ClinVar Miner

List of variants reported as uncertain significance by Prostate Cancer Research Center, Institute of Biosciences and Medical Technology, University of Tampere

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001098794.2(FHIP1B):c.2542C>T (p.Arg848Cys) rs117940741 0.00490
NM_017551.3(GRID1):c.884C>T (p.Thr295Met) rs143353694 0.00014
NM_001004416.3(UMODL1):c.3655G>A (p.Val1219Ile) rs539189509 0.00011
NM_152635.3(OIT3):c.1598C>T (p.Thr533Met) rs145480078 0.00011
NM_001012967.3(DDX60L):c.1633C>T (p.Arg545Trp) rs201155959 0.00008
NM_001351264.2(C17orf80):c.973C>T (p.Arg325Trp) rs776418014 0.00006
NM_020731.4(AHRR):c.1472G>A (p.Arg491Gln) rs769781351 0.00006
NM_033427.3(CTTNBP2):c.3823G>A (p.Glu1275Lys) rs750789291 0.00006
NM_078471.4(MYO18A):c.40G>A (p.Gly14Arg) rs755153578 0.00006
NM_000696.4(ALDH9A1):c.265T>C (p.Trp89Arg) rs140581841 0.00004
NM_024045.2(DDX50):c.122C>T (p.Ser41Leu) rs374203626 0.00004
NM_001346516.2(LCOR):c.2564G>A (p.Arg855His) rs746615879 0.00003
NM_006260.5(DNAJC3):c.580C>T (p.Arg194Ter) rs727502865 0.00003
NM_012397.4(SERPINB13):c.893C>T (p.Ala298Val) rs864622008 0.00003
NM_014708.6(KNTC1):c.6626C>T (p.Ser2209Leu) rs772156434 0.00003
NM_002332.3(LRP1):c.2309G>A (p.Arg770Gln) rs769851229 0.00002
NM_002485.5(NBN):c.1925A>G (p.Lys642Arg) rs587781547 0.00002
NM_001085377.2(MCC):c.800G>A (p.Arg267His) rs760873189 0.00001
NM_001282426.2(PIK3CG):c.1414C>T (p.Arg472Cys) rs864622026 0.00001
NM_001379270.1(CNGA1):c.1421G>A (p.Arg474His) rs759487836 0.00001
NM_004665.6(VNN2):c.450C>A (p.Asp150Glu) rs864622023 0.00001
NM_007046.4(EMILIN1):c.197G>A (p.Arg66Gln) rs753987568 0.00001
NM_014766.5(SCRN1):c.178G>A (p.Asp60Asn) rs864622024 0.00001
NM_016281.4(TAOK3):c.512T>C (p.Met171Thr) rs864622030 0.00001
NM_000921.5(PDE3A):c.2832G>C (p.Met944Ile) rs567843370
NM_001004434.3(SLC30A2):c.655G>A (p.Ala219Thr) rs864622019
NM_001018072.2(ABTB3):c.148A>G (p.Ser50Gly) rs200629571
NM_001039840.4(CHIC1):c.331C>T (p.Pro111Ser) rs864622038
NM_001245.7(SIGLEC6):c.883G>T (p.Ala295Ser) rs370040093
NM_001256864.2(DNAJC6):c.454C>T (p.Arg152Ter) rs864622011
NM_001276277.3(PPIP5K2):c.2063-1_2065del rs864622022
NM_001330288.2(SMARCC2):c.3670A>C (p.Thr1224Pro) rs864622039
NM_001767.5(CD2):c.974G>C (p.Gly325Ala) rs864622018
NM_002612.4(PDK4):c.59T>G (p.Val20Gly) rs864622014
NM_002715.4(PPP2CA):c.922_924del (p.Phe308del) rs864622012
NM_003369.4(UVRAG):c.500A>G (p.Glu167Gly) rs864622029
NM_004317.4(GET3):c.224C>G (p.Pro75Arg) rs864622036
NM_004713.6(NEMF):c.2431_2432del (p.Gln811fs) rs864622015
NM_004946.3(DOCK2):c.3352G>T (p.Glu1118Ter) rs864622013
NM_005225.3(E2F1):c.497G>A (p.Arg166His) rs864622017
NM_005845.5(ABCC4):c.2672G>T (p.Arg891Leu) rs781305510
NM_006086.4(TUBB3):c.1288G>C (p.Ala430Pro) rs864622009
NM_012120.3(CD2AP):c.560C>T (p.Pro187Leu) rs864622037
NM_012161.4(FBXL5):c.1654del (p.Cys552fs) rs864622020
NM_014475.4(DHDH):c.611A>T (p.His204Leu) rs757900117
NM_014853.3(SGSM2):c.1696G>A (p.Val566Met) rs864622032
NM_014916.4(LMTK2):c.651_652del (p.Cys217_Asp218delinsTer) rs864622025
NM_015208.5(ANKRD12):c.2593G>T (p.Asp865Tyr) rs864622035
NM_015459.5(ATL3):c.1200G>T (p.Lys400Asn) rs864622016
NM_016339.6(RAPGEFL1):c.851A>G (p.Gln284Arg) rs864622033
NM_017631.6(DDX60):c.1913A>G (p.Gln638Arg) rs864622021
NM_018071.5(ARHGEF40):c.1177C>G (p.Arg393Gly) rs753872972
NM_018715.4(RCC2):c.782G>C (p.Cys261Ser) rs864622010
NM_024940.8(DOCK5):c.5125G>T (p.Ala1709Ser) rs864622027
NM_030780.5(SLC25A32):c.548A>G (p.Tyr183Cys) rs864622028
NM_033255.5(EPSTI1):c.350C>T (p.Thr117Ile) rs864622031
NM_152890.7(COL24A1):c.2341C>T (p.Gln781Ter) rs774125436
NM_173079.5(RUNDC1):c.866G>C (p.Gly289Ala) rs864622034

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