ClinVar Miner

List of variants reported as uncertain significance for adenocarcinoma by Molecular Oncology - Human Genetics Lab, University of Sao Paulo

Included ClinVar conditions (112):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_014907.3(FRMPD1):c.770G>A (p.Arg257His) rs148192224 0.00335
NM_000245.4(MET):c.1715G>A (p.Ser572Asn) rs199771406 0.00188
NM_032776.3(JMJD1C):c.6395A>T (p.Lys2132Ile) rs200769337 0.00068
NM_005475.3(SH2B3):c.622G>C (p.Glu208Gln) rs202080221 0.00066
NM_020937.4(FANCM):c.2859A>C (p.Lys953Asn) rs142864437 0.00064
NM_000551.4(VHL):c.241C>T (p.Pro81Ser) rs104893829 0.00039
NM_001022.4(RPS19):c.164C>T (p.Thr55Met) rs147508369 0.00039
NM_001018115.3(FANCD2):c.2273G>C (p.Cys758Ser) rs540805431 0.00037
NM_001360.3(DHCR7):c.988G>A (p.Val330Met) rs139724817 0.00029
NM_000051.4(ATM):c.1595G>A (p.Cys532Tyr) rs35963548 0.00026
NM_002253.4(KDR):c.2525G>A (p.Arg842His) rs149901681 0.00015
NM_000043.6(FAS):c.667A>C (p.Asn223His) rs143318339 0.00005
NM_032444.4(SLX4):c.4712C>T (p.Thr1571Met) rs765601038 0.00005
NM_203447.4(DOCK8):c.4760T>C (p.Met1587Thr) rs749789023 0.00005
NM_000168.6(GLI3):c.245G>A (p.Arg82Lys) rs754143860 0.00003
NM_001242835.2(NDRG4):c.202G>A (p.Val68Met) rs753975630 0.00003
NM_000143.4(FH):c.664T>A (p.Ser222Thr) rs1448268784 0.00002
NM_001429.4(EP300):c.4235C>T (p.Ala1412Val) rs887226313 0.00002
NM_203447.4(DOCK8):c.1416C>G (p.Phe472Leu) rs1443199004 0.00002
NM_000094.4(COL7A1):c.1774C>T (p.Arg592Cys) rs147470888 0.00001
NM_000168.6(GLI3):c.233C>T (p.Ser78Leu) rs777937822 0.00001
NM_001018115.3(FANCD2):c.3710T>C (p.Val1237Ala) rs767806932 0.00001
NM_001382508.1(DROSHA):c.3218A>C (p.Asp1073Ala) rs1394064377 0.00001
NM_144997.7(FLCN):c.284A>G (p.Tyr95Cys) rs1555610947 0.00001
NM_000038.6(APC):c.3747C>A (p.Cys1249Ter) rs2149898263
NM_000051.4(ATM):c.6998C>A (p.Thr2333Lys) rs150503164
NM_000059.4(BRCA2):c.3858_3860del (p.Lys1286del) rs80359406
NM_000137.4(FAH):c.506C>T (p.Ser169Phe) rs2142097943
NM_000179.3(MSH6):c.334A>G (p.Asn112Asp) rs864622397
NM_001005498.4(RHBDF2):c.269G>A (p.Arg90His) rs368409953
NM_001048174.2(MUTYH):c.572C>T (p.Thr191Ile) rs2149150096
NM_001110556.2(FLNA):c.1997C>T (p.Ala666Val) rs374295965
NM_002907.4(RECQL):c.572C>A (p.Pro191Gln) rs2137374485
NM_003242.6(TGFBR2):c.1667A>G (p.Lys556Arg) rs2125455732
NM_020937.4(FANCM):c.4585G>A (p.Asp1529Asn) rs1245071059
NM_025081.3(NYNRIN):c.5493G>C (p.Gln1831His) rs2139356308
NM_152383.5(DIS3L2):c.2534A>G (p.Gln845Arg) rs371430235
NM_203447.4(DOCK8):c.959C>T (p.Thr320Met) rs766320232

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