ClinVar Miner

List of variants in gene FKBP14 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_017946.4(FKBP14):c.357T>G (p.Ile119Met) rs202182643 0.00010
NM_017946.4(FKBP14):c.144G>A (p.Met48Ile) rs141850025 0.00009
NM_017946.4(FKBP14):c.179G>A (p.Gly60Asp) rs781073404 0.00009
NM_017946.4(FKBP14):c.350-5G>A rs763069544 0.00007
NM_017946.4(FKBP14):c.478G>A (p.Val160Ile) rs768353747 0.00003
NM_017946.4(FKBP14):c.92T>C (p.Val31Ala) rs372805238 0.00003
NM_017946.4(FKBP14):c.16T>G (p.Trp6Gly) rs935382945 0.00002
NM_017946.4(FKBP14):c.265G>A (p.Asp89Asn) rs760591517 0.00002
NM_017946.4(FKBP14):c.314T>C (p.Ile105Thr) rs765841495 0.00002
NM_017946.4(FKBP14):c.404G>A (p.Arg135Gln) rs747727076 0.00002
NM_017946.4(FKBP14):c.53T>C (p.Ile18Thr) rs140239991 0.00002
NM_017946.4(FKBP14):c.74C>G (p.Pro25Arg) rs142423230 0.00002
NM_017946.4(FKBP14):c.79G>C (p.Val27Leu) rs148775136 0.00002
NM_017946.4(FKBP14):c.136G>T (p.Asp46Tyr) rs750062960 0.00001
NM_017946.4(FKBP14):c.173A>C (p.Lys58Thr) rs769609634 0.00001
NM_017946.4(FKBP14):c.198-3T>C rs772253719 0.00001
NM_017946.4(FKBP14):c.206A>G (p.His69Arg) rs564539430 0.00001
NM_017946.4(FKBP14):c.224T>G (p.Ile75Ser) rs763688956 0.00001
NM_017946.4(FKBP14):c.233C>T (p.Thr78Ile) rs758100842 0.00001
NM_017946.4(FKBP14):c.257A>G (p.Lys86Arg) rs543492611 0.00001
NM_017946.4(FKBP14):c.25G>A (p.Val9Ile) rs1198123802 0.00001
NM_017946.4(FKBP14):c.365A>G (p.Glu122Gly) rs1789965131 0.00001
NM_017946.4(FKBP14):c.386T>C (p.Ile129Thr) rs201579172 0.00001
NM_017946.4(FKBP14):c.467C>A (p.Ser156Tyr) rs751708321 0.00001
NM_017946.4(FKBP14):c.512A>C (p.His171Pro) rs147665999 0.00001
NM_017946.4(FKBP14):c.533G>C (p.Ser178Thr) rs373762287 0.00001
NM_017946.4(FKBP14):c.537T>A (p.His179Gln) rs142257224 0.00001
NM_017946.4(FKBP14):c.556G>A (p.Asp186Asn) rs766873942 0.00001
NM_017946.4(FKBP14):c.589G>A (p.Gly197Arg) rs748942204 0.00001
NM_017946.4(FKBP14):c.619A>C (p.Lys207Gln) rs1281054139 0.00001
NM_017946.4(FKBP14):c.130G>A (p.Gly44Arg)
NM_017946.4(FKBP14):c.133G>T (p.Gly45Trp) rs146195079
NM_017946.4(FKBP14):c.134G>A (p.Gly45Glu) rs1790172789
NM_017946.4(FKBP14):c.144G>C (p.Met48Ile)
NM_017946.4(FKBP14):c.155A>G (p.Tyr52Cys) rs138774873
NM_017946.4(FKBP14):c.16T>C (p.Trp6Arg) rs935382945
NM_017946.4(FKBP14):c.215G>A (p.Gly72Asp) rs949937945
NM_017946.4(FKBP14):c.223A>G (p.Ile75Val) rs2483522670
NM_017946.4(FKBP14):c.247G>A (p.Glu83Lys) rs1264425307
NM_017946.4(FKBP14):c.259G>A (p.Gly87Ser)
NM_017946.4(FKBP14):c.263G>C (p.Trp88Ser)
NM_017946.4(FKBP14):c.295G>C (p.Glu99Gln) rs2483522388
NM_017946.4(FKBP14):c.329G>T (p.Gly110Val) rs1244619961
NM_017946.4(FKBP14):c.32C>T (p.Thr11Ile) rs1235130674
NM_017946.4(FKBP14):c.354A>T (p.Lys118Asn)
NM_017946.4(FKBP14):c.40G>C (p.Val14Leu) rs2483531450
NM_017946.4(FKBP14):c.424G>C (p.Glu142Gln) rs2483513114
NM_017946.4(FKBP14):c.445C>T (p.Leu149Phe) rs2127948264
NM_017946.4(FKBP14):c.448A>G (p.Asn150Asp)
NM_017946.4(FKBP14):c.454G>A (p.Asp152Asn)
NM_017946.4(FKBP14):c.47C>G (p.Ser16Cys)
NM_017946.4(FKBP14):c.493AAG[1] (p.Lys166del) rs542254849
NM_017946.4(FKBP14):c.50T>C (p.Leu17Ser) rs1554371125
NM_017946.4(FKBP14):c.512A>G (p.His171Arg) rs147665999
NM_017946.4(FKBP14):c.514G>A (p.Gly172Ser)
NM_017946.4(FKBP14):c.520G>T (p.Val174Leu)
NM_017946.4(FKBP14):c.524T>A (p.Val175Glu) rs1057282546
NM_017946.4(FKBP14):c.52A>T (p.Ile18Phe) rs1046480485
NM_017946.4(FKBP14):c.53T>A (p.Ile18Asn) rs140239991
NM_017946.4(FKBP14):c.554A>G (p.Glu185Gly) rs1789837483
NM_017946.4(FKBP14):c.559A>G (p.Ile187Val)
NM_017946.4(FKBP14):c.560T>G (p.Ile187Ser) rs773564727
NM_017946.4(FKBP14):c.573A>T (p.Glu191Asp) rs1283044971
NM_017946.4(FKBP14):c.595A>T (p.Ile199Leu)
NM_017946.4(FKBP14):c.601G>A (p.Ala201Thr)
NM_017946.4(FKBP14):c.63G>C (p.Leu21Phe)
NM_017946.4(FKBP14):c.6G>T (p.Arg2Ser) rs2127950957

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