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Variants search result for Homo sapiens
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44 records found for search term mrpl9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15182772CV777015single nucleotide variantNM_031420.4(MRPL9):c.311-9A>Gnot provided [RCV000952302]benign1151762509151762509Humanname
596945605CV3547959duplicationNM_031420.4(MRPL9):c.589-10_589-5dupnot provided [RCV004809290]likely benign1151760903151760904Humanname
598128744CV3886541duplicationNM_031420.4(MRPL9):c.589-17_589-5dupnot provided [RCV005244201]likely benign1151760903151760904Humanname
12896881CV390565duplicationNM_031420.4(MRPL9):c.589-27_589-26dupnot specified [RCV000455947]benign1151760903151760904Humanname
598179088CV3993464single nucleotide variantNM_031420.4(MRPL9):c.5C>T (p.Ala2Val)not specified [RCV005371872]uncertain significance1151763475151763475Humanname
405759499CV3364178single nucleotide variantNM_031420.4(MRPL9):c.20C>G (p.Thr7Arg)not specified [RCV004500379]uncertain significance1151763460151763460Humanname
401727895CV2678561single nucleotide variantNM_031420.4(MRPL9):c.68G>A (p.Arg23Gln)not specified [RCV004292571]uncertain significance1151763412151763412Humanname
401932802CV2809259single nucleotide variantNM_031420.4(MRPL9):c.597T>G (p.Val199=)not provided [RCV003408875]likely benign1151760891151760891Humanname
405771761CV3364226single nucleotide variantNM_031420.4(MRPL9):c.77T>G (p.Val26Gly)not specified [RCV004502411]uncertain significance1151763403151763403Humanname
407479801CV3450399single nucleotide variantNM_031420.4(MRPL9):c.37C>G (p.Leu13Val)not specified [RCV004631666]uncertain significance1151763443151763443Humanname
597634130CV3557350single nucleotide variantNM_031420.4(MRPL9):c.74G>C (p.Gly25Ala)not specified [RCV004830939]uncertain significance1151763406151763406Humanname
598179100CV3993466single nucleotide variantNM_031420.4(MRPL9):c.35C>T (p.Ala12Val)not specified [RCV005371874]uncertain significance1151763445151763445Humanname
156161752CV2246446single nucleotide variantNM_031420.4(MRPL9):c.233G>C (p.Arg78Pro)not specified [RCV004110215]uncertain significance1151763067151763067Humanname
156272479CV2283608single nucleotide variantNM_031420.4(MRPL9):c.139C>T (p.Leu47Phe)not specified [RCV004140113]uncertain significance1151763341151763341Humanname
156089427CV2359372single nucleotide variantNM_031420.4(MRPL9):c.265C>T (p.Arg89Trp)not specified [RCV004214699]uncertain significance1151763035151763035Humanname
329374962CV2430979single nucleotide variantNM_031420.4(MRPL9):c.271A>G (p.Lys91Glu)not specified [RCV004248567]uncertain significance1151763029151763029Humanname
329365058CV2439996single nucleotide variantNM_031420.4(MRPL9):c.223C>T (p.Arg75Trp)not specified [RCV004260475]uncertain significance1151763077151763077Humanname
401739264CV2676468single nucleotide variantNM_031420.4(MRPL9):c.137G>A (p.Ser46Asn)not specified [RCV004286482]uncertain significance1151763343151763343Humanname
401873029CV2761350single nucleotide variantNM_031420.4(MRPL9):c.261G>C (p.Lys87Asn)not specified [RCV004341215]uncertain significance1151763039151763039Humanname
405759536CV3364184single nucleotide variantNM_031420.4(MRPL9):c.214C>T (p.Arg72Cys)not specified [RCV004500385]uncertain significance1151763086151763086Humanname
407480622CV3450396single nucleotide variantNM_031420.4(MRPL9):c.182A>T (p.Lys61Met)not specified [RCV004638215]uncertain significance1151763118151763118Humanname
407479797CV3450398single nucleotide variantNM_031420.4(MRPL9):c.247G>C (p.Val83Leu)not specified [RCV004631665]uncertain significance1151763053151763053Humanname
598213155CV3993468single nucleotide variantNM_031420.4(MRPL9):c.269C>A (p.Pro90His)not specified [RCV005378295]uncertain significance1151763031151763031Humanname
598213160CV3993469single nucleotide variantNM_031420.4(MRPL9):c.151C>G (p.Arg51Gly)not specified [RCV005378296]uncertain significance1151763329151763329Humanname
598213166CV3993470single nucleotide variantNM_031420.4(MRPL9):c.121C>G (p.Leu41Val)not specified [RCV005378297]uncertain significance1151763359151763359Humanname
156166254CV2243581single nucleotide variantNM_031420.4(MRPL9):c.604G>A (p.Ala202Thr)not specified [RCV004114312]uncertain significance1151760884151760884Humanname
156294347CV2243680single nucleotide variantNM_031420.4(MRPL9):c.673G>C (p.Val225Leu)not specified [RCV004114387]uncertain significance1151760181151760181Humanname
329400120CV2440612single nucleotide variantNM_031420.4(MRPL9):c.470C>T (p.Thr157Ile)not specified [RCV004256524]uncertain significance1151762121151762121Humanname
401728608CV2672987single nucleotide variantNM_031420.4(MRPL9):c.712G>T (p.Val238Leu)not specified [RCV004283986]uncertain significance1151760142151760142Humanname
401733081CV2712965single nucleotide variantNM_031420.4(MRPL9):c.571C>T (p.Arg191Cys)not specified [RCV004314674]uncertain significance1151761468151761468Humanname
401884384CV2761252single nucleotide variantNM_031420.4(MRPL9):c.793C>T (p.Pro265Ser)not specified [RCV004341129]likely benign1151760061151760061Humanname
405759693CV3364211single nucleotide variantNM_031420.4(MRPL9):c.579C>A (p.Phe193Leu)not specified [RCV004500412]uncertain significance1151761460151761460Humanname
405759750CV3364220single nucleotide variantNM_031420.4(MRPL9):c.691G>C (p.Val231Leu)not specified [RCV004500421]uncertain significance1151760163151760163Humanname
405771748CV3364224single nucleotide variantNM_031420.4(MRPL9):c.712G>A (p.Val238Met)not specified [RCV004502409]uncertain significance1151760142151760142Humanname
407475224CV3450397single nucleotide variantNM_031420.4(MRPL9):c.536A>G (p.Asn179Ser)not specified [RCV004638216]uncertain significance1151761503151761503Humanname
597634117CV3557347single nucleotide variantNM_031420.4(MRPL9):c.511C>T (p.Arg171Cys)not specified [RCV004830936]uncertain significance1151761528151761528Humanname
597634122CV3557348single nucleotide variantNM_031420.4(MRPL9):c.643C>T (p.Arg215Trp)not specified [RCV004830937]uncertain significance1151760845151760845Humanname
597634127CV3557349single nucleotide variantNM_031420.4(MRPL9):c.394G>T (p.Ala132Ser)not specified [RCV004830938]uncertain significance1151762417151762417Humanname
597638007CV3557351single nucleotide variantNM_031420.4(MRPL9):c.743A>C (p.Tyr248Ser)not specified [RCV004824842]uncertain significance1151760111151760111Humanname
597634135CV3557352single nucleotide variantNM_031420.4(MRPL9):c.720T>G (p.Phe240Leu)not specified [RCV004830940]uncertain significance1151760134151760134Humanname
597634145CV3557354single nucleotide variantNM_031420.4(MRPL9):c.601G>A (p.Val201Ile)not specified [RCV004830942]uncertain significance1151760887151760887Humanname
598179082CV3993463single nucleotide variantNM_031420.4(MRPL9):c.644G>A (p.Arg215Gln)not specified [RCV005371871]uncertain significance1151760844151760844Humanname
598179094CV3993465single nucleotide variantNM_031420.4(MRPL9):c.527T>C (p.Met176Thr)not specified [RCV005371873]uncertain significance1151761512151761512Humanname
598179106CV3993471single nucleotide variantNM_031420.4(MRPL9):c.561A>C (p.Glu187Asp)not specified [RCV005371875]uncertain significance1151761478151761478Humanname