R250H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161774	NM_030569.7(ITIH5):c.2545G>T (p.Asp849Tyr)	ITIH5 (D849Y +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161773	NM_025145.7(CFAP43):c.2051A>G (p.His684Arg)	CFAP43 (H684R)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161772	NM_025113.5(RUBCNL):c.1141C>T (p.Arg381Ter)	RUBCNL (R381* +4 more)	Single nucleotide variant (nonsense)	Malignant tumor of prostate	GUncertain significance
Select item 161771	NM_024870.4(PREX2):c.1444-4G>A	PREX2	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 161770	NM_001286201.2(RERGL):c.412C>A (p.Gln138Lys)	RERGL (Q139K +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161769	NM_024603.4(BEND5):c.1210A>G (p.Ile404Val)	AGBL4, BEND5 (I404V +2 more)	Single nucleotide variant (missense variant +2 more)	Malignant tumor of prostate	GUncertain significance
Select item 161768	NM_024012.4(HTR5A):c.79G>C (p.Asp27His)	HTR5A, HTR5A-AS1 (D27H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161767	NM_023078.6(PYCR3):c.16C>T (p.Pro6Ser)	PYCR3 (P6S)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161766	NM_023015.5(INTS3):c.1700T>C (p.Ile567Thr)	INTS3 (I567T)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161765	NM_022829.6(SLC13A3):c.1637G>A (p.Arg546Gln)	SLC13A3 (R546Q +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 161764	NM_022828.5(YTHDC2):c.2617C>A (p.Pro873Thr)	YTHDC2 (P873T +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161763	NM_022785.4(EFCAB6):c.314C>T (p.Pro105Leu)	EFCAB6 (P105L)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 161762	NM_022769.5(CRTC3):c.1387C>A (p.Arg463Ser)	CRTC3, CRTC3-AS1 (R463S)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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