C0376358[trait identifier] AND "Prostate Cancer Research Center, Insti - ClinVar

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Items: 61

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 219300	NM_018715.4(RCC2):c.782G>C (p.Cys261Ser)	RCC2 (C261S)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219312	NM_001004434.3(SLC30A2):c.655G>A (p.Ala219Thr)	SLC30A2 (A219T +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219301	NM_001256864.2(DNAJC6):c.454C>T (p.Arg152Ter)	DNAJC6 (R82* +2 more)	Single nucleotide variant (nonsense)	Juvenile onset Parkinson disease 19A	GPathogenic
Select item 219313	NM_152890.7(COL24A1):c.2341C>T (p.Gln781Ter)	COL24A1 (Q781* +1 more)	Single nucleotide variant (nonsense +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219311	NM_001767.5(CD2):c.974G>C (p.Gly325Ala)	CD2 (G325A +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219314	NM_000696.4(ALDH9A1):c.265T>C (p.Trp89Arg)	ALDH9A1 (W89R)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219343	NM_007046.4(EMILIN1):c.197G>A (p.Arg66Gln)	EMILIN1 (R66Q)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 13657	NM_006218.4(PIK3CA):c.1636C>A (p.Gln546Lys)	PIK3CA (Q546K)	Single nucleotide variant (missense variant)	Segmental undergrowth associated with mainly venous malformation with capillary component +1 more	GConflicting classifications of pathogenicity
Select item 219315	NM_012161.4(FBXL5):c.1654del (p.Cys552fs)	FBXL5 (C551fs +2 more)	Deletion (frameshift variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219316	NM_001379270.1(CNGA1):c.1421G>A (p.Arg474His)	CNGA1, LOC101927157 (R474H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 219317	NM_017631.6(DDX60):c.1913A>G (p.Gln638Arg)	DDX60 (Q638R)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219297	NM_001012967.3(DDX60L):c.1633C>T (p.Arg545Trp)	DDX60L (R545W)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219350	NM_020731.4(AHRR):c.1472G>A (p.Arg491Gln)	AHRR, PDCD6-AHRR	Single nucleotide variant	Malignant tumor of prostate	GUncertain significance
Select item 219318	NM_001276277.3(PPIP5K2):c.2063-1_2065del	PPIP5K2	Deletion (splice acceptor variant)	Malignant tumor of prostate	GUncertain significance
Select item 219319	NM_001085377.2(MCC):c.800G>A (p.Arg267His)	MCC (R267H +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219302	NM_002715.4(PPP2CA):c.922_924del (p.Phe308del)	PPP2CA (F308del +1 more)	Deletion (inframe_deletion +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219303	NM_004946.3(DOCK2):c.3352G>T (p.Glu1118Ter)	DOCK2 (E1118*)	Single nucleotide variant (nonsense +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219344	NM_012120.3(CD2AP):c.560C>T (p.Pro187Leu)	CD2AP (P187L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 219320	NM_004665.6(VNN2):c.450C>A (p.Asp150Glu)	VNN2 (D150E +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219321	NM_014766.5(SCRN1):c.178G>A (p.Asp60Asn)	SCRN1 (D60N +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219304	NM_002612.4(PDK4):c.59T>G (p.Val20Gly)	PDK4 (V20G)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219322	NM_014916.4(LMTK2):c.651_652del (p.Cys217_Asp218delinsTer)	LMTK2	Microsatellite (nonsense)	Malignant tumor of prostate	GUncertain significance
Select item 219323	NM_001282426.2(PIK3CG):c.1414C>T (p.Arg472Cys)	PIK3CG (R472C)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219324	NM_033427.3(CTTNBP2):c.3823G>A (p.Glu1275Lys)	CTTNBP2 (E1275K +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219325	NM_024940.8(DOCK5):c.5125G>T (p.Ala1709Ser)	DOCK5 (A1709S)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 141169	NM_002485.5(NBN):c.1925A>G (p.Lys642Arg)	NBN (K642R +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 219326	NM_030780.5(SLC25A32):c.548A>G (p.Tyr183Cys)	SLC25A32 (Y183C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 219327	NM_024045.2(DDX50):c.122C>T (p.Ser41Leu)	DDX50 (S41L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219345	NM_152635.3(OIT3):c.1598C>T (p.Thr533Met)	OIT3 (T533M)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219328	NM_017551.3(GRID1):c.884C>T (p.Thr295Met)	GRID1 (T295M)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219346	NM_001346516.2(LCOR):c.2564G>A (p.Arg855His)	C10orf12, LCOR (R855H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219307	NM_001098794.2(FHIP1B):c.2542C>T (p.Arg848Cys)	FHIP1B (R848C +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 219308	NM_015459.5(ATL3):c.1200G>T (p.Lys400Asn)	ATL3, LOC126861231 (K382N +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219329	NM_003369.4(UVRAG):c.500A>G (p.Glu167Gly)	UVRAG (E167G)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219347	NM_000921.5(PDE3A):c.2832G>C (p.Met944Ile)	PDE3A (M944I +3 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219351	NM_001330288.2(SMARCC2):c.3670A>C (p.Thr1224Pro)	SMARCC2 (T1109P +3 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219352	NM_002332.3(LRP1):c.2309G>A (p.Arg770Gln)	LRP1 (R770Q)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219309	NM_001018072.2(ABTB3):c.148A>G (p.Ser50Gly)	ABTB3 (S50G)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219330	NM_016281.4(TAOK3):c.512T>C (p.Met171Thr)	TAOK3 (M171T +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219331	NM_014708.6(KNTC1):c.6626C>T (p.Ser2209Leu)	KNTC1 (S2209L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219332	NM_033255.5(EPSTI1):c.350C>T (p.Thr117Ile)	EPSTI1 (T117I)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219333	NM_005845.5(ABCC4):c.2672G>T (p.Arg891Leu)	ABCC4 (R844L +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 162620	NM_006260.5(DNAJC3):c.580C>T (p.Arg194Ter)	DNAJC3 (R194*)	Single nucleotide variant (nonsense)	Malignant tumor of prostate +1 more	GConflicting classifications of pathogenicity
Select item 219348	NM_018071.5(ARHGEF40):c.1177C>G (p.Arg393Gly)	ARHGEF40 (R393G)	Single nucleotide variant (5 prime UTR variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 219305	NM_004713.6(NEMF):c.2431_2432del (p.Gln811fs)	NEMF (Q811fs +1 more)	Microsatellite (frameshift variant)	Malignant tumor of prostate	GUncertain significance
Select item 219299	NM_006086.4(TUBB3):c.1288G>C (p.Ala430Pro)	TUBB3 (A358P +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219334	NM_014853.3(SGSM2):c.1696G>A (p.Val566Met)	SGSM2 (V521M +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219335	NM_078471.4(MYO18A):c.40G>A (p.Gly14Arg)	MYO18A (G14R)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219336	NM_016339.6(RAPGEFL1):c.851A>G (p.Gln284Arg)	RAPGEFL1 (Q127R +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219337	NM_173079.5(RUNDC1):c.866G>C (p.Gly289Ala)	RUNDC1 (G289A +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 161486	NM_001007228.2(SPOP):c.305T>G (p.Phe102Cys)	SPOP (F102C)	Single nucleotide variant (missense variant)	Prostate adenocarcinoma +1 more	GConflicting classifications of pathogenicity
Select item 219338	NM_001351264.2(C17orf80):c.973C>T (p.Arg325Trp)	C17orf80 (R325W)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219339	NM_015208.5(ANKRD12):c.2593G>T (p.Asp865Tyr)	ANKRD12 (D842Y +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219298	NM_012397.4(SERPINB13):c.893C>T (p.Ala298Val)	SERPINB13 (A298V +3 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219340	NM_004317.4(GET3):c.224C>G (p.Pro75Arg)	GET3 (P75R)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219306	NM_014475.4(DHDH):c.611A>T (p.His204Leu)	DHDH (H204L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219341	NM_001245.7(SIGLEC6):c.883G>T (p.Ala295Ser)	SIGLEC6 (A243S +4 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219310	NM_005225.3(E2F1):c.497G>A (p.Arg166His)	E2F1 (R166H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219342	NM_001004416.3(UMODL1):c.3655G>A (p.Val1219Ile)	UMODL1 (V1147I +3 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 219296	NM_000044.6(AR):c.2105T>A (p.Leu702His)	AR (L702H +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GLikely pathogenic
Select item 219349	NM_001039840.4(CHIC1):c.331C>T (p.Pro111Ser)	CHIC1 (P111S)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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Items: 61