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Variants search result for Homo sapiens
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28 records found for search term Psmd8
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598170960CV3908197single nucleotide variantNM_002812.5(PSMD8):c.26G>A (p.Arg9Lys)not specified [RCV005263235]uncertain significance193837462738374627Humanname
329393063CV2469264single nucleotide variantNM_002812.5(PSMD8):c.56C>T (p.Thr19Ile)not specified [RCV004280604]uncertain significance193837465738374657Humanname
598170969CV3908199single nucleotide variantNM_002812.5(PSMD8):c.47G>A (p.Arg16Gln)not specified [RCV005263237]likely benign193837464838374648Humanname
598170973CV3908200single nucleotide variantNM_002812.5(PSMD8):c.52G>A (p.Ala18Thr)not specified [RCV005263238]uncertain significance193837465338374653Humanname
15187989CV704951single nucleotide variantNM_002812.5(PSMD8):c.345G>A (p.Glu115=)not provided [RCV000953751]benign193837494638374946Humanname
15129090CV741843single nucleotide variantNM_002812.5(PSMD8):c.729A>G (p.Lys243=)not provided [RCV000897383]benign193838092538380925Humanname
155906002CV2303225single nucleotide variantNM_002812.5(PSMD8):c.172C>T (p.Leu58Phe)not specified [RCV004156981]likely benign193837477338374773Humanname
401776928CV2721531single nucleotide variantNM_002812.5(PSMD8):c.259G>C (p.Val87Leu)not specified [RCV004316047]uncertain significance193837486038374860Humanname
405662257CV3378600single nucleotide variantNM_002812.5(PSMD8):c.185G>C (p.Arg62Pro)not specified [RCV004513374]uncertain significance193837478638374786Humanname
407531746CV3471924single nucleotide variantNM_002812.5(PSMD8):c.238C>G (p.Pro80Ala)not specified [RCV004657763]uncertain significance193837483938374839Humanname
407531748CV3471925single nucleotide variantNM_002812.5(PSMD8):c.181T>G (p.Ser61Ala)not specified [RCV004657764]uncertain significance193837478238374782Humanname
597750756CV3592116single nucleotide variantNM_002812.5(PSMD8):c.170T>C (p.Leu57Pro)not specified [RCV004846399]uncertain significance193837477138374771Humanname
597750751CV3592117single nucleotide variantNM_002812.5(PSMD8):c.154C>G (p.Arg52Gly)not specified [RCV004846400]uncertain significance193837475538374755Humanname
597750738CV3592120single nucleotide variantNM_002812.5(PSMD8):c.197C>T (p.Ala66Val)not specified [RCV004846403]uncertain significance193837479838374798Humanname
598170965CV3908198single nucleotide variantNM_002812.5(PSMD8):c.137T>C (p.Val46Ala)not specified [RCV005263236]uncertain significance193837473838374738Humanname
598170981CV3908202single nucleotide variantNM_002812.5(PSMD8):c.160T>G (p.Ser54Ala)not specified [RCV005263240]uncertain significance193837476138374761Humanname
15202557CV704950single nucleotide variantNM_002812.5(PSMD8):c.178G>A (p.Ala60Thr)not provided [RCV000957952]benign193837477938374779Humanname
156162050CV2319518single nucleotide variantNM_002812.5(PSMD8):c.949A>G (p.Ser317Gly)not specified [RCV004185087]uncertain significance193838328638383286Humanname
155972335CV2335787single nucleotide variantNM_002812.5(PSMD8):c.473G>A (p.Arg158His)not specified [RCV004193978]uncertain significance193837639138376391Humanname
405662260CV3378601single nucleotide variantNM_002812.5(PSMD8):c.344A>C (p.Glu115Ala)not specified [RCV004513375]uncertain significance193837494538374945Humanname
407531750CV3471926single nucleotide variantNM_002812.5(PSMD8):c.533A>G (p.Tyr178Cys)not specified [RCV004657765]uncertain significance193837645138376451Humanname
597750742CV3592119single nucleotide variantNM_002812.5(PSMD8):c.676A>G (p.Ile226Val)not specified [RCV004846402]uncertain significance193837937938379379Humanname
597750733CV3592121single nucleotide variantNM_002812.5(PSMD8):c.574T>G (p.Leu192Val)not specified [RCV004846404]uncertain significance193837927738379277Humanname
597750728CV3592122single nucleotide variantNM_002812.5(PSMD8):c.629C>T (p.Thr210Met)not specified [RCV004846405]uncertain significance193837933238379332Humanname
598170976CV3908201single nucleotide variantNM_002812.5(PSMD8):c.594C>A (p.Phe198Leu)not specified [RCV005263239]uncertain significance193837929738379297Humanname
598170989CV3908204single nucleotide variantNM_002812.5(PSMD8):c.977A>G (p.Glu326Gly)not specified [RCV005263242]uncertain significance193838331438383314Humanname
598170993CV3908205single nucleotide variantNM_002812.5(PSMD8):c.758C>T (p.Ala253Val)not specified [RCV005263243]uncertain significance193838095438380954Humanname
156112794CV2387955single nucleotide variantNM_002812.5(PSMD8):c.1030C>T (p.Arg344Trp)not specified [RCV004236493]uncertain significance193838336738383367Humanname